(Q43766348)

26 November 2017

title

Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation (English)

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26 November 2017

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Dérand R

1

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26 November 2017

Bulteau-Pignoux L

2

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26 November 2017

Mettey Y

3

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26 November 2017

Zegarra-Moran O

4

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26 November 2017

Howell LD

5

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26 November 2017

Randak C

6

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26 November 2017

Galietta LJ

7

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26 November 2017

Cohn JA

8

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26 November 2017

Norez C

9

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26 November 2017

Romio L

10

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26 November 2017

Vierfond JM

11

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26 November 2017

Joffre M

12

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26 November 2017

Becq F

13

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26 November 2017

language of work or name

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1 November 2001

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American Journal of Physiology - Cell Physiology

26 November 2017

published in

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26 November 2017

volume

281

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26 November 2017

issue

5

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26 November 2017

page(s)

C1657-66

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Phosphatase inhibitors activate normal and defective CFTR chloride channels

26 November 2017

cites work

1 reference

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21 January 2018

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cAMP- and Ca2+-independent activation of cystic fibrosis transmembrane conductance regulator channels by phenylimidazothiazole drugs

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21 January 2018

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Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

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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21 January 2018

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Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis.

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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21 January 2018

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21 January 2018

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cAMP-independent activation of CFTR Cl channels by the tyrosine kinase inhibitor genistein

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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Phosphorylation by protein kinase C is required for acute activation of cystic fibrosis transmembrane conductance regulator by protein kinase A.

21 January 2018

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ATPase activity of the cystic fibrosis transmembrane conductance regulator

21 January 2018

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Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding

21 January 2018

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A recombinant polypeptide model of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator functions as an active ATPase, GTPase and adenylate kinase.

21 January 2018

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

21 January 2018

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Pharmacology of CFTR chloride channel activity.

21 January 2018

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Organic extraction of P i with isobutanol/toluene

21 January 2018

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Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

21 January 2018

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21 January 2018

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Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator

21 January 2018

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Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

21 January 2018

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A simple assay for agonist-regulated Cl and K conductances in salt-secreting epithelial cells

21 January 2018

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Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.281.5.C1657

10.1152/AJPCELL.2001.281.5.C1657

21 January 2018

Identifiers

DOI

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