发表研究结果有使用 ab58067?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab58067 被引用在 5 文献中.

  • Christodoulou DC  et al. 5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy. J Clin Invest 124:1364-70 (2014). WB ; Mouse . PubMed: 24509080
  • Domenighetti AA  et al. Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice. Hum Mol Genet N/A:N/A (2013). PubMed: 23975679
  • Black KM  et al. Preliminary biomarkers for identification of human ascending thoracic aortic aneurysm. J Am Heart Assoc 2:e000138 (2013). WB ; Human . PubMed: 24231657
  • Hartmannova H  et al. Isolated X-linked hypertrophic cardiomyopathy caused by a novel mutation of the four-and-a-half LIM domain 1 gene. Circ Cardiovasc Genet 6:543-51 (2013). IHC-P ; Human . PubMed: 24114807
  • Gueneau L  et al. Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy. Am J Hum Genet 85:338-53 (2009). WB ; Human . PubMed: 19716112

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