Marc Lalande - Publications

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

108 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
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  1
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  1
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  1
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  1
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  1
2013 Crandall L, Lalande M. Is urine the next source of stem cells? Regenerative Medicine. 8: 235-6. PMID 23627817 DOI: 10.2217/Rme.13.24  1
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  1
2011 Martins-Taylor K, Nisler BS, Taapken SM, Compton T, Crandall L, Montgomery KD, Lalande M, Xu RH. Recurrent copy number variations in human induced pluripotent stem cells. Nature Biotechnology. 29: 488-91. PMID 21654665 DOI: 10.1038/Nbt.1890  1
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  1
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  1
2010 Chamberlain SJ, Lalande M. Angelman syndrome, a genomic imprinting disorder of the brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 9958-63. PMID 20668179 DOI: 10.1523/Jneurosci.1728-10.2010  1
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  1
2010 Glatt-Deeley H, Bancescu DL, Lalande M. Prader-Willi syndrome, Snord115, and Htr2c editing. Neurogenetics. 11: 143-4. PMID 19653017 DOI: 10.1007/S10048-009-0209-X  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2004 Meurice G, Jacob D, Deborde C, Chaillou S, Rouault A, Leverrier P, Jan G, Thierry A, Maillard MB, Amet P, Lalande M, Zagorec M, Boyaval P, Dimova D. Whole genome sequencing project of a dairy Propionibacterium freudenreichii subsp. shermanii genome: Progress and first bioinformatic analysis Lait. 84: 15-24. DOI: 10.1051/lait:2003041  1
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  1
2001 Wolverton T, Lalande M. Identification and characterization of three members of a novel subclass of protocadherins. Genomics. 76: 66-72. PMID 11549318 DOI: 10.1006/Geno.2001.6592  1
2001 Lalande M. Imprints of disease at GNAS1. The Journal of Clinical Investigation. 107: 793-4. PMID 11285295 DOI: 10.1172/Jci12645  1
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  1
1999 Hibbard MK, Strehl S, Lalande M. Replication timing of CD4 and CD8 in single-positive peripheral blood lymphocytes. Cellular Immunology. 198: 61-8. PMID 10612652 DOI: 10.1006/Cimm.1999.1582  1
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  1
1999 Lalande M, Minassian BA, DeLorey TM, Olsen RW. Parental imprinting and Angelman syndrome. Advances in Neurology. 79: 421-9. PMID 10514831  1
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  1
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  1
1999 Bialopiotrowicz T, Blanpain-Avet P, Lalande M. Characterization of inorganic carbon-supported microfiltration and ultrafiltration membranes by aqueous phenol adsorption Separation Science and Technology. 34: 1803-1818. DOI: 10.1081/SS-100100739  1
1999 Blanpain-Avet P, Doubrovine N, Lafforgue C, Lalande M. The effect of oscillatory flow on crossflow microfiltration of beer in a tubular mineral membrane system - Membrane fouling resistance decrease and energetic considerations Journal of Membrane Science. 152: 151-174. DOI: 10.1016/S0376-7388(98)00214-2  1
1999 Blanpain-Avet P, Fillaudeau L, Lalande M. Investigation of mechanisms governing membrane fouling and protein rejection in the sterile microfiltration of beer with an organic membrane Food and Bioproducts Processing: Transactions of the Institution of of Chemical Engineers, Part C. 77: 75-89.  1
1998 Rougeulle C, Lalande M. Angelman syndrome: how many genes to remain silent? Neurogenetics. 1: 229-37. PMID 10732796 DOI: 10.1007/S100480050034  1
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  1
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  1
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  1
1998 Rougeulle C, Cardoso C, Fontés M, Colleaux L, Lalande M. An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript. Nature Genetics. 19: 15-6. PMID 9590281 DOI: 10.1038/Ng0598-15  1
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  1
1998 Fillaudeau L, Lalande M. A practical method to predict steady-state flux and fouling in the crossflow microfiltration of rough beer with 1.40 μn tubular ceramic membranes Food and Bioproducts Processing: Transactions of the Institution of of Chemical Engineers, Part C. 76: 217-223.  1
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  1
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  1
1997 Rougeulle C, Glatt H, Lalande M. The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nature Genetics. 17: 14-5. PMID 9288088 DOI: 10.1038/Ng0997-14  1
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  1
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  1
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  1
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  1
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  1
1997 Blanpain P, Lalande M. Investigation of fouling mechanisms governing permeate flux in the crossf low microfiltration of beer Filtration and Separation. 34: 1065-1069.  1
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  1
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  1
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  1
1996 Lalande M. Synchronization of primary human fibroblasts and lymphocytes with mimosine Methods in Cell Science. 18: 135-142. DOI: 10.1007/BF00122164  1
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  1
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  1
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  1
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  1
1995 Greger V, Knoll JH, Woolf E, Glatt K, Tyndale RF, DeLorey TM, Olsen RW, Tobin AJ, Sikela JM, Nakatsu Y. The gamma-aminobutyric acid receptor gamma 3 subunit gene (GABRG3) is tightly linked to the alpha 5 subunit gene (GABRA5) on human chromosome 15q11-q13 and is transcribed in the same orientation. Genomics. 26: 258-64. PMID 7601451 DOI: 10.1016/0888-7543(95)80209-5  1
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  1
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  1
1994 Hanauske-Abel HM, Park MH, Hanauske AR, Popowicz AM, Lalande M, Folk JE. Inhibition of the G1-S transition of the cell cycle by inhibitors of deoxyhypusine hydroxylation. Biochimica Et Biophysica Acta. 1221: 115-24. PMID 8148388 DOI: 10.1016/0167-4889(94)90003-5  1
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  1
1994 Lalande M. In and around SNRPN. Nature Genetics. 8: 5-7. PMID 7987391 DOI: 10.1038/Ng0994-5  1
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  1
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  1
1994 Leclercq-Perlat MN, Lalande M. Cleanability in relation to surface chemical composition and surface finishing of some materials commonly used in food industries Journal of Food Engineering. 23: 501-517. DOI: 10.1016/0260-8774(94)90108-2  1
1993 Lyn D, Cherney BW, Lalande M, Berenson JR, Lichtenstein A, Lupold S, Bhatia KG, Smulson M. A duplicated region is responsible for the poly(ADP-ribose) polymerase polymorphism, on chromosome 13, associated with a predisposition to cancer. American Journal of Human Genetics. 52: 124-34. PMID 8434580  1
1993 Nakatsu Y, Tyndale RF, DeLorey TM, Durham-Pierre D, Gardner JM, McDanel HJ, Nguyen Q, Wagstaff J, Lalande M, Sikela JM. A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus. Nature. 364: 448-50. PMID 8392662 DOI: 10.1038/364448a0  1
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  1
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  1
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  1
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  1
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  1
1993 Wagstaff J, Shugart YY, Lalande M. Linkage analysis in familial Angelman syndrome. American Journal of Human Genetics. 53: 105-12. PMID 8317476  1
1993 Lalande M, Wagstaff J, Sinnett D, Greger V, Knoll JH. Mapping of the Angelman and Prader-Willi syndromes. Progress in Clinical and Biological Research. 384: 225-34. PMID 8115405  1
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  1
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  1
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  1
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  1
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  1
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  1
1992 Lalande M. Imprinting and human genetics Current Opinion in Pediatrics. 4: 978-982. DOI: 10.1097/00008480-199212000-00012  1
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  1
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  1
1991 Hoffman BD, Hanauske-Abel HM, Flint A, Lalande M. A new class of reversible cell cycle inhibitors. Cytometry. 12: 26-32. PMID 1900227 DOI: 10.1002/Cyto.990120105  1
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  1
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  1
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  1
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  1
1991 René F, Lalande M. Momentum and mass transfer during ultrafiltration of dextran with tubular mineral membranes in turbulent flow regime Journal of Membrane Science. 56: 29-48. DOI: 10.1016/0376-7388(91)85014-V  1
1991 Rene F, Leuliet JC, Lalande M. Heat transfer to Newtonian and non-Newtonian food fluids in plate heat exchangers. Experimental and numerical approaches Food and Bioproducts Processing: Transactions of the Institution of of Chemical Engineers, Part C. 69: 115-126.  1
1991 LeClercq-Perlat MN, Lalande M. Review on the modeling of the removal of porous contaminants deposited on heat transfer surfaces International Chemical Engineering. 31: 74-93.  1
1990 Cram LS, Lalande M, Mayall BH. In memoriam: Samuel A. Latt (1938-1988). Cytometry. 11: 1-7. PMID 2407472 DOI: 10.1002/Cyto.990110103  1
1990 Chu B, Wang ZL, Xu RL, Lalande M. Study of large DNA fragments in agarose gels by transient electric birefringence. Biopolymers. 29: 737-50. PMID 2383640 DOI: 10.1002/Bip.360290408  1
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  1
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  1
1990 Leuliet JC, Maingonnat JF, LaLande M. Flow and heat transfer in plate heat exchangers treating viscous Newtonian and pseudoplastic products. I. Modeling the variations of the hydraulic diameter | Ecoulements et transferts de chaleur dans les echangeurs a plaques traitant des produits visqueux newtoniens et pseudoplastiques Canadian Journal of Chemical Engineering. 68: 220-229.  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
1981 Miller RG, Lalande ME, McCutcheon MJ, Stewart SS, Price GB. Usage of the flow cytometer-cell sorter. Journal of Immunological Methods. 47: 13-24. PMID 7031138 DOI: 10.1016/0022-1759(81)90252-0  1
1980 Lalande ME, McCutcheon MJ, Miller RG. Quantitative studies on the precursors of cytotoxic lymphocytes. VI. Second signal requirements of specifically activated precursors isolated 12 h after stimulation. The Journal of Experimental Medicine. 151: 12-9. PMID 6965304  1
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