Mutations in Non-muscle Myosin 2A Disrupt the Actomyosin Cytoskeleton in Sertoli Cells and Cause Male Infertility

Mutations in non-muscle myosin 2A (NM2A) encompass a wide spectrum of anomalies collectively known as MYH9-Related Disease (MYH9-RD) in humans that can include macrothrombocytopenia, glomerulosclerosis, deafness, and cataracts. We previously created mouse models of the three mutations most frequentl...

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Bibliographische Detailangaben
Veröffentlicht in:Dev Biol
Hauptverfasser: Sung, Derek C., Ahmad, Mohsin, Cervantes, Connie B. Lerma, Zhang, Yingfan, Adelstein, Robert S., Ma, Xuefei
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2020
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7855486/
https://ncbi.nlm.nih.gov/pubmed/33188738
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ydbio.2020.11.003
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