Influence of cell background on pharmacological rescue of mutant CFTR. (Q39755118)

14 September 2017

Influence of cell background on pharmacological rescue of mutant CFTR. (English)

1 reference

14 September 2017

1 reference

Elvira Sondo

3

1 reference

ORCID Public Data File 2021

Luis Galietta

series ordinal

4

object named as

Luis J V Galietta

1 reference

14 September 2017

Nicoletta Pedemonte

1

1 reference

PubMed ID

20053923

14 September 2017

Valeria Tomati

series ordinal

2

1 reference

14 September 2017

6 January 2010

1 reference

American Journal of Physiology - Cell Physiology

14 September 2017

1 reference

14 September 2017

298

1 reference

14 September 2017

4

1 reference

14 September 2017

C866-74

1 reference

Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening

14 September 2017

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Green fluorescent protein-based halide indicators with improved chloride and iodide affinities

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Novel CFTR chloride channel activators identified by screening of combinatorial libraries based on flavone and benzoquinolizinium lead compounds

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Delta F508-CFTR channels: kinetics, activation by forskolin, and potentiation by xanthines

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Binding site of activators of the cystic fibrosis transmembrane conductance regulator in the nucleotide binding domains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

A quantitative description of the activation and inhibition of CFTR by potentiators: Genistein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Phenylglycine and sulfonamide correctors of defective delta F508 and G551D cystic fibrosis transmembrane conductance regulator chloride-channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Biological and chemical approaches to diseases of proteostasis deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

3-(2-Benzyloxyphenyl)isoxazoles and isoxazolines: synthesis and evaluation as CFTR activators

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Structure and function of the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

The role of the UPS in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Rescue of DeltaF508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Chloride channels as drug targets

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Nanomolar affinity small molecule correctors of defective Delta F508-CFTR chloride channel gating.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Sequential quality-control checkpoints triage misfolded cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00404.2009

10.1152/AJPCELL.00404.2009

21 January 2018

Identifiers

DOI

1 reference

14 September 2017

1 reference

PubMed ID

20053923