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Last Name
Institution

Marc Lalande PhD

TitleProfessor and Chair
InstitutionUConn Health Center
DepartmentGenetics and Developmental Biology
AddressMC 6403
Cell and Genome Sciences Building, MC 6403
400 Farmington Avenue
Phone860-679-8350
Fax860-679-8345
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    Other Positions
    TitleAssociate Dean for Research Planning and Coordination
    InstitutionUniversity of Connecticut
    DepartmentSchool of Medicine

    TitleHead
    InstitutionUniversity of Connecticut
    DepartmentUConn Stem Cell Institute


    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. 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. 2016; 9:18. PMID: 27168766.
      View in: PubMed
    2. 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. 2015 May 7; 16(5):533-46. PMID: 25921272.
      View in: PubMed
    3. 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. Mol Autism. 2014; 5:44. PMID: 25694803; PMCID: PMC4332023.
    4. 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. Hum Mol Genet. 2014 Sep 1; 23(17):4674-85. PMID: 24760766; PMCID: PMC4481691.
    5. 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. Hum Mol Genet. 2014 May 1; 23(9):2364-73. PMID: 24363065; PMCID: PMC3976333.
    6. Crandall L, Lalande M. Is urine the next source of stem cells? Regen Med. 2013 May; 8(3):235-6. PMID: 23627817.
      View in: PubMed
    7. 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. 2012 Jan 1; 7(1):71-82. PMID: 22207353; PMCID: PMC3329505.
    8. 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. Nat Biotechnol. 2011 Jun; 29(6):488-91. PMID: 21654665.
      View in: PubMed
    9. Leung KN, Chamberlain SJ, Lalande M, LaSalle JM. Neuronal chromatin dynamics of imprinting in development and disease. J Cell Biochem. 2011 Feb; 112(2):365-73. PMID: 21268055; PMCID: PMC3090268.
    10. 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. Proc Natl Acad Sci U S A. 2010 Oct 12; 107(41):17668-73. PMID: 20876107; PMCID: PMC2955112.
    11. Chamberlain SJ, Lalande M. Angelman syndrome, a genomic imprinting disorder of the brain. J Neurosci. 2010 Jul 28; 30(30):9958-63. PMID: 20668179.
      View in: PubMed
    12. Chamberlain SJ, Lalande M. Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13. Neurobiol Dis. 2010 Jul; 39(1):13-20. PMID: 20304067.
      View in: PubMed
    13. Glatt-Deeley H, Bancescu DL, Lalande M. Prader-Willi syndrome, Snord115, and Htr2c editing. Neurogenetics. 2010 Feb; 11(1):143-4. PMID: 19653017.
      View in: PubMed
    14. Chamberlain SJ, Li XJ, Lalande M. Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders. Neurogenetics. 2008 Oct; 9(4):227-35. PMID: 18791750.
      View in: PubMed
    15. Lalande M, Calciano MA. Molecular epigenetics of Angelman syndrome. Cell Mol Life Sci. 2007 Apr; 64(7-8):947-60. PMID: 17347796.
      View in: PubMed
    16. Colosi DC, Martin D, Moré K, Lalande M. Genomic organization and allelic expression of UBE3A in chicken. Gene. 2006 Nov 15; 383:93-8. PMID: 16996702.
      View in: PubMed
    17. 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. 2006 May; 55(3):216-26. PMID: 16439020.
      View in: PubMed
    18. 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. Dev Biol. 2005 Oct 15; 286(2):587-600. PMID: 16126194.
      View in: PubMed
    19. 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 Res. 2005; 33(13):3976-84. PMID: 16027444; PMCID: PMC1178004.
    20. Bancescu DL, Glatt-Deeley H, Lalande M. Epigenetic activation of the 5-hydroxytryptamine (serotonin) receptor 2C in embryonal carcinoma cells is DNA replication-dependent. Exp Cell Res. 2004 Aug 1; 298(1):262-7. PMID: 15242780.
      View in: PubMed
    21. Simon J, Wakimoto H, Fujita N, Lalande M, Barnard EA. Analysis of the set of GABA(A) receptor genes in the human genome. J Biol Chem. 2004 Oct 1; 279(40):41422-35. PMID: 15258161.
      View in: PubMed
    22. 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 Res. 2004; 32(11):3480-92. PMID: 15226413; PMCID: PMC443545.
    23. Wolverton T, Lalande M. Identification and characterization of three members of a novel subclass of protocadherins. Genomics. 2001 Aug; 76(1-3):66-72. PMID: 11549318.
      View in: PubMed
    24. Lalande M. Imprints of disease at GNAS1. J Clin Invest. 2001 Apr; 107(7):793-4. PMID: 11285295; PMCID: PMC199585.
    25. 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. Proc Natl Acad Sci U S A. 2000 Dec 19; 97(26):14311-6. PMID: 11106375; PMCID: PMC18915.
    26. 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. Hum Mol Genet. 1999 Dec; 8(13):2497-505. PMID: 10556298.
      View in: PubMed
    27. 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. Am J Hum Genet. 1997 Mar; 60(3):574-80. PMID: 9042916; PMCID: PMC1712510.
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