Marc Lalande

Affiliations: 
University of Connecticut Health Center, Farmington, CT, United States 
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"Marc Lalande"
Mean distance: 17811 (cluster 32)
 
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Publications

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Smith OK, Kim R, Fu H, et al. (2016) Distinct epigenetic features of differentiation-regulated replication origins. Epigenetics & Chromatin. 9: 18
Vallot C, Ouimette JF, Makhlouf M, et al. (2015) 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
Germain ND, Chen PF, Plocik AM, et al. (2014) Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. Molecular Autism. 5: 44
Cruvinel E, Budinetz T, Germain N, et al. (2014) Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs. Human Molecular Genetics. 23: 4674-85
Martins-Taylor K, Hsiao JS, Chen PF, et al. (2014) Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion. Human Molecular Genetics. 23: 2364-73
Crandall L, Lalande M. (2013) Is urine the next source of stem cells? Regenerative Medicine. 8: 235-6
Martins-Taylor K, Schroeder DI, LaSalle JM, et al. (2012) Role of DNMT3B in the regulation of early neural and neural crest specifiers. Epigenetics : Official Journal of the Dna Methylation Society. 7: 71-82
Martins-Taylor K, Nisler BS, Taapken SM, et al. (2011) Recurrent copy number variations in human induced pluripotent stem cells. Nature Biotechnology. 29: 488-91
Leung KN, Chamberlain SJ, Lalande M, et al. (2011) Neuronal chromatin dynamics of imprinting in development and disease. Journal of Cellular Biochemistry. 112: 365-73
Chamberlain SJ, Chen PF, Ng KY, et al. (2010) 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
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