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There are 154669 results for: content related to: Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene

  1. 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

  2. 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

  3. You have free access to this content
    Recombinant EDA or Sonic Hedgehog rescue the branching defect in Ectodysplasin A pathway mutant salivary glands in vitro

    Developmental Dynamics

    Volume 239, Issue 10, October 2010, Pages: 2674–2684, K.L. Wells, C. Mou, D.J. Headon and A.S. Tucker

    Version of Record online : 27 AUG 2010, DOI: 10.1002/dvdy.22406

  4. 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

  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

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

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    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

  7. 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

  8. Constraints on utilization of the EDA-signaling pathway in threespine stickleback evolution

    Evolution & Development

    Volume 9, Issue 2, March/April 2007, Pages: 141–154, Anne K. Knecht, Kim E. Hosemann and David M. Kingsley

    Version of Record online : 16 MAR 2007, DOI: 10.1111/j.1525-142X.2007.00145.x

  9. 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

  10. 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

  11. 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

  12. Molecular genetic analysis of patients from India with hypohidrotic ectodermal dysplasia reveals novel mutations in the EDA and EDAR genes

    British Journal of Dermatology

    Volume 158, Issue 1, January 2008, Pages: 163–167, A.R. RamaDevi, E.C. Reddy, S. Ranjan and M.D. Bashyam

    Version of Record online : 26 OCT 2007, DOI: 10.1111/j.1365-2133.2007.08231.x

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    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

  14. 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

  15. 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

    Version of Record online : 9 DEC 2010, DOI: 10.1002/humu.21384

  16. Molecular characterization of dental development in a toothed archosaur, the American alligator Alligator mississippiensis

    Evolution & Development

    Volume 15, Issue 6, November 2013, Pages: 393–405, Olivia Weeks, Bhart-Anjan S. Bhullar and Arhat Abzhanov

    Version of Record online : 22 NOV 2013, DOI: 10.1111/ede.12049

    Corrected by:

    Corrigendum: CORRIGENDUM

    Vol. 16, Issue 2, 121, Version of Record online: 11 MAR 2014

  17. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia

    British Journal of Dermatology

    Volume 153, Issue 1, July 2005, Pages: 46–50, M. Naeem, D. Muhammad and W. Ahmad

    Version of Record online : 27 JUN 2005, DOI: 10.1111/j.1365-2133.2005.06642.x

  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. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes

    American Journal of Medical Genetics Part A

    Volume 155, Issue 7, July 2011, Pages: 1616–1622, Birgitta Bergendal, Joakim Klar, Christina Stecksén-Blicks, Johanna Norderyd and Niklas Dahl

    Version of Record online : 27 MAY 2011, DOI: 10.1002/ajmg.a.34045

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    Abortive placode formation in the feather tract of the scaleless chicken embryo

    Developmental Dynamics

    Volume 236, Issue 11, November 2007, Pages: 3020–3030, Leslie Houghton, Catherine M. Lindon, Allison Freeman and Bruce A. Morgan

    Version of Record online : 18 OCT 2007, DOI: 10.1002/dvdy.21337