Загрузка...
A mouse model for the cystic fibrosis delta F508 mutation.
Most cystic fibrosis (CF) patients produce a mutant form (delta F508) of the cystic fibrosis transmembrane conductance regulator (CFTR), which is not properly processed in normal cells but is active as a chloride channel in several experimental systems. We used a double homologous recombination (...
Сохранить в:
Главные авторы: | , , , , , , |
---|---|
Формат: | Artigo |
Язык: | Inglês |
Опубликовано: |
1995
|
Предметы: | |
Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC394531/ https://ncbi.nlm.nih.gov/pubmed/7556083 |
Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|