(Q38812271)

6 September 2017

Cytoplasmic pathway followed by chloride ions to enter the CFTR channel pore (English)

1 reference

6 September 2017

3

Paul Linsdell

1 reference

6 September 2017

Yassine El Hiani

1

1 reference

PubMed ID

26659082

6 September 2017

Alexander Negoda

series ordinal

2

1 reference

6 September 2017

13 December 2015

1 reference

Cellular and Molecular Life Sciences

6 September 2017

1 reference

6 September 2017

73

1 reference

6 September 2017

9

1 reference

6 September 2017

1917-1925

1 reference

https://scigraph.springernature.com/pub.10.1007/s00018-015-2113-x

6 September 2017

0 references

cites work

Understanding how cystic fibrosis mutations disrupt CFTR function: from single molecules to animal models

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

The human ATP-binding cassette (ABC) transporter superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

CLC-0 and CFTR: chloride channels evolved from transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Functional architecture of the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Ion channels versus ion pumps: the principal difference, in principle

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Conformational changes opening and closing the CFTR chloride channel: insights from cysteine scanning mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Full-open and closed CFTR channels, with lateral tunnels from the cytoplasm and an alternative position of the F508 region, as revealed by molecular dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR): CLOSED AND OPEN STATE CHANNEL MODELS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Channel-lining residues in the M3 membrane-spanning segment of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Cystic fibrosis transmembrane conductance regulator: a molecular model defines the architecture of the anion conduction path and locates a "bottleneck" in the pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

The Fifth Transmembrane Segment of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Its Anion Permeation Pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Cysteine-independent inhibition of the CFTR chloride channel by the cysteine-reactive reagent sodium (2-sulphonatoethyl) methanethiosulphonate

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Functional differences in pore properties between wild-type and cysteine-less forms of the CFTR chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Changes in accessibility of cytoplasmic substances to the pore associated with activation of the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Dual roles of the sixth transmembrane segment of the CFTR chloride channel in gating and permeation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Alignment of transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Functional arrangement of the 12th transmembrane region in the CFTR chloride channel pore based on functional investigation of a cysteine-less CFTR variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Relative contribution of different transmembrane segments to the CFTR chloride channel pore.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Role of the juxtamembrane region of cytoplasmic loop 3 in the gating and conductance of the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Structural basis for the channel function of a degraded ABC transporter, CFTR (ABCC7).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Cysteine scanning of CFTR's first transmembrane segment reveals its plausible roles in gating and permeation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-015-2113-X

Cystic fibrosis transmembrane conductance regulator (ABCC7) structure

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26659082

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The CFTR ion channel: gating, regulation, and anion permeation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26659082

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00018-015-2113-X

1 reference

6 September 2017

1 reference

PubMed ID

26659082