ロード中...
Lens induction requires attenuation of ERK signaling by Nf1
Aphakia (lack of lens) is a rare human congenital disorder with its genetic etiology largely unknown. Even in model organisms, very few mutations are known to result in such a drastic ocular defect. In this study, we have shown that homozygous deletion of Nf1, the Ras GTPase gene underlying human ne...
保存先:
| 主要な著者: | , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2011
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3049355/ https://ncbi.nlm.nih.gov/pubmed/21233129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr014 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|