Center-Authored Papers

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Arnett, ALH, Garikipati D, Wang Z, Tapscott SJ, Chamberlain JS.  2011.  Immune Responses to rAAV6: The Influence of Canine Parvovirus Vaccination and Neonatal Administration of Viral Vector.. Frontiers in microbiology. 2:220. Abstract
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Balog, J, Thijssen PE, de Greef JC, Shah B, van Engelen BGM, Yokomori K, Tapscott SJ, Tawil R, van der Maarel SM.  2012.  Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD.. Epigenetics : official journal of the DNA Methylation Society. 7(6):579-584. Abstract
Balog, J, Miller D, Sanchez-Curtailles E, Carbo-Marques J, Block G, Potman M, de Knijff P, Lemmers RJLF, Tapscott SJ, van der Maarel SM.  2012.  Epigenetic regulation of the X-chromosomal macrosatellite repeat encoding for the cancer/testis gene CT47.. European journal of human genetics : EJHG. 20(2):185-191. Abstract
Borensztein, M, Monnier P, Court F, Louault Y, Ripoche M-A, Tiret L, Yao Z, Tapscott SJ, Forné T, Montarras D et al..  2013.  Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse.. Development (Cambridge, England). 140(6):1231-9. Abstract
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Cao, Y, Yao Z, Sarkar D, Lawrence M, Sanchez GJ, Parker MH, MacQuarrie KL, Davison J, Morgan MT, Ruzzo WL et al..  2010.  Genome-wide MyoD binding in skeletal muscle cells: a potential for broad cellular reprogramming.. Developmental cell. 18(4):662-74. Abstract
Conerly, ML, MacQuarrie KL, Fong AP, Yao Z, Tapscott SJ.  2011.  Polycomb-mediated repression during terminal differentiation: what don't you want to be when you grow up? Genes & development. 25(10):997-1003. Abstract
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Diede, SJ, Tanaka H, Bergstrom DA, Yao M-C, Tapscott SJ.  2010.  Genome-wide analysis of palindrome formation.. Nature genetics. 42(4):279.
Diede, SJ, Guenthoer J, Geng LN, Mahoney SE, Marotta M, Olson JM, Tanaka H, Tapscott SJ.  2010.  DNA methylation of developmental genes in pediatric medulloblastomas identified by denaturation analysis of methylation differences.. Proceedings of the National Academy of Sciences of the United States of America. 107(1):234-9. Abstract
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Fong, AP, Yao Z, Zhong JW, Cao Y, Ruzzo WL, Gentleman RC, Tapscott SJ.  2012.  Genetic and epigenetic determinants of neurogenesis and myogenesis.. Developmental cell. 22(4):721-35. Abstract
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Geng, LN, Tyler AE, Tapscott SJ.  2011.  Immunodetection of human double homeobox 4.. Hybridoma (2005). 30(2):125-30. Abstract
Geng, LN, Yao Z, Snider L, Fong AP, Cech JN, Young JM, van der Maarel SM, Ruzzo WL, Gentleman RC, Tawil R et al..  2012.  DUX4 Activates Germline Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy.. Developmental cell. 22(1):38-51. Abstract
Gianakopoulos, PJ, Mehta V, Voronova A, Cao Y, Yao Z, Coutu J, Wang X, Waddington MS, Tapscott SJ, Skerjanc IS.  2011.  MyoD directly up-regulates premyogenic mesoderm factors during induction of skeletal myogenesis in stem cells.. The Journal of biological chemistry. 286(4):2517-25. Abstract
Guenthoer, J, Diede SJ, Tanaka H, Chai X, Hsu L, Tapscott SJ, Porter PL.  2012.  Assessment of palindromes as platforms for DNA amplification in breast cancer.. Genome research. 22(2):232-45. Abstract
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Halbert, CL, Madtes DK, Vaughan AE, Wang Z, Storb R, Tapscott SJ, Miller AD.  2010.  Expression of human alpha1-antitrypsin in mice and dogs following AAV6 vector-mediated gene transfer to the lungs.. Molecular therapy : the journal of the American Society of Gene Therapy. 18(6):1165-72. Abstract
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Kerwin, WS, Naumova A, Storb R, Tapscott SJ, Wang Z.  2012.  Mapping contrast agent uptake and retention in MRI studies of myocardial perfusion: case control study of dogs with Duchenne muscular dystrophy.. The international journal of cardiovascular imaging. Abstract
Kim, H-J, Archer E, Escobedo N, Tapscott SJ, Unguez GA.  2008.  Inhibition of mammalian muscle differentiation by regeneration blastema extract of Sternopygus macrurus.. Developmental dynamics : an official publication of the American Association of Anatomists. 237(10):2830-43. Abstract
Kimura, E, Han JJ, Li S, Fall B, Ra J, Haraguchi M, Tapscott SJ, Chamberlain JS.  2008.  Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy.. Human molecular genetics. 17(16):2507-17. Abstract
Klezovitch, O, Fernandez TE, Tapscott SJ, Vasioukhin VI.  2004.  Loss of cell polarity causes severe brain dysplasia in Lgl1 knockout mice.. Genes & development. 18(5):559-71. Abstract
Knight, MA, Hernandez D, Diede SJ, Dauwerse HG, Rafferty I, van de Leemput J, Forrest SM, Gardner MKRJ, Storey E, van Ommen G-JB et al..  2008.  A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20.. Human molecular genetics. 17(24):3847-53. Abstract
Krom, YD, Thijssen PE, Young JM, den Hamer B, Balog J, Yao Z, Maves L, Snider L, Knopp P, Zammit PS et al..  2013.  Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD.. PLoS genetics. 9(4):e1003415. Abstract
Krom, YD, Dumonceaux J, Mamchaoui K, den Hamer B, Mariot V, Negroni E, Geng LN, Martin N, Tawil R, Tapscott SJ et al..  2012.  Generation of Isogenic D4Z4 Contracted and Noncontracted Immortal Muscle Cell Clones from a Mosaic Patient: A Cellular Model for FSHD.. The American journal of pathology. Abstract
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Lee, K-S, Cao Y, Witwicka HE, Tom S, Tapscott SJ, Wang EH.  2010.  RNA-binding protein Muscleblind-like 3 (MBNL3) disrupts myocyte enhancer factor 2 (Mef2) {beta}-exon splicing.. The Journal of biological chemistry. 285(44):33779-87. Abstract
Lemmers, RJLF, Tawil R, Petek LM, Balog J, Block GJ, Santen GWE, Amell AM, van der Vliet PJ, Almomani R, Straasheijm KR et al..  2012.  Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.. Nature genetics. 44(12):1370-4. Abstract
Lemmers, RJLF, van der Vliet PJ, Klooster R, Sacconi S, Camaño P, Dauwerse JG, Snider L, Straasheijm KR, van Ommen GJ, Padberg GW et al..  2010.  A unifying genetic model for facioscapulohumeral muscular dystrophy.. Science (New York, N.Y.). 329(5999):1650-3. Abstract
Libby, RT, Hagerman KA, Pineda VV, Lau R, Cho DH, Baccam SL, Axford MM, Cleary JD, Moore JM, Sopher BL et al..  2008.  CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination.. PLoS genetics. 4(11):e1000257. Abstract