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There are 3377 results for: content related to: Epigenetic modulation by TFII-I during embryonic stem cell differentiation

  1. PI3K/Akt-dependent functions of TFII-I transcription factors in mouse embryonic stem cells

    Journal of Cellular Biochemistry

    Volume 113, Issue 4, April 2012, Pages: 1122–1131, Nyam-Osor Chimge, Aleksandr V. Makeyev, Sabine J. Waigel, Badam Enkhmandakh and Dashzeveg Bayarsaihan

    Version of Record online : 23 FEB 2012, DOI: 10.1002/jcb.23441

  2. You have free access to this content
    Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome

    Protein Science

    Volume 13, Issue 10, October 2004, Pages: 2588–2599, Timothy A. Hinsley, Pamela Cunliffe, Hannah J. Tipney, Andrew Brass and May Tassabehji

    Version of Record online : 1 JAN 2009, DOI: 10.1110/ps.04747604

  3. You have free access to this content
    GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif ‘GUCE’

    FEBS Letters

    Volume 581, Issue 6, March 20, 2007, Pages: 1233–1242, P.D. Thompson, M. Webb, W. Beckett, T. Hinsley, T. Jowitt, A.D. Sharrocks and M. Tassabehji

    Version of Record online : 28 FEB 2007, DOI: 10.1016/j.febslet.2007.02.040

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    Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice

    Genes, Brain and Behavior

    Volume 7, Issue 2, March 2008, Pages: 224–234, E. J. Young, T. Lipina, E. Tam, A. Mandel, S. J. Clapcote, A. R. Bechard, J. Chambers, H. T. J. Mount, P. J. Fletcher, J. C. Roder and L. R. Osborne

    Version of Record online : 7 JUL 2007, DOI: 10.1111/j.1601-183X.2007.00343.x

  5. Novel splice variants in the 5'UTR of Gtf2i expressed in the rat brain: alternative 5'UTRs and differential expression in the neuronal dendrites

    Journal of Neurochemistry

    Volume 134, Issue 3, August 2015, Pages: 578–589, Yoshinori Shirai, Masahiko Watanabe, Hiroyuki Sakagami and Tatsuo Suzuki

    Version of Record online : 14 MAY 2015, DOI: 10.1111/jnc.13136

  6. Is it Williams syndrome? GTF2IRD1 implicated in visual–spatial construction and GTF2I in sociability revealed by high resolution arrays

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 302–314, L. Dai, U. Bellugi, X.-N. Chen, A.M. Pulst-Korenberg, A. Järvinen-Pasley, T. Tirosh-Wagner, P.S. Eis, J. Graham, D. Mills, Y. Searcy and J.R. Korenberg

    Version of Record online : 9 FEB 2009, DOI: 10.1002/ajmg.a.32652

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    TFII-I gene family during tooth development: Candidate genes for tooth anomalies in Williams syndrome

    Developmental Dynamics

    Volume 236, Issue 10, October 2007, Pages: 2884–2888, Atsushi Ohazama and Paul T. Sharpe

    Version of Record online : 6 SEP 2007, DOI: 10.1002/dvdy.21311

  8. Animal models of Williams syndrome

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 154C, Issue 2, 15 May 2010, Pages: 209–219, Lucy R. Osborne

    Version of Record online : 22 APR 2010, DOI: 10.1002/ajmg.c.30257

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    Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions

    Autism Research

    Volume 4, Issue 1, February 2011, Pages: 28–39, Takeshi Sakurai, Nathan P. Dorr, Nagahide Takahashi, L. Alison McInnes, Gregory A. Elder and Joseph D. Buxbaum

    Version of Record online : 3 DEC 2010, DOI: 10.1002/aur.169

  10. You have full text access to this OnlineOpen article
    Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice

    EMBO Molecular Medicine

    Volume 1, Issue 1, April 2009, Pages: 50–65, Hong Hua Li, Madhuri Roy, Unsal Kuscuoglu, Corinne M. Spencer, Birgit Halm, Katharine C. Harrison, Joseph H. Bayle, Alessandra Splendore, Feng Ding, Leslie A. Meltzer, Elena Wright, Richard Paylor, Karl Deisseroth and Uta Francke

    Version of Record online : 26 MAR 2009, DOI: 10.1002/emmm.200900003

  11. Generation of a mouse model for a conditional inactivation of Gtf2i allele

    genesis

    Accepted manuscript online: 19 MAY 2016, Badam Enkhmnandakh, Chris Stoddard, Kris Mack, Wei He, Deb Kaback, Siu-Pok Yee and Dashzeveg Bayarsaihan

    DOI: 10.1002/dvg.22948

  12. Molecular Genetics of Williams–Beuren Syndrome

    Standard Article

    eLS

    Giuseppe Merla, Lucia Micale, Carmela Fusco and Maria Nicla Loviglio

    Published Online : 15 JAN 2012, DOI: 10.1002/9780470015902.a0022436

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    GTF2I-RARA is a novel fusion transcript in a t(7;17) variant of acute promyelocytic leukaemia with clinical resistance to retinoic acid

    British Journal of Haematology

    Volume 168, Issue 6, March 2015, Pages: 904–908, Ji Li, Hai-Ying Zhong, Yang Zhang, Le Xiao, Li-Hong Bai, Su-Fang Liu, Guang-Biao Zhou and Guang-Sen Zhang

    Version of Record online : 4 OCT 2014, DOI: 10.1111/bjh.13157

  14. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype–phenotype analysis of five families with deletions in the Williams syndrome region

    American Journal of Medical Genetics Part A

    Volume 123A, Issue 1, November 15, 2003, Pages: 45–59, Colleen A. Morris, Carolyn B. Mervis, Holly H. Hobart, Ronald G. Gregg, Jacquelyn Bertrand, Gregory J. Ensing, Annemarie Sommer, Cynthia A. Moore, Robert J. Hopkin, Patricia A. Spallone, Mark T. Keating, Lucy Osborne, Kendra W. Kimberley and A. Dean Stock

    Version of Record online : 17 SEP 2003, DOI: 10.1002/ajmg.a.20496

  15. Expression profiling of BEN regulated genes in mouse embryonic fibroblasts

    Journal of Experimental Zoology Part B: Molecular and Developmental Evolution

    Volume 308B, Issue 3, 15 May 2007, Pages: 209–224, Nyam-Osor Chimge, Ognoon Mungunsukh, Frank Ruddle and Dashzeveg Bayarsaihan

    Version of Record online : 14 OCT 2006, DOI: 10.1002/jez.b.21129

  16. Molecular and phenotypic characterization of atypical Williams–Beuren syndrome

    Clinical Genetics

    Volume 86, Issue 5, November 2014, Pages: 487–491, J. Euteneuer, C.M.B. Carvalho, S. Kulkarni, M. Vineyard, R. Mark Grady, J.R. Lupski and M. Shinawi

    Version of Record online : 18 NOV 2013, DOI: 10.1111/cge.12305

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    Solution structure of the general transcription factor 2I domain in mouse TFII-I protein

    Protein Science

    Volume 16, Issue 8, August 2007, Pages: 1788–1792, Yukiko Doi-Katayama, Fumiaki Hayashi, Makoto Inoue, Takashi Yabuki, Masaaki Aoki, Eiko Seki, Takayoshi Matsuda, Takanori Kigawa, Mayumi Yoshida, Mikako Shirouzu, Takaho Terada, Yoshihide Hayashizaki, Shigeyuki Yokoyama and Hiroshi Hirota

    Version of Record online : 2 JAN 2009, DOI: 10.1110/ps.072792007

  18. Abstracts

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 76, Issue 3, March 2006, Pages: 145–169, NDE Greene, LPE Dunlevy, K Burren, LS Chitty and AJ Copp

    Version of Record online : 14 MAR 2006, DOI: 10.1002/bdra.20242

  19. You have full text access to this OnlineOpen article
    More than the sum of its parts: new mouse models for dissecting the genetic complexities of Williams–Beuren syndrome

    EMBO Molecular Medicine

    Volume 1, Issue 1, April 2009, Pages: 6–9, Andreas Meyer-Lindenberg

    Version of Record online : 26 MAR 2009, DOI: 10.1002/emmm.200900007

  20. A t(7;12) balanced translocation with breakpoints overlapping those of the Williams–Beuren and 12q14 microdeletion syndromes

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1285–1294, Stefania Gimelli, Jacqueline Chrast, Anwar Baban, Charlotte N. Henrichsen, Margherita Lerone, Orsetta Zuffardi, Giorgio Gimelli and Alexandre Reymond

    Version of Record online : 13 APR 2010, DOI: 10.1002/ajmg.a.33365