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There are 22969 results for: content related to: A novel form of chondrocyte stress is triggered by a COMP mutation causing pseudoachondroplasia

  1. You have free access to this content
    Chondrocyte-Specific Pathology During Skeletal Growth and Therapeutics in a Murine Model of Pseudoachondroplasia

    Journal of Bone and Mineral Research

    Volume 29, Issue 5, May 2014, Pages: 1258–1268, Karen L Posey, Francoise Coustry, Alka C Veerisetty, Peiman Liu, Joseph L Alcorn and Jacqueline T Hecht

    Version of Record online : 22 APR 2014, DOI: 10.1002/jbmr.2139

  2. COMP mutations: Domain-dependent relationship between abnormal chondrocyte trafficking and clinical PSACH and MED phenotypes

    Journal of Cellular Biochemistry

    Volume 103, Issue 3, 15 February 2008, Pages: 778–787, Tung-Ling L. Chen, Karen L. Posey, Jacqueline T. Hecht and Barbara M. Vertel

    Version of Record online : 14 JUN 2007, DOI: 10.1002/jcb.21445

  3. MED and PSACH COMP mutations affect chondrogenesis in chicken limb bud micromass cultures

    Journal of Cellular Physiology

    Volume 224, Issue 3, September 2010, Pages: 817–826, J. Roman-Blas, A.S. Dion, M.R. Seghatoleslami, K. Giunta, P. Oca, S.A. Jimenez and C.J. Williams

    Version of Record online : 21 MAY 2010, DOI: 10.1002/jcp.22185

  4. You have free access to this content
    Mechanisms and models of endoplasmic reticulum stress in chondrodysplasia

    Developmental Dynamics

    Volume 243, Issue 7, July 2014, Pages: 875–893, Sara E. Patterson and Caroline N. Dealy

    Version of Record online : 16 APR 2014, DOI: 10.1002/dvdy.24131

  5. You have full text access to this OnlineOpen article
    Pseudoachondroplasia and multiple epiphyseal dysplasia: A 7-year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution

    Human Mutation

    Volume 33, Issue 1, January 2012, Pages: 144–157, Gail C. Jackson, Laureane Mittaz-Crettol, Jacqueline A. Taylor, Geert R. Mortier, Juergen Spranger, Bernhard Zabel, Martine Le Merrer, Valerie Cormier-Daire, Christine M. Hall, Amaka Offiah, Michael J. Wright, Ravi Savarirayan, Gen Nishimura, Simon C. Ramsden, Rob Elles, Luisa Bonafe, Andrea Superti-Furga, Sheila Unger, Andreas Zankl and Michael D. Briggs

    Version of Record online : 31 OCT 2011, DOI: 10.1002/humu.21611

  6. Novel mutation in exon 18 of the cartilage oligomeric matrix protein gene causes a severe pseudoachondroplasia

    American Journal of Medical Genetics

    Volume 104, Issue 2, 22 November 2001, Pages: 135–139, Akihiko Mabuchi, Nobuhiko Haga, Toshiyuki Ikeda, Noriyo Manabe, Hirofumi Ohashi, Yoshio Takatori, Kozo Nakamura and Shiro Ikegawa

    Version of Record online : 8 OCT 2001, DOI: 10.1002/ajmg.10067

  7. Circulating COMP is decreased in pseudoachondroplasia and multiple epiphyseal dysplasia patients carrying COMP mutations

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 1, 15 August 2004, Pages: 35–38, Akihiko Mabuchi, Shigeki Momohara, Hirofumi Ohashi, Yoshio Takatori, Nobuhiko Haga, Gen Nishimura and Shiro Ikegawa

    Version of Record online : 7 JUN 2004, DOI: 10.1002/ajmg.a.30164

  8. Pseudoachondroplasia and multiple epiphyseal dysplasia: New etiologic developments

    American Journal of Medical Genetics

    Volume 106, Issue 4, Winter 2001, Pages: 244–250, Sheila Unger and Jacqueline T. Hecht

    Version of Record online : 25 JAN 2002, DOI: 10.1002/ajmg.10234

  9. Cartilage Oligomeric Matrix Protein

    Standard Article

    Encyclopedia Of Molecular Medicine

    Jack Lawler and Hui Chen

    Published Online : 15 JAN 2002, DOI: 10.1002/0471203076.emm0181

  10. Pseudoachondroplasia and painful sequelae

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2618–2622, Candace Gamble, Joanne Nguyen, S. Shahrukh Hashmi and Jacqueline T. Hecht

    Version of Record online : 14 JUL 2015, DOI: 10.1002/ajmg.a.37253

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    A secreted variant of cartilage oligomeric matrix protein carrying a chondrodysplasia-causing mutation (p.H587R) disrupts collagen fibrillogenesis

    Arthritis & Rheumatism

    Volume 63, Issue 1, January 2011, Pages: 159–167, Uwe Hansen, Nicole Platz, Alexander Becker, Peter Bruckner, Mats Paulsson and Frank Zaucke

    Version of Record online : 28 DEC 2010, DOI: 10.1002/art.30073

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    Molecular mapping of a site for Cd2+-induced modification of human ether-à-go-go-related gene (hERG) channel activation

    The Journal of Physiology

    Volume 567, Issue 3, September 2005, Pages: 737–755, David Fernandez, Azad Ghanta, Krista I. Kinard and Michael C. Sanguinetti

    Version of Record online : 12 SEP 2005, DOI: 10.1113/jphysiol.2005.089094

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    Expression of mutant cartilage oligomeric matrix protein in human chondrocytes induces the pseudoachondroplasia phenotype

    Journal of Orthopaedic Research

    Volume 24, Issue 4, April 2006, Pages: 700–707, Thomas M. Merritt, Joseph L. Alcorn, Richard Haynes and Jacqueline T. Hecht

    Version of Record online : 2 MAR 2006, DOI: 10.1002/jor.20100

  14. Coming together is a beginning: The making of an intervertebral disc

    Birth Defects Research Part C: Embryo Today: Reviews

    Volume 102, Issue 1, March 2014, Pages: 83–100, Wilson C. W. Chan, Tiffany Y. K. Au, Vivian Tam, Kathryn S. E. Cheah and Danny Chan

    Version of Record online : 27 MAR 2014, DOI: 10.1002/bdrc.21061

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    Homozygosity for a missense variant in COMP gene associated with severe pseudoachondroplasia

    Clinical Genetics

    Volume 93, Issue 1, January 2018, Pages: 182–186, M. Tariq, T.N. Khan, L. Lundin, M. Jameel, T. Lönnerholm, S.M. Baig, N. Dahl and J. Klar

    Version of Record online : 21 NOV 2017, DOI: 10.1111/cge.13091

  16. The ups and downs of parting COMPany Poly-aspartic acid tract instability: a novel expansion–contraction mutation

    Clinical Genetics

    Volume 56, Issue 4, October 1999, Pages: 259–260, Paul Goldberg

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.560402.x

  17. Genetics and manifold effects of strong's luxoid gene in the mouse, including its interactions with green's luxoid and carter's luxate genes

    Journal of Morphology

    Volume 110, Issue 3, May 1962, Pages: 391–420, Paulinus F. Forsthoefel

    Version of Record online : 6 FEB 2005, DOI: 10.1002/jmor.1051100306

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    Combined role of type IX collagen and cartilage oligomeric matrix protein in cartilage matrix assembly: Cartilage oligomeric matrix protein counteracts type IX collagen–induced limitation of cartilage collagen fibril growth in mouse chondrocyte cultures

    Arthritis & Rheumatism

    Volume 60, Issue 12, December 2009, Pages: 3676–3685, K. Blumbach, Y. M. Bastiaansen-Jenniskens, J. DeGroot, M. Paulsson, G. J. V. M. van Osch and F. Zaucke

    Version of Record online : 30 NOV 2009, DOI: 10.1002/art.24979

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    Bodenin: A novel murine gene expressed in restricted areas of the brain

    Developmental Dynamics

    Volume 212, Issue 2, June 1998, Pages: 293–303, Anja M. Faisst and Peter Gruss

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-0177(199806)212:2<293::AID-AJA14>3.0.CO;2-5

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    The Yersinia pestis type III secretion needle plays a role in the regulation of Yop secretion

    Molecular Microbiology

    Volume 57, Issue 6, September 2005, Pages: 1719–1733, Julie Torruellas, Michael W. Jackson, Jeffry W. Pennock and Gregory V. Plano

    Version of Record online : 27 JUL 2005, DOI: 10.1111/j.1365-2958.2005.04790.x