Učitavanje...
On the Mechanism of MgATP-dependent Gating of CFTR Cl(−) Channels
CFTR, the product of the gene mutated in cystic fibrosis, is an ATPase that functions as a Cl(−) channel in which bursts of openings separate relatively long interburst closed times (τib). Channel gating is controlled by phosphorylation and MgATP, but the underlying molecular mechanisms remain contr...
Spremljeno u:
| Glavni autori: | , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Rockefeller University Press
2003
|
| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2217317/ https://ncbi.nlm.nih.gov/pubmed/12508051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.20028673 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|