发表研究结果有使用 ab23937?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab23937 被引用在 9 文献中.

  • Albrecht I  et al. Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies. J Clin Invest 125:4612-24 (2015). PubMed: 26551678
  • Feeney SJ  et al. FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1). PLoS One 10:e0117665 (2015). WB . PubMed: 25695429
  • Sabatelli P  et al. Aggresome-Autophagy Involvement in a Sarcopenic Patient with Rigid Spine Syndrome and a p.C150R Mutation in FHL1 Gene. Front Aging Neurosci 6:215 (2014). WB . PubMed: 25191266
  • D'Arcy C  et al. X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 Gene. J Child Neurol N/A:N/A (2014). IHC-Fr ; Human . PubMed: 25246303
  • D'Arcy CE  et al. Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. Hum Mol Genet N/A:N/A (2013). PubMed: 24087791
  • Wu MP  et al. G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivo. FEBS J 280:6097-113 (2013). PubMed: 24102982
  • Veith C  et al. Paxillin regulates pulmonary arterial smooth muscle cell function in pulmonary hypertension. Am J Pathol 181:1621-33 (2012). IP, ICC/IF . PubMed: 22959909
  • Isumi Y  et al. Transgenic overexpression of USP15 in the heart induces cardiac remodeling in mice. Biochem Biophys Res Commun 405:216-21 (2011). WB ; Human . PubMed: 21219870
  • Schessl J  et al. Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. Brain 132:452-64 (2009). PubMed: 19181672

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