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There are 33436 results for: content related to: Mouse myodystrophy ( myd ) mutation: Refined mapping in an interval flanked by homology with distal human 4q

  1. Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis

    Annals of Neurology

    Volume 43, Issue 3, March 1998, Pages: 279–282, Dr Rabi Tawil, Denise A. Figlewicz, Robert C. Griggs and Barbara Weiffenbach

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410430303

  2. MYD88 L265P and CXCR4 mutations in lymphoplasmacytic lymphoma identify cases with high disease activity

    British Journal of Haematology

    Volume 169, Issue 6, June 2015, Pages: 795–803, Janine Schmidt, Birgit Federmann, Natalie Schindler, Julia Steinhilber, Irina Bonzheim, Falko Fend and Leticia Quintanilla-Martinez

    Version of Record online : 29 MAR 2015, DOI: 10.1111/bjh.13361

  3. You have full text access to this OnlineOpen article
    Defects in Glycosylation Impair Satellite Stem Cell Function and Niche Composition in the Muscles of the Dystrophic Largemyd Mouse

    STEM CELLS

    Volume 30, Issue 10, October 2012, Pages: 2330–2341, Jacob Ross, Abigail Benn, Jacqueline Jonuschies, Luisa Boldrin, Francesco Muntoni, Jane E. Hewitt, Susan C. Brown and Jennifer E. Morgan

    Version of Record online : 20 SEP 2012, DOI: 10.1002/stem.1197

  4. Incomplete manifestations of myotonic dystrophy in a large kinship in labrador

    Annals of Neurology

    Volume 11, Issue 6, June 1982, Pages: 582–591, Dr. William Pryse-Phillips, Gordon J. Johnson and Bodil Larsen

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410110606

  5. Sarcolemmal reorganization in facioscapulohumeral muscular dystrophy

    Annals of Neurology

    Volume 59, Issue 2, February 2006, Pages: 289–297, Patrick Reed, Neil C. Porter, John Strong, David W. Pumplin, Andrea M. Corse, Paul W. Luther, Kevin M. Flanigan and Robert J. Bloch

    Version of Record online : 25 JAN 2006, DOI: 10.1002/ana.20750

  6. You have free access to this content
    Stoichiometry of sodium and potassium transport in erythrocytes from patients with myotonic muscular dystrophy.

    The Journal of Physiology

    Volume 254, Issue 1, January 1, 1976, Pages: 169–181, K L Hull Jr and A D Roses

    Version of Record online : 1 JAN 1976, DOI: 10.1113/jphysiol.1976.sp011227

  7. You have full text access to this Open Access content
    Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects

    Journal of Cellular and Molecular Medicine

    Volume 14, Issue 1-2, January-February 2010, Pages: 275–289, Marietta Barro, Gilles Carnac, Sébastien Flavier, Jacques Mercier, Yegor Vassetzky and Dalila Laoudj-Chenivesse

    Version of Record online : 24 MAY 2008, DOI: 10.1111/j.1582-4934.2008.00368.x

  8. Excessive plasma K+ increase after ischemic exercise in myotonic muscular dystrophy

    Muscle & Nerve

    Volume 13, Issue 1, January 1990, Pages: 27–32, Dr. Ron A. Wevers, Dr. Ed M. G. Joosten, Dr., MD J. B. Margot van de Biezenbos, Dr. Ad G. M. Theewes and Dr. Jacques H. Veerkamp

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880130107

  9. DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo

    Annals of Neurology

    Volume 69, Issue 3, March 2011, Pages: 540–552, Lindsay M. Wallace, Sara E. Garwick, Wenyan Mei, Alexandra Belayew, Frederique Coppee, Katherine J. Ladner, Denis Guttridge, Jing Yang and Scott Q. Harper

    Version of Record online : 8 DEC 2010, DOI: 10.1002/ana.22275

  10. Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy

    Annals of Neurology

    Volume 78, Issue 3, September 2015, Pages: 387–400, Virginie Mariot, Stephane Roche, Christophe Hourdé, Debora Portilho, Sabrina Sacconi, Francesca Puppo, Stephanie Duguez, Philippe Rameau, Nathalie Caruso, Anne-Lise Delezoide, Claude Desnuelle, Bettina Bessières, Sophie Collardeau, Leonard Feasson, Thierry Maisonobe, Frederique Magdinier, Françoise Helmbacher, Gillian Butler-Browne, Vincent Mouly and Julie Dumonceaux

    Version of Record online : 3 JUL 2015, DOI: 10.1002/ana.24446

  11. Facioscapulohumeral muscular dystrophy

    Muscle & Nerve

    Volume 34, Issue 1, July 2006, Pages: 1–15, Rabi Tawil and Silvère M. Van Der Maarel

    Version of Record online : 28 FEB 2006, DOI: 10.1002/mus.20522

  12. CXCR4 WHIM-like frameshift and nonsense mutations promote ibrutinib resistance but do not supplant MYD88L265P-directed survival signalling in Waldenström macroglobulinaemia cells

    British Journal of Haematology

    Volume 168, Issue 5, March 2015, Pages: 701–707, Yang Cao, Zachary R. Hunter, Xia Liu, Lian Xu, Guang Yang, Jie Chen, Nickolas Tsakmaklis, Sandra Kanan, Jorge J. Castillo and Steven P. Treon

    Version of Record online : 5 NOV 2014, DOI: 10.1111/bjh.13200

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    Allele-specific PCR is a powerful tool for the detection of the MYD88 L265P mutation in diffuse large B cell lymphoma and decalcified bone marrow samples

    British Journal of Haematology

    Volume 171, Issue 1, October 2015, Pages: 145–148, Annette M. Staiger, M. Michaela Ott, Stefani Parmentier, Andreas Rosenwald, German Ott, Heike Horn and Ernst-Ulrich Griese

    Version of Record online : 30 MAR 2015, DOI: 10.1111/bjh.13369

  14. Patients with myotonic dystrophy, a possible segmental progeroid syndrome, and duchenne muscular dystrophy have fibroblasts with normal limits for in vitro lifespan and growth characteristics

    Journal of Cellular Physiology

    Volume 107, Issue 2, May 1981, Pages: 255–260, Richard L. Wertz, Geoffrey B. Hartwig, Arlo P. Frost, Jere J. Brophy, Susan K. Atwater and Allen D. Roses

    Version of Record online : 4 FEB 2005, DOI: 10.1002/jcp.1041070212

  15. Cognitive function in early adult and adult onset myotonic dystrophy

    Acta Neurologica Scandinavica

    Volume 91, Issue 6, June 1995, Pages: 456–461, K. P. M. van Spaendonck, J. P. Ter Bruggen, E. W. A. Weyn Banningh, B. A.M. Maassen, J. B. M. van, de Biezenbos and F.J. M. Gabreëls

    Version of Record online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1995.tb00446.x

  16. Properties of Ca2+-activated K+ channels in erythrocytes from patients with myotonic muscular dystrophy

    Muscle & Nerve

    Volume 21, Issue 11, November 1998, Pages: 1465–1472, Mario Pellegrino, Monica Pellegrini, Paolo Bigini and Annalisa Scimemi

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4598(199811)21:11<1465::AID-MUS15>3.0.CO;2-#

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    MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome

    British Journal of Haematology

    Volume 167, Issue 4, November 2014, Pages: 506–513, Stéphanie Poulain, Eileen M. Boyle, Christophe Roumier, Hélène Demarquette, Mathieu Wemeau, Sandrine Geffroy, Charles Herbaux, Elisabeth Bertrand, Bénédicte Hivert, Louis Terriou, Albert Verrier, Jean Paul Pollet, Claude Alain Maurage, Brigitte Onraed, Franck Morschhauser, Bruno Quesnel, Patrick Duthilleul, Claude Preudhomme and Xavier Leleu

    Version of Record online : 27 AUG 2014, DOI: 10.1111/bjh.13078

  18. Eye movement disorder: An early expression of the myotonic dystrophy gene?

    Muscle & Nerve

    Volume 15, Issue 3, March 1992, Pages: 358–361, Dr. Jan P. ter Bruggen, Dr. Cees C. Tijssen, Dr. Han G. Brunner, Dr. Bernard A. van Oost and Dr. Louis A. K. Bastiaensen

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880150315

  19. Myotonic muscular dystrophy: Morphology, histochemistry, and growth characteristics of cultured skin fibroblasts

    Muscle & Nerve

    Volume 5, Issue 2, February 1982, Pages: 125–130, Dr. Geoffrey B. Hartwig, Dr. Sara E. Miller, Mr. Arlo P. Frost and Dr. Allen D. Roses

    Version of Record online : 13 OCT 2004, DOI: 10.1002/mus.880050208

  20. You have free access to this content
    Cloning of two members of the SIRPα family of protein tyrosine phosphatase binding proteins in cattle that are expressed on monocytes and a subpopulation of dendritic cells and which mediate binding to CD4 T cells

    European Journal of Immunology

    Volume 28, Issue 1, January 1998, Pages: 1–11, Gareth P. Brooke, Keith R. Parsons and Chris J. Howard

    Version of Record online : 14 DEC 1998, DOI: 10.1002/(SICI)1521-4141(199801)28:01<1::AID-IMMU1>3.0.CO;2-V