| Year |
Citation |
Score |
| 2021 |
Crittenden JR, Zhai S, Sauvage M, Kitsukawa T, Burguière E, Thomsen M, Zhang H, Costa C, Martella G, Ghiglieri V, Picconi B, Pescatore KA, Unterwald EM, Jackson WS, Housman DE, et al. CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors. Neurobiology of Disease. 105473. PMID 34371144 DOI: 10.1016/j.nbd.2021.105473 |
0.668 |
|
| 2021 |
Crittenden JR, Gipson TA, Smith AC, Bowden HA, Yildirim F, Fischer KB, Yim M, Housman DE, Graybiel AM. Striatal transcriptome changes linked to drug-induced repetitive behaviors. The European Journal of Neuroscience. PMID 33759265 DOI: 10.1111/ejn.15116 |
0.683 |
|
| 2018 |
Wang ET, Treacy D, Eichinger K, Struck A, Estabrook J, Olafson H, Wang TT, Bhatt K, Westbrook T, Sedehizadeh S, Ward A, Day J, Brook D, Berglund JA, Cooper T, ... Housman D, et al. Transcriptome alterations in myotonic dystrophy skeletal muscle and heart. Human Molecular Genetics. PMID 30561649 DOI: 10.1093/Hmg/Ddy432 |
0.653 |
|
| 2018 |
Fratta P, Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Brito-Armas JM, Kalmar B, Ule A, Yu Y, Birsa N, Bodo C, Collins T, Conicella AE, Mejia Maza A, ... ... Housman DE, et al. Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. The Embo Journal. PMID 29764981 DOI: 10.15252/Embj.201798684 |
0.482 |
|
| 2018 |
Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Kalmar B, Wang E, Housman D, Baralle F, Greensmith L, Buratti E, Plagnol V, Fisher EMC, Arozena AA, Fratta P. Dissecting TDP-43 gain- and loss-of-function in neurodegeneration Neuromuscular Disorders. 28. DOI: 10.1016/S0960-8966(18)30366-3 |
0.464 |
|
| 2017 |
McGinty RJ, Puleo F, Aksenova AY, Hisey JA, Shishkin AA, Pearson EL, Wang ET, Housman DE, Moore C, Mirkin SM. A Defective mRNA Cleavage and Polyadenylation Complex Facilitates Expansions of Transcribed (GAA)n Repeats Associated with Friedreich's Ataxia. Cell Reports. 20: 2490-2500. PMID 28877480 DOI: 10.1016/J.Celrep.2017.08.051 |
0.481 |
|
| 2017 |
Sivakumar P, Humphrey J, Ule A, Bodo C, Emmett W, Ricketts T, Oliveira H, Wang E, Housman D, Greensmith L, Buratti E, Baralle F, Plagnol V, Acevedo-Arozena A, Fisher E, et al. Investigating dysfunctional RNA processing in TDP-43 mouse mutants Neuromuscular Disorders. 27: S32. DOI: 10.1016/S0960-8966(17)30314-0 |
0.497 |
|
| 2016 |
Crittenden JR, Tillberg PW, Riad MH, Shima Y, Gerfen CR, Curry J, Housman DE, Nelson SB, Boyden ES, Graybiel AM. Striosome-dendron bouquets highlight a unique striatonigral circuit targeting dopamine-containing neurons. Proceedings of the National Academy of Sciences of the United States of America. PMID 27647894 DOI: 10.1073/Pnas.1613337113 |
0.661 |
|
| 2014 |
Bugiardini E, Meola G, Alvarez C, Angeard N, Bassez G, Day JW, Dent G, Ekström AB, Eymard B, Fossati B, Gagnon C, Gomes-Pereira M, Gourdon G, Heatwole C, Housman DE, et al. Consensus on cerebral involvement in myotonic dystrophy. Workshop report: May 24-27, 2013, Ferrere (AT), Italy Neuromuscular Disorders. 24: 445-452. PMID 24613228 DOI: 10.1016/J.Nmd.2014.01.013 |
0.394 |
|
| 2013 |
Gipson TA, Neueder A, Wexler NS, Bates GP, Housman D. Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis. Rna Biology. 10: 1647-52. PMID 24256709 DOI: 10.4161/rna.26706 |
0.336 |
|
| 2013 |
van Blitterswijk M, Wang ET, Friedman BA, Keagle PJ, Lowe P, Leclerc AL, van den Berg LH, Housman DE, Veldink JH, Landers JE. Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq. Plos One. 8: e60788. PMID 23577159 DOI: 10.1371/Journal.Pone.0060788 |
0.497 |
|
| 2012 |
Wang ET, Cody NA, Jog S, Biancolella M, Wang TT, Treacy DJ, Luo S, Schroth GP, Housman DE, Reddy S, Lécuyer E, Burge CB. Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins. Cell. 150: 710-24. PMID 22901804 DOI: 10.1016/J.Cell.2012.06.041 |
0.634 |
|
| 2012 |
Janas MM, Wang E, Love T, Harris AS, Stevenson K, Semmelmann K, Shaffer JM, Chen PH, Doench JG, Yerramilli SV, Neuberg DS, Iliopoulos D, Housman DE, Burge CB, Novina CD. Reduced expression of ribosomal proteins relieves microRNA-mediated repression. Molecular Cell. 46: 171-86. PMID 22541556 DOI: 10.1016/J.Molcel.2012.04.008 |
0.603 |
|
| 2012 |
Parkesh R, Childs-Disney JL, Nakamori M, Kumar A, Wang E, Wang T, Hoskins J, Tran T, Housman D, Thornton CA, Disney MD. Design of a bioactive small molecule that targets the myotonic dystrophy type 1 RNA via an RNA motif-ligand database and chemical similarity searching. Journal of the American Chemical Society. 134: 4731-42. PMID 22300544 DOI: 10.1021/Ja210088V |
0.516 |
|
| 2010 |
Crittenden JR, Dunn DE, Merali FI, Woodman B, Yim M, Borkowska AE, Frosch MP, Bates GP, Housman DE, Lo DC, Graybiel AM. CalDAG-GEFI down-regulation in the striatum as a neuroprotective change in Huntington's disease. Human Molecular Genetics. 19: 1756-65. PMID 20147317 DOI: 10.1093/Hmg/Ddq055 |
0.679 |
|
| 2009 |
Weiss A, Abramowski D, Bibel M, Bodner R, Chopra V, DiFiglia M, Fox J, Kegel K, Klein C, Grueninger S, Hersch S, Housman D, Régulier E, Rosas HD, Stefani M, et al. Single-step detection of mutant huntingtin in animal and human tissues: a bioassay for Huntington's disease. Analytical Biochemistry. 395: 8-15. PMID 19664996 DOI: 10.1016/J.Ab.2009.08.001 |
0.304 |
|
| 2009 |
Brocklebank D, Gayán J, Andresen JM, Roberts SA, Young AB, Snodgrass SR, Penney JB, Ramos-Arroyo MA, Cha JJ, Rosas HD, Hersch SM, Feigin A, Cherny SS, Wexler NS, Housman DE, et al. Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 425-9. PMID 18712713 DOI: 10.1002/Ajmg.B.30826 |
0.518 |
|
| 2008 |
Gayán J, Brocklebank D, Andresen JM, Alkorta-Aranburu G, Zameel Cader M, Roberts SA, Cherny SS, Wexler NS, Cardon LR, Housman DE. Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genetic Epidemiology. 32: 445-53. PMID 18481795 DOI: 10.1002/Gepi.20317 |
0.552 |
|
| 2007 |
Bergmeier W, Goerge T, Wang HW, Crittenden JR, Baldwin AC, Cifuni SM, Housman DE, Graybiel AM, Wagner DD. Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III. The Journal of Clinical Investigation. 117: 1699-707. PMID 17492052 DOI: 10.1172/Jci30575 |
0.672 |
|
| 2007 |
Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/J.1469-1809.2006.00335.X |
0.591 |
|
| 2007 |
Andresen JM, Gayán J, Cherny SS, Brocklebank D, Alkorta-Aranburu G, Addis EA, Cardon LR, Housman DE, Wexler NS. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. Journal of Medical Genetics. 44: 44-50. PMID 17018562 DOI: 10.1136/Jmg.2006.045153 |
0.511 |
|
| 2007 |
Goerge T, Bergmeier W, Wang H, Crittenden J, Baldwin A, Cifuni S, Housman D, Graybiel A, Wagner D. CALDAG-GEFI-DEFICIENCY CAUSES IMPAIRED BETA1, BETA2, AND BETA3 INTEGRIN ACTIVATION IN NEUTROPHILS AND PLATELETS: A MODEL FOR LEUKOCYTE ADHESION DEFICIENCY-III (LAD-III) Journal of Thrombosis and Haemostasis. 5: P-T-278-P-T-278. DOI: 10.1111/J.1538-7836.2007.Tb02036.X |
0.648 |
|
| 2004 |
Crittenden JR, Bergmeier W, Zhang Y, Piffath CL, Liang Y, Wagner DD, Housman DE, Graybiel AM. CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation. Nature Medicine. 10: 982-6. PMID 15334074 DOI: 10.1038/Nm1098 |
0.662 |
|
| 2004 |
Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayán J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, ... ... Housman DE, et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America. 101: 3498-503. PMID 14993615 DOI: 10.1073/Pnas.0308679101 |
0.602 |
|
| 2004 |
Bergmeier W, Crittenden JR, Piffath CL, Wagner DD, Housman DE, Graybiel AM. CalDAG-GEFI Is a Key Signal Integrator in Platelet Activation and Thrombus Formation. Blood. 104: 326-326. DOI: 10.1182/Blood.V104.11.326.326 |
0.675 |
|
| 2004 |
Crittenden JR, Bergmeier W, Zhang Y, Piffath CL, Liang Y, Wagner DD, Housman DE, Graybiel AM. Erratum: CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation Nature Medicine. 10: 1139-1139. DOI: 10.1038/Nm1004-1139A |
0.643 |
|
| 2003 |
Charest A, Lane K, McMahon K, Park J, Preisinger E, Conroy H, Housman D. Fusion of FIG to the receptor tyrosine kinase ROS in a glioblastoma with an interstitial del(6)(q21q21). Genes, Chromosomes & Cancer. 37: 58-71. PMID 12661006 DOI: 10.1002/Gcc.10207 |
0.313 |
|
| 2003 |
Alberta JA, Springett GM, Rayburn H, Natoli TA, Loring J, Kreidberg JA, Housman D. Role of the WT1 tumor suppressor in murine hematopoiesis. Blood. 101: 2570-4. PMID 12468434 DOI: 10.1182/blood-2002-06-1656 |
0.318 |
|
| 2002 |
Dash AB, Williams IR, Kutok JL, Tomasson MH, Anastasiadou E, Lindahl K, Li S, Van Etten RA, Borrow J, Housman D, Druker B, Gilliland DG. A murine model of CML blast crisis induced by cooperation between BCR/ABL and NUP98/HOXA9. Proceedings of the National Academy of Sciences of the United States of America. 99: 7622-7. PMID 12032333 DOI: 10.1073/Pnas.102583199 |
0.3 |
|
| 2001 |
Ten Asbroek AL, Olsen J, Housman D, Baas F, Stanton V. Genetic variation in mRNA coding sequences of highly conserved genes. Physiological Genomics. 5: 113-8. PMID 11285364 DOI: 10.1152/Physiolgenomics.2001.5.3.113 |
0.333 |
|
| 2000 |
Volkert MR, Elliott NA, Housman DE. Functional genomics reveals a family of eukaryotic oxidation protection genes. Proceedings of the National Academy of Sciences of the United States of America. 97: 14530-5. PMID 11114193 DOI: 10.1073/pnas.260495897 |
0.324 |
|
| 2000 |
Chattopadhyay S, Kaul R, Charest A, Housman D, Chen J. SMAR1, a novel, alternatively spliced gene product, binds the Scaffold/Matrix-associated region at the T cell receptor beta locus. Genomics. 68: 93-6. PMID 10950932 DOI: 10.1006/geno.2000.6279 |
0.32 |
|
| 1999 |
Kazantsev A, Preisinger E, Dranovsky A, Goldgaber D, Housman D. Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 96: 11404-9. PMID 10500189 DOI: 10.1073/Pnas.96.20.11404 |
0.311 |
|
| 1999 |
Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V, Taylor K, Cameron J, Munroe D, Johansson J, et al. Molecular genetic characterisation of frontotemporal dementia on chromosome 3. Dementia and Geriatric Cognitive Disorders. 10: 93-101. PMID 10436350 DOI: 10.1159/000051222 |
0.334 |
|
| 1999 |
Hunter K, Greenwood J, Yang YL, Cunningham JM, Birren B, Housman D. An integrated somatic cell hybrid, YAC, and BAC map of the Rmc1 region of mouse chromosome 1. Genomics. 58: 318-22. PMID 10373331 DOI: 10.1006/geno.1999.5841 |
0.335 |
|
| 1998 |
Nichols KE, Harkin DP, Levitz S, Krainer M, Kolquist KA, Genovese C, Bernard A, Ferguson M, Zuo L, Snyder E, Buckler AJ, Wise C, Ashley J, Lovett M, Valentine MB, ... ... Housman DE, et al. Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome. Proceedings of the National Academy of Sciences of the United States of America. 95: 13765-70. PMID 9811875 DOI: 10.1073/Pnas.95.23.13765 |
0.482 |
|
| 1998 |
Heesen M, Berman MA, Charest A, Housman D, Gerard C, Dorf ME. Cloning and chromosomal mapping of an orphan chemokine receptor: mouse RDC1. Immunogenetics. 47: 364-70. PMID 9510554 DOI: 10.1007/S002510050371 |
0.311 |
|
| 1998 |
Das M, Chu LL, Ghahremani M, Abrams-Ogg T, Roy MS, Housman D, Pelletier J. Characterization of an abundant short interspersed nuclear element (SINE) present in Canis familiaris. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 64-9. PMID 9434948 DOI: 10.1007/S003359900681 |
0.305 |
|
| 1997 |
Haluska FG, Thiele C, Goldstein A, Tsao H, Benoit EP, Housman D. Lack of phospholipase A2 mutations in neuroblastoma, melanoma and colon-cancer cell lines. International Journal of Cancer. Journal International Du Cancer. 72: 337-9. PMID 9219842 DOI: 10.1002/(SICI)1097-0215(19970717)72:2<337::AID-IJC22>3.0.CO;2-B |
0.325 |
|
| 1997 |
Beckers MC, Ernst E, Diez E, Morissette C, Gervais F, Hunter K, Housman D, Yoshida S, Skamene E, Gros P. High-resolution linkage map of mouse chromosome 13 in the vicinity of the host resistance locus Lgn1. Genomics. 39: 254-63. PMID 9119362 DOI: 10.1006/Geno.1996.4489 |
0.329 |
|
| 1996 |
Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36. Human Molecular Genetics. 5: 1667-72. PMID 8894705 |
0.527 |
|
| 1996 |
Dackowski WR, Connors TD, Bowe AE, Stanton V, Housman D, Doggett NA, Landes GM, Klinger KW. The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. Genome Research. 6: 515-24. PMID 8828040 DOI: 10.1101/Gr.6.6.515 |
0.332 |
|
| 1996 |
Borrow J, Stanton VP, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE. The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nature Genetics. 14: 33-41. PMID 8782817 DOI: 10.1038/Ng0996-33 |
0.525 |
|
| 1995 |
Housman D. Human DNA polymorphism. The New England Journal of Medicine. 332: 318-20. PMID 7816069 DOI: 10.1056/NEJM199502023320508 |
0.316 |
|
| 1995 |
Liu J, Stanton VP, Fujiwara TM, Wang JX, Rezonzew R, Crumley MJ, Morgan K, Gros P, Housman D, Schurr E. Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach. Genomics. 26: 178-91. PMID 7601441 DOI: 10.1016/0888-7543(95)80199-V |
0.313 |
|
| 1995 |
Moffett P, Bruening W, Nakagama H, Bardeesy N, Housman D, Housman DE, Pelletier J. Antagonism of WT1 activity by protein self-association. Proceedings of the National Academy of Sciences of the United States of America. 92: 11105-9. PMID 7479946 DOI: 10.1073/Pnas.92.24.11105 |
0.327 |
|
| 1993 |
Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nature Genetics. 3: 36-43. PMID 8490651 DOI: 10.1038/Ng0193-36 |
0.768 |
|
| 1993 |
Haas M, Aburatani H, Stanton VP, Bhatt M, Housman D, Ward DC. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3. Genomics. 16: 90-6. PMID 8486389 DOI: 10.1006/Geno.1993.1145 |
0.321 |
|
| 1993 |
Park S, Schalling M, Bernard A, Maheswaran S, Shipley GC, Roberts D, Fletcher J, Shipman R, Rheinwald J, Demetri G, Griffin J, Minden M, Housman DE, Haber DA. The Wilms tumour gene WT1 is expressed in murine mesoderm-derived tissues and mutated in a human mesothelioma Nature Genetics. 4: 415-420. PMID 8401592 DOI: 10.1038/ng0893-415 |
0.461 |
|
| 1993 |
Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R. WT-1 is required for early kidney development. Cell. 74: 679-91. PMID 8395349 DOI: 10.1016/0092-8674(93)90515-R |
0.312 |
|
| 1993 |
Skare J, Wu B, Madan S, Pulijaal V, Purtilo D, Haber D, Nelson D, Sylla B, Grierson H, Nitowsky H, Glaser J, Wissink J, White B, Holden J, Housman D, et al. Characterization of three overlapping deletions causing X-linked lymphoproliferative disease Genomics. 16: 254-255. PMID 8387453 DOI: 10.1006/Geno.1993.1169 |
0.513 |
|
| 1993 |
Moir DT, Dorman TE, Xue F, Ma NS, Stanton VP, Housman D, Bowden DW, Noll WW, Mao J. Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products. Gene. 136: 177-83. PMID 7904972 DOI: 10.1016/0378-1119(93)90461-B |
0.331 |
|
| 1993 |
Church DM, Banks LT, Rogers AC, Graw SL, Housman DE, Gusella JF, Buckler AJ. Identification of human chromosome 9 specific genes using exon amplification. Human Molecular Genetics. 2: 1915-20. PMID 7506603 DOI: 10.1093/hmg/2.11.1915 |
0.418 |
|
| 1992 |
Oettinger MA, Stanger B, Schatz DG, Glaser T, Call K, Housman D, Baltimore D. The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice. Immunogenetics. 35: 97-101. PMID 1735560 DOI: 10.1007/Bf00189518 |
0.353 |
|
| 1992 |
Ambrose C, James M, Barnes G, Lin C, Bates G, Altherr M, Duyao M, Groot N, Church D, Wasmuth JJ, Lehrach H, Housman D, Buckler A, Gusella JF, MacDonald ME. A novel G protein-coupled receptor kinase gene cloned from 4p16.3 Human Molecular Genetics. 1: 697-703. PMID 1338872 DOI: 10.1093/Hmg/1.9.697 |
0.325 |
|
| 1992 |
Baird PN, Groves N, Haber DA, Housman DE, Cowell JK. Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome. Oncogene. 7: 2141-9. PMID 1331933 |
0.469 |
|
| 1992 |
Haber DA, Housman DE. The genetics of Wilms' tumor. Advances in Cancer Research. 59: 41-68. PMID 1325734 DOI: 10.1016/S0065-230X(08)60302-4 |
0.419 |
|
| 1992 |
Haber DA, Housman DE. Role of the WT1 gene in Wilms' tumour. Cancer Surveys. 12: 105-17. PMID 1322241 |
0.469 |
|
| 1992 |
Haber DA, Timmers HT, Pelletier J, Sharp PA, Housman DE. A dominant mutation in the Wilms tumor gene WT1 cooperates with the viral oncogene E1A in transformation of primary kidney cells. Proceedings of the National Academy of Sciences of the United States of America. 89: 6010-4. PMID 1321431 DOI: 10.1073/Pnas.89.13.6010 |
0.473 |
|
| 1992 |
Bruening W, Bardeesy N, Silverman BL, Cohn RA, Machin GA, Aronson AJ, Housman D, Pelletier J. Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. Nature Genetics. 1: 144-8. PMID 1302008 DOI: 10.1038/Ng0592-144 |
0.311 |
|
| 1991 |
Hunter K, Housman D, Hopkins N. Isolation and characterization of irradiation fusion hybrids from mouse chromosome 1 for mapping Rmc-1, a gene encoding a cellular receptor for MCF class murine retroviruses. Somatic Cell and Molecular Genetics. 17: 169-83. PMID 2011795 DOI: 10.1007/Bf01232974 |
0.328 |
|
| 1991 |
Cowell JK, Wadey RB, Haber DA, Call KM, Housman DE, Pritchard J. Structural rearrangements of the WT1 gene in Wilms' tumour cells. Oncogene. 6: 595-9. PMID 1851548 |
0.47 |
|
| 1991 |
Buckler AJ, Chang DD, Graw SL, Brook JD, Haber DA, Sharp PA, Housman DE. Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. Proceedings of the National Academy of Sciences of the United States of America. 88: 4005-9. PMID 1850845 DOI: 10.1073/Pnas.88.9.4005 |
0.476 |
|
| 1991 |
Haber DA, Housman DE. Rate-limiting steps: the genetics of pediatric cancers. Cell. 64: 5-8. PMID 1846091 DOI: 10.1016/0092-8674(91)90200-I |
0.364 |
|
| 1991 |
Doucette-Stamm LA, Riba L, Handelin B, Difilippantonio M, Ward DC, Wasmuth JJ, Gusella JF, Housman DE. Generation and characterization of irradiation hybrids of human chromosome 4. Somatic Cell and Molecular Genetics. 17: 471-80. PMID 1837181 DOI: 10.1007/Bf01233171 |
0.444 |
|
| 1991 |
Huff V, Miwa H, Haber DA, Call KM, Housman D, Strong LC, Saunders GF. Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. American Journal of Human Genetics. 48: 997-1003. PMID 1673293 |
0.484 |
|
| 1991 |
Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE. Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development. Molecular and Cellular Biology. 11: 1707-12. PMID 1671709 DOI: 10.1128/Mcb.11.3.1707 |
0.471 |
|
| 1991 |
Thompson LM, Plummer S, Schalling M, Altherr MR, Gusella JF, Housman DE, Wasmuth JJ. A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4. Genomics. 11: 1133-42. PMID 1664411 DOI: 10.1016/0888-7543(91)90041-C |
0.465 |
|
| 1991 |
Haber DA, Sohn RL, Buckler AJ, Pelletier J, Call KM, Housman DE. Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proceedings of the National Academy of Sciences of the United States of America. 88: 9618-22. PMID 1658787 DOI: 10.1073/Pnas.88.21.9618 |
0.485 |
|
| 1991 |
Schwartz CE, Haber DA, Stanton VP, Strong LC, Skolnick MH, Housman DE. Familial predisposition to Wilms tumor does not segregate with the WT1 gene. Genomics. 10: 927-30. PMID 1655633 DOI: 10.1016/0888-7543(91)90181-D |
0.449 |
|
| 1991 |
Pelletier J, Bruening W, Kashtan CE, Mauer SM, Manivel JC, Striegel JE, Houghton DC, Junien C, Habib R, Fouser L, Fine RN, Silverman BL, Haber DA, Housman D. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell. 67: 437-447. PMID 1655284 DOI: 10.1016/0092-8674(91)90194-4 |
0.496 |
|
| 1991 |
Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature. 353: 431-4. PMID 1654525 DOI: 10.1038/353431A0 |
0.479 |
|
| 1991 |
Davis LM, Zabel B, Senger G, Lüdecke HJ, Metzroth B, Call K, Housman D, Claussen U, Horsthemke B, Shows TB. A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. Genomics. 10: 588-92. PMID 1653761 DOI: 10.1016/0888-7543(91)90440-P |
0.32 |
|
| 1991 |
Pelletier J, Schalling M, Buckler AJ, Rogers A, Haber DA, Housman D. Expression of the Wilms' tumor gene WT1 in the murine urogenital system. Genes & Development. 5: 1345-56. PMID 1651275 DOI: 10.1101/Gad.5.8.1345 |
0.528 |
|
| 1991 |
Royer-Pokora B, Ragg S, Heckl-Ostreicher B, Held M, Loos U, Call K, Glaser T, Housman D, Saunders G, Zabel B. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare. Genes, Chromosomes & Cancer. 3: 89-100. PMID 1648959 DOI: 10.1002/Gcc.2870030203 |
0.317 |
|
| 1990 |
Warburton D, Gersen S, Yu MT, Jackson C, Handelin B, Housman D. Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. Genomics. 6: 358-66. PMID 2307476 DOI: 10.1016/0888-7543(90)90577-H |
0.334 |
|
| 1990 |
Lichter P, Tang CJ, Call K, Hermanson G, Evans GA, Housman D, Ward DC. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science (New York, N.Y.). 247: 64-9. PMID 2294592 DOI: 10.1126/Science.2294592 |
0.325 |
|
| 1990 |
Glaser T, Lane J, Housman D. A mouse model of the aniridia-Wilms tumor deletion syndrome. Science (New York, N.Y.). 250: 823-7. PMID 2173141 DOI: 10.1126/Science.2173141 |
0.346 |
|
| 1990 |
Pritchard-Jones K, Fleming S, Davidson D, Bickmore W, Porteous D, Gosden C, Bard J, Buckler A, Pelletier J, Housman D. The candidate Wilms' tumour gene is involved in genitourinary development. Nature. 346: 194-7. PMID 2164159 DOI: 10.1038/346194A0 |
0.356 |
|
| 1990 |
Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell. 61: 1257-69. PMID 2163761 DOI: 10.1016/0092-8674(90)90690-G |
0.49 |
|
| 1990 |
Glaser T, Rose E, Morse H, Housman D, Jones C. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex. Genomics. 6: 48-64. PMID 2154397 DOI: 10.1016/0888-7543(90)90447-3 |
0.374 |
|
| 1990 |
Arceci RJ, Baas F, Raponi R, Horwitz SB, Housman D, Croop JM. Multidrug resistance gene expression is controlled by steroid hormones in the secretory epithelium of the uterus. Molecular Reproduction and Development. 25: 101-9. PMID 1968749 DOI: 10.1002/mrd.1080250202 |
0.305 |
|
| 1989 |
Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Somatic Cell and Molecular Genetics. 15: 477-501. PMID 2595451 DOI: 10.1007/Bf01534910 |
0.364 |
|
| 1989 |
Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Genomics. 5: 880-93. PMID 2574149 DOI: 10.1016/0888-7543(89)90130-4 |
0.365 |
|
| 1989 |
Emanuel JR, Graw S, Housman D, Levenson R. Identification of a region within the Na,K-ATPase alpha subunit that contributes to differential ouabain sensitivity. Molecular and Cellular Biology. 9: 3744-9. PMID 2550800 DOI: 10.1128/Mcb.9.9.3744 |
0.433 |
|
| 1989 |
Haber DA, Housman DE. MspI/HpaII polymorphism in the human multidrug resistance gene 1. Nucleic Acids Research. 17: 10142. PMID 2481261 DOI: 10.1093/Nar/17.23.10142 |
0.415 |
|
| 1989 |
Croop JM, Raymond M, Haber D, Devault A, Arceci RJ, Gros P, Housman DE. The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues. Molecular and Cellular Biology. 9: 1346-50. PMID 2471060 DOI: 10.1128/Mcb.9.3.1346 |
0.46 |
|
| 1988 |
Geissler EN, Cheng SV, Gusella JF, Housman DE. Genetic analysis of the dominant white-spotting (W) region on mouse chromosome 5: identification of cloned DNA markers near W. Proceedings of the National Academy of Sciences of the United States of America. 85: 9635-9. PMID 3200849 |
0.452 |
|
| 1987 |
Housman D. Insertion of dominant selectable markers into the human genome. Somatic Cell and Molecular Genetics. 13: 441-6. PMID 3331833 DOI: 10.1007/Bf01534945 |
0.304 |
|
| 1987 |
Gerhard DS, Jones C, Morse HG, Handelin B, Weeks V, Housman D. Analysis of human chromosome 11 by somatic cell genetics: reexamination of derivatives of human-hamster cell line J1. Somatic Cell and Molecular Genetics. 13: 293-304. PMID 3331828 DOI: 10.1007/Bf01534923 |
0.358 |
|
| 1987 |
Kent RB, Emanuel JR, Ben Neriah Y, Levenson R, Housman DE. Ouabain resistance conferred by expression of the cDNA for a murine Na+, K+-ATPase alpha subunit. Science (New York, N.Y.). 237: 901-3. PMID 3039660 DOI: 10.1126/Science.3039660 |
0.54 |
|
| 1987 |
Weis JH, Seidman JG, Housman DE, Nelson DL. Eucaryotic chromosome transfer: production of a murine-specific cosmid library from a neor-linked fragment of murine chromosome 17. Molecular and Cellular Biology. 6: 441-51. PMID 3023847 DOI: 10.1128/MCB.6.2.441 |
0.348 |
|
| 1987 |
Kent RB, Fallows DA, Geissler E, Glaser T, Emanuel JR, Lalley PA, Levenson R, Housman DE. Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouse. Proceedings of the National Academy of Sciences of the United States of America. 84: 5369-73. PMID 2885848 DOI: 10.1073/Pnas.84.15.5369 |
0.494 |
|
| 1987 |
Fallows D, Kent RB, Nelson DL, Emanuel JR, Levenson R, Housman DE. Chromosome-mediated transfer of the murine Na,K-ATPase alpha subunit confers ouabain resistance. Molecular and Cellular Biology. 7: 2985-7. PMID 2823111 DOI: 10.1128/Mcb.7.8.2985 |
0.466 |
|
| 1985 |
van Den Elsen P, Bruns G, Gerhard DS, Pravtcheva D, Jones C, Housman D, Ruddle FA, Orkin S, Terhorst C. Assignment of the gene coding for the T-3-δ subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9 Proceedings of the National Academy of Sciences of the United States of America. 82: 2920-2924. PMID 3857625 DOI: 10.1073/Pnas.82.9.2920 |
0.313 |
|
| 1985 |
Wexler NS, Conneally PM, Housman D, Gusella JF. A DNA Polymorphism for Huntington's Disease Marks the Future Archives of Neurology. 42: 20-24. PMID 3155610 DOI: 10.1001/Archneur.1985.04060010026009 |
0.478 |
|
| 1984 |
Weis JH, Nelson DL, Przyborski MJ, Chaplin DD, Mulligan RC, Housman DE, Seidman JG. Eukaryotic chromosome transfer: linkage of the murine major histocompatibility complex to an inserted dominant selectable marker. Proceedings of the National Academy of Sciences of the United States of America. 81: 4879-83. PMID 6589632 DOI: 10.1073/Pnas.81.15.4879 |
0.366 |
|
| 1984 |
Levenson R, Racaniello V, Albritton L, Housman D. Molecular cloning of the mouse ouabain-resistance gene. Proceedings of the National Academy of Sciences of the United States of America. 81: 1489-93. PMID 6324196 DOI: 10.1073/Pnas.81.5.1489 |
0.538 |
|
| 1984 |
Minden M, Gusella J, Housman D. Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cells Blood. 64: 842-846. DOI: 10.1182/Blood.V64.4.842.Bloodjournal644842 |
0.497 |
|
| 1983 |
Housman D. Cloning in on the gene for Duchenne's muscular dystrophy Trends in Neurosciences. 6: 115-118. DOI: 10.1016/0166-2236(83)90060-7 |
0.314 |
|
| 1982 |
Gusella JF, Jones C, Kao FT, Housman D, Puck TT. Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 79: 7804-8. PMID 6961451 DOI: 10.1073/Pnas.79.24.7804 |
0.506 |
|
| 1982 |
Gusella JF, Tsiftsoglou AS, Volloch V, Weil SC, Neumann J, Housman DE. Dissociation of hemoglobin accumulation and commitment during murine erythroleukemia cell differentiation by treatment with imidazole. Journal of Cellular Physiology. 113: 179-85. PMID 6957412 DOI: 10.1002/JCP.1041130127 |
0.429 |
|
| 1982 |
Housman D, Kidd K, Gusella JF. Recombinant DNA approach to neurogenetic disorders Trends in Neurosciences. 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8 |
0.488 |
|
| 1981 |
Levenson R, Housman D. Commitment: how do cells make the decision to differentiate? Cell. 25: 5-6. PMID 7023699 DOI: 10.1016/0092-8674(81)90225-7 |
0.493 |
|
| 1981 |
Levenson R, Housman D. Erasure of the memory response in MEL cells. Developmental Biology. 86: 81-6. PMID 6974666 DOI: 10.1016/0012-1606(81)90317-1 |
0.503 |
|
| 1981 |
Housman D, Levenson R, Volloch V, Tsiftsoglou A, Gusella J, Parker D, Kernen J, Mitrani A, Weeks V, Witte O, Besmer P. Control of proliferation and differentiation in cells transformed by Friend virus. Cold Spring Harbor Symposia On Quantitative Biology. 1177-85. PMID 6933050 DOI: 10.1101/Sqb.1980.044.01.127 |
0.581 |
|
| 1981 |
Bridges K, Levenson R, Housman D, Cantley L. Calcium regulates the commitment of murine erythroleukemia cells to terminal erythroid differentiation. The Journal of Cell Biology. 90: 542-4. PMID 6793600 DOI: 10.1083/Jcb.90.2.542 |
0.514 |
|
| 1981 |
Bruns GAP, Gusella JF, Keys C, Housman D, Gerald PS. 704 ISOLATION OF DNA SEGMENTS FROM THE HUMAN X CHROMOSOME Pediatric Research. 15: 559-559. DOI: 10.1203/00006450-198104001-00727 |
0.48 |
|
| 1980 |
Gusella JF, Keys C, VarsanyiBreiner A, Kao FT, Jones C, Puck TT, Housman D. Isolation and localization of DNA segments from specific human chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 77: 2829-33. PMID 6930670 DOI: 10.1073/Pnas.77.5.2829 |
0.504 |
|
| 1980 |
Levenson R, Kernen J, Mitrani A, Housman D. DNA synthesis is not required for the commitment of murine erythroleukemia cells. Developmental Biology. 74: 224-30. PMID 6444216 DOI: 10.1016/0012-1606(80)90064-0 |
0.529 |
|
| 1980 |
Levenson R, Kernen J, Housman D. Synchronization of MEL cell commitment with cordycepin. Cell. 18: 1073-8. PMID 316363 DOI: 10.1016/0092-8674(79)90220-4 |
0.532 |
|
| 1980 |
Gusella J, Weil S, Tsiftsoglou A, Volloch V, Neumann J, Keys C, Housman D. Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation Blood. 56: 481-487. DOI: 10.1182/Blood.V56.3.481.481 |
0.489 |
|
| 1980 |
Gusella J, Weil S, Tsiftsoglou A, Volloch V, Neumann J, Keys C, Housman D. Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation Blood. 56: 481-487. DOI: 10.1182/BLOOD.V56.3.481.481 |
0.421 |
|
| 1979 |
Gusella J, Varsanyi-Breiner A, Kao FT, Jones C, Puck TT, Keys C, Orkin S, Housman D. Precise localization of human beta-globin gene complex on chromosome 11. Proceedings of the National Academy of Sciences of the United States of America. 76: 5239-42. PMID 291941 DOI: 10.1073/Pnas.76.10.5239 |
0.529 |
|
| 1979 |
Varsanyi-Breiner A, Gusella JF, Keys C, Housman DE, Sullivan D, Brisson N, Verma DP. The organization of a nuclear DNA sequence from a higher plant: molecular cloning and characterization of soybean ribosomal DNA. Gene. 7: 317-34. PMID 160361 DOI: 10.1016/0378-1119(79)90051-9 |
0.401 |
|
| 1978 |
Geller R, Levenson R, Housman D. Significance of the cell cycle in commitment of murine erythroleukemia cells to erythroid differentiation. Journal of Cellular Physiology. 95: 213-22. PMID 274446 DOI: 10.1002/Jcp.1040950211 |
0.516 |
|
| 1976 |
Gusella J, Geller R, Clarke B, Weeks V, Housman D. Commitment to erythroid differentiation by friend erythroleukemia cells: a stochastic analysis Cell. 9: 221-229. PMID 975244 DOI: 10.1016/0092-8674(76)90113-6 |
0.49 |
|
| 1976 |
Gusella JF, Housman D. Induction of erythroid differentiation in vitro by purines and purine analogues. Cell. 8: 263-9. PMID 971485 DOI: 10.1016/0092-8674(76)90010-6 |
0.468 |
|
| 1976 |
Forget BG, Hillman DG, Lazarus H, Barell EF, Benz EJ, Caskey CT, Hulsman THJ, Schroeder WA, Housman D. Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobin Cell. 7: 323-329. PMID 947544 DOI: 10.1016/0092-8674(76)90161-6 |
0.504 |
|
| 1973 |
Jacobson A, Housman D, Prensky W. Oligonucleotide fingerprinting of Hela cell 5 S RNA labeled in vitro with (125)I. Molecular Biology Reports. 1: 209-213. PMID 24197568 DOI: 10.1007/Bf00357643 |
0.531 |
|
| 1973 |
Preisler HS, Housman D, Scher W, Friend C. Effects of 5-bromo-2' -deoxyuridine on production of globin messenger RNA in dimethyl sulfoxide-stimulated Friend leukemia cells. Proceedings of the National Academy of Sciences of the United States of America. 70: 2956-9. PMID 4517948 DOI: 10.1073/Pnas.70.10.2956 |
0.314 |
|
| 1972 |
Nathan DG, Lodish HF, Kan YW, Housman D. Beta thalassemia and translation of globin messenger RNA. Proceedings of the National Academy of Sciences of the United States of America. 68: 2514-8. PMID 5289885 DOI: 10.1073/Pnas.68.10.2514 |
0.445 |
|
| 1972 |
Pemberton RE, Housman D, Lodish HF, Baglioni C. Isolation of duck haemoglobin messenger RNA and its translation by rabbit reticulocyte cell free system. Nature: New Biology. 235: 99-102. PMID 4501199 DOI: 10.1038/Newbio235099A0 |
0.44 |
|
| 1971 |
Lodish HF, Housman D, Jacobsen M. Initiation of hemoglobin synthesis. Specific inhibition by antibiotics and bacteriophage ribonucleic acid. Biochemistry. 10: 2348-2356. PMID 5114993 DOI: 10.1021/Bi00788A027 |
0.416 |
|
| 1970 |
Housman D, Jacobs-lorena M, Rajbhandary UL, Lodish HF. Initiation of haemoglobin synthesis by methionyl-tRNA Nature. 227: 913-918. PMID 4915406 DOI: 10.1038/227913A0 |
0.438 |
|
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