טוען...
Modeling the Conformational Changes Underlying Channel Opening in CFTR
Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator protein (CFTR) cause cystic fibrosis (CF), the most common life-shortening genetic disease among Caucasians. Although general features of the structure of CFTR have been predicted from homology models, the conform...
שמור ב:
| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Public Library of Science
2013
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3785483/ https://ncbi.nlm.nih.gov/pubmed/24086355 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0074574 |
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