(Q39755118)

14 September 2017

title

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

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14 September 2017

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Elvira Sondo

3

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ORCID Public Data File 2021

Luis Galietta

series ordinal

4

object named as

Luis J V Galietta

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14 September 2017

Nicoletta Pedemonte

1

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14 September 2017

Valeria Tomati

series ordinal

2

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14 September 2017

publication date

6 January 2010

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American Journal of Physiology - Cell Physiology

14 September 2017

published in

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14 September 2017

volume

298

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14 September 2017

issue

4

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14 September 2017

page(s)

C866-74

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

14 September 2017

cites work

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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Biological and chemical approaches to diseases of proteostasis deficiency

21 January 2018

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

21 January 2018

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

21 January 2018

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Structure and function of the CFTR chloride channel

21 January 2018

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The role of the UPS in cystic fibrosis

21 January 2018

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

21 January 2018

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Chloride channels as drug targets

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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10.1152/AJPCELL.00404.2009

21 January 2018

Identifiers

DOI

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14 September 2017

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