Center-Authored Papers

Filters: Author is Tapscott, Stephen J  [Clear All Filters]
2004
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
2008
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
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
Parker MH, Kuhr C, Tapscott SJ, Storb R.  2008.  Hematopoietic cell transplantation provides an immune-tolerant platform for myoblast transplantation in dystrophic dogs.. Molecular therapy : the journal of the American Society of Gene Therapy. 16(7):1340-6. 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
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
2009
Wang Z, Chamberlain JS, Tapscott SJ, Storb R.  2009.  Gene therapy in large animal models of muscular dystrophy.. ILAR journal / National Research Council, Institute of Laboratory Animal Resources. 50(2):187-98. Abstract
Snider L, Asawachaicharn A, Tyler AE, Geng LN, Petek LM, Maves L, Miller DG, Lemmers RJLF, Winokur ST, Tawil R et al..  2009.  RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy.. Human molecular genetics. 18(13):2414-30. Abstract
Yang Z, MacQuarrie KL, Analau E, Tyler AE, Dilworth JF, Cao Y, Diede SJ, Tapscott SJ.  2009.  MyoD and E-protein heterodimers switch rhabdomyosarcoma cells from an arrested myoblast phase to a differentiated state.. Genes & development. 23(6):694-707. Abstract
Maves L, Tyler A, Moens CB, Tapscott SJ.  2009.  Pbx acts with Hand2 in early myocardial differentiation.. Developmental biology. 333(2):409-18. Abstract
2010
Diede SJ, Tanaka H, Bergstrom DA, Yao M-C, Tapscott SJ.  2010.  Genome-wide analysis of palindrome formation.. Nature genetics. 42(4):279.
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
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
Rajapakse I, Scalzo D, Tapscott SJ, Kosak ST, Groudine M.  2010.  Networking the nucleus.. Molecular systems biology. 6:395. Abstract
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
Wang Z, Storb R, Lee D, Kushmerick MJ, Chu B, Berger C, Arnett A, Allen J, Chamberlain JS, Riddell SR et al..  2010.  Immune responses to AAV in canine muscle monitored by cellular assays and noninvasive imaging.. Molecular therapy : the journal of the American Society of Gene Therapy. 18(3):617-24. Abstract
Snider L, Geng LN, Lemmers RJLF, Kyba M, Ware CB, Nelson AM, Tawil R, Filippova GN, van der Maarel SM, Tapscott SJ et al..  2010.  Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene.. PLoS genetics. 6(10):e1001181. Abstract
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, 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
2011
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
Wang Z, Tapscott SJ, Chamberlain JS, Storb R.  2011.  Immunity and AAV-Mediated Gene Therapy for Muscular Dystrophies in Large Animal Models and Human Trials.. Frontiers in microbiology. 2:201. Abstract
Wang Z, Tapscott SJ, Storb R.  2011.  Local gene delivery and methods to control immune responses in muscles of normal and dystrophic dogs.. Methods in molecular biology (Clifton, N.J.). 709:265-75. Abstract
MacQuarrie KL, Fong AP, Morse RH, Tapscott SJ.  2011.  Genome-wide transcription factor binding: beyond direct target regulation.. Trends in genetics : TIG. 27(4):141-8. Abstract
Geng LN, Tyler AE, Tapscott SJ.  2011.  Immunodetection of human double homeobox 4.. Hybridoma (2005). 30(2):125-30. Abstract
Palii CG, Perez-Iratxeta C, Yao Z, Cao Y, Dai F, Davison J, Atkins H, Allan D, Dilworth JF, Gentleman R et al..  2011.  Differential genomic targeting of the transcription factor TAL1 in alternate haematopoietic lineages.. The EMBO journal. 30(3):494-509. Abstract