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Zebrafish short fin mutations in Connexin43 lead to aberrant gap junctional intercellular communication

Mutations in the zebrafish connexin43 (cx43) gene cause the short fin phenotype, indicating that direct cell-cell communication contributes to bone length. Three independently generated cx43 alleles exhibit short segments of variable sizes, suggesting that gap junctional intercellular communication...

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書誌詳細
主要な著者: Hoptak-Solga, Angela D., Klein, Kathryn A., DeRosa, Adam M., White, Thomas W., Iovine, M. Kathryn
フォーマット: Artigo
言語:Inglês
出版事項: 2007
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2044562/
https://ncbi.nlm.nih.gov/pubmed/17599838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.febslet.2007.06.030
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