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There are 8067 results for: content related to: Wnt10a regulates dentin sialophosphoprotein mRNA expression and possibly links odontoblast differentiation and tooth morphogenesis

  1. You have free access to this content
    Wnt10a is involved in AER formation during chick limb development

    Developmental Dynamics

    Volume 233, Issue 2, June 2005, Pages: 282–287, Tomohiro Narita, Shunsuke Sasaoka, Kiyoshi Udagawa, Takahiro Ohyama, Naoyuki Wada, Shin-ichiro Nishimatsu, Shinji Takada and Tsutomu Nohno

    Article first published online : 23 MAR 2005, DOI: 10.1002/dvdy.20321

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    Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 429–440, A Mostowska, B Biedziak, M Zadurska, I Dunin-Wilczynska, M Lianeri and PP Jagodzinski

    Article first published online : 7 DEC 2012, DOI: 10.1111/cge.12061

  3. WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations

    American Journal of Medical Genetics Part A

    Volume 164, Issue 2, February 2014, Pages: 353–359, Pakeeza Shaiq Arzoo, Joakim Klar, Birgitta Bergendal, Johanna Norderyd and Niklas Dahl

    Article first published online : 25 NOV 2013, DOI: 10.1002/ajmg.a.36243

  4. Mechanical forces induce odontoblastic differentiation of mesenchymal stem cells on three-dimensional biomimetic scaffolds

    Journal of Tissue Engineering and Regenerative Medicine

    Shunro Miyashita, Nermeen El Motaz Bellah Ahmed, Masashi Murakami, Koichiro Iohara, Tokunori Yamamoto, Hiroshi Horibe, Kenichi Kurita, Teruko Takano-Yamamoto and Misako Nakashima

    Article first published online : 12 JUN 2014, DOI: 10.1002/term.1928

  5. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 671–678, Julie Plaisancié, Isabelle Bailleul-Forestier, Véronique Gaston, Fréderic Vaysse, Didier Lacombe, Muriel Holder-Espinasse, Marc Abramowicz, Christine Coubes, Ghislaine Plessis, Laurence Faivre, Bénédicte Demeer, Catherine Vincent-Delorme, Hélène Dollfus, Sabine Sigaudy, Encarna Guillén-Navarro, Alain Verloes, Philippe Jonveaux, Dominique Martin-Coignard, Estelle Colin, Eric Bieth, Patrick Calvas and Nicolas Chassaing

    Article first published online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35747

  6. The WNT10A gene in ectodermal dysplasias and selective tooth agenesis

    American Journal of Medical Genetics Part A

    Gabriele Mues, John Bonds, Lilin Xiang, Alexandre R. Vieira, Figen Seymen, Ophir Klein and Rena N. D'Souza

    Article first published online : 3 APR 2014, DOI: 10.1002/ajmg.a.36520

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    Histone H3K9 methyltransferase G9a represses PPARγ expression and adipogenesis

    The EMBO Journal

    Volume 32, Issue 1, January 9, 2013, Pages: 45–59, Lifeng Wang, Shiliyang Xu, Ji-Eun Lee, Anne Baldridge, Sean Grullon, Weiqun Peng and Kai Ge

    Article first published online : 23 NOV 2012, DOI: 10.1038/emboj.2012.306

  8. Wnt11 expression in rat dental pulp and promotional effects of Wnt signaling on odontoblast differentiation

    Congenital Anomalies

    Volume 53, Issue 3, September 2013, Pages: 101–108, Yu Koizumi, Nobuyuki Kawashima, Mioko Yamamoto, Koyo Takimoto, Mengyu Zhou, Noriyuki Suzuki, Masahiro Saito, Hidemitsu Harada and Hideaki Suda

    Article first published online : 2 SEP 2013, DOI: 10.1111/cga.12011

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    Census of vertebrate Wnt genes: Isolation and developmental expression of Xenopus Wnt2, Wnt3, Wnt9a, Wnt9b, Wnt10a, and Wnt16

    Developmental Dynamics

    Volume 236, Issue 5, May 2007, Pages: 1249–1258, Robert J. Garriock, Andrew S. Warkman, Stryder M. Meadows, Susan D'Agostino and Paul A. Krieg

    Article first published online : 13 APR 2007, DOI: 10.1002/dvdy.21156

  10. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

    Human Mutation

    Volume 32, Issue 1, January 2011, Pages: 70–72, Céline Cluzeau, Smail Hadj-Rabia, Marguerite Jambou, Sourour Mansour, Philippe Guigue, Sahben Masmoudi, Elodie Bal, Nicolas Chassaing, Marie-Claire Vincent, Géraldine Viot, François Clauss, Marie-Cécile Manière, Steve Toupenay, Martine Le Merrer, Stanislas Lyonnet, Valérie Cormier-Daire, Jeanne Amiel, Laurence Faivre, Yves de Prost, Arnold Munnich, Jean-Paul Bonnefont, Christine Bodemer and Asma Smahi

    Article first published online : 9 DEC 2010, DOI: 10.1002/humu.21384

  11. WNT10A and isolated hypodontia

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Pages: 1119–1122, Piranit Kantaputra and Warissara Sripathomsawat

    Article first published online : 11 APR 2011, DOI: 10.1002/ajmg.a.33840

  12. Schöpf–Schulz–Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A

    Australasian Journal of Dermatology

    Volume 52, Issue 3, August 2011, Pages: 224–226, Gabriela Petrof, Kenneth Fong, Joey E Lai-Cheong, Sarah E Cockayne and John A McGrath

    Article first published online : 29 JUN 2011, DOI: 10.1111/j.1440-0960.2011.00788.x

  13. The role of WNT10B in physiology and disease

    Acta Physiologica

    Volume 204, Issue 1, January 2012, Pages: 34–51, P. Wend, K. Wend, S. A. Krum and G. A. Miranda-Carboni

    Article first published online : 7 MAY 2011, DOI: 10.1111/j.1748-1716.2011.02296.x

  14. Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations

    American Journal of Medical Genetics Part A

    Volume 164, Issue 4, April 2014, Pages: 1041–1048, P. Kantaputra, M. Kaewgahya, D. Jotikasthira and W. Kantaputra

    Article first published online : 23 JAN 2014, DOI: 10.1002/ajmg.a.36388

  15. Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

    Clinical Genetics

    Volume 79, Issue 1, January 2011, Pages: 92–95, M Castori, D Castiglia, F Brancati, M Foglio, S Heath, G Floriddia, S Madonna, J Fischer and G Zambruno

    Article first published online : 9 DEC 2010, DOI: 10.1111/j.1399-0004.2010.01513.x

  16. Dental Anomalies: Genetics

    Standard Article

    eLS

    Pekka Nieminen

    Published Online : 15 MAR 2013, DOI: 10.1002/9780470015902.a0006088.pub2

  17. WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity

    American Journal of Medical Genetics Part A

    Volume 164, Issue 2, February 2014, Pages: 360–363, P. Kantaputra, M. Kaewgahya and W. Kantaputra

    Article first published online : 5 DEC 2013, DOI: 10.1002/ajmg.a.36280

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    Identification of the mammary line in mouse by Wnt10b expression

    Developmental Dynamics

    Volume 229, Issue 2, February 2004, Pages: 349–356, Jacqueline M. Veltmaat, Wendy Van Veelen, Jean Paul Thiery and Saverio Bellusci

    Article first published online : 8 JAN 2004, DOI: 10.1002/dvdy.10441

  19. Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 2, March/April 2013, Pages: 183–212, Martyn T. Cobourne and Paul T. Sharpe

    Article first published online : 25 MAY 2012, DOI: 10.1002/wdev.66

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    Wnt'er in liver: Expression of Wnt and frizzled genes in mouse

    Hepatology

    Volume 45, Issue 1, January 2007, Pages: 195–204, Gang Zeng, Farrukh Awan, Wade Otruba, Peggy Muller, Udayan Apte, Xinping Tan, Chandrashekhar Gandhi, Anthony J. Demetris and Satdarshan P. S. Monga

    Article first published online : 22 DEC 2006, DOI: 10.1002/hep.21473