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 (�...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: van Doorninck, J H, French, P J, Verbeek, E, Peters, R H, Morreau, H, Bijman, J, Scholte, B J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1995
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC394531/
https://ncbi.nlm.nih.gov/pubmed/7556083
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia