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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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| Publicado no: | Dev Biol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | 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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