| Year |
Citation |
Score |
| 2020 |
da Costa Almeida CB, Welter AT, Abech GD, Brandão GR, Flores JAM, Schüle B, Francke U, Fiegenbaum M, Zen PRG, Rosa RFM. Report of the Phenotype of a Patient with Roberts Syndrome and a Rare Variant. Journal of Pediatric Genetics. 9: 58-62. PMID 31976146 DOI: 10.1055/S-0039-1696636 |
0.703 |
|
| 2013 |
Kiefer AK, Tung JY, Do CB, Hinds DA, Mountain JL, Francke U, Eriksson N. Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia. Plos Genetics. 9: e1003299. PMID 23468642 DOI: 10.1371/Journal.Pgen.1003299 |
0.313 |
|
| 2012 |
Eriksson N, Wu S, Do CB, Kiefer AK, Tung JY, Mountain JL, Hinds DA, Francke U. A genetic variant near olfactory receptor genes influences cilantro preference Flavour. 1: 22. DOI: 10.1186/2044-7248-1-22 |
0.307 |
|
| 2012 |
Barnholt KE, Hinds DA, Kiefer AK, Do CB, Eriksson N, Mountain JL, Francke U, Tung JA, Nguyen H(, Levine RL, Mesa RA, Gotlib J, Zehnder JL. Estimation of JAK2 V617F Prevalence by Detection of the Mutation in Saliva Samples From Online MPN and General Population Cohorts Blood. 120: 1737-1737. DOI: 10.1182/Blood.V120.21.1737.1737 |
0.312 |
|
| 2011 |
Stheneur C, Faivre L, Collod-Béroud G, Gautier E, Binquet C, Bonithon-Kopp C, Claustres M, Child AH, Arbustini E, Adès LC, Francke U, Mayer K, Arslan-Kirchner M, De Paepe A, Chevallier B, et al. Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year. Pediatric Research. 69: 265-70. PMID 21135753 DOI: 10.1203/Pdr.0B013E3182097219 |
0.301 |
|
| 2011 |
Goergen CJ, Li HH, Francke U, Taylor CA. Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities. Journal of Vascular Research. 48: 119-29. PMID 20926892 DOI: 10.1159/000316808 |
0.37 |
|
| 2010 |
Ding F, Li HH, Li J, Myers RM, Francke U. Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice. Plos One. 5: e9402. PMID 20195375 DOI: 10.1371/Journal.Pone.0009402 |
0.329 |
|
| 2009 |
Li HH, Roy M, Kuscuoglu U, Spencer CM, Halm B, Harrison KC, Bayle JH, Splendore A, Ding F, Meltzer LA, Wright E, Paylor R, Deisseroth K, Francke U. Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice. Embo Molecular Medicine. 1: 50-65. PMID 20049703 DOI: 10.1002/emmm.200900003 |
0.326 |
|
| 2009 |
Faivre L, Collod-Beroud G, Callewaert B, Child A, Binquet C, Gautier E, Loeys BL, Arbustini E, Mayer K, Arslan-Kirchner M, Stheneur C, Kiotsekoglou A, Comeglio P, Marziliano N, Wolf JE, ... ... Francke U, et al. Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation. European Journal of Human Genetics : Ejhg. 17: 491-501. PMID 19002209 DOI: 10.1038/Ejhg.2008.207 |
0.317 |
|
| 2008 |
Schüle B, Armstrong DD, Vogel H, Oviedo A, Francke U. Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure. Clinical Genetics. 74: 116-26. PMID 18477000 DOI: 10.1111/J.1399-0004.2008.01005.X |
0.343 |
|
| 2008 |
Ding F, Li HH, Zhang S, Solomon NM, Camper SA, Cohen P, Francke U. SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. Plos One. 3: e1709. PMID 18320030 DOI: 10.1371/Journal.Pone.0001709 |
0.33 |
|
| 2008 |
Curry CJR, Loughman WD, Francke U, Hall BD, Golbus MS, Dersttne J, Epstein CJ. Partial trisomy for the distal long arm of chromosome 5 (region q34→qter). A new clinically recognizable syndrome Clinical Genetics. 15: 454-461. DOI: 10.1111/J.1399-0004.1979.Tb01779.X |
0.47 |
|
| 2007 |
Yao Z, Jaeger JC, Ruzzo WL, Morale CZ, Emond M, Francke U, Milewicz DM, Schwartz SM, Mulvihill ER. A Marfan syndrome gene expression phenotype in cultured skin fibroblasts. Bmc Genomics. 8: 319. PMID 17850668 DOI: 10.1186/1471-2164-8-319 |
0.323 |
|
| 2007 |
Schüle B, Li HH, Fisch-Kohl C, Purmann C, Francke U. DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency. American Journal of Human Genetics. 81: 492-506. PMID 17701895 DOI: 10.1086/520063 |
0.711 |
|
| 2007 |
Faivre L, Collod-Beroud G, Loeys BL, Child A, Binquet C, Gautier E, Callewaert B, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Marziliano N, Dietz HC, Halliday D, ... ... Francke U, et al. Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study. American Journal of Human Genetics. 81: 454-66. PMID 17701892 DOI: 10.1086/520125 |
0.305 |
|
| 2007 |
Jordan C, Li HH, Kwan HC, Francke U. Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets. Bmc Medical Genetics. 8: 36. PMID 17584923 DOI: 10.1186/1471-2350-8-36 |
0.324 |
|
| 2006 |
Francke U. Mechanisms of disease: neurogenetics of MeCP2 deficiency. Nature Clinical Practice. Neurology. 2: 212-21. PMID 16932552 DOI: 10.1038/Ncpneuro0148 |
0.373 |
|
| 2006 |
Jordan C, Francke U. Ube3a expression is not altered in Mecp2 mutant mice. Human Molecular Genetics. 15: 2210-5. PMID 16754645 DOI: 10.1093/Hmg/Ddl146 |
0.337 |
|
| 2006 |
Liu J, Francke U. Identification of cis-regulatory elements for MECP2 expression. Human Molecular Genetics. 15: 1769-82. PMID 16613900 DOI: 10.1093/Hmg/Ddl099 |
0.42 |
|
| 2006 |
Arron JR, Winslow MM, Polleri A, Chang CP, Wu H, Gao X, Neilson JR, Chen L, Heit JJ, Kim SK, Yamasaki N, Miyakawa T, Francke U, Graef IA, Crabtree GR. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21. Nature. 441: 595-600. PMID 16554754 DOI: 10.1038/Nature04678 |
0.445 |
|
| 2006 |
Polleri A, Graef IA, Arron JR, Winslow MM, Kim SK, Miyakawa T, Francke U, Crabtree GR. Increased dosage of DSCR1 and DYRK1A on chromosome 21 destabilizes NFAT regulation and accounts for Down syndrome phenotypes Developmental Biology. 295: 324. DOI: 10.1016/J.Ydbio.2006.04.007 |
0.449 |
|
| 2005 |
Schüle B, Oviedo A, Johnston K, Pai S, Francke U. Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation. American Journal of Human Genetics. 77: 1117-28. PMID 16380922 DOI: 10.1086/498695 |
0.346 |
|
| 2005 |
Ding F, Prints Y, Dhar MS, Johnson DK, Garnacho-Montero C, Nicholls RD, Francke U. Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 424-31. PMID 16075369 DOI: 10.1007/S00335-005-2460-2 |
0.476 |
|
| 2005 |
Schüle B, Albalwi M, Northrop E, Francis DI, Rowell M, Slater HR, Gardner RJ, Francke U. Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome. Bmc Medical Genetics. 6: 18. PMID 15877813 DOI: 10.1186/1471-2350-6-18 |
0.515 |
|
| 2005 |
Ranheim EA, Kwan HC, Reya T, Wang YK, Weissman IL, Francke U. Frizzled 9 knock-out mice have abnormal B-cell development. Blood. 105: 2487-94. PMID 15572594 DOI: 10.1182/Blood-2004-06-2334 |
0.338 |
|
| 2004 |
Gartler SM, Varadarajan KR, Luo P, Canfield TK, Traynor J, Francke U, Hansen RS. Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins. Bmc Biology. 2: 21. PMID 15377381 DOI: 10.1186/1741-7007-2-21 |
0.352 |
|
| 2002 |
Traynor J, Agarwal P, Lazzeroni L, Francke U. Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations. Bmc Medical Genetics. 3: 12. PMID 12418965 DOI: 10.1186/1471-2350-3-12 |
0.379 |
|
| 2002 |
Gallagher RC, Pils B, Albalwi M, Francke U. Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome. American Journal of Human Genetics. 71: 669-78. PMID 12154412 DOI: 10.1086/342408 |
0.375 |
|
| 2002 |
Schrijver I, Liu W, Odom R, Brenn T, Oefner P, Furthmayr H, Francke U. Premature termination mutations in FBN1: distinct effects on differential allelic expression and on protein and clinical phenotypes. American Journal of Human Genetics. 71: 223-37. PMID 12068374 DOI: 10.1086/341581 |
0.335 |
|
| 2001 |
Lee SS, Wan M, Francke U. Spectrum of MECP2 mutations in Rett syndrome. Brain & Development. 23: S138-43. PMID 11738860 DOI: 10.1016/S0387-7604(01)00339-4 |
0.351 |
|
| 2001 |
Liu W, Schrijver I, Brenn T, Furthmayr H, Francke U. Multi-exon deletions of the FBN1 gene in Marfan syndrome. Bmc Medical Genetics. 2: 11. PMID 11710961 DOI: 10.1186/1471-2350-2-11 |
0.412 |
|
| 2001 |
Kerr AM, Nomura Y, Armstrong D, Anvret M, Belichenko PV, Budden S, Cass H, Christodoulou J, Clarke A, Ellaway C, d'Esposito M, Francke U, Hulten M, Julu P, Leonard H, et al. Guidelines for reporting clinical features in cases with MECP2 mutations. Brain & Development. 23: 208-11. PMID 11376997 DOI: 10.1016/S0387-7604(01)00193-0 |
0.371 |
|
| 2001 |
Graef IA, Gastier JM, Francke U, Crabtree GR. Evolutionary relationships among Rel domains indicate functional diversification by recombination. Proceedings of the National Academy of Sciences of the United States of America. 98: 5740-5. PMID 11344309 DOI: 10.1073/Pnas.101602398 |
0.32 |
|
| 2001 |
Wan M, Zhao K, Lee SS, Francke U. MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome. Human Molecular Genetics. 10: 1085-92. PMID 11331619 DOI: 10.1093/Hmg/10.10.1085 |
0.34 |
|
| 2001 |
Fulmer-Smentek SB, Francke U. Association of acetylated histones with paternally expressed genes in the Prader--Willi deletion region. Human Molecular Genetics. 10: 645-52. PMID 11230184 DOI: 10.1093/Hmg/10.6.645 |
0.317 |
|
| 2000 |
Gastier JM, Berg MA, Vesterhus P, Reiter EO, Francke U. Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndrome. Human Mutation. 16: 323-33. PMID 11013443 DOI: 10.1002/1098-1004(200010)16:4<323::Aid-Humu5>3.0.Co;2-D |
0.415 |
|
| 2000 |
de los Santos T, Schweizer J, Rees CA, Francke U. Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain. American Journal of Human Genetics. 67: 1067-82. PMID 11007541 DOI: 10.1086/303106 |
0.417 |
|
| 2000 |
Ferguson PJ, Blanton SH, Saulsbury FT, McDuffie MJ, Lemahieu V, Gastier JM, Francke U, Borowitz SM, Sutphen JL, Kelly TE. Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome. American Journal of Medical Genetics. 90: 390-7. PMID 10706361 DOI: 10.1002/(Sici)1096-8628(20000228)90:5<390::Aid-Ajmg9>3.0.Co;2-M |
0.401 |
|
| 2000 |
Peoples R, Franke Y, Wang YK, Pérez-Jurado L, Paperna T, Cisco M, Francke U. A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23. American Journal of Human Genetics. 66: 47-68. PMID 10631136 DOI: 10.1086/302722 |
0.514 |
|
| 2000 |
Francke U, Wan M, Lee SSJ, Zhang X, Houwink-Manville I, Song H-, Amir RE, Budden S, Naidu S, Pereira JLP, Lo IFM, Zoghbi HY, Schanen NC. 28. Rett syndrome and beyond: recurrent spontaneous and familial mutations at CpG hotspots in the methyl-CpG binding protein-2 gene Biological Psychiatry. 47. DOI: 10.1016/S0006-3223(00)00286-9 |
0.328 |
|
| 1999 |
Wan M, Lee SS, Zhang X, Houwink-Manville I, Song HR, Amir RE, Budden S, Naidu S, Pereira JL, Lo IF, Zoghbi HY, Schanen NC, Francke U. Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots. American Journal of Human Genetics. 65: 1520-9. PMID 10577905 DOI: 10.1086/302690 |
0.337 |
|
| 1999 |
Franke Y, Peoples RJ, Francke U. Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23. Cytogenetics and Cell Genetics. 86: 296-304. PMID 10575229 DOI: 10.1159/000015322 |
0.398 |
|
| 1999 |
Pérez Jurado LA, Wang YK, Francke U, Cruces J. TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog. Cytogenetics and Cell Genetics. 86: 277-84. PMID 10575226 DOI: 10.1159/000015319 |
0.487 |
|
| 1999 |
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. 23: 185-8. PMID 10508514 DOI: 10.1038/13810 |
0.361 |
|
| 1999 |
Schrijver I, Liu W, Brenn T, Furthmayr H, Francke U. Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes. American Journal of Human Genetics. 65: 1007-20. PMID 10486319 DOI: 10.1086/302582 |
0.325 |
|
| 1999 |
Francke U. Williams-Beuren syndrome: genes and mechanisms. Human Molecular Genetics. 8: 1947-54. PMID 10469848 DOI: 10.1093/Hmg/8.10.1947 |
0.482 |
|
| 1999 |
Lemahieu V, Gastier JM, Francke U. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. Human Mutation. 14: 54-66. PMID 10447259 DOI: 10.1002/(Sici)1098-1004(1999)14:1<54::Aid-Humu7>3.0.Co;2-E |
0.349 |
|
| 1999 |
Ring HZ, Chang H, Guilbot A, Brice A, LeGuern E, Francke U. The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q. Human Genetics. 104: 326-32. PMID 10369162 DOI: 10.1007/S004390050961 |
0.485 |
|
| 1999 |
Wang YK, Spörle R, Paperna T, Schughart K, Francke U. Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome. Genomics. 57: 235-48. PMID 10198163 DOI: 10.1006/Geno.1999.5773 |
0.443 |
|
| 1999 |
Ring HZ, Vameghi-Meyers V, Min H, Nikolic JM, Black DL, Francke U. The mouse Fubp gene maps near the distal end of chromosome 3. Genomics. 56: 357-8. PMID 10087207 DOI: 10.1006/Geno.1998.5731 |
0.493 |
|
| 1999 |
Ring HZ, Vameghi-Meyers V, Nikolic JM, Min H, Black DL, Francke U. Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17. Genomics. 56: 350-2. PMID 10087204 DOI: 10.1006/Geno.1998.5725 |
0.554 |
|
| 1999 |
Schweizer J, Zynger D, Francke U. In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit. Human Molecular Genetics. 8: 555-66. PMID 10072422 DOI: 10.1093/Hmg/8.4.555 |
0.433 |
|
| 1998 |
Liu WO, Oefner PJ, Qian C, Odom RS, Francke U. Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in marfan syndrome and related connective tissue disorders Genetic Testing. 1: 237-242. PMID 10464652 DOI: 10.1089/Gte.1997.1.237 |
0.385 |
|
| 1998 |
Paperna T, Peoples R, Wang YK, Kaplan P, Francke U. Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion. Genomics. 54: 453-9. PMID 9878248 DOI: 10.1006/Geno.1998.5619 |
0.505 |
|
| 1998 |
Wan M, Cravatt BF, Ring HZ, Zhang X, Francke U. Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutation. Genomics. 54: 408-14. PMID 9878243 DOI: 10.1006/Geno.1998.5597 |
0.518 |
|
| 1998 |
Li L, Francke U, Cohen SN. Retraction. The TSG101 tumor susceptibility gene is located in chromosome 11 band p15 and is mutated in human breast cancer. Cell. 93: following 660. PMID 9867424 |
0.307 |
|
| 1998 |
Peoples RJ, Cisco MJ, Kaplan P, Francke U. Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23. Cytogenetics and Cell Genetics. 82: 238-46. PMID 9858827 DOI: 10.1159/000015110 |
0.452 |
|
| 1998 |
Wojcik J, Berg MA, Esposito N, Geffner ME, Sakati N, Reiter EO, Dower S, Francke U, Postel-Vinay MC, Finidori J. Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptor. The Journal of Clinical Endocrinology and Metabolism. 83: 4481-9. PMID 9851797 DOI: 10.1210/Jcem.83.12.5357 |
0.341 |
|
| 1998 |
Babcock D, Gasner C, Francke U, Maslen C. A single mutation that results in an Asp to His substitution and partial exon skipping in a family with congenital contractural arachnodactyly. Human Genetics. 103: 22-8. PMID 9737771 DOI: 10.1007/S004390050777 |
0.342 |
|
| 1998 |
Ring HZ, Vameghi-Meyers V, Wang W, Crabtree GR, Francke U. Five SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARC) genes are dispersed in the human genome. Genomics. 51: 140-3. PMID 9693044 DOI: 10.1006/Geno.1998.5343 |
0.491 |
|
| 1998 |
Heidary G, Hampton LL, Schanen NC, Rivkin MJ, Darras BT, Battey J, Francke U. Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome. American Journal of Medical Genetics. 78: 173-5. PMID 9674911 DOI: 10.1002/(Sici)1096-8628(19980630)78:2<173::Aid-Ajmg15>3.0.Co;2-K |
0.456 |
|
| 1998 |
Wan M, Francke U. Evaluation of two X chromosomal candidate genes for Rett syndrome: glutamate dehydrogenase-2 (GLUD2) and rab GDP-dissociation inhibitor (GDI1). American Journal of Medical Genetics. 78: 169-72. PMID 9674910 DOI: 10.1002/(Sici)1096-8628(19980630)78:2<169::Aid-Ajmg14>3.0.Co;2-L |
0.479 |
|
| 1998 |
Rosenbloom AL, Guevara-Aguirre J, Berg MA, Francke U. Stature in Ecuadorians heterozygous for growth hormone receptor gene E180 splice mutation does not differ from that of homozygous normal relatives. The Journal of Clinical Endocrinology and Metabolism. 83: 2373-5. PMID 9661611 DOI: 10.1210/Jcem.83.7.4972 |
0.308 |
|
| 1998 |
Schanen C, Francke U. A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map. American Journal of Human Genetics. 63: 267-9. PMID 9637791 DOI: 10.1086/301932 |
0.321 |
|
| 1998 |
Hwang BJ, Toering S, Francke U, Chu G. p48 Activates a UV-damaged-DNA binding factor and is defective in xeroderma pigmentosum group E cells that lack binding activity. Molecular and Cellular Biology. 18: 4391-9. PMID 9632823 DOI: 10.1128/Mcb.18.7.4391 |
0.313 |
|
| 1998 |
Burwinkel B, Miglierini G, Jenne DE, Gilbert DJ, Copeland NG, Jenkins NA, Ring HZ, Francke U, Kilimann MW. Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant mice. Genomics. 49: 462-6. PMID 9615234 DOI: 10.1006/Geno.1998.5276 |
0.519 |
|
| 1998 |
Francke U. Imprinted genes in the Prader-Willi deletion. Novartis Foundation Symposium. 214: 264-75; discussion 2. PMID 9601023 DOI: 10.1002/9780470515501.Ch16 |
0.507 |
|
| 1998 |
Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI. A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nature Genetics. 19: 25-31. PMID 9590284 DOI: 10.1038/Ng0598-25 |
0.418 |
|
| 1998 |
Wang YK, Pérez-Jurado LA, Francke U. A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region. Genomics. 48: 163-70. PMID 9521869 DOI: 10.1006/Geno.1997.5182 |
0.524 |
|
| 1998 |
Pérez Jurado LA, Wang YK, Peoples R, Coloma A, Cruces J, Francke U. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK. Human Molecular Genetics. 7: 325-34. PMID 9466987 DOI: 10.1093/Hmg/7.3.325 |
0.536 |
|
| 1998 |
Collod-Béroud G, Béroud C, Ades L, Black C, Boxer M, Brock DJ, Holman KJ, de Paepe A, Francke U, Grau U, Hayward C, Klein HG, Liu W, Nuytinck L, Peltonen L, et al. Marfan Database (third edition): new mutations and new routines for the software. Nucleic Acids Research. 26: 229-3. PMID 9399842 DOI: 10.1093/Nar/26.1.229 |
0.323 |
|
| 1997 |
Fang J, Li X, Smiley E, Francke U, Mecham RP, Bonadio J. Mouse latent TGF-beta binding protein-2: molecular cloning and developmental expression. Biochimica Et Biophysica Acta. 1354: 219-30. PMID 9427531 DOI: 10.1016/S0167-4781(97)00104-8 |
0.451 |
|
| 1997 |
Wedemeyer N, Peoples R, Himmelbauer H, Lehrach H, Francke U, Wanker EE. Localization of the human HIP1 gene close to the elastin (ELN) locus on 7q11.23. Genomics. 46: 313-5. PMID 9417924 DOI: 10.1006/Geno.1997.5027 |
0.465 |
|
| 1997 |
Carmeci C, Thompson DA, Ring HZ, Francke U, Weigel RJ. Identification of a gene (GPR30) with homology to the G-protein-coupled receptor superfamily associated with estrogen receptor expression in breast cancer. Genomics. 45: 607-17. PMID 9367686 DOI: 10.1006/Geno.1997.4972 |
0.326 |
|
| 1997 |
Pérez Jurado LA, Argente J, Barrios V, Pozo J, Muñoz MT, Hernández M, Francke U. Molecular diagnosis and endocrine evaluation of a patient with a homozygous 7.0 kb deletion of the growth hormone (GH) gene cluster: Response to biosynthetic GH therapy Journal of Pediatric Endocrinology and Metabolism. 10: 185-190. PMID 9364351 DOI: 10.1515/Jpem.1997.10.2.185 |
0.348 |
|
| 1997 |
Schanen NC, Dahle EJ, Capozzoli F, Holm VA, Zoghbi HY, Francke U. A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map. American Journal of Human Genetics. 61: 634-41. PMID 9326329 DOI: 10.1086/515525 |
0.406 |
|
| 1997 |
Liu W, Qian C, Francke U. Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome Nature Genetics. 16: 328-329. PMID 9241263 DOI: 10.1038/Ng0897-328 |
0.361 |
|
| 1997 |
Schrijver I, Liu W, Francke U. The pathogenicity of the Pro1148Ala substitution in the FBN1 gene: Causing or predisposing to Marfan syndrome and aortic aneurysm, or clinically innocent? Human Genetics. 99: 607-611. PMID 9150726 DOI: 10.1007/S004390050414 |
0.336 |
|
| 1997 |
Liu W, Faraco J, Qian C, Francke U. The gene for microfibril-associated protein-1 (MFAP1) is located several megabases centromeric to FBN1 and is not mutated in Marfan syndrome Human Genetics. 99: 578-584. PMID 9150721 DOI: 10.1007/S004390050409 |
0.456 |
|
| 1997 |
Wang YK, Samos CH, Peoples R, Pérez-Jurado LA, Nusse R, Francke U. A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23. Human Molecular Genetics. 6: 465-72. PMID 9147651 DOI: 10.1093/Hmg/6.3.465 |
0.498 |
|
| 1997 |
Shang J, Li X, Ring HZ, Clayton DA, Francke U. Backfoot, a novel homeobox gene, maps to human chromosome 5 (BFT) and mouse chromosome 13 (Bft) Genomics. 40: 108-113. PMID 9070926 DOI: 10.1006/Geno.1996.4558 |
0.513 |
|
| 1997 |
Wevrick R, Francke U. An imprinted mouse transcript homglogous to the human imprinted in Prader-Willi syndrome (IPW) gene Human Molecular Genetics. 6: 325-332. PMID 9063754 DOI: 10.1093/Hmg/6.2.325 |
0.494 |
|
| 1997 |
Gebe JA, Kiener PA, Ring HZ, Li X, Francke U, Aruffo A. Molecular cloning, mapping to human chromosome 1 q21-q23, and cell binding characteristics of Spα, a new member of the scavenger receptor cysteine-rich (SRCR) family of proteins Journal of Biological Chemistry. 272: 6151-6158. PMID 9045627 DOI: 10.1074/Jbc.272.10.6151 |
0.423 |
|
| 1997 |
Li L, Li X, Francke U, Cohen SN. The TSG101 tumor susceptibility gene is located in chromosome 11 band p15 and is mutated in human breast cancer Cell. 88: 143-154. PMID 9019400 DOI: 10.1016/S0092-8674(00)81866-8 |
0.359 |
|
| 1997 |
Zhou YD, Barnard M, Tian H, Li X, Ring HZ, Francke U, Shelton J, Richardson J, Russell DW, McKnight SL. Molecular characterization of two mammalian bHLH-PAS domain proteins selectively expressed in the central nervous system. Proceedings of the National Academy of Sciences of the United States of America. 94: 713-8. PMID 9012850 DOI: 10.1073/Pnas.94.2.713 |
0.506 |
|
| 1996 |
Schanen NC, Scherer SW, Tsui LC, Francke U. Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1 Cytogenetics and Cell Genetics. 72: 187-188. PMID 8978771 DOI: 10.1159/000134184 |
0.455 |
|
| 1996 |
Larrick JW, Lee J, Ma S, Li X, Francke U, Wright SC, Balint RF. Structural, functional analysis and localization of the human CAP18 gene. Febs Letters. 398: 74-80. PMID 8946956 DOI: 10.1016/S0014-5793(96)01199-4 |
0.511 |
|
| 1996 |
Giacalone J, Li X, Lehrach H, Francke U. High-density radiation hybrid map of human chromosome 18 and contig of 18p Genomics. 37: 9-18. PMID 8921364 DOI: 10.1006/Geno.1996.0514 |
0.389 |
|
| 1996 |
Ellison JW, Li X, Francke U, Shapiro LJ. Rapid evolution of human pseudoautosomal genes and their mouse homologs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 25-30. PMID 8903724 DOI: 10.1007/S003359900007 |
0.529 |
|
| 1996 |
Liu W, Qian C, Comeau K, Brenn T, Furthmayr H, Francke U. Mutant fibrillin-1 monomers lacking EGF-like domains disrupt microfibril assembly and cause severe Marfan syndrome Human Molecular Genetics. 5: 1581-1587. PMID 8894692 DOI: 10.1093/Hmg/5.10.1581 |
0.349 |
|
| 1996 |
Wevrick R, Francke U. Diagnostic test for the Prader-Willi syndrome by SNRPN expression in blood Lancet. 348: 1068-1069. PMID 8874459 DOI: 10.1016/S0140-6736(96)04342-5 |
0.406 |
|
| 1996 |
Wevrick R, Kerns JA, Francke U. The IPW gene is imprinted and is not expressed in the Prader-Willi syndrome. Acta Geneticae Medicae Et Gemellologiae. 45: 191-7. PMID 8872030 DOI: 10.1017/S000156600000129X |
0.357 |
|
| 1996 |
Maresco DL, Chang E, Theil KS, Francke U, Anderson CL. The three genes of the human FCGR1 gene family encoding FcγRI flank the centromere of chromosome 1 at 1p12 and 1q21 Cytogenetics and Cell Genetics. 73: 157-163. PMID 8697799 |
0.417 |
|
| 1996 |
Coetzee T, Li X, Fujita N, Marcus J, Suzuki K, Francke U, Popko B. Molecular cloning, chromosomal mapping, and characterization of the mouse UDP-galactose:ceramide galactosyltransferase gene Genomics. 35: 215-222. PMID 8661123 DOI: 10.1006/Geno.1996.0341 |
0.527 |
|
| 1996 |
Symons M, Derry JMJ, Karlak B, Jiang S, Lemahieu V, McCormick F, Francke U, Abo A. Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization Cell. 84: 723-734. PMID 8625410 DOI: 10.1016/S0092-8674(00)81050-8 |
0.301 |
|
| 1996 |
Gratas C, Li X, Wang Y, Francke U, Becker D. Chromosomal assignment of three human melanocyte-specific genes International Journal of Oncology. 9: 481-485. DOI: 10.3892/Ijo.9.3.481 |
0.546 |
|
| 1995 |
Derry JM, Wiedemann P, Blair P, Wang Y, Kerns JA, Lemahieu V, Godfrey VL, Wilkinson JE, Francke U. The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome. Genomics. 29: 471-7. PMID 8666397 DOI: 10.1006/Geno.1995.9979 |
0.531 |
|
| 1995 |
Derry JM, Kerns JA, Francke U. RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain. Human Molecular Genetics. 4: 2307-11. PMID 8634703 DOI: 10.1093/Hmg/4.12.2307 |
0.343 |
|
| 1995 |
Derry JMJ, Jess U, Francke U. Cloning and characterization of a novel zinc finger gene in Xp11.2 Genomics. 30: 361-365. PMID 8586441 DOI: 10.1006/Geno.1995.0031 |
0.432 |
|
| 1995 |
Aoyama T, Francke U, Gasner C, Furthmayr H. Fibrillin abnormalities and prognosis in Marfan syndrome and related disorders American Journal of Medical Genetics. 58: 169-176. PMID 8533811 DOI: 10.1002/Ajmg.1320580216 |
0.312 |
|
| 1995 |
Derry JM, Kerns JA, Weinberg KI, Ochs HD, Volpini V, Estivill X, Walker AP, Francke U. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Human Molecular Genetics. 4: 1127-35. PMID 8528199 DOI: 10.1093/Hmg/4.7.1127 |
0.368 |
|
| 1995 |
Rosenbloom AL, Francke U, Berg MA, Kasatkina EP, Volkova TN, Skorobogatova VF, Sokolovskaya VN. Severe Growth Hormone Insensitivity (Laron Syndrome) Due to Nonsense Mutation of the GH Receptor in Brothers from Russia Journal of Pediatric Endocrinology and Metabolism. 8: 159-166. PMID 8521189 DOI: 10.1515/Jpem.1995.8.3.159 |
0.364 |
|
| 1995 |
Li X, Ho SN, Luna J, Giacalone J, Thomas DJ, Timmerman LA, Crabtree GR, Francke U. Cloning and chromosomal localization of the human and murine genes for the T-cell transcription factors NFATc and NFATp. Cytogenetics and Cell Genetics. 68: 185-91. PMID 7842733 DOI: 10.1159/000133910 |
0.564 |
|
| 1995 |
Moore KJ, Testa JR, Francke U, Milatovich A, Copeland NG, Jenkins NA. Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome band 15q21 Cytogenetic and Genome Research. 69: 53-58. PMID 7835087 DOI: 10.1159/000133937 |
0.541 |
|
| 1995 |
Wiemer EAC, Nuttley WM, Bertolaet BL, Li X, Francke U, Wheelock MJ, Anné UK, Johnson KR, Subramani S. Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders Journal of Cell Biology. 130: 51-65. PMID 7790377 DOI: 10.1083/Jcb.130.1.51 |
0.391 |
|
| 1995 |
Jurado LAP, Li X, Francke U. The human calcitonin receptor gene (CALCR) at 7q21.3 is outside the deletion associated with the williams syndrome Cytogenetic and Genome Research. 70: 246-249. PMID 7789182 DOI: 10.1159/000134044 |
0.524 |
|
| 1995 |
Peoples R, Milatovich A, Francke U. Hemizygosity at the insulin-like growth factor I eceptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome Cytogenetic and Genome Research. 70: 228-234. PMID 7789178 DOI: 10.1159/000134040 |
0.48 |
|
| 1995 |
Bowen MA, Patel DD, Li X, Modrell B, Malacko AR, Wang WC, Marquardt H, Neubauer M, Pesando JM, Francke U, Haynes BF, Aruffo A. Cloning, mapping, and characterization of activated leukocyte-cell adhesion molecule (ALCAM), a CD6 ligand Journal of Experimental Medicine. 181: 2213-2220. PMID 7760007 DOI: 10.1084/Jem.181.6.2213 |
0.324 |
|
| 1995 |
Faraco J, Bashir M, Rosenbloom J, Francke U. Characterization of the human gene for microfibril-associated glycoprotein (MFAP2), assignment to chromosome 1p36.1-p35, and linkage to D1S170 Genomics. 25: 630-637. PMID 7759096 DOI: 10.1016/0888-7543(95)80004-6 |
0.558 |
|
| 1995 |
Yamamoto R, Li X, Winter S, Francke U, Kilimann MW. Primary structure of human amphiphysin, the dominant autoantigen of paraneoplastic Stiff-Man syndrome, and mapping of its gene (AMPH) to chromosome 7p13-p14 Human Molecular Genetics. 4: 265-268. PMID 7757077 DOI: 10.1093/Hmg/4.2.265 |
0.488 |
|
| 1995 |
Li X, Yin W, Pérez-Jurado L, Bonadio J, Francke U. Mapping of human and murine genes for latent TGF-β binding protein-2 (LTBP2) Mammalian Genome. 6: 42-45. PMID 7719025 DOI: 10.1007/Bf00350892 |
0.493 |
|
| 1995 |
Laureys G, Speleman F, Versteeg R, Van Der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers Oncogene. 10: 1087-1093. PMID 7700633 |
0.354 |
|
| 1995 |
Ho SN, Thomas DJ, Timmerman LA, Li X, Francke U, Crabtree GR. NFATc3, a lymphoid-specific NFATc family member that is calcium-regulated and exhibits distinct DNA binding specificity. The Journal of Biological Chemistry. 270: 19898-907. PMID 7650004 DOI: 10.1074/Jbc.270.34.19898 |
0.344 |
|
| 1995 |
Li X, Rosahl TW, Sudhof TC, Francke U. Mapping of synapsin II (SYN2) genes to human chromosome 3p and mouse chromosome 6 band F Cytogenetics and Cell Genetics. 71: 301-305. PMID 7587399 DOI: 10.1159/000134132 |
0.545 |
|
| 1995 |
Li X, Francke U. Assignment of the gene SLC1A2 coding for the human glutamate transporter EAAT2 to human chromosome 11 bands p13-p12 Cytogenetics and Cell Genetics. 71: 212-213. PMID 7587378 DOI: 10.1159/000134111 |
0.414 |
|
| 1995 |
Zhu Q, Zhang M, Blaese RM, Derry JM, Junker A, Francke U, Chen SH, Ochs HD. The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene. Blood. 86: 3797-804. PMID 7579347 DOI: 10.1182/Blood.V86.10.3797.Bloodjournal86103797 |
0.37 |
|
| 1995 |
Laureys G, Versteeg R, Speleman F, van der Drift P, Francke U, Opdenakker G, Van Roy N. Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma European Journal of Cancer. 31: 523-526. PMID 7576958 DOI: 10.1016/0959-8049(95)00012-8 |
0.476 |
|
| 1995 |
Li X, Luna J, Lombroso PJ, Francke U. Molecular cloning of the human homolog of a striatum-enriched phosphatase (STEP) gene and chromosomal mapping of the human and murine loci. Genomics. 28: 442-9. PMID 7490079 DOI: 10.1006/Geno.1995.1173 |
0.524 |
|
| 1994 |
Li X, Pereira L, Zhang H, Sanguineti C, Ramirez F, Bonadio J, Francke U. Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18. Genomics. 18: 667-72. PMID 8307578 DOI: 10.1016/S0888-7543(05)80371-4 |
0.566 |
|
| 1994 |
Li X, Nghiem P, Schulman H, Francke U. Localization of the CAMKG gene encoding gamma isoforms of multifunctional calcium/calmodulin-dependent protein kinase (CaM kinase) to human chromosome 10 band q22 and mouse chromosome 14. Cytogenetics and Cell Genetics. 66: 113-6. PMID 8287681 DOI: 10.1159/000133679 |
0.482 |
|
| 1994 |
Francke U. Digitized and differentially shaded human chromosome ideograms for genomic applications Cytogenetic and Genome Research. 65: 206-219. PMID 8222762 DOI: 10.1159/000133633 |
0.46 |
|
| 1994 |
Wilgenbus KK, Hsieh CL, Lankes WT, Milatovich A, Francke U, Furthmayr H. Structure and localization on the X chromosome of the gene coding for the human filopodial protein moesin (MSN) Genomics. 19: 326-333. PMID 8188263 DOI: 10.1006/Geno.1994.1065 |
0.528 |
|
| 1994 |
Pérez Jurado LA, Phillips JA, Francke U. Exclusion of growth hormone (GH)-releasing hormone gene mutations in familial isolated GH deficiency by linkage and single strand conformation analysis Journal of Clinical Endocrinology and Metabolism. 78: 622-628. PMID 8126133 DOI: 10.1210/Jcem.78.3.8126133 |
0.378 |
|
| 1994 |
Francke U, Chang E, Comeau K, Geigl EM, Giacalone J, Li X, Luna J, Moon A, Welch S, Wilgenbus P. A radiation hybrid map of human chromosome 18 Cytogenetics and Cell Genetics. 66: 196-213. PMID 8125019 DOI: 10.1159/000133697 |
0.504 |
|
| 1994 |
Tachibana M, Perez-Jurado LA, Nakayama A, Hodgkinson CA, Li X, Schneider M, Miki T, Fex J, Francke U, Arnheiter H. Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3 Human Molecular Genetics. 3: 553-557. PMID 8069297 DOI: 10.1093/Hmg/3.4.553 |
0.52 |
|
| 1994 |
Milatovich A, Qiu RG, Grosschedl R, Francke U. Gene for a tissue-specific transcriptional activator (EBF or Olf-1), expressed in early B lymphocytes, adipocytes, and olfactory neurons, is located on human Chromosome 5, band q34, and proximal mouse Chromosome 11 Mammalian Genome. 5: 211-215. PMID 8012110 DOI: 10.1007/Bf00360547 |
0.529 |
|
| 1994 |
Milatovich A, Bolger G, Michaeli T, Francke U. Chromosome localizations of genes for five cAMP-specific phosphodiesterases in man and mouse Somatic Cell and Molecular Genetics. 20: 75-86. PMID 8009369 DOI: 10.1007/Bf02290677 |
0.553 |
|
| 1994 |
Derry JM, Ochs HD, Francke U. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome Cell. 79: following 922. PMID 8001129 DOI: 10.1016/0092-8674(94)90528-2 |
0.416 |
|
| 1994 |
Berg MA, Peoples R, Pérez-Jurado L, Guevara-Aguirre J, Rosenbloom AL, Laron Z, Milner RD, Francke U. Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patient Acta Paediatrica (Oslo, Norway : 1992). Supplement. 399: 112-114. PMID 7949594 DOI: 10.1111/J.1651-2227.1994.Tb13302.X |
0.324 |
|
| 1994 |
Durham-Pierre D, Gardner JM, Nakatsu Y, King RA, Francke U, Ching A, Aquaron R, del Marmol V, Brilliant MH. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism. Nature Genetics. 7: 176-9. PMID 7920637 DOI: 10.1038/Ng0694-176 |
0.406 |
|
| 1994 |
Giacalone J, Francke U. Single nucleotide dimorphism in the transcribed region of the SNRPN gene at 15q12 Human Molecular Genetics. 3: 379. PMID 7911699 DOI: 10.1093/Hmg/3.2.379 |
0.42 |
|
| 1994 |
Wevrick R, Kerns JA, Francke U. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Human Molecular Genetics. 3: 1877-82. PMID 7849716 DOI: 10.1093/Hmg/3.10.1877 |
0.477 |
|
| 1994 |
Garcia CK, Li X, Luna J, Francke U. cDNA Cloning of the Human Monocarboxylate Transporter 1 and Chromosomal Localization of the SLC16A1 Locus to 1p13.2-p12 Genomics. 23: 500-503. PMID 7835905 DOI: 10.1006/Geno.1994.1532 |
0.488 |
|
| 1994 |
Brilliant MH, King R, Francke U, Schuffenhauer S, Meitinger T, Gardner JM, Durham-Pierre D, Nakatsu Y. The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 7: 398-402. PMID 7761348 DOI: 10.1111/J.1600-0749.1994.Tb00068.X |
0.527 |
|
| 1994 |
Kelly D, Chancellor K, Milatovich A, Francke U, Suzuki K, Popko B. Autosomal recessive neuromuscular disorder in a transgenic line of mice The Journal of Neuroscience. 14: 198-207. DOI: 10.1523/Jneurosci.14-01-00198.1994 |
0.309 |
|
| 1993 |
Hanna Z, Jankowski M, Tremblay P, Jiang X, Milatovich A, Francke U, Jolicoeur P. The Vin-1 gene, identified by provirus insertional mutagenesis, is the cyclin D2. Oncogene. 8: 1661-6. PMID 8502486 |
0.325 |
|
| 1993 |
Milatovich A, Mendel DB, Crabtree GR, Francke U. Genes for the dimerization cofactor of hepatocyte nuclear factor-1 alpha (DCOH) are on human and murine chromosomes 10. Genomics. 16: 292-5. PMID 8486378 DOI: 10.1006/Geno.1993.1182 |
0.444 |
|
| 1993 |
Wilgenbus KK, Milatovich A, Francke U, Furthmayr H. Molecular cloning, cDNA sequence, and chromosomal assignment of the human radixin gene and two dispersed pseudogenes Genomics. 16: 199-206. PMID 8486357 DOI: 10.1006/Geno.1993.1159 |
0.468 |
|
| 1993 |
Morrissey J, Tkachuk DC, Milatovich A, Francke U, Link M, Cleary ML. A serine/proline-rich protein is fused to HRX in t(4;11) acute leukemias Blood. 81: 1124-1131. PMID 8443374 DOI: 10.1182/Blood.V81.5.1124.1124 |
0.448 |
|
| 1993 |
Chang E, Luna J, Giacalone J, Uyar D, Silverman GA, Francke U. Regional localization of 56 new human chromosome 18-specific yeast artificial chromosomes Cytogenetics and Cell Genetics. 65: 136-139. PMID 8404067 DOI: 10.1159/000133620 |
0.51 |
|
| 1993 |
Pérez-Jurado LA, Francke U. Dinucleotide repeat polymorphism at the human pituitary adenylate cyclase activating polypeptide (PACAP) gene Human Molecular Genetics. 2: 827. PMID 8353512 DOI: 10.1093/Hmg/2.6.827-A |
0.378 |
|
| 1993 |
Rivera H, Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Remarks on constitutional 5q deletions [3] American Journal of Human Genetics. 53: 532-534. PMID 8328466 |
0.564 |
|
| 1993 |
Van den Berg DJ, Francke U. Roberts syndrome: A review of 100 cases and a new rating system for severity American Journal of Medical Genetics. 47: 1104-1123. PMID 8291532 DOI: 10.1002/Ajmg.1320470735 |
0.384 |
|
| 1993 |
Leib-Mosch C, Haltmeier M, Werner T, Geigl EM, Brack-Werner R, Francke U, Erfle V, Hehlmann R. Genomic distribution and transcription of solitary HERV-K LTRs Genomics. 18: 261-269. PMID 8288228 DOI: 10.1006/Geno.1993.1464 |
0.313 |
|
| 1993 |
Karasawa M, Zwacka RM, Reuter A, Fink T, Hsieh CL, Lichter P, Francke U, Weiher H. The human homolog of the glomerulosclerosis gene Mpv17: Structure and genomic organization Human Molecular Genetics. 2: 1829-1834. PMID 8281143 DOI: 10.1093/Hmg/2.11.1829 |
0.469 |
|
| 1993 |
Tynan K, Comeau K, Pearson M, Wilgenbus P, Levitt D, Gasner C, Berg MA, Miller DC, Francke U. Mutation screening of complete fibrillin-1 coding sequence: Report of five new mutations, including two in 8-cysteine domains Human Molecular Genetics. 2: 1813-1821. PMID 8281141 DOI: 10.1093/Hmg/2.11.1813 |
0.365 |
|
| 1993 |
Andres DA, Milatovich A, Ozçelik T, Wenzlau JM, Brown MS, Goldstein JL, Francke U. cDNA cloning of the two subunits of human CAAX farnesyltransferase and chromosomal mapping of FNTA and FNTB loci and related sequences. Genomics. 18: 105-12. PMID 8276393 DOI: 10.1006/Geno.1993.1432 |
0.677 |
|
| 1993 |
Ibraghimov-Beskrovnaya O, Milatovich A, Ozcelik T, Yang B, Koepnick K, Francke U, Campbell KP. Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. Human Molecular Genetics. 2: 1651-7. PMID 8268918 DOI: 10.1093/Hmg/2.10.1651 |
0.638 |
|
| 1993 |
Chen Y, Faraco J, Yin W, Germiller J, Francke U, Bonadio J. Structure, chromosomal localization, and expression pattern of the murine Magp gene Journal of Biological Chemistry. 268: 27381-27389. PMID 8262979 |
0.35 |
|
| 1993 |
Van den Berg DJ, Francke U. Sensitivity of Roberts syndrome cells to gamma radiation, mitomycin C, and protein synthesis inhibitors. Somatic Cell and Molecular Genetics. 19: 377-92. PMID 8211379 DOI: 10.1007/Bf01232749 |
0.353 |
|
| 1993 |
Aoyama T, Tynan K, Dietz HC, Francke U, Furthmayr H. Missense mutations impair intracellular processing of fibrillin and microfibril assembly in Marfan syndrome Human Molecular Genetics. 2: 2135-2140. PMID 8111384 DOI: 10.1093/Hmg/2.12.2135 |
0.319 |
|
| 1993 |
McKenzie ANJ, Li X, Largaespada DA, Sato A, Kaneda A, Zurawski SM, Doyle EL, Milatovich A, Francke U, Copeland NG, Jenkins NA, Zurawski G. Structural Comparison and Chromosomal Localization of the Human and Mouse IL-13 Genes Journal of Immunology. 150: 5436-5444. PMID 8099936 |
0.325 |
|
| 1993 |
Le Beau MM, Overhauser J, Straub RE, Silverman G, Gilliam TC, Ott J, O'Connell P, Francke U, Geurts van Kessel A. Report of the first international workshop on human chromosome 18 mapping. Cytogenetics and Cell Genetics. 63: 78-96. PMID 8096808 |
0.349 |
|
| 1993 |
Chang E, Welch S, Luna J, Giacalone J, Francke U. Generation of a human chromosome 18-specific YAC clone collection and mapping of 55 unique YACs by FISH and fingerprinting Genomics. 17: 393-402. PMID 7691716 DOI: 10.1006/Geno.1993.1338 |
0.524 |
|
| 1993 |
Gao JL, Kuhns DB, Tiffany HL, McDermott D, Li X, Francke U, Murphy PM. Structure and functional expression of the human macrophage inflammatory protein 1α/RANTES receptor Journal of Experimental Medicine. 177: 1421-1427. PMID 7683036 DOI: 10.1084/Jem.177.5.1421 |
0.352 |
|
| 1993 |
Aruffo A, Farrington M, Hollenbaugh D, Li X, Milatovich A, Nonoyama S, Bajorath J, Grosmaire LS, Stenkamp R, Neubauer M, Roberts RL, Noelle RJ, Ledbetter JA, Francke U, Ochs HD. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome Cell. 72: 291-300. PMID 7678782 DOI: 10.1016/0092-8674(93)90668-G |
0.32 |
|
| 1993 |
Berg MA, Guevara-Aguirre J, Rosenbloom AL, Francke U. Detection Of Ecuadorean Laron Syndrome Gene Carriers By Molecular Genetic Analysis Of Guthrie Card Blood Samples Pediatric Research. 33. DOI: 10.1203/00006450-199305001-00393 |
0.357 |
|
| 1993 |
Jurado LAP, Cogan JD, Phillips JA, Francke U. Exclusion Of The Ghrh Gene As A Candidate For Most Cases Of Familial Isolated Growth Hormone Deficiency Pediatric Research. 33. DOI: 10.1203/00006450-199305001-00172 |
0.415 |
|
| 1993 |
Francke U. Growth Hormone Insensitivity Syndrome Pediatric Research. 33. DOI: 10.1203/00006450-199305001-00027 |
0.381 |
|
| 1992 |
Matsuo M, Nishio H, Kitoh Y, Francke U, Nakamura H. Partial deletion of a dystrophin gene leads to exon skipping and to loss of an intra-exon hairpin structure from the predicted mRNA precursor. Biochemical and Biophysical Research Communications. 182: 495-500. PMID 1734864 DOI: 10.1016/0006-291X(92)91759-J |
0.315 |
|
| 1992 |
Marcus S, Steen AM, Andersson B, Lambert B, Kristoffersson U, Francke U. Mutation analysis and prenatal diagnosis in a Lesch-Nyhan family showing non-random X-inactivation interfering with carrier detection tests. Human Genetics. 89: 395-400. PMID 1618489 DOI: 10.1007/Bf00194310 |
0.335 |
|
| 1992 |
Welch SK, Francke U. Assignment of the human alpha 2-plasmin inhibitor gene (PLI) to chromosome 17, region pter-p12, by PCR analysis of somatic cell hybrids. Genomics. 13: 213-4. PMID 1577485 DOI: 10.1016/0888-7543(92)90224-G |
0.544 |
|
| 1992 |
Suter U, Welcher AA, Ozcelik T, Snipes GJ, Kosaras B, Francke U, Billings-Gagliardi S, Sidman RL, Shooter EM. Trembler mouse carries a point mutation in a myelin gene. Nature. 356: 241-4. PMID 1552943 DOI: 10.1038/356241A0 |
0.656 |
|
| 1992 |
Thigpen AE, Davis DL, Milatovich A, Mendonca BB, Imperato-McGinley J, Griffin JE, Francke U, Wilson JD, Russell DW. Molecular genetics of steroid 5 alpha-reductase 2 deficiency. The Journal of Clinical Investigation. 90: 799-809. PMID 1522235 DOI: 10.1172/Jci115954 |
0.428 |
|
| 1992 |
Berkemeier LR, Ozçelik T, Francke U, Rosenthal A. Human chromosome 19 contains the neurotrophin-5 gene locus and three related genes that may encode novel acidic neurotrophins. Somatic Cell and Molecular Genetics. 18: 233-45. PMID 1496419 DOI: 10.1007/Bf01233860 |
0.677 |
|
| 1992 |
Milatovich A, Francke U. Human cyclin B1 gene (CCNB1) assigned to chromosome 5 (q13-qter). Somatic Cell and Molecular Genetics. 18: 303-307. PMID 1386686 DOI: 10.1007/Bf01233865 |
0.498 |
|
| 1992 |
Francke U, Hsieh CL, Kelly D, Lai E, Popko B. Induced reciprocal translocation in transgenic mice near sites of transgene integration. Mammalian Genome. 3: 209-216. PMID 1377063 DOI: 10.1007/Bf00355721 |
0.506 |
|
| 1992 |
Murphy PM, Ozçelik T, Kenney RT, Tiffany HL, McDermott D, Francke U. A structural homologue of the N-formyl peptide receptor. Characterization and chromosome mapping of a peptide chemoattractant receptor family. The Journal of Biological Chemistry. 267: 7637-43. PMID 1373134 |
0.537 |
|
| 1992 |
Davidson JJ, Ozçelik T, Hamacher C, Willems PJ, Francke U, Kilimann MW. cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis. Proceedings of the National Academy of Sciences of the United States of America. 89: 2096-100. PMID 1372435 DOI: 10.1073/Pnas.89.6.2096 |
0.636 |
|
| 1992 |
Ozçelik T, Porteus MH, Rubenstein JL, Francke U. DLX2 (TES1), a homeobox gene of the Distal-less family, assigned to conserved regions on human and mouse chromosomes 2. Genomics. 13: 1157-61. PMID 1354641 DOI: 10.1016/0888-7543(92)90031-M |
0.544 |
|
| 1992 |
Arnaudo E, Hirano M, Seelan RS, Milatovich A, Hsieh CL, Fabrizi GM, Grossman LI, Francke U, Schon EA. Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase. Gene. 119: 299-305. PMID 1327965 DOI: 10.1016/0378-1119(92)90287-Y |
0.41 |
|
| 1992 |
Rupp F, Ozçelik T, Linial M, Peterson K, Francke U, Scheller R. Structure and chromosomal localization of the mammalian agrin gene. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 12: 3535-44. PMID 1326608 DOI: 10.1523/Jneurosci.12-09-03535.1992 |
0.468 |
|
| 1992 |
Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis. American Journal of Human Genetics. 50: 988-97. PMID 1315124 |
0.639 |
|
| 1992 |
Ozçelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, Francke U. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nature Genetics. 2: 265-9. PMID 1303277 DOI: 10.1038/Ng1292-265 |
0.54 |
|
| 1992 |
Leff SE, Brannan CI, Reed ML, Ozçelik T, Francke U, Copeland NG, Jenkins NA. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nature Genetics. 2: 259-64. PMID 1303276 DOI: 10.1038/Ng1292-259 |
0.715 |
|
| 1992 |
Ahuja SK, Ozçelik T, Milatovitch A, Francke U, Murphy PM. Molecular evolution of the human interleukin-8 receptor gene cluster. Nature Genetics. 2: 31-6. PMID 1303245 DOI: 10.1038/Ng0992-31 |
0.616 |
|
| 1992 |
Patel PI, Roa BB, Welcher AA, Schoener-Scott R, Trask BJ, Pentao L, Snipes GJ, Garcia CA, Francke U, Shooter EM, Lupski JR, Suter U. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nature Genetics. 1: 159-65. PMID 1303228 DOI: 10.1038/Ng0692-159 |
0.531 |
|
| 1992 |
Milatovich A, Hsieh CL, Bonaminio G, Tecott L, Julius D, Francke U. Serotonin receptor 1c gene assigned to X chromosome in human (band q24) and mouse (bands D-F4). Human Molecular Genetics. 1: 681-4. PMID 1302605 DOI: 10.1093/Hmg/1.9.681 |
0.479 |
|
| 1992 |
Giacalone J, Friedes J, Francke U. A novel GC–rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomes Nature Genetics. 1: 137-143. PMID 1302007 DOI: 10.1038/Ng0592-137 |
0.428 |
|
| 1992 |
Berg MA, Guevara-Aguirre J, Rosenbloom AL, Rosenfeld RG, Francke U. Mutation creating a new splice site in the growth hormone receptor genes of 37 Ecuadorean patients with Laron syndrome Human Mutation. 1: 24-34. PMID 1284474 DOI: 10.1002/Humu.1380010105 |
0.365 |
|
| 1992 |
Francke U. Chromosome banding: By A. T. Sumner. London: Unwin Hyman. (1990). 434 pp. UK £60.00 Cell. 68: 1005-1006. DOI: 10.1016/0092-8674(92)90072-K |
0.383 |
|
| 1991 |
Hoegen Iv, Hsieh C, Scharting R, Francke U, Parnes JR. Identity of human Lyb-2 and CD72 and localization of the gene to chromosome 9. European Journal of Immunology. 21: 1425-1431. PMID 2044654 DOI: 10.1002/Eji.1830210615 |
0.422 |
|
| 1991 |
Keats BJ, Sherman SL, Morton NE, Robson EB, Buetow KH, Cartwright PE, Chakravarti A, Francke U, Green PP, Ott J. Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990). Annals of Human Genetics. 55: 1-6. PMID 2042931 DOI: 10.1111/J.1469-1809.1991.Tb00392.X |
0.338 |
|
| 1991 |
Hofmann SL, Topham M, Hsieh CL, Francke U. cDNA and genomic cloning of HRC, a human sarcoplasmic reticulum protein, and localization of the gene to human chromosome 19 and mouse chromosome 7. Genomics. 9: 656-69. PMID 2037293 DOI: 10.1016/0888-7543(91)90359-M |
0.552 |
|
| 1991 |
Keats BJ, Sherman SL, Morton NE, Robson EB, Buetow KH, Cartwright PE, Chakravarti A, Francke U, Green PP, Ott J. Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990). Genomics. 9: 557-60. PMID 2032725 DOI: 10.1016/0888-7543(91)90426-F |
0.338 |
|
| 1991 |
Kwon BS, Chintamaneni C, Kozak CA, Copeland NG, Gilbert DJ, Jenkins N, Barton D, Francke U, Kobayashi Y, Kim KK. A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12. Proceedings of the National Academy of Sciences of the United States of America. 88: 9228-32. PMID 1924386 DOI: 10.1073/Pnas.88.20.9228 |
0.49 |
|
| 1991 |
Ozçelik T, Rosenthal A, Francke U. Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse. Genomics. 10: 569-75. PMID 1889807 DOI: 10.1016/0888-7543(91)90437-J |
0.689 |
|
| 1991 |
Hsieh C, Kumar NM, Gilula NB, Francke U. Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes. Somatic Cell and Molecular Genetics. 17: 191-200. PMID 1849321 DOI: 10.1007/Bf01232976 |
0.532 |
|
| 1991 |
Perin MS, Johnston PA, Ozcelik T, Jahn R, Francke U, Südhof TC. Structural and functional conservation of synaptotagmin (p65) in Drosophila and humans. The Journal of Biological Chemistry. 266: 615-22. PMID 1840599 |
0.592 |
|
| 1991 |
Tse WT, Menninger JC, Yang-Feng TL, Francke U, Sahr KE, Lux SE, Ward DC, Forget BG. Isolation and chromosomal localization of a novel nonerythroid ankyrin gene. Genomics. 10: 858-66. PMID 1833308 DOI: 10.1016/0888-7543(91)90173-C |
0.494 |
|
| 1991 |
Milatovich A, Travis A, Grosschedl R, Francke U. Gene for lymphoid enhancer-binding factor 1 (LEF1) mapped to human chromosome 4 (q23-q25) and mouse chromosome 3 near Egf. Genomics. 11: 1040-1048. PMID 1783375 DOI: 10.1016/0888-7543(91)90030-I |
0.555 |
|
| 1991 |
Agarwal N, Hsieh CL, Sills D, Swaroop M, Desai B, Francke U, Swaroop A. Sequence analysis, expression and chromosomal localization of a gene, isolated from a subtracted human retina cDNA library, that encodes an insulin-like growth factor binding protein (IGFBP2). Experimental Eye Research. 52: 549-61. PMID 1712312 DOI: 10.1016/0014-4835(91)90056-K |
0.451 |
|
| 1991 |
Hsieh CL, Navankasattusas S, Escobedo JA, Williams LT, Francke U. Chromosomal localization of the gene for AA-type platelet-derived growth factor receptor (PDGFRA) in humans and mice Cytogenetic and Genome Research. 56: 160-163. PMID 1711435 DOI: 10.1159/000133076 |
0.524 |
|
| 1991 |
You KH, Hsieh CL, Hayes C, Stahl N, Francke U, Popko B. DNA sequence, genomic organization, and chromosomal localization of the mouse peripheral myelin protein zero gene: identification of polymorphic alleles. Genomics. 9: 751-757. PMID 1709914 DOI: 10.1016/0888-7543(91)90370-T |
0.489 |
|
| 1991 |
Jenkins EP, Hsieh CL, Milatovich A, Normington K, Berman DM, Francke U, Russell DW. Characterization and chromosomal mapping of a human steroid 5α-reductase gene and pseudogene and mapping of the mouse homologue Genomics. 11: 1102-1112. PMID 1686016 DOI: 10.1016/0888-7543(91)90038-G |
0.511 |
|
| 1991 |
Blonden LAJ, Grootscholten PM, den Dunnen JT, Bakker E, Abbs S, Bobrow M, Boehm C, van Broeckhoven C, Baumbach L, Chamberlain J, Caskey CT, Denton M, Felicetti L, Galluzi G, Fischbeck KH, ... Francke U, et al. 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread Genomics. 10: 631-639. PMID 1679746 DOI: 10.1016/0888-7543(91)90445-K |
0.454 |
|
| 1991 |
Archidiacono N, Lerone M, Rocchi M, Anvret M, Ozcelik T, Francke U, Romeo G. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations. Human Genetics. 86: 604-6. PMID 1673961 DOI: 10.1007/Bf00201549 |
0.627 |
|
| 1991 |
Cowan JM, Francke U. Cytogenetic analysis in melanoma and nevi. Cancer Treatment and Research. 54: 3-16. PMID 1673858 DOI: 10.1007/978-1-4615-3938-4_1 |
0.309 |
|
| 1991 |
Milatovich A, Song K, Heller RA, Francke U. Tumor necrosis factor receptor genes, TNFR1 and TNFR2, on human chromosomes 12 and 1. Somatic Cell and Molecular Genetics. 17: 519-523. PMID 1662415 DOI: 10.1007/Bf01233176 |
0.482 |
|
| 1991 |
Lomax MI, Hsieh CL, Darras BT, Francke U. Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenes Genomics. 10: 1-9. PMID 1646156 DOI: 10.1016/0888-7543(91)90476-U |
0.522 |
|
| 1991 |
Roy NV, Laureys G, Speleman F, Opdenakker G, Leroy JG, Francke U. Rapid characterization of somatic cell hybrids using fluorescent in situ hybridization Cancer Genetics and Cytogenetics. 56: 94-95. DOI: 10.1016/0165-4608(91)90371-Z |
0.338 |
|
| 1990 |
Hsieh CL, Sturm R, Herr W, Francke U. The gene for the ubiquitous octamer-binding protein Oct-1 is on human chromosome 1, region cen-q32, and near Ly-22 and Ltw-4 on mouse chromosome 1. Genomics. 6: 666-72. PMID 2341156 DOI: 10.1016/0888-7543(90)90502-L |
0.527 |
|
| 1990 |
Hsieh CL, Donlon TA, Darras BT, Chang DD, Topper JN, Clayton DA, Francke U. The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4. Genomics. 6: 540-4. PMID 2328993 DOI: 10.1016/0888-7543(90)90483-B |
0.395 |
|
| 1990 |
Affholter JA, Hsieh C, Francke U, Roth RA. Insulin-degrading enzyme: stable expression of the human complementary DNA, characterization of its protein product, and chromosomal mapping of the human and mouse genes. Molecular Endocrinology. 4: 1125-1135. PMID 2293021 DOI: 10.1210/Mend-4-8-1125 |
0.405 |
|
| 1990 |
Kuo CJ, Conley PB, Hsieh CL, Francke U, Crabtree GR. Molecular cloning, functional expression, and chromosomal localization of mouse hepatocyte nuclear factor 1. Proceedings of the National Academy of Sciences of the United States of America. 87: 9838-42. PMID 2263635 DOI: 10.1073/Pnas.87.24.9838 |
0.488 |
|
| 1990 |
Lomax MI, Welch MD, Darras BT, Francke U, Grossman LI. Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunitIV Gene. 86: 209-216. PMID 2157630 DOI: 10.1016/0378-1119(90)90281-U |
0.522 |
|
| 1990 |
Yang-Feng TL, Xue F, Zhong W, Cotecchia S, Frielle T, Caron MG, Lefkowitz RJ, Francke U. Chromosomal organization of adrenergic receptor genes Proceedings of the National Academy of Sciences of the United States of America. 87: 1516-1520. PMID 2154750 DOI: 10.1073/Pnas.87.4.1516 |
0.445 |
|
| 1990 |
Francke U. A gene for Wilms tumour Nature. 343: 692-693. PMID 2154698 DOI: 10.1038/343692A0 |
0.335 |
|
| 1990 |
Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V, McIntosh S, Collins FS, Francke U, Ward DC, Forget BG. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 Nature. 345: 736-739. PMID 2141669 DOI: 10.1038/345736A0 |
0.498 |
|
| 1990 |
Seharaseyon J, Bober E, Hsieh C, Fodor WL, Francke U, Arnold H, Vanin EF. Human embryonic/atrial myosin alkali light chain gene: characterization, sequence, and chromosomal location. Genomics. 7: 289-293. PMID 2129532 DOI: 10.1016/0888-7543(90)90554-8 |
0.482 |
|
| 1990 |
Hsieh CL, Swaroop A, Francke U. Chromosomal localization and cDNA sequence of human ralB, a GTP binding protein Somatic Cell and Molecular Genetics. 16: 407-410. PMID 2120779 DOI: 10.1007/Bf01232469 |
0.494 |
|
| 1990 |
Hsieh CL, Bowcock AM, Farrer LA, Hebert JM, Huang KN, Cavalli-Sforza LL, Julius D, Francke U. The serotonin receptor subtype 2 locus HTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14. Somatic Cell and Molecular Genetics. 16: 567-74. PMID 1980030 DOI: 10.1007/Bf01233097 |
0.535 |
|
| 1990 |
Archer BT, Ozçelik T, Jahn R, Francke U, Südhof TC. Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2. The Journal of Biological Chemistry. 265: 17267-73. PMID 1976629 |
0.666 |
|
| 1990 |
Ozçelik T, Lafreniere RG, Archer BT, Johnston PA, Willard HF, Francke U, Südhof TC. Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse. American Journal of Human Genetics. 47: 551-61. PMID 1975480 |
0.463 |
|
| 1990 |
Harbers K, Francke U, Soriano P, Jaenisch R, Müller U. Structure and chromosomal mapping of a highly polymorphic repetitive DNA sequence from the pseudoautosomal region of the mouse sex chromosomes. Cytogenetics and Cell Genetics. 53: 129-33. PMID 1973377 DOI: 10.1159/000132912 |
0.497 |
|
| 1990 |
Levanon D, Hsieh CL, Francke U, Dawson PA, Ridgway ND, Brown MS, Goldstein JL. cDNA cloning of human oxysterol-binding protein and localization of the gene to human chromosome 11 and mouse chromosome 19. Genomics. 7: 65-74. PMID 1970801 DOI: 10.1016/0888-7543(90)90519-Z |
0.538 |
|
| 1990 |
Hsieh CL, Cheng-Deutsch A, Gloor S, Schachner M, Francke U. Assignment of Amog (adhesion molecule on glia) gene to mouse chromosome 11 near Zfp-3 and Asgr-1,2 and to human chromosome 17. Somatic Cell and Molecular Genetics. 16: 401-5. PMID 1699290 DOI: 10.1007/Bf01232468 |
0.536 |
|
| 1990 |
Francke U, Ochs HD, Darras BT, Swaroop A. Origin of mutations in two families with X-linked chronic granulomatous disease. Blood. 76: 602-606. DOI: 10.1182/Blood.V76.3.602.602 |
0.423 |
|
| 1989 |
Sundaresan S, Francke U. Gene for alpha 2(I) collagen is on mouse chromosome 6 not 16. Somatic Cell and Molecular Genetics. 15: 471-3. PMID 2781418 DOI: 10.1007/Bf01534898 |
0.514 |
|
| 1989 |
Sundaresan S, Yang-Feng TL, Francke U. Genes for HMG-CoA reductase and serotonin 1a receptor are on mouse chromosome 13. Somatic Cell and Molecular Genetics. 15: 465-9. PMID 2781417 DOI: 10.1007/Bf01534897 |
0.542 |
|
| 1989 |
Barton DE, Foellmer BE, Wood WI, Francke U. Chromosome mapping of the growth hormone receptor gene in man and mouse. Cytogenetic and Genome Research. 50: 137-141. PMID 2776481 DOI: 10.1159/000132743 |
0.351 |
|
| 1989 |
Barton DE, Yang-Feng TL, Mason AJ, Seeburg PH, Francke U. Mapping of genes for inhibin subunits alpha, beta A, and beta B on human and mouse chromosomes and studies of jsd mice. Genomics. 5: 91-9. PMID 2767687 DOI: 10.1016/0888-7543(89)90091-8 |
0.453 |
|
| 1989 |
Francke U, Foellmer BE. The glucocorticoid receptor gene is in 5q–q32 Genomics. 4: 610-612. PMID 2744768 DOI: 10.1016/0888-7543(89)90287-5 |
0.316 |
|
| 1989 |
Leib-Mösch C, Barton DE, Brack-Werner R, Foellmer B, Werner T, Rohrmeier D, Francke U, Erfle V, Hehlmann R. Genetic characterization of a human endogenous retroviral element located on chromosome 18q21. Haematology and Blood Transfusion. 32: 461-463. PMID 2576240 DOI: 10.1007/978-3-642-74621-5_80 |
0.427 |
|
| 1989 |
Friedman JM, Schneider BS, Barton DE, Francke U. Level of expression and chromosome mapping of the mouse cholecystokinin gene: implications for murine models of genetic obesity. Genomics. 5: 463-9. PMID 2575582 DOI: 10.1016/0888-7543(89)90010-4 |
0.472 |
|
| 1989 |
Hsieh CL, Vogel US, Dixon RAF, Francke U. Chromosome localization and cDNA sequence of murine and human genes for ras p21 GTPase activating protein (GAP). Somatic Cell and Molecular Genetics. 15: 579-590. PMID 2574500 DOI: 10.1007/Bf01534919 |
0.536 |
|
| 1989 |
Sundaresan S, Francke U. Genes for beta 2-adrenergic receptor and platelet-derived growth factor receptor map to mouse chromosome 18. Somatic Cell and Molecular Genetics. 15: 367-71. PMID 2569767 DOI: 10.1007/Bf01534975 |
0.455 |
|
| 1989 |
Battat L, Francke U. A common SacI polymorphism in the gene for the M1 subunit of ribonucleotide reductase (RRM1). Nucleic Acids Research. 17: 4005-4005. PMID 2567505 DOI: 10.1093/Nar/17.10.4005 |
0.312 |
|
| 1989 |
Leib-Mösch C, Barton D, Geigl E-, Brack-Werner R, Erfle V, Hehlmann R, Francke U. Two RFLPs associated with the human endogenous retroviral element S71 on chromosome 18q21. Nucleic Acids Research. 17: 2367-2367. PMID 2565025 DOI: 10.1093/Nar/17.6.2367 |
0.454 |
|
| 1989 |
Sundaresan S, Francke U. Insulin-like growth factor I receptor gene is concordant with c-Fes protooncogene and mouse chromosome 7 in somatic cell hybrids. Somatic Cell and Molecular Genetics. 15: 373-6. PMID 2548293 DOI: 10.1007/Bf01534976 |
0.477 |
|
| 1989 |
Brack-Werner R, Barton DE, Werner T, Foellmer BE, Leib-Mösch C, Francke U, Erfle V, Hehlmann R. Human SSAV-related endogenous retroviral element: LTR-like sequence and chromosomal localization to 18q21. Genomics. 4: 68-75. PMID 2536635 DOI: 10.1016/0888-7543(89)90316-9 |
0.474 |
|
| 1989 |
Kwon BS, Haq AK, Wakulchik M, Kestler D, Barton DE, Francke U, Lamoreux ML, Whitney JB, Halaban R. Isolation, chromosomal mapping, and expression of the mouse tyrosinase gene Journal of Investigative Dermatology. 93: 589-594. PMID 2507645 DOI: 10.1111/1523-1747.Ep12319693 |
0.476 |
|
| 1989 |
Staunton DE, Fisher RC, LeBeau MM, Lawrence JB, Barton DE, Francke U, Dustin M, Thorley-Lawson DA. Blast-1 possesses a glycosyl-phosphatidylinositol (GPI) membrane anchor, is related to LFA-3 and OX-45, and MAPS to chromosome 1q21-23 Journal of Experimental Medicine. 169: 10876-1099. PMID 2466936 DOI: 10.1084/Jem.169.3.1087 |
0.442 |
|
| 1988 |
Zeviani M, Darras BT, Rizzuto R, Salviati G, Betto R, Bonilla E, Miranda AF, Du J, Samitt C, Dickson G, Walsh FS, DiMauro S, Francke U, Schon EA. Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32. Genomics. 2: 249-256. PMID 3397062 DOI: 10.1016/0888-7543(88)90009-2 |
0.535 |
|
| 1988 |
Leto TL, Fortugno-Erikson D, Barton D, Yang-Feng TL, Francke U, Harris AS, Morrow JS, Marchesi VT, Benz EJ. Comparison of nonerythroid alpha-spectrin genes reveals strict homology among diverse species. Molecular and Cellular Biology. 8: 1-9. PMID 3336352 DOI: 10.1128/Mcb.8.1.1 |
0.396 |
|
| 1988 |
Brissenden JE, Caras I, Thelander L, Francke U. The structural gene for the M1 subunit of ribonucleotide reductase maps to chromosome 11, band p15, in human and to chromosome 7 in mouse. Experimental Cell Research. 174: 302-308. PMID 3275546 DOI: 10.1016/0014-4827(88)90165-6 |
0.531 |
|
| 1988 |
Alonso MA, Barton DE, Francke U. Assignment of the T-cell differentiation gene MAL to human chromosome 2, region cen----q13. Immunogenetics. 27: 91-95. PMID 3257199 DOI: 10.1007/Bf00351081 |
0.538 |
|
| 1988 |
Barton DE, Kwon BS, Francke U. Human tyrosinase gene, mapped to chromosome 11 (q14----q21), defines second region of homology with mouse chromosome 7. Genomics. 3: 17-24. PMID 3146546 DOI: 10.1016/0888-7543(88)90153-X |
0.553 |
|
| 1988 |
Richmond A, Balentien E, Thomas HG, Flaggs G, Barton DE, Spiess J, Bordoni R, Francke U, Derynck R. Molecular characterization and chromosomal mapping of melanoma growth stimulatory activity, a growth factor structurally related to beta-thromboglobulin. The Embo Journal. 7: 2025-33. PMID 2970963 DOI: 10.1002/J.1460-2075.1988.Tb03042.X |
0.462 |
|
| 1988 |
Burke BA, Wick MR, King R, Thompson T, Hansen J, Darrae BT, Francke U, Seltzer WK, McCabe ERB, Scheithauer BW, Opitz JM, Reynolds JF. Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome. American Journal of Medical Genetics. 31: 75-97. PMID 2906226 DOI: 10.1002/Ajmg.1320310111 |
0.351 |
|
| 1988 |
Darras BT, Koenig M, Kunkel LM, Francke U. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA. American Journal of Medical Genetics. 29: 713-26. PMID 2897793 DOI: 10.1002/Ajmg.1320290341 |
0.402 |
|
| 1988 |
Laureys G, Barton DE, Ullrich A, Francke U. Chromosomal mapping of the gene for the type II insulin-like growth factor receptor/cation-independent mannose 6-phosphate receptor in man and mouse Genomics. 3: 224-229. PMID 2852162 DOI: 10.1016/0888-7543(88)90083-3 |
0.469 |
|
| 1988 |
Yang-Feng TL, Schneider JW, Lindgren V, Shull MM, Benz EJ, Lingrel JB, Francke U. Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes. Genomics. 2: 128-38. PMID 2842249 DOI: 10.1016/0888-7543(88)90094-8 |
0.505 |
|
| 1988 |
Swaroop A, Hogan BLM, Francke U. Molecular analysis of the cDNA for human SPARC/osteonectin/BM-40: Sequence, expression, and localization of the gene to chromosome 5q31-q33 Genomics. 2: 37-47. PMID 2838412 DOI: 10.1016/0888-7543(88)90107-3 |
0.512 |
|
| 1987 |
Warburton D, Anyane‐Yeboa K, Francke U, Reynolds JF. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases. American Journal of Medical Genetics. 27: 275-283. PMID 3605213 DOI: 10.1002/Ajmg.1320270205 |
0.38 |
|
| 1987 |
Darras BT, Harper JF, Francke U. Prenatal diagnosis and detection of carriers with DNA probes in Duchenne's muscular dystrophy. The New England Journal of Medicine. 316: 985-992. PMID 3561454 DOI: 10.1056/Nejm198704163161604 |
0.396 |
|
| 1987 |
Cahilly-Snyder L, Yang-Feng T, Francke U, George DL. Molecular analysis and chromosomal mapping of amplified genes isolated from a transformed mouse 3T3 cell line. Somatic Cell and Molecular Genetics. 13: 235-44. PMID 3474784 DOI: 10.1007/Bf01535205 |
0.453 |
|
| 1987 |
Münke M, Harbers K, Jaenisch R, Francke U. Chromosomal mapping of four different integration sites of Moloney murine leukemia virus including the locus for alpha 1(I) collagen in mouse. Cytogenetics and Cell Genetics. 43: 140-9. PMID 3467899 DOI: 10.1159/000132312 |
0.52 |
|
| 1987 |
Yang-Feng TL, Landau NR, Baltimore D, Francke U. The terminal deoxynucleotidyltransferase gene is located on human chromosome 10 (10q23----q24) and on mouse chromosome 19. Cytogenetics and Cell Genetics. 43: 121-6. PMID 3467897 DOI: 10.1159/000132309 |
0.549 |
|
| 1987 |
Kraus JP, Matsubara Y, Barton D, Yang-Feng TL, Glassberg R, Ito M, Ikeda Y, Mole J, Francke U, Tanaka K. Isolation of cDNA clones coding for rat isovaleryl-CoA dehydrogenase and assignment of the gene to human chromosome 15 Genomics. 1: 264-269. PMID 3446585 DOI: 10.1016/0888-7543(87)90053-X |
0.447 |
|
| 1987 |
Radna RL, Foellmer B, Feldman LA, Francke U, Ozer HL. Restriction of human adenovirus replication in Chinese hamster cell lines and their hybrids with human cells Virus Research. 8: 277-299. PMID 3433922 DOI: 10.1016/0168-1702(87)90001-3 |
0.392 |
|
| 1987 |
Yang-Feng TL, Barton DE, Thelander L, Lewis WH, Srinivasan PR, Francke U. Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell lines. Genomics. 1: 77-86. PMID 3311968 DOI: 10.1016/0888-7543(87)90108-X |
0.516 |
|
| 1987 |
DeGennaro LJ, McCaffery CA, Kirchgessner CU, Yang-Feng TL, Francke U. Molecular analysis of synapsin I, a candidate gene for Rett syndrome. Brain & Development. 9: 469-74. PMID 3124657 DOI: 10.1016/S0387-7604(87)80066-9 |
0.423 |
|
| 1987 |
Kobilka BK, Frielle T, Collins S, Yang-Feng T, Kobilka TS, Francke U, Lefkowitz RJ, Caron MG. An intronless gene encoding a potential member of the family of receptors coupled to guanine nucleotide regulatory proteins. Nature. 329: 75-9. PMID 3041227 DOI: 10.1038/329075A0 |
0.347 |
|
| 1987 |
Chenevix-Trench G, Cowan JM, Behm FG, Goorha R, Brown JA, Westin EH, Francke U. Cytogenetic and molecular genetic studies of a patient with atypical lymphoid hyperplasia. Cancer Genetics and Cytogenetics. 27: 251-9. PMID 3036340 DOI: 10.1016/0165-4608(87)90007-0 |
0.465 |
|
| 1987 |
Kobilka BK, Dixon RA, Frielle T, Dohlman HG, Bolanowski MA, Sigal IS, Yang-Feng TL, Francke U, Caron MG, Lefkowitz RJ. cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor. Proceedings of the National Academy of Sciences of the United States of America. 84: 46-50. PMID 3025863 DOI: 10.1073/Pnas.84.1.46 |
0.402 |
|
| 1987 |
Darras BT, Francke U. A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male. Nature. 329: 556-558. PMID 2889145 DOI: 10.1038/329556A0 |
0.49 |
|
| 1987 |
Barton DE, Francke U. Activation of human alpha 1-antitrypsin genes in rat hepatoma x human fibroblast hybrid cell lines is correlated with demethylation. Somatic Cell and Molecular Genetics. 13: 635-644. PMID 2823394 DOI: 10.1007/Bf01534484 |
0.429 |
|
| 1987 |
Kobilka BK, Matsui H, Kobilka TS, Yang-Feng TL, Francke U, Caron MG, Lefkowitz RJ, Regan JW. Cloning, sequencing, and expression of the gene coding for the human platelet alpha 2-adrenergic receptor. Science (New York, N.Y.). 238: 650-6. PMID 2823383 DOI: 10.1126/Science.2823383 |
0.342 |
|
| 1987 |
Yarden Y, Kuang WJ, Yang-Feng T, Coussens L, Munemitsu S, Dull TJ, Chen E, Schlessinger J, Francke U, Ullrich A. Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand. The Embo Journal. 6: 3341-51. PMID 2448137 DOI: 10.1002/J.1460-2075.1987.Tb02655.X |
0.405 |
|
| 1987 |
Spritz RA, Strunk K, Surowy CS, Hoch SO, Barton DE, Francke U. The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-binding Nucleic Acids Research. 15: 10373-10391. PMID 2447561 DOI: 10.1093/Nar/15.24.10373 |
0.36 |
|
| 1987 |
Barton DE, Arquint M, Roder J, Dunn R, Francke U. The myelin-associated glycoprotein gene: mapping to human chromosome 19 and mouse chromosome 7 and expression in quivering mice. Genomics. 1: 107-112. PMID 2447011 DOI: 10.1016/0888-7543(87)90002-4 |
0.559 |
|
| 1987 |
Rozen R, Hum DW, Barton D, Francke U, Mackenzie RE. CHROMOSOMAL ASSIGNMENT OF THE HUMAN GENE FOR THE TRIFUNCTIONAL FOLATE-DEPENDENT ENZYME: EVIDENCE FOR MULTIPLE LOCI Pediatric Research. 21: 294A-294A. DOI: 10.1203/00006450-198704010-00760 |
0.545 |
|
| 1986 |
Cowan JM, Halaban R, Lane AT, Francke U. The involvement of 6p in melanoma Cancer Genetics and Cytogenetics. 20: 255-261. PMID 3943065 DOI: 10.1016/0165-4608(86)90081-6 |
0.497 |
|
| 1986 |
Lindgren V, Luskey KL, Russell DW, Francke U. Human genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probes. Proceedings of the National Academy of Sciences of the United States of America. 82: 8567-71. PMID 3866240 DOI: 10.1073/Pnas.82.24.8567 |
0.533 |
|
| 1986 |
Yang-Feng TL, Bruns GAP, Carroll AJ, Simola KOJ, Francke U. Localization of the LDHA gene to 11p14----11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13. Human Genetics. 74: 331-334. PMID 3793094 DOI: 10.1007/Bf00280481 |
0.454 |
|
| 1986 |
Floyd-Smith G, Whitehead AS, Colten HR, Francke U. The human C-reactive protein gene (CRP) and serum amyloid P component gene (APCS) are located on the proximal long arm of chromosome 1. Immunogenetics. 24: 171-6. PMID 3759147 DOI: 10.1007/Bf00364745 |
0.54 |
|
| 1986 |
Coussens L, Parker PJ, Rhee L, Yang-Feng TL, Chen E, Waterfield MD, Francke U, Ullrich A. Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways Science. 233: 859-866. PMID 3755548 DOI: 10.1126/Science.3755548 |
0.415 |
|
| 1986 |
Yang-Feng TL, Seeburg PH, Francke U. Human luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2----p21). Somatic Cell and Molecular Genetics. 12: 95-100. PMID 3511544 DOI: 10.1007/Bf01560732 |
0.515 |
|
| 1986 |
Matsubara Y, Kraus JP, Yang-Feng TL, Francke U, Rosenberg LE, Tanaka K. Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1 Proceedings of the National Academy of Sciences of the United States of America. 83: 6543-6547. PMID 3462713 DOI: 10.1073/Pnas.83.17.6543 |
0.425 |
|
| 1986 |
Fujii D, Brissenden JE, Derynck R, Francke U. Transforming growth factor beta gene maps to human chromosome 19 long arm and to mouse chromosome 7. Somatic Cell and Molecular Genetics. 12: 281-8. PMID 3459257 DOI: 10.1007/Bf01570787 |
0.467 |
|
| 1986 |
Kraus JP, Williamson CL, Firgaira FA, Yang-Feng TL, Münke M, Francke U, Rosenberg LE. Cloning and screening with nanogram amounts of immunopurified mRNAs: cDNA cloning and chromosomal mapping of cystathionine β-synthase and the β subunit of propionyl-CoA carboxylase Proceedings of the National Academy of Sciences of the United States of America. 83: 2047-2051. PMID 3457373 DOI: 10.1073/Pnas.83.7.2047 |
0.426 |
|
| 1986 |
Francke U, Yang-Feng TL, Brissenden JE, Ullrich A. Chromosomal mapping of genes involved in growth control. Cold Spring Harbor Symposia On Quantitative Biology. 51: 855-866. PMID 3107886 DOI: 10.1101/Sqb.1986.051.01.099 |
0.452 |
|
| 1986 |
Yang-Feng TL, Degennaro LJ, Francke U. Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes Proceedings of the National Academy of Sciences of the United States of America. 83: 8679-8683. PMID 3095840 DOI: 10.1073/Pnas.83.22.8679 |
0.539 |
|
| 1986 |
Colb M, Yang-Feng T, Francke U, Mermer B, Parkinson DR, Krontiris TG. A variable tandem repeat locus mapped to chromosome band 10q26 is amplified and rearranged in leukocyte DNAs of two cancer patients Nucleic Acids Research. 14: 7929-7937. PMID 3022240 DOI: 10.1093/Nar/14.20.7929 |
0.442 |
|
| 1986 |
Pear WS, Ingvarsson S, Steffen D, Münke M, Francke U, Bazin H, Klein G, Sümegi J. Multiple chromosomal rearrangements in a spontaneously arising t(6;7) rat immunocytoma juxtapose c-myc and immunoglobulin heavy chain sequences. Proceedings of the National Academy of Sciences of the United States of America. 83: 7376-80. PMID 3020544 DOI: 10.1073/Pnas.83.19.7376 |
0.42 |
|
| 1986 |
Yarden Y, Escobedo JA, Kuang WJ, Yang-Feng TL, Daniel TO, Tremble PM, Chen EY, Ando ME, Harkins RN, Francke U. Structure of the receptor for platelet-derived growth factor helps define a family of closely related growth factor receptors. Nature. 323: 226-32. PMID 3020426 DOI: 10.1038/323226A0 |
0.313 |
|
| 1986 |
Brissenden JE, Page DC, de Martinville B, Trowsdale J, Botstein D, Francke U. Regional assignments of three polymorphic DNA segments on human chromosome 15. Genetic Epidemiology. 3: 231-9. PMID 3017806 DOI: 10.1002/Gepi.1370030404 |
0.514 |
|
| 1986 |
Floyd-Smith G, Martinville BD, Francke U. An expressed β-tubulin gene, TUBB, is located on the short arm of human chromosome 6 and two related sequences are dispersed on chromosomes 8 and 13 Experimental Cell Research. 163: 539-548. PMID 3007184 DOI: 10.1016/0014-4827(86)90084-4 |
0.516 |
|
| 1986 |
Hofker MH, Bergen AAB, Skraastad MI, Bakker E, Francke U, Wieringa B, Bartley J, Ommen GJBv, Pearson PL. Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy Human Genetics. 74: 275-279. PMID 2877936 DOI: 10.1007/Bf00282548 |
0.385 |
|
| 1986 |
Breier G, Bućan M, Francke U, Colberg-Poley AM, Gruss P. Sequential expression of murine homeo box genes during F9 EC cell differentiation. The Embo Journal. 5: 2209-15. PMID 2877873 DOI: 10.1002/J.1460-2075.1986.Tb04486.X |
0.396 |
|
| 1986 |
Münke M, Cox DR, Jackson IJ, Hogan BLM, Francke U. The murine Hox-2 cluster of homeo box containing genes maps distal on chromosome 11 near the tail-short (Ts) locus. Cytogenetic and Genome Research. 42: 236-240. PMID 2875852 DOI: 10.1159/000132284 |
0.492 |
|
| 1986 |
Barton DE, Yang-Feng TL, Francke U. The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22----q24) by somatic cell hybrid analysis and in situ hybridization. Human Genetics. 72: 221-224. PMID 2870017 DOI: 10.1007/Bf00291881 |
0.548 |
|
| 1986 |
Bućan M, Yang-Feng T, Colberg-Poley A, Wolgemuth D, Guenet J, Francke U, Lehrach H. Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7. The Embo Journal. 5: 2899-2905. DOI: 10.1002/J.1460-2075.1986.Tb04585.X |
0.503 |
|
| 1986 |
Mason IJ, Murphy D, Münke M, Francke U, Elliott RW, Hogan BLM. Developmental and transformation-sensitive expression of the Sparc gene on mouse chromosome 11. The Embo Journal. 5: 1831-1837. DOI: 10.1002/J.1460-2075.1986.Tb04434.X |
0.415 |
|
| 1985 |
Yang-Feng TL, Finley SC, Finley WH, Francke U. High resolution cytogenetic evaluation of couples with recurring fetal wastage. Human Genetics. 69: 246-9. PMID 3980017 DOI: 10.1007/Bf00293034 |
0.341 |
|
| 1985 |
Engström Y, Francke U. Assignment of the structural gene for subunit M1 of human ribonucleotide reductase to the short arm of chromosome 11 Experimental Cell Research. 158: 477-483. PMID 3891388 DOI: 10.1016/0014-4827(85)90470-7 |
0.443 |
|
| 1985 |
Yang-Feng TL, Francke U, Ullrich A. Gene for human insulin receptor: localization to site on chromosome 19 involved in pre-B-cell leukemia. Science. 228: 728-731. PMID 3873110 DOI: 10.1126/Science.3873110 |
0.478 |
|
| 1985 |
Cox DW, Francke U. Direct assignment of orosomucoid to human chromosome 9 and α2HS-glycoprotein to chromosome 3 using human fetal liver x rat hepatoma hybrids Human Genetics. 70: 109-115. PMID 3859464 DOI: 10.1007/Bf00273067 |
0.491 |
|
| 1985 |
Gehring U, Segnitz B, Foellmer B, Francke U. Assignment of the human gene for the glucocorticoid receptor to chromosome 5 Proceedings of the National Academy of Sciences of the United States of America. 82: 3751-3755. PMID 3858847 DOI: 10.1073/Pnas.82.11.3751 |
0.471 |
|
| 1985 |
Lindgren V, Bernstein LB, Weiner AM, Francke U. Human U1 small nuclear RNA pseudogenes do not map to the site of the U1 genes in 1p36 but are clustered in 1q12-q22 Molecular and Cellular Biology. 5: 2172-2180. PMID 3837186 DOI: 10.1128/Mcb.5.9.2172 |
0.492 |
|
| 1985 |
Coussens L, Yang-Feng TL, Liao YC, Chen E, Gray A, McGrath J, Seeburg PH, Libermann TA, Schlessinger J, Francke U. Tyrosine kinase receptor with extensive homology to EGF receptor shares chromosomal location with neu oncogene. Science (New York, N.Y.). 230: 1132-9. PMID 2999974 DOI: 10.1126/Science.2999974 |
0.435 |
|
| 1985 |
Münke M, Martinville Bd, Francke U, Lieber E, Opitz JM, Reynolds JF. Minute chromosomes replacing the Y chromosome carry Y-specific sequences by restriction fragment analysis and in situ hybridization. American Journal of Medical Genetics. 22: 361-374. PMID 2996350 DOI: 10.1002/Ajmg.1320220221 |
0.461 |
|
| 1985 |
Schechter AL, Hung MC, Vaidyanathan L, Weinberg RA, Yang-Feng TL, Francke U, Ullrich A, Coussens L. The neu gene: An erbB-homologous gene distinct from and unlinked to the gene encoding the EGF receptor Science. 229: 976-978. PMID 2992090 DOI: 10.1126/Science.2992090 |
0.439 |
|
| 1985 |
Yamamoto K, Floyd-Smith G, Francke U, Koch N, Lauer W, Dobberstein B, Schäfer R, Hämmerling GJ. The gene encoding the Ia-associated invariant chain is located on chromosome 18 in the mouse. Immunogenetics. 21: 83-90. PMID 2981770 DOI: 10.1007/Bf00372244 |
0.495 |
|
| 1985 |
Lindgren V, Ares M, Weiner AM, Francke U. Human genes for U2 small nuclear RNA map to a major adenovirus 12 modification site on chromosome 17 Nature. 314: 115-116. PMID 2579339 DOI: 10.1038/314115A0 |
0.494 |
|
| 1984 |
Francke U, de Martinville B, Coussens L, Ullrich A. The human gene for the beta subunit of nerve growth factor is located on the proximal short arm of chromosome 1. Science (New York, N.Y.). 222: 1248-51. PMID 6648531 DOI: 10.1126/Science.6648531 |
0.463 |
|
| 1984 |
Skovby F, Krassikoff N, Francke U. Assignment of the gene for cystathionine beta-synthase to human chromosome 21 in somatic cell hybrids. Human Genetics. 65: 291-294. PMID 6583157 DOI: 10.1007/Bf00286520 |
0.506 |
|
| 1984 |
George DL, Scott AF, de Martinville B, Francke U. Amplified DNA in Y1 mouse adrenal tumor cells: isolation of cDNAs complementary to an amplified c-Ki-ras gene and localization of homologous sequences to mouse chromosome 6. Nucleic Acids Research. 12: 2731-43. PMID 6546797 DOI: 10.1093/Nar/12.6.2731 |
0.427 |
|
| 1984 |
Francke U. Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease. Cytogenetic and Genome Research. 38: 298-307. PMID 6510024 DOI: 10.1159/000132078 |
0.32 |
|
| 1984 |
Lindgren V, de Martinville B, Horwich AL, Rosenberg LE, Francke U. Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus. Science (New York, N.Y.). 226: 698-700. PMID 6494904 DOI: 10.1126/Science.6494904 |
0.506 |
|
| 1984 |
Brissenden JE, Ullrich A, Francke U. Human chromosomal mapping of genes for insulin-like growth factors I and II and epidermal growth factor. Nature. 310: 781-784. PMID 6382023 DOI: 10.1038/310781A0 |
0.421 |
|
| 1984 |
Francke U, Brown MS, Goldstein JL. Assignment of the human gene for the low density lipoprotein receptor to chromosome 19: synteny of a receptor, a ligand, and a genetic disease. Proceedings of the National Academy of Sciences of the United States of America. 81: 2826-30. PMID 6326146 DOI: 10.1073/Pnas.81.9.2826 |
0.444 |
|
| 1984 |
Münke M, Lindgren V, de Martinville B, Francke U. Comparative analysis of mouse-human hybrids with rearranged chromosomes 1 by in situ hybridization and Southern blotting: high-resolution mapping of NRAS, NGFB, and AMY on human chromosome 1. Somatic Cell and Molecular Genetics. 10: 589-99. PMID 6209808 DOI: 10.1007/Bf01535224 |
0.545 |
|
| 1983 |
Pearson SJ, Tetri P, George DL, Francke U. Activation of human alpha 1-antitrypsin gene in rat hepatoma x human fetal liver cell hybrids depends on presence of human chromosome 14. Somatic Cell Genetics. 9: 567-92. PMID 6604949 DOI: 10.1007/Bf01574259 |
0.475 |
|
| 1983 |
Martinville Bd, Cunningham JM, Murray MJ, Francke U. The N-ras oncogene assigned to the short arm of human chromosome 1 Nucleic Acids Research. 11: 5267-5275. PMID 6576326 DOI: 10.1093/Nar/11.15.5267 |
0.454 |
|
| 1983 |
Horwich A, Riccardi VM, Francke U, Opitz JM. Aqueductal stenosis leading to hydrocephalus—an unusual manifestation of neurofibromatosis American Journal of Medical Genetics. 14: 577-581. PMID 6407319 DOI: 10.1002/Ajmg.1320140322 |
0.309 |
|
| 1983 |
Martinville Bd, Francke U. The c-Ha-ras1, insulin and beta-globin loci map outside the deletion associated with aniridia-Wilms' tumour. Nature. 305: 641-643. PMID 6312329 DOI: 10.1038/305641A0 |
0.465 |
|
| 1983 |
de Martinville B, Giacalone J, Shih C, Weinberg RA, Francke U. Oncogene from human EJ bladder carcinoma is located on the short arm of chromosome 11 Science. 219: 498-501. PMID 6297001 DOI: 10.1126/Science.6297001 |
0.437 |
|
| 1983 |
Vora S, Miranda AF, Hernandez E, Francke U. Regional assignment of the human gene for platelet-type phosphofructokinase (PFKP) to chromosome 10p: novel use of polyspecific rodent antisera to localize human enzyme genes Human Genetics. 63: 374-379. PMID 6222962 DOI: 10.1007/Bf00274765 |
0.523 |
|
| 1983 |
Francke U, Foellmer BE, Haynes BF. Chromosome mapping of human cell surface molecules: Monoclonal anti-human lymphocyte antibodies 4F2, A3D8, and A1G3 define antigens controlled by different regions of chromosome 11 Somatic Cell and Molecular Genetics. 9: 333-344. PMID 6190235 DOI: 10.1007/Bf01539142 |
0.463 |
|
| 1983 |
Cory S, Adams JM, Gerondakis SD, Miller JF, Gamble J, Wiener F, Spira J, Francke U. Fusion of DNA region to murine immunoglobulin heavy chain locus corresponds to plasmacytoma-associated chromosome translocation. The Embo Journal. 2: 213-216. DOI: 10.1002/J.1460-2075.1983.Tb01407.X |
0.481 |
|
| 1982 |
Taggart RT, Francke U. Mapping of polypeptide genes by two-dimensional gel electrophoresis of hybrid cell extracts. Cytogenetics and Cell Genetics. 32: 99-110. PMID 7140373 DOI: 10.1159/000131690 |
0.533 |
|
| 1982 |
Haseltine FP, Lynch VA, van Dyke DL, Breg WR, Francke U. H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesis American Journal of Medical Genetics. 13: 115-123. PMID 7137226 DOI: 10.1002/Ajmg.1320130203 |
0.431 |
|
| 1982 |
Hershfield MS, Francke U. The human genes for S-adenosylhomocysteine hydrolase and adenosine deaminase are syntenic on chromosome 20 Science. 216: 739-742. PMID 7079734 DOI: 10.1126/Science.7079734 |
0.489 |
|
| 1982 |
Francke U, De Martinville B, D'Eustachio P, Ruddle FH. Comparative gene mapping: murine lambda light chain genes are located in region cen to B5 of mouse chromosome 16 not homologous to human chromosome 21. Cytogenetics and Cell Genetics. 33: 267-71. PMID 6813029 DOI: 10.1159/000131769 |
0.5 |
|
| 1982 |
Page D, de Martinville B, Barker D, Wyman A, White R, Francke U, Botstein D. Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 79: 5352-6. PMID 6291041 DOI: 10.1073/Pnas.79.17.5352 |
0.484 |
|
| 1982 |
Francke U, Francke B. Requirement of the human chromosome 11 long arm for replication of herpes simplex virus type 1 in nonpermissive Chinese hamster x human diploid fibroblast hybrids. Somatic Cell and Molecular Genetics. 7: 171-191. PMID 6270835 DOI: 10.1007/Bf01567656 |
0.463 |
|
| 1982 |
Vora S, Durham S, de Martinville B, George DL, Francke U. Assignment of the human gene for muscle-type phosphofructokinase (PFKM) to chromosome 1 (region cen leads to q32) using somatic cell hybrids and monoclonal anti-M antibody. Somatic Cell Genetics. 8: 95-104. PMID 6213050 DOI: 10.1007/Bf01538653 |
0.516 |
|
| 1981 |
Puck SM, Haseltine FP, Francke U. Absence of H-Y antigen in an XY female with campomelic dysplasia. Human Genetics. 57: 23-27. PMID 7196381 DOI: 10.1007/Bf00271161 |
0.371 |
|
| 1981 |
Vora S, Francke U. Assignment of the human gene for liver-type 6-phosphofructokinase isozyme (PFKL) to chromosome 21 by using somatic cell hybrids and monoclonal anti-L antibody Proceedings of the National Academy of Sciences of the United States of America. 78: 3738-3742. PMID 6455664 DOI: 10.1073/Pnas.78.6.3738 |
0.435 |
|
| 1981 |
George DL, Phillips JA, Francke U, Seeburg PH. The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21 to qter. Human Genetics. 57: 138-41. PMID 6262212 DOI: 10.1007/Bf00282009 |
0.508 |
|
| 1981 |
Francke U, Tetri P, Taggart RT, Oliver N. Conserved autosomal syntenic group on mouse (MMU) chromosome 15 and human (HSA) chromosome 22: Assignment of a gene for arylsulfatase A to MMU 15 and regional mapping of DIAl, ARSA, and ACO2 on HSA 22 Cytogenetic and Genome Research. 31: 58-69. PMID 6118238 DOI: 10.1159/000131626 |
0.544 |
|
| 1981 |
Pintar J, Barbosa J, Francke U, Castiglione C, Hawkins M, Breakefield X. Gene for monoamine oxidase type A assigned to the human X chromosome. The Journal of Neuroscience. 1: 166-175. DOI: 10.1523/Jneurosci.01-02-00166.1981 |
0.501 |
|
| 1981 |
Vora S, Francke U. 769 Assignment Of The Human Gene For Liver Type Phospho-Fructokinase Isozyme To Chromosome 21 Using Somatic Cell Hybrids Pediatric Research. 15: 570-570. DOI: 10.1203/00006450-198104001-00793 |
0.487 |
|
| 1981 |
Martinville BD, Wyman AR, White R, Francke U. 710 Assignment Of The First Highly Polymorphic Dna Marker Locus To A Human Chromosome Region Pediatric Research. 15: 560-560. DOI: 10.1203/00006450-198104001-00733 |
0.456 |
|
| 1981 |
Berenson R, Francke U, Dolnick B, Bertino J. Karyotypic analysis of methotrexate-resistant and sensitive mouse L5178Y cells Cytogenetic and Genome Research. 29: 143-152. DOI: 10.1159/000131563 |
0.378 |
|
| 1980 |
Blumberg B, Moore R, Mohandas T, Francke U. Partial 3q trisomy due to an unbalanced 3/10 translocation. American Journal of Medical Genetics. 7: 335-339. PMID 7468658 DOI: 10.1002/Ajmg.1320070315 |
0.382 |
|
| 1980 |
Harrod MJE, Byrne JB, Dev VG, Francke U. Duplication 12q mosaicism in two unrelated patients with similar syndrome American Journal of Medical Genetics. 7: 123-129. PMID 7468644 DOI: 10.1002/Ajmg.1320070206 |
0.492 |
|
| 1980 |
Francke U, Gehring U. Chromosome assignment of a murine glucocorticoid receptor gene (Grl-1) using intraspecies somatic cell hybrids Cell. 22: 657-664. PMID 7460010 DOI: 10.1016/0092-8674(80)90541-3 |
0.471 |
|
| 1980 |
Sanders-Haigh L, Anderson WF, Francke U. The β-globin gene is on the short arm of human chromosome 11 Nature. 283: 683-686. PMID 7354859 DOI: 10.1038/283683A0 |
0.52 |
|
| 1980 |
Halaban R, Nordlund J, Francke U, Moellmann G, Eisenstadt JM. Supermelanotic hybrids derived from mouse melanomas and normal mouse cells. Somatic Cell and Molecular Genetics. 6: 29-44. PMID 6768142 DOI: 10.1007/Bf01538694 |
0.353 |
|
| 1980 |
Riccardi VM, Hittner HM, Francke U, Yunis JJ, Ledbetter D, Borges W. The aniridia-Wilms tumor association: The critical role of chromosome band 11p13☆ Cancer Genetics and Cytogenetics. 2: 131-137. DOI: 10.1016/0165-4608(80)90056-4 |
0.366 |
|
| 1979 |
Francke U, Brown MG, Jones KL. Immediate chromosome diagnosis on bone marrow cells: An aid to management of the malformed newborn infant The Journal of Pediatrics. 94: 289-292. PMID 762626 DOI: 10.1016/S0022-3476(79)80846-X |
0.394 |
|
| 1979 |
Bakay B, Nissinen E, Sweetman L, Francke U, Nyhan WL. Utilization of purines by an HPRT variant in an intelligent, nonmutilative patient with features of the Lesch-Nyhan syndrome. Pediatric Research. 13: 1365-1370. PMID 523196 DOI: 10.1203/00006450-197912000-00013 |
0.311 |
|
| 1979 |
Jeffreys AJ, Craig IW, Francke U. Localisation of the G gamma-, A gamma-, delta- and beta-globin genes on the short arm of human chromosome 11. Nature. 281: 606-8. PMID 492329 DOI: 10.1038/281606A0 |
0.51 |
|
| 1979 |
Hustinx TWJ, Nabben FAE, Scheres JMJC, Francke U. Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6. American Journal of Medical Genetics. 3: 353-358. PMID 474635 DOI: 10.1002/Ajmg.1320030406 |
0.452 |
|
| 1979 |
Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Catalog of mapped human gene markers Cytogenetic and Genome Research. 25: 3-8. PMID 295267 DOI: 10.1159/000131393 |
0.402 |
|
| 1979 |
Hittner HM, Riccardi VM, Francke U. Aniridia caused by a heritable chromosome 11 deletion Ophthalmology. 86: 1173-1183. PMID 230439 DOI: 10.1016/S0161-6420(79)35425-2 |
0.461 |
|
| 1979 |
Brown S, Oie HK, Gazdar AF, Minna JD, Francke U. Requirement of human chromosomes 19, 6 and possibly 3 for infection of hamster × human hybrid cells with baboon M7 type C virus Cell. 18: 135-143. PMID 228859 DOI: 10.1016/0092-8674(79)90362-3 |
0.458 |
|
| 1979 |
Francke U, Holmes LB, Atkins L, Riccardi VM. Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13. Cytogenetics and Cell Genetics. 24: 185-92. PMID 225131 DOI: 10.1159/000131375 |
0.45 |
|
| 1978 |
Lalley PA, Francke U, Minna JD. Comparative gene mapping in man and mouse: assignment of the genes for lactate dehydrogenase-A, peptidase-D, and isocitrate dehydrogenase-2 to mouse chromosome 7. Cytogenetic and Genome Research. 22: 577-580. PMID 752544 DOI: 10.1159/000131027 |
0.479 |
|
| 1978 |
Lalley PA, Francke U, Minna JD. Comparative gene mapping: the linkage relationships of the homologous genes for Phosphoglucomutase and peptidase S are conserved in man and mouse Cytogenetic and Genome Research. 22: 573-576. PMID 752543 DOI: 10.1159/000131026 |
0.412 |
|
| 1978 |
Lalley PA, Francke U, Minna JD. Assignment of the genes coding for pyrophosphatase and hexokinase-1 to mouse chromosome 10: implications for comparative gene mapping in man and mouse Cytogenetic and Genome Research. 22: 570-572. PMID 752542 DOI: 10.1159/000131025 |
0.481 |
|
| 1978 |
Francke U. Hageman (factor XII) locus on 7q?: report of a second case with del(7)q35 and normal factor XII level. Human Genetics. 45: 363-367. PMID 738736 DOI: 10.1007/Bf00278736 |
0.337 |
|
| 1978 |
Francke U, Oliver N. Quantitative analysis of high-resolution trypsin-Giemsa bands on human prometaphase chromosomes Human Genetics. 45: 137-165. PMID 738718 DOI: 10.1007/Bf00286957 |
0.413 |
|
| 1978 |
Zabel BU, Baumann WA, Pirntke W, Gerhard‐Ratschow K, Francke U. X-inactivation pattern in three cases of X/autosome translocation. American Journal of Medical Genetics. 1: 309-317. PMID 677170 DOI: 10.1002/Ajmg.1320010307 |
0.352 |
|
| 1978 |
Lalley PA, Minna JD, Francke U. Conservation of autosomal gene synteny groups in mouse and man Nature. 274: 160-163. PMID 662012 DOI: 10.1038/274160A0 |
0.553 |
|
| 1978 |
Taylor KM, Francke U, Brown MG, George DL, Kaufhold M. Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q. American Journal of Medical Genetics. 1: 3-19. PMID 610424 DOI: 10.1002/Ajmg.1320010103 |
0.5 |
|
| 1978 |
George DL, Francke U. Regional mapping of human genes for hexosaminidase B and diphtheria toxin sensitivity on chromosome 5 using mouse X human hybrid cells. Somatic Cell Genetics. 3: 629-38. PMID 601683 DOI: 10.1007/Bf01539070 |
0.502 |
|
| 1978 |
Francke U, George DL, Brown MG, Riccardi VM. Gene dose effect: intraband mapping of the LDH A locus using cells from four individuals with different interstitial deletions of 11p. Cytogenetics and Cell Genetics. 19: 197-207. PMID 598250 DOI: 10.1159/000130809 |
0.4 |
|
| 1978 |
Minna JD, Bruns GAP, Krinsky AH, Lalley PA, Francke U, Gerald PS. Assignment of a Mus musculus gene for triosephosphate isomerase to chromosome 6 and for glyoxalase-I to chromosome 17 using somatic cell hybrids. Somatic Cell and Molecular Genetics. 4: 241-252. PMID 566476 DOI: 10.1007/Bf01538988 |
0.535 |
|
| 1978 |
Oie HK, Gazdar AF, Lalley PA, Russell EK, Minna JD, Delarco J, Todaro GJ, Francke U. Mouse chromosome 5 codes for ecotropic murine leukaemia virus cell-surface receptor Nature. 274: 60-62. PMID 566388 DOI: 10.1038/274060A0 |
0.402 |
|
| 1978 |
Francke U, Denney RM, Ruddle FH. Intrachromosomal gene mapping in man: the gene for tryptophyl-tRNA synthetase maps in region q21 leads to qter of chromosome 14. Somatic Cell Genetics. 3: 381-9. PMID 564085 DOI: 10.1007/Bf01542967 |
0.551 |
|
| 1978 |
Brown S, Oie H, Francke U, Gazdar AF, Minna JD. Assignment of a gene required for infection with endogenous baboon virus to human chromosome 19. Cytogenetic and Genome Research. 22: 239-242. PMID 222542 DOI: 10.1159/000130945 |
0.443 |
|
| 1978 |
Lalley PA, Francke U, Minna JD. Homologous genes for enolase, phosphogluconate dehydrogenase, phosphoglucomutase, and adenylate kinase are syntenic on mouse chromosome 4 and human chromosome 1p. Proceedings of the National Academy of Sciences of the United States of America. 75: 2382-2386. PMID 209463 DOI: 10.1073/Pnas.75.5.2382 |
0.554 |
|
| 1978 |
George DL, Francke U. Regional mapping on human genes for phosphoglucomutase-1 on chromosome 1 and beta-glucuronidase on chromosome 7 using mouse x human hybrids. Human Heredity. 28: 161-70. PMID 206510 DOI: 10.1159/000152957 |
0.544 |
|
| 1978 |
Oliver N, Francke U, Pellegrino MA. Regional assignment of genes for mannose phosphate isomerase, pyruvate kinase-3, and beta 2-microglobulin expression on human chromosome 15 by hybridization of cells from a t(15;22) (q14;q13.3) translocation carrier. Cytogenetic and Genome Research. 22: 506-510. PMID 88301 DOI: 10.1159/000131009 |
0.476 |
|
| 1978 |
Oliver N, Francke U, Taylor KM. Silver staining studies on the short arm variant of human chromosome 17. Human Genetics. 42: 79-82. PMID 77246 DOI: 10.1007/Bf00291628 |
0.454 |
|
| 1977 |
Francke U, Arias DE, Nyhan WL. Proximal 4p-deletion: Phenotype differs from classical 4p-syndrome The Journal of Pediatrics. 90: 250-252. PMID 830918 DOI: 10.1016/S0022-3476(77)80642-2 |
0.316 |
|
| 1977 |
George DL, Francke U. Gene dose effect: regional mapping of human nuceloside phosphorylase on chromosome 14. Science (New York, N.Y.). 194: 851-2. PMID 824731 DOI: 10.1126/Science.824731 |
0.51 |
|
| 1977 |
Francke U, Pellegrino MA. Assignment of the major histocompatibility complex to a region of the short arm of human chromosome 6 Proceedings of the National Academy of Sciences of the United States of America. 74: 1147-1151. PMID 265561 DOI: 10.1073/Pnas.74.3.1147 |
0.502 |
|
| 1977 |
Francke U, Lalley PA, Moss W, Ivy J, Minna JD. Gene mapping in Mus musculus by interspecific cell hybridization: assignment of the genes for tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2. Cytogenetic and Genome Research. 19: 57-84. PMID 198184 DOI: 10.1159/000130799 |
0.515 |
|
| 1977 |
Gazdar AF, Oie H, Lalley P, Moss WW, Minna JD, Francke U. Identification of mouse chromosomes required for murine leukemia virus replication Cell. 11: 949-956. PMID 196770 DOI: 10.1016/0092-8674(77)90306-3 |
0.463 |
|
| 1977 |
Francke U. Random X-Inactivation In A Female With An Interstitial Short Arm Deletion Of The X Chromosome Pediatric Research. 11: 455-455. DOI: 10.1203/00006450-197704000-00512 |
0.409 |
|
| 1977 |
Francke U. The 2p Partial Trisomy Syndrome-Reply Jama Pediatrics. 131: 1406-1406. DOI: 10.1001/Archpedi.1977.02120250087021 |
0.489 |
|
| 1976 |
Taylor KM, Wolfinger HL, Brown MG, Chadwick DL, Francke U. Partial trisomy 20p derived from a t(18;20) translocation Human Genetics. 34: 155-162. PMID 1002139 DOI: 10.1007/Bf00278884 |
0.314 |
|
| 1976 |
Francke U, Jones KL. The 2p Partial Trisomy Syndrome: Duplication of Region 2p23 → 2pter in Two Members of a t(2;7) Translocation Kindred American Journal of Diseases of Children. 130: 1244-1249. PMID 984008 DOI: 10.1001/Archpedi.1976.02120120078014 |
0.389 |
|
| 1976 |
Francke U. Retinoblastoma and chromosome 13. Cytogenetic and Genome Research. 16: 131-134. PMID 975871 DOI: 10.1159/000130573 |
0.469 |
|
| 1976 |
Francke U, Busby N, Shaw D, Hansen S, Brown MG. Intrachromosomal gene mapping in man: Assignment of nucleoside phosphorylase to region 14cen→14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation Somatic Cell and Molecular Genetics. 2: 27-40. PMID 829289 DOI: 10.1007/Bf01539240 |
0.487 |
|
| 1976 |
Minna JD, Lalley PA, Francke U. Comparative mapping using somatic cell hybrids In Vitro Cellular & Developmental Biology – Plant. 12: 726-733. PMID 828614 DOI: 10.1007/Bf02835447 |
0.506 |
|
| 1976 |
Francke U, Busby N, Shaw D, Hansen S, Brown MG. Assignment of the nucleoside phosphorylase (NP) gene locus to region 14pter→14q21 Cytogenetic and Genome Research. 16: 135-137. PMID 824099 DOI: 10.1159/000130574 |
0.32 |
|
| 1976 |
Buck DW, Bodmer WF, Bobrow M, Francke U. The gene for the species antigen on human chromosome 11 is on the short arm. Cytogenetic and Genome Research. 16: 97-98. PMID 61840 DOI: 10.1159/000130562 |
0.477 |
|
| 1976 |
George DL, Francke U, Biederman B, Bowen P, Aronson MM, Greene AE, Coriell LL, Rushton AR, Therman E, Kuhn EM, Rumpler Y, Dutrillaux B, Markvong A, Ward OG, Hsu TC, et al. International Standing Committee on Human Cytogenetic Nomenclature Cytogenetic and Genome Research. 17: 304-304. DOI: 10.1159/000130730 |
0.33 |
|
| 1975 |
Francke U, Busby N. Assignments of the human genes for lactate dehydrogenase-A and thymidine kinase to specific chromosomal regions. Cytogenetic and Genome Research. 14: 313-319. PMID 1192784 DOI: 10.1159/000130371 |
0.491 |
|
| 1975 |
Francke U, Benirschke K, Jones OW. Prenatal diagnosis of trisomy 9. Human Genetics. 29: 243-250. PMID 1165103 DOI: 10.1007/Bf00297630 |
0.311 |
|
| 1975 |
Francke U, Kernahan C, Bradshaw C. Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies. Human Genetics. 26: 343-351. PMID 1150232 DOI: 10.1007/Bf00285386 |
0.372 |
|
| 1975 |
Schuh B, Korf B, Francke U, Jones O, Moran M. Sex-Chromosome Abnormalities In Husbands And Wives The Lancet. 305: 333-334. DOI: 10.1016/S0140-6736(75)91240-4 |
0.448 |
|
| 1974 |
Schrott HG, Sakaguchi S, Francke U, Luzzatti L, Fialkow PJ. Translocation, t(4q−;13q+), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation Journal of Medical Genetics. 11: 201-205. PMID 4135220 DOI: 10.1136/Jmg.11.2.201 |
0.435 |
|
| 1973 |
Spence A, Francke U, Forsythe AB. Evidence against the peripheral location of the Y chromosome in human metaphase cells Cytogenetic and Genome Research. 12: 49-52. PMID 4707247 DOI: 10.1159/000130437 |
0.472 |
|
| 1973 |
Nesbitt MN, Francke U. A system of nomenclature for band patterns of mouse chromosomes Chromosoma. 41: 145-158. PMID 4120886 DOI: 10.1007/Bf00319691 |
0.477 |
|
| 1973 |
Francke U, Hammond DS, Schneider JA. The band patterns of twelve D 98/AH-2 marker chromosomes and their use for identification of intraspecific cell hybrids Chromosoma. 41: 111-121. PMID 4120821 DOI: 10.1007/Bf00284079 |
0.488 |
|
| 1972 |
Lerner RA, Jensen F, Kennel SJ, Dixon FJ, Des Roches G, Francke U. Karyotypic, virologic, and immunologic analyses of two continuous lymphocyte lines established from New Zealand black mice: possible relationship of chromosomal mosaicism to autoimmunity. Proceedings of the National Academy of Sciences of the United States of America. 69: 2965-9. PMID 4342970 DOI: 10.1073/Pnas.69.10.2965 |
0.35 |
|
| 1971 |
Francke U, Nesbitt M. Cattanach's Translocation: Cytological Characterization by Quinacrine Mustard Staining Proceedings of the National Academy of Sciences of the United States of America. 68: 2918-2920. PMID 5289234 DOI: 10.1073/Pnas.68.12.2918 |
0.464 |
|
| 1971 |
Francke U, Nesbitt M. Identification of the mouse chromosomes by quinacrine mustard staining. Cytogenetic and Genome Research. 10: 356-366. PMID 4109887 DOI: 10.1159/000130154 |
0.416 |
|
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