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There are 7006653 results for: content related to: Enhanced ectodysplasin-A receptor (EDAR) signaling alters multiple fiber characteristics to produce the East Asian hair form

  1. You have free access to this content
    Ectodysplasin receptor-mediated signaling is essential for embryonic submandibular salivary gland development

    The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology

    Volume 271A, Issue 2, April 2003, Pages: 322–331, Tina Jaskoll, Yan-Min Zhou, Gary Trump and Michael Melnick

    Version of Record online : 5 MAR 2003, DOI: 10.1002/ar.a.10045

  2. Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 20, 15 October 2008, Pages: 2657–2662, Hala Mégarbané, Céline Cluzeau, Christine Bodemer, Sylvie Fraïtag, Myrna Chababi-Atallah, André Mégarbané and Asma Smahi

    Version of Record online : 24 SEP 2008, DOI: 10.1002/ajmg.a.32509

  3. Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

    Human Mutation

    Volume 28, Issue 7, July 2007, Pages: 703–709, E. Bal, L. Baala, C. Cluzeau, F. El Kerch, K. Ouldim, S. Hadj-Rabia, C. Bodemer, A. Munnich, G. Courtois, A. Sefiani and A. Smahi

    Version of Record online : 12 MAR 2007, DOI: 10.1002/humu.20500

  4. A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India

    British Journal of Dermatology

    Volume 166, Issue 4, April 2012, Pages: 819–829, M.D. Bashyam, A.K. Chaudhary, E.C. Reddy, V. Reddy, V. Acharya, H.A. Nagarajaram, A.R.R. Devi, L. Bashyam, A.B. Dalal, N. Gupta, M. Kabra, M. Agarwal, S.R. Phadke, R. Tainwala, R. Kumar and S.V. Hariharan

    Version of Record online : 5 MAR 2012, DOI: 10.1111/j.1365-2133.2011.10707.x

  5. You have free access to this content
    Molecular aspects of hypohidrotic ectodermal dysplasia

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 2031–2036, Marja L. Mikkola

    Version of Record online : 13 AUG 2009, DOI: 10.1002/ajmg.a.32855

  6. Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia

    Australasian Journal of Dermatology

    Volume 52, Issue 1, February 2011, Pages: 37–42, Nosheen Bibi, Saeed Ahmad, Wasim Ahmad and Muhammad Naeem

    Version of Record online : 23 AUG 2010, DOI: 10.1111/j.1440-0960.2010.00685.x

  7. Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases

    British Journal of Dermatology

    Volume 162, Issue 5, May 2010, Pages: 1044–1048, N. Chassaing, C. Cluzeau, E. Bal, P. Guigue, M-C. Vincent, G. Viot, D. Ginisty, A. Munnich, A. Smahi and P. Calvas

    Version of Record online : 5 MAR 2010, DOI: 10.1111/j.1365-2133.2010.09670.x

  8. X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings

    Clinical Genetics

    Volume 78, Issue 3, September 2010, Pages: 257–266, F Clauss, N Chassaing, A Smahi, MC Vincent, P Calvas, M Molla, H Lesot, Y Alembik, S Hadj-Rabia, C Bodemer, MC Manière and M Schmittbuhl

    Version of Record online : 24 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01376.x

  9. Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia

    Human Mutation

    Volume 27, Issue 3, March 2006, Pages: 255–259, N. Chassaing, S. Bourthoumieu, M. Cossee, P. Calvas and M.-C. Vincent

    Version of Record online : 24 JAN 2006, DOI: 10.1002/humu.20295

  10. Molecular principles of hair follicle induction and morphogenesis

    BioEssays

    Volume 27, Issue 3, March 2005, Pages: 247–261, Ruth Schmidt-Ullrich and Ralf Paus

    Version of Record online : 15 FEB 2005, DOI: 10.1002/bies.20184

  11. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype–phenotype correlation

    Oral Diseases

    Volume 21, Issue 8, November 2015, Pages: 994–1000, B Zeng, H Lu, X Xiao, L Zhou, J Lu, L Zhu, D Yu and W Zhao

    Version of Record online : 24 OCT 2015, DOI: 10.1111/odi.12376

  12. The EDAR370A allele attenuates the severity of hypohidrotic ectodermal dysplasia caused by EDA gene mutation

    British Journal of Dermatology

    Volume 166, Issue 3, March 2012, Pages: 678–681, C. Cluzeau, S. Hadj-Rabia, E. Bal, F. Clauss, A. Munnich, C. Bodemer, D. Headon and A. Smahi

    Version of Record online : 5 DEC 2011, DOI: 10.1111/j.1365-2133.2011.10620.x

  13. A Mongolian patient with hypohidrotic ectodermal dysplasia with a novel P121S variant in EDARADD

    Orthodontics & Craniofacial Research

    Volume 13, Issue 2, May 2010, Pages: 114–117, N Suda, A Bazar, O Bold, B Jigjid, A Garidkhuu, G Ganburged and K Moriyama

    Version of Record online : 19 APR 2010, DOI: 10.1111/j.1601-6343.2010.01484.x

  14. Identification of mutations in the EDA and EDAR genes in Pakistani families with hypohidrotic ectodermal dysplasia

    Clinical Genetics

    Volume 75, Issue 6, June 2009, Pages: 582–584, Y Shimomura, M Wajid, J Weiser, L Kraemer, Y Ishii, V Lombillo, SJ Bale and AM Christiano

    Version of Record online : 5 MAY 2009, DOI: 10.1111/j.1399-0004.2009.01178.x

  15. 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

    Version of Record online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35747

  16. You have free access to this content
    Eda/Edar signaling guides fin ray formation with preceding osteoblast differentiation, as revealed by analyses of the medaka all-fin less mutant afl

    Developmental Dynamics

    Volume 243, Issue 6, June 2014, Pages: 765–777, Yuuki Iida, Kenta Hibiya, Keiji Inohaya and Akira Kudo

    Version of Record online : 19 MAR 2014, DOI: 10.1002/dvdy.24120

  17. You have free access to this content
    Ectodermal dysplasias: An overview and update of clinical and molecular-functional mechanisms

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 2003–2013, Manuela Priolo

    Version of Record online : 5 JUN 2009, DOI: 10.1002/ajmg.a.32804

  18. 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

    Version of Record online : 25 MAY 2012, DOI: 10.1002/wdev.66

  19. You have full text access to this OnlineOpen article
    Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

    Molecular Genetics & Genomic Medicine

    Volume 3, Issue 1, January 2015, Pages: 40–58, Jie Yang, Shih-Kai Wang, Murim Choi, Bryan M. Reid, Yuanyuan Hu, Yuan-Ling Lee, Curtis R. Herzog, Hera Kim-Berman, Moses Lee, Paul J. Benke, K. C. Kent Lloyd, James P. Simmer and Jan C.-C. Hu

    Version of Record online : 15 SEP 2014, DOI: 10.1002/mgg3.111

  20. Development and application of a LC–MS/MS assay for the simultaneous quantification of edaravone and taurine in beagle plasma

    Journal of Separation Science

    Volume 36, Issue 24, December 2013, Pages: 3837–3844, Yan-yan Yu, Xiao-xiao Zheng, Ting-ting Bian, Yin-jie Li, Xiao-wen Wu, Dong-zhi Yang, Shui-shi Jiang and Dao-quan Tang

    Version of Record online : 5 NOV 2013, DOI: 10.1002/jssc.201300983