Marc Lalande - Publications

University of Connecticut Health Center, Farmington, CT, United States 

103 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Langouët M, Gorka D, Orniacki C, Dupont-Thibert CM, Chung MS, Glatt-Deeley HR, Germain N, Crandall LJ, Cotney JL, Stoddard CE, Lalande M, Chamberlain SJ. Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics. PMID 32977341 DOI: 10.1093/hmg/ddaa210  0.326
2017 Langouët M, Glatt-Deeley HR, Chung MS, Dupont-Thibert CM, Mathieux E, Banda EC, Stoddard CE, Crandall L, Lalande M. Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics. PMID 29228278 DOI: 10.1093/Hmg/Ddx420  0.446
2016 Smith OK, Kim R, Fu H, Martin MM, Lin CM, Utani K, Zhang Y, Marks AB, Lalande M, Chamberlain S, Libbrecht MW, Bouhassira EE, Ryan MC, Noble WS, Aladjem MI. Distinct epigenetic features of differentiation-regulated replication origins. Epigenetics & Chromatin. 9: 18. PMID 27168766 DOI: 10.1186/S13072-016-0067-3  0.314
2015 Vallot C, Ouimette JF, Makhlouf M, Féraud O, Pontis J, Côme J, Martinat C, Bennaceur-Griscelli A, Lalande M, Rougeulle C. Erosion of X Chromosome Inactivation in Human Pluripotent Cells Initiates with XACT Coating and Depends on a Specific Heterochromatin Landscape. Cell Stem Cell. 16: 533-46. PMID 25921272 DOI: 10.1016/J.Stem.2015.03.016  0.437
2014 Germain ND, Chen PF, Plocik AM, Glatt-Deeley H, Brown J, Fink JJ, Bolduc KA, Robinson TM, Levine ES, Reiter LT, Graveley BR, Lalande M, Chamberlain SJ. Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. Molecular Autism. 5: 44. PMID 25694803 DOI: 10.1186/2040-2392-5-44  0.469
2014 Cruvinel E, Budinetz T, Germain N, Chamberlain S, Lalande M, Martins-Taylor K. Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs. Human Molecular Genetics. 23: 4674-85. PMID 24760766 DOI: 10.1093/Hmg/Ddu187  0.431
2014 Martins-Taylor K, Hsiao JS, Chen PF, Glatt-Deeley H, De Smith AJ, Blakemore AI, Lalande M, Chamberlain SJ. Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion. Human Molecular Genetics. 23: 2364-73. PMID 24363065 DOI: 10.1093/Hmg/Ddt628  0.468
2012 Martins-Taylor K, Schroeder DI, LaSalle JM, Lalande M, Xu RH. Role of DNMT3B in the regulation of early neural and neural crest specifiers. Epigenetics : Official Journal of the Dna Methylation Society. 7: 71-82. PMID 22207353 DOI: 10.4161/Epi.7.1.18750  0.585
2011 Leung KN, Chamberlain SJ, Lalande M, LaSalle JM. Neuronal chromatin dynamics of imprinting in development and disease. Journal of Cellular Biochemistry. 112: 365-73. PMID 21268055 DOI: 10.1002/Jcb.22958  0.686
2010 Chamberlain SJ, Chen PF, Ng KY, Bourgois-Rocha F, Lemtiri-Chlieh F, Levine ES, Lalande M. Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes. Proceedings of the National Academy of Sciences of the United States of America. 107: 17668-73. PMID 20876107 DOI: 10.1073/Pnas.1004487107  0.391
2010 Chamberlain SJ, Lalande M. Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13. Neurobiology of Disease. 39: 13-20. PMID 20304067 DOI: 10.1016/J.Nbd.2010.03.011  0.489
2008 Chamberlain SJ, Li XJ, Lalande M. Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders. Neurogenetics. 9: 227-35. PMID 18791750 DOI: 10.1007/S10048-008-0147-Z  0.312
2007 Lalande M, Calciano MA. Molecular epigenetics of Angelman syndrome. Cellular and Molecular Life Sciences : Cmls. 64: 947-60. PMID 17347796 DOI: 10.1007/S00018-007-6460-0  0.464
2006 Colosi DC, Martin D, Moré K, Lalande M. Genomic organization and allelic expression of UBE3A in chicken. Gene. 383: 93-8. PMID 16996702 DOI: 10.1016/J.Gene.2006.07.019  0.461
2006 Sotirova VN, Calciano MA, Krueger W, Lalande M. Inclusion of a matrix-attached region in a 7SK pol III vector increases the efficiency of shRNA-mediated gene silencing in embryonic carcinoma cells. Plasmid. 55: 216-26. PMID 16439020 DOI: 10.1016/J.Plasmid.2005.11.008  0.319
2005 Le Meur E, Watrin F, Landers M, Sturny R, Lalande M, Muscatelli F. Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region. Developmental Biology. 286: 587-600. PMID 16126194 DOI: 10.1016/J.Ydbio.2005.07.030  0.39
2005 Landers M, Calciano MA, Colosi D, Glatt-Deeley H, Wagstaff J, Lalande M. Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans. Nucleic Acids Research. 33: 3976-84. PMID 16027444 DOI: 10.1093/Nar/Gki705  0.344
2004 Simon J, Wakimoto H, Fujita N, Lalande M, Barnard EA. Analysis of the set of GABA(A) receptor genes in the human genome. The Journal of Biological Chemistry. 279: 41422-35. PMID 15258161 DOI: 10.1074/Jbc.M401354200  0.357
2004 Bancescu DL, Glatt-Deeley H, Lalande M. Epigenetic activation of the 5-hydroxytryptamine (serotonin) receptor 2C in embryonal carcinoma cells is DNA replication-dependent. Experimental Cell Research. 298: 262-7. PMID 15242780 DOI: 10.1016/J.Yexcr.2004.04.021  0.346
2004 Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M. Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Research. 32: 3480-92. PMID 15226413 DOI: 10.1093/Nar/Gkh670  0.354
2001 LaSalle J, Lalande M. Flow cytometry and FISH to investigate allele-specific replication timing and homologous association of imprinted chromosomes. Methods in Molecular Biology (Clifton, N.J.). 181: 181-92. PMID 12843450 DOI: 10.1385/1-59259-211-2:181  0.666
2001 Lalande M. Imprints of disease at GNAS1. The Journal of Clinical Investigation. 107: 793-4. PMID 11285295 DOI: 10.1172/Jci12645  0.367
2000 Cavaillé J, Buiting K, Kiefmann M, Lalande M, Brannan CI, Horsthemke B, Bachellerie JP, Brosius J, Hüttenhofer A. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proceedings of the National Academy of Sciences of the United States of America. 97: 14311-6. PMID 11106375 DOI: 10.1073/Pnas.250426397  0.38
1999 Boccaccio I, Glatt-Deeley H, Watrin F, Roëckel N, Lalande M, Muscatelli F. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Human Molecular Genetics. 8: 2497-505. PMID 10556298 DOI: 10.1093/Hmg/8.13.2497  0.451
1999 Lalande M, Minassian BA, DeLorey TM, Olsen RW. Parental imprinting and Angelman syndrome. Advances in Neurology. 79: 421-9. PMID 10514831  0.362
1999 Moncla A, Malzac P, Voelckel MA, Auquier P, Girardot L, Mattei MG, Philip N, Mattei JF, Lalande M, Livet MO. Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients. European Journal of Human Genetics : Ejhg. 7: 131-9. PMID 10196695 DOI: 10.1038/Sj.Ejhg.5200258  0.447
1999 Katz SG, Schneider SS, Bartuski A, Trask BJ, Massa H, Overhauser J, Lalande M, Lansdorp PM, Silverman GA. An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA. Human Molecular Genetics. 8: 87-92. PMID 9887335 DOI: 10.1093/Hmg/8.1.87  0.518
1998 Rougeulle C, Lalande M. Angelman syndrome: how many genes to remain silent? Neurogenetics. 1: 229-37. PMID 10732796 DOI: 10.1007/S100480050034  0.448
1998 Strehl S, Glatt K, Liu QM, Glatt H, Lalande M. Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14. Genomics. 53: 81-9. PMID 9787079 DOI: 10.1006/Geno.1998.5467  0.467
1998 Ritchie RJ, Mattei MG, Lalande M. A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications. Human Molecular Genetics. 7: 1253-60. PMID 9668167 DOI: 10.1093/Hmg/7.8.1253  0.499
1998 Buiting K, Dittrich B, Gross S, Lich C, Färber C, Buchholz T, Smith E, Reis A, Bürger J, Nöthen MM, Barth-Witte U, Janssen B, Abeliovich D, Lerer I, van den Ouweland AM, ... ... Lalande M, et al. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. American Journal of Human Genetics. 63: 170-80. PMID 9634532 DOI: 10.1086/301935  0.434
1998 LaSalle JM, Ritchie RJ, Glatt H, Lalande M. Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes. Proceedings of the National Academy of Sciences of the United States of America. 95: 1675-80. PMID 9465075 DOI: 10.1073/Pnas.95.4.1675  0.554
1997 Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roëckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics. 17: 357-61. PMID 9354807 DOI: 10.1038/Ng1197-357  0.466
1997 Strehl S, LaSalle JM, Lalande M. High-resolution analysis of DNA replication domain organization across an R/G-band boundary. Molecular and Cellular Biology. 17: 6157-66. PMID 9315676 DOI: 10.1128/Mcb.17.10.6157  0.595
1997 Kim Y, Glatt H, Xie W, Sinnett D, Lalande M. Human gamma-aminobutyric acid-type A receptor alpha5 subunit gene (GABRA5): characterization and structural organization of the 5' flanking region. Genomics. 42: 378-87. PMID 9205108 DOI: 10.1006/Geno.1997.4770  0.397
1997 Mizuta R, LaSalle JM, Cheng HL, Shinohara A, Ogawa H, Copeland N, Jenkins NA, Lalande M, Alt FW. RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein. Proceedings of the National Academy of Sciences of the United States of America. 94: 6927-32. PMID 9192668 DOI: 10.1073/Pnas.94.13.6927  0.532
1997 Glatt K, Glatt H, Lalande M. Structure and organization of GABRB3 and GABRA5. Genomics. 41: 63-9. PMID 9126483 DOI: 10.1006/Geno.1997.4639  0.449
1997 Greger V, Knoll JH, Wagstaff J, Woolf E, Lieske P, Glatt H, Benn PA, Rosengren SS, Lalande M. Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3. American Journal of Human Genetics. 60: 574-80. PMID 9042916  0.375
1997 Kishino T, Lalande M, Wagstaff J. UBE3A/E6-AP mutations cause Angelman syndrome. Nature Genetics. 15: 70-3. PMID 8988171 DOI: 10.1038/Ng0197-70  0.395
1996 Lalande M. Parental imprinting and human disease. Annual Review of Genetics. 30: 173-95. PMID 8982453 DOI: 10.1146/Annurev.Genet.30.1.173  0.5
1996 Sinnett D, Woolf E, Xie W, Glatt K, Kirkness EF, Nielsen TO, Zannis-Hadjopoulos M, Price GB, Lalande M. Identification of a putative DNA replication origin in the gamma-aminobutyric acid receptor subunit beta3 and alpha5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timing. Gene. 173: 171-7. PMID 8964494 DOI: 10.1016/0378-1119(96)00106-0  0.443
1996 LaSalle JM, Lalande M. Homologous association of oppositely imprinted chromosomal domains. Science (New York, N.Y.). 272: 725-8. PMID 8614834 DOI: 10.1126/Science.272.5262.725  0.646
1995 LaSalle JM, Lalande M. Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution. Nature Genetics. 9: 386-94. PMID 7795644 DOI: 10.1038/Ng0495-386  0.63
1995 Silverman GA, Schneider SS, Massa HF, Flint A, Lalande M, Leonard JC, Overhauser J, van den Engh G, Trask BJ. The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2. American Journal of Human Genetics. 56: 926-37. PMID 7717403  0.372
1995 Robinson WP, Lalande M. Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region. Human Molecular Genetics. 4: 801-6. PMID 7633438 DOI: 10.1093/Hmg/4.5.801  0.435
1995 Hui SM, Trask B, van den Engh G, Bartuski AJ, Smith A, Flint A, Lalande M, Silverman GA. Analysis of randomly amplified flow-sorted chromosomes using the polymerase chain reaction. Genomics. 26: 364-71. PMID 7601463 DOI: 10.1016/0888-7543(95)80221-7  0.483
1994 Glatt K, Sinnett D, Lalande M. The human gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster in chromosome 15q11-q13 is rich in highly polymorphic (CA)n repeats. Genomics. 19: 157-60. PMID 8188218 DOI: 10.1006/Geno.1994.1027  0.413
1994 Reis A, Dittrich B, Greger V, Buiting K, Lalande M, Gillessen-Kaesbach G, Anvret M, Horsthemke B. Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. American Journal of Human Genetics. 54: 741-7. PMID 8178815  0.387
1994 Knoll JH, Cheng SD, Lalande M. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region. Nature Genetics. 6: 41-6. PMID 8136833 DOI: 10.1038/Ng0194-41  0.526
1994 Lalande M. In and around SNRPN. Nature Genetics. 8: 5-7. PMID 7987391 DOI: 10.1038/Ng0994-5  0.398
1994 Greger V, Reis A, Lalande M. The critical region for Angelman syndrome lies between D15S122 and D15S113. American Journal of Medical Genetics. 53: 396-8. PMID 7864058 DOI: 10.1002/Ajmg.1320530425  0.443
1994 Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, Lalande M, Mutirangura A, Kuwano A, Ledbetter DH, Niikawa N. Molecular and clinical study of 61 Angelman syndrome patients American Journal of Medical Genetics. 52: 158-163. PMID 7802001 DOI: 10.1002/Ajmg.1320520207  0.377
1993 Bull PC, Barwell JA, Hannah HT, Pautler SE, Higgins MJ, Lalande M, Cox DW. Isolation of new probes in the region of the Wilson disease locus, 13q14.2-->q14.3. Cytogenetics and Cell Genetics. 64: 12-7. PMID 8508673 DOI: 10.1159/000133550  0.45
1993 Sinnett D, Wagstaff J, Glatt K, Woolf E, Kirkness EJ, Lalande M. High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients. American Journal of Human Genetics. 52: 1216-29. PMID 8389098  0.374
1993 Knoll JH, Sinnett D, Wagstaff J, Glatt K, Wilcox AS, Whiting PM, Wingrove P, Sikela JM, Lalande M. FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions. Human Molecular Genetics. 2: 183-9. PMID 8388764 DOI: 10.1093/Hmg/2.2.183  0.48
1993 Knoll JH, Wagstaff J, Lalande M. Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview. American Journal of Medical Genetics. 46: 2-6. PMID 8388170 DOI: 10.1002/Ajmg.1320460103  0.386
1993 Greger V, Woolf E, Lalande M. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient. Human Molecular Genetics. 2: 921-4. PMID 8364575 DOI: 10.1093/Hmg/2.7.921  0.483
1993 Sinnett D, Flint A, Lalande M. Determination of DNA replication kinetics in synchronized human cells using a PCR-based assay. Nucleic Acids Research. 21: 3227-32. PMID 8341597 DOI: 10.1093/Nar/21.14.3227  0.36
1993 Buiting K, Dittrich B, Gross S, Greger V, Lalande M, Robinson W, Mutirangura A, Ledbetter D, Horsthemke B. Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene. Human Molecular Genetics. 2: 1991-4. PMID 8111365 DOI: 10.1093/Hmg/2.12.1991  0.497
1992 Webb T, Clayton-Smith J, Cheng XJ, Knoll JH, Lalande M, Pembrey ME, Malcolm S. Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13. Journal of Medical Genetics. 29: 921-4. PMID 1362225 DOI: 10.1136/Jmg.29.12.921  0.442
1992 Saitoh S, Kubota T, Ohta T, Jinno Y, Niikawa N, Sugimoto T, Wagstaff J, Lalande M. Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene. Lancet. 339: 366-7. PMID 1346439 DOI: 10.1016/0140-6736(92)91686-3  0.305
1992 Glatt KA, Sinnett D, Lalande M. Dinucleotide repeat polymorphism at the GABAA receptor alpha 5 (GABRA5) locus at chromosome 15q11-q13. Human Molecular Genetics. 1: 348. PMID 1338907 DOI: 10.1093/Hmg/1.5.348  0.423
1992 Wagstaff J, Knoll JH, Glatt KA, Shugart YY, Sommer A, Lalande M. Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression. Nature Genetics. 1: 291-4. PMID 1338769 DOI: 10.1038/Ng0792-291  0.479
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  0.51
1991 Knoll JH, Glatt KA, Nicholls RD, Malcolm S, Lalande M. Chromosome 15 uniparental disomy is not frequent in Angelman syndrome. American Journal of Human Genetics. 48: 16-21. PMID 1985457  0.413
1991 Watson PA, Hanauske-Abel HH, Flint A, Lalande M. Mimosine reversibly arrests cell cycle progression at the G1-S phase border. Cytometry. 12: 242-6. PMID 1903691 DOI: 10.1002/Cyto.990120306  0.304
1991 Engel E, Knoll JHM, Nicholls RD, Malcolm S, Lalande M. Chromosome 15 uniparental disomy is not frequent in Angelman syndrome [2] American Journal of Human Genetics. 49: 459-460. PMID 1867202  0.353
1991 Wagstaff J, Knoll JHM, Fleming J, Kirkness EF, Martin-Gallardo A, Greenberg F, Graham JM, Menninger J, Ward D, Venter JC, Lalande M. Localization of the gene encoding the GABAA receptor β3 subunit to the Angelman/Prader-Willi region of human chromosome 15 American Journal of Human Genetics. 49: 330-337. PMID 1714232  0.398
1991 Chaillet JR, Knoll JH, Horsthemke B, Lalande M. The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7. Genomics. 11: 773-6. PMID 1685485 DOI: 10.1016/0888-7543(91)90090-2  0.493
1991 Wagstaff J, Chaillet JR, Lalande M. The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7. Genomics. 11: 1071-8. PMID 1664410 DOI: 10.1016/0888-7543(91)90034-C  0.469
1990 Müller U, Lalande M. A physical map of the human Y-chromosome short arm. Genomics. 7: 517-23. PMID 1974877 DOI: 10.1016/0888-7543(90)90194-Y  0.445
1990 Knoll JH, Nicholls RD, Magenis RE, Glatt K, Graham JM, Kaplan L, Lalande M. Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers. American Journal of Human Genetics. 47: 149-54. PMID 1971993  0.382
1990 Higgins MJ, Turmel C, Noolandi J, Neumann PE, Lalande M. Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map. Proceedings of the National Academy of Sciences of the United States of America. 87: 3415-9. PMID 1970636 DOI: 10.1073/Pnas.87.9.3415  0.466
1989 Higgins MJ, Hansen MF, Cavenee WK, Lalande M. Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus. Molecular and Cellular Biology. 9: 1-5. PMID 2927388 DOI: 10.1128/Mcb.9.1.1  0.439
1989 Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature. 342: 281-5. PMID 2812027 DOI: 10.1038/342281A0  0.511
1989 Knoll JH, Nicholls RD, Lalande M. On the parental origin of the deletion in Angelman syndrome. Human Genetics. 83: 205-7. PMID 2777263 DOI: 10.1007/Bf00286723  0.304
1989 Higgins MJ, Turmel C, Noolandi J, Lalande M. Detection of Saccharomyces cerevisiae chromosome size markers directly on Southern blots of pulsed-field gels with a single DNA hybridization probe. Nucleic Acids Research. 17: 10136. PMID 2690003 DOI: 10.1093/nar/17.23.10136  0.321
1989 Nicholls RD, Lalande M. Three allele TaqI RFLP for probe 3-21 [D15S10] on chromosome 15q. Nucleic Acids Research. 17: 10140. PMID 2574845 DOI: 10.1093/Nar/17.23.10140  0.463
1989 Knoll JH, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. American Journal of Medical Genetics. 32: 285-90. PMID 2564739 DOI: 10.1002/Ajmg.1320320235  0.512
1989 Müller U, Fontaine D, Adinolfi M, Fraccaro M, Lalande M. Analysis of complex Y chromosome aberrations using a single DNA probe (Y-367). Cytogenetics and Cell Genetics. 50: 161-4. PMID 2550180 DOI: 10.1159/000132750  0.484
1989 Müller U, Lalande M, Donlon TA, Heartlein MW. Breakage of the human Y-chromosome short arm between two blocks of tandemly repeated DNA sequences. Genomics. 5: 153-6. PMID 2548948 DOI: 10.1016/0888-7543(89)90101-8  0.483
1988 Tantravahi U, Stewart GD, Van Keuren M, McNeil G, Roy S, Patterson D, Drabkin H, Lalande M, Kurnit DM, Latt SA. Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes. Human Genetics. 79: 196-202. PMID 3402991 DOI: 10.1007/Bf00366237  0.504
1988 Turmel C, Lalande M. Resolution of Schizosaccharomyces pombe chromosomes by field inversion gel electrophoresis. Nucleic Acids Research. 16: 4727. PMID 3380699 DOI: 10.1093/Nar/16.10.4727  0.397
1988 Slater GW, Rousseau J, Noolandi J, Turmel C, Lalande M. Quantitative analysis of the three regimes of DNA electrophoresis in agarose gels. Biopolymers. 27: 509-24. PMID 3359012 DOI: 10.1002/Bip.360270311  0.315
1988 Lalande M, Noolandi J, Turmel C, Brousseau R, Rousseau J, Slater GW. Scrambling of bands in gel electrophoresis of DNA. Nucleic Acids Research. 16: 5427-37. PMID 2838816 DOI: 10.1093/Nar/16.12.5427  0.308
1988 Griesser H, Champagne E, Tkachuk D, Takihara Y, Lalande M, Baillie E, Minden M, Mak TW. The human T cell receptor alpha-delta locus: a physical map of the variable, joining and constant region genes. European Journal of Immunology. 18: 641-4. PMID 2835248 DOI: 10.1002/Eji.1830180424  0.346
1987 Müller U, Donlon TA, Kunkel SM, Lalande M, Latt SA. Y-190, a DNA probe for the sensitive detection of Y-derived marker chromosomes and mosaicism. Human Genetics. 75: 109-13. PMID 3469135 DOI: 10.1007/Bf00591069  0.434
1987 Lalande M, Noolandi J, Turmel C, Rousseau J, Slater GW. Pulsed-field electrophoresis: application of a computer model to the separation of large DNA molecules. Proceedings of the National Academy of Sciences of the United States of America. 84: 8011-5. PMID 3317398 DOI: 10.1073/Pnas.84.22.8011  0.327
1987 Harris P, Lalande M, Stroh H, Bruns G, Flint A, Latt SA. Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p. Human Genetics. 77: 95-103. PMID 2888723 DOI: 10.1007/Bf00272372  0.427
1986 Müller U, Lalande M, Donlon T, Latt SA. Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female. Nucleic Acids Research. 14: 1325-40. PMID 3951989 DOI: 10.1093/Nar/14.3.1325  0.461
1986 Lalande M, Donlon T, Petersen RA, Liberfarb R, Manter S, Latt SA. Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma. Cancer Genetics and Cytogenetics. 23: 151-7. PMID 3756834  0.403
1986 Müller U, Donlon T, Schmid M, Fitch N, Richer CL, Lalande M, Latt SA. Deletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) females. Nucleic Acids Research. 14: 6489-505. PMID 3748818 DOI: 10.1093/Nar/14.16.6489  0.392
1986 Latt SA, Lalande M, Donlon T, Wyman A, Rose E, Shiloh Y, Korf B, Müller U, Sakai K, Kanda N. DNA-based detection of chromosome deletion and amplification: diagnostic and mechanistic significance. Cold Spring Harbor Symposia On Quantitative Biology. 51: 299-307. PMID 3472727 DOI: 10.1101/Sqb.1986.051.01.035  0.465
1986 Müller U, Lalande M, Disteche CM, Latt SA. Construction, analysis, and application to 46,XY gonadal dysgenesis of a recombinant phage DNA library from flow-sorted human Y chromosomes. Cytometry. 7: 418-24. PMID 3019620 DOI: 10.1002/Cyto.990070505  0.446
1986 Donlon TA, Lalande M, Wyman A, Bruns G, Latt SA. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Proceedings of the National Academy of Sciences of the United States of America. 83: 4408-12. PMID 3012567 DOI: 10.1073/Pnas.83.12.4408  0.524
1985 Latt SA, Lalande M, Kunkel LM, Schreck R, Tantravahi U. Applications of fluorescence spectroscopy to molecular cytogenetics. Biopolymers. 24: 77-95. PMID 3886034 DOI: 10.1002/Bip.360240108  0.436
1985 Kunkel LM, Lalande M, Monaco AP, Flint A, Middlesworth W, Latt SA. Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci. Gene. 33: 251-8. PMID 2989089 DOI: 10.1016/0378-1119(85)90232-X  0.48
1985 Lalande M, Schreck RR, Hoffman R, Latt SA. Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis. Cytometry. 6: 1-6. PMID 2578344 DOI: 10.1002/Cyto.990060102  0.491
1984 Latt SA, Kurnit DM, Bruns GP, Schreck RR, Morton CC, Kunkel LM, Lalande M, Aldridge J, Neve R, Tantravahi U. Molecular genetic approaches to human diseases involving mental retardation. American Journal of Mental Deficiency. 88: 561-71. PMID 6731492  0.35
1984 Lalande M, Kunkel LM, Flint A, Latt SA. Development and use of metaphase chromosome flow-sorting methodology to obtain recombinant phage libraries enriched for parts of the human X chromosome. Cytometry. 5: 101-7. PMID 6232119 DOI: 10.1002/Cyto.990050202  0.458
1984 Lalande M, Dryja TP, Schreck RR, Shipley J, Flint A, Latt SA. Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus. Cancer Genetics and Cytogenetics. 13: 283-95. PMID 6210139 DOI: 10.1016/0165-4608(84)90073-6  0.517
1983 D'Andrea AD, Tantravahi U, Lalande M, Perle MA, Latt SA. High resolution analysis of the timing of replication of specific DNA sequences during S phase of mammalian cells. Nucleic Acids Research. 11: 4753-74. PMID 6192392 DOI: 10.1093/Nar/11.14.4753  0.337
1982 Latt SA, Kaiser TN, Lojewski A, Dougherty C, Juergens L, Brefach S, Sahar E, Gustashaw K, Schreck RR, Powers M, Lalande M. Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia. Cytogenetics and Cell Genetics. 33: 133-8. PMID 7116934 DOI: 10.1159/000131737  0.348
Show low-probability matches.