ロード中...

High-content Functional Screen to Identify Proteins that Correct F508del-CFTR Function

Cystic Fibrosis is caused by mutations in CFTR, with a deletion of a phenylalanine at position 508 (F508del-CFTR) representing the most common mutation. The F508del-CFTR protein exhibits a trafficking defect and is retained in the endoplasmic reticulum. Here we describe the development of a high-con...

詳細記述

保存先:
書誌詳細
主要な著者: Trzcińska-Daneluti, Agata M., Ly, Diane, Huynh, Lise, Jiang, Chong, Fladd, Christopher, Rotin, Daniela
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Biochemistry and Molecular Biology 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2667356/
https://ncbi.nlm.nih.gov/pubmed/19088066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/mcp.M800268-MCP200
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!