Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling.
about
A genomic signature approach to rescue ΔF508-cystic fibrosis transmembrane conductance regulator biosynthesis and function.Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.Pharmacological Correctors of Mutant CFTR Mistrafficking.Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain.Prolyl-4-hydroxylase α subunit 2 promotes breast cancer progression and metastasis by regulating collagen deposition.Pharmacological correction of misfolding of ABC proteins.Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis Mutation.Pharmacological rescue of the mutant cystic fibrosis transmembrane conductance regulator (CFTR) detected by use of a novel fluorescence platformMurine and human CFTR exhibit different sensitivities to CFTR potentiators.Ouabain Mimics Low Temperature Rescue of F508del-CFTR in Cystic Fibrosis Epithelial Cells.A synonymous codon change alters the drug sensitivity of ΔF508 cystic fibrosis transmembrane conductance regulator.Functional Rescue of F508del-CFTR Using Small Molecule CorrectorsRole of STARD4 and NPC1 in intracellular sterol transport.Trimethylangelicin promotes the functional rescue of mutant F508del CFTR protein in cystic fibrosis airway cells.Revisiting CFTR inhibition: a comparative study of CFTRinh -172 and GlyH-101 inhibitorsGoblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release.SYVN1, NEDD8, and FBXO2 Proteins Regulate ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Ubiquitin-mediated Proteasomal Degradation.High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel.Matrine in association with FD‑2 stimulates F508del‑cystic fibrosis transmembrane conductance regulator activity in the presence of corrector VX809.Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.
P2860
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P2860
Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Rescue of the mutant CFTR chlo ...... by gene expression profiling.
@ast
Rescue of the mutant CFTR chlo ...... by gene expression profiling.
@en
type
label
Rescue of the mutant CFTR chlo ...... by gene expression profiling.
@ast
Rescue of the mutant CFTR chlo ...... by gene expression profiling.
@en
prefLabel
Rescue of the mutant CFTR chlo ...... by gene expression profiling.
@ast
Rescue of the mutant CFTR chlo ...... by gene expression profiling.
@en
P2093
P2860
P50
P1476
Rescue of the mutant CFTR chlo ...... d by gene expression profiling
@en
P2093
Alessia Isabella Esposito
Emanuela Caci
Valeria Tomati
P2860
P304
P356
10.1152/AJPCELL.00507.2010
P577
2011-07-13T00:00:00Z