A combined analysis of the cystic fibrosis transmembrane conductance regulator: implications for structure and disease models. (Q48347827)

10 February 2018

title

A combined analysis of the cystic fibrosis transmembrane conductance regulator: implications for structure and disease models. (English)

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10 February 2018

main subject

transmembrane protein

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cystic fibrosis

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author name string

J M Chen

1

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10 February 2018

C Cutler

2

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10 February 2018

C Jacques

3

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10 February 2018

G Boeuf

4

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10 February 2018

E Denamur

5

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10 February 2018

G Lecointre

6

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10 February 2018

B Mercier

7

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10 February 2018

G Cramb

8

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10 February 2018

C Férec

9

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10 February 2018

publication date

1 September 2001

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10 February 2018

Molecular Biology and Evolution

published in

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10 February 2018

volume

18

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10 February 2018

issue

9

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10 February 2018

page(s)

1771-1788

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10 February 2018

Differential interactions of nucleotides at the two nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator

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Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulator

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Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.

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Severed channels probe regulation of gating of cystic fibrosis transmembrane conductance regulator by its cytoplasmic domains

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Localization of sequences within the C-terminal domain of the cystic fibrosis transmembrane conductance regulator which impact maturation and stability

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C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutation

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Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore

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Non-pore lining amino acid side chains influence anion selectivity of the human CFTR Cl- channel expressed in mammalian cell lines

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Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels

21 January 2018

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Structural model of the nucleotide-binding conserved component of periplasmic permeases

21 January 2018

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Differential function of the two nucleotide binding domains on cystic fibrosis transmembrane conductance regulator

21 January 2018

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Analysis of a DNase I hypersensitive site located -20.9 kb upstream of the CFTR gene

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21 January 2018

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21 January 2018

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Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity.

21 January 2018

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Structure and function of the CFTR chloride channel

21 January 2018

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Nucleotide occlusion in the human cystic fibrosis transmembrane conductance regulator. Different patterns in the two nucleotide binding domains

21 January 2018

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21 January 2018

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Molecular analysis of the ovine cystic fibrosis transmembrane conductance regulator gene

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The two halves of CFTR form a dual-pore ion channel

21 January 2018

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21 January 2018

Identifiers

DOI

1 reference

10 February 2018

PubMed ID

11504857

1 reference

10 February 2018