The cystic fibrosis transmembrane conductance regulator gene.
about
The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era.Gene therapy: light is finally in the tunnelPharmacological induction of CFTR function in patients with cystic fibrosis: mutation-specific therapy.Calculating expected lung deposition of aerosolized administration of AAV vector in human clinical studies.Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndromeRectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations.Salmonella typhi uses CFTR to enter intestinal epithelial cells.Cystic fibrosis in adults. From researcher to practitioner.CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.Heterogeneous spectrum of CFTR gene mutations in Korean patients with cystic fibrosis.Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screen.Side chain and backbone contributions of Phe508 to CFTR folding.The cystic fibrosis gene: a molecular genetic perspectiveBiomarkers of lung-related diseases: current knowledge by proteomic approaches.Cystic fibrosis: need for mass deployable screening methods.The thymidine-dependent small-colony-variant phenotype is associated with hypermutability and antibiotic resistance in clinical Staphylococcus aureus isolates.Induction of HSP70 promotes DeltaF508 CFTR trafficking.Differential effects of apical and basolateral uridine triphosphate on intestinal epithelial chloride secretion.A human epithelium-specific vector optimized in rat pneumocytes for lung gene therapy.A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules.Functional expression and apical localization of the cystic fibrosis transmembrane conductance regulator in MDCK I cells.DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research.Pharmacology of CFTR chloride channel activity.Molecular basis of cystic fibrosis: from bench to bedside
P2860
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P2860
The cystic fibrosis transmembrane conductance regulator gene.
description
1995 nî lūn-bûn
@nan
1995 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մարտին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
The cystic fibrosis transmembrane conductance regulator gene.
@ast
The cystic fibrosis transmembrane conductance regulator gene.
@en
The cystic fibrosis transmembrane conductance regulator gene.
@nl
type
label
The cystic fibrosis transmembrane conductance regulator gene.
@ast
The cystic fibrosis transmembrane conductance regulator gene.
@en
The cystic fibrosis transmembrane conductance regulator gene.
@nl
prefLabel
The cystic fibrosis transmembrane conductance regulator gene.
@ast
The cystic fibrosis transmembrane conductance regulator gene.
@en
The cystic fibrosis transmembrane conductance regulator gene.
@nl
P2860
P356
P1476
The cystic fibrosis transmembrane conductance regulator gene.
@en
P2093
P2860
P304
P356
10.1164/AJRCCM/151.3_PT_2.S47
P407
P433
P577
1995-03-01T00:00:00Z