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Claudin h Is Essential for Hair Cell Morphogenesis and Auditory Function in Zebrafish
Hereditary hearing loss caused by defective hair cells is one of the most common congenital diseases, whose nosogenesis is still unclear because many of the causative genes remain unidentified. Claudins are one kind of transmembrane proteins that constitute the most important components of the tight...
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| 出版年: | Front Cell Dev Biol |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8147561/ https://ncbi.nlm.nih.gov/pubmed/34046408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2021.663995 |
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