Wordt geladen...
Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.
Cystic fibrosis transmembrane conductance regulator (CFTR) generates cAMP-regulated Cl- channels; mutations in CFTR cause defective Cl- channel function in cystic fibrosis epithelia. We used the patch-clamp technique to determine the single channel properties of Cl- channels in cell expressing recom...
Bewaard in:
| Hoofdauteurs: | , , , , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
1991
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC295615/ https://ncbi.nlm.nih.gov/pubmed/1717515 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|