(Q51795601)

English

Direct and indirect effects of mutations at the outer mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

scientific article published in April 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

Direct and indirect effects of mutations at the outer mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

cystic fibrosis

0 references

transmembrane protein

0 references

3

object named as

Paul Linsdell

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

author name string

Jing-Jun Zhou

1

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

Mohammad Fatehi

2

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

publication date

1 April 2007

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

number of pages

14

1 reference

based on heuristic

inferred from page(s)

Journal of Membrane Biology

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

216

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

2-3

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

129-142

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

https://scigraph.springernature.com/pub.10.1007/s00232-007-9056-6

0 references

Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue

1 reference

https://api.crossref.org/works/10.1007%2FS00232-007-9056-6

21 January 2018

CFTR: What's it like inside the pore?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular determinants of Au(CN)(2)(-) binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl(-) channel pore

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positive charges at the intracellular mouth of the pore regulate anion conduction in the CFTR chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and crystallization of the cystic fibrosis transmembrane conductance regulator (CFTR).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a second blocker binding site at the cytoplasmic mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of lonidamine inhibition of the CFTR chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of nucleotide-binding domain 1 of the cystic fibrosis transmembrane conductance regulator

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interactions between impermeant blocking ions in the cystic fibrosis transmembrane conductance regulator chloride channel pore: evidence for anion-induced conformational changes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the origin of asymmetric interactions between permeant anions and the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and function of the CFTR chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Location of a common inhibitor binding site in the cytoplasmic vestibule of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maximization of the rate of chloride conduction in the CFTR channel pore by ion-ion interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

State-dependent chemical reactivity of an engineered cysteine reveals conformational changes in the outer vestibule of the cystic fibrosis transmembrane conductance regulator

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ionic Blockage of Sodium Channels in Nerve

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surface charges and ion channel function

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular determinants and role of an anion binding site in the external mouth of the CFTR chloride channel pore

1 reference

https://pubmed.ncbi.nlm.nih.gov/17673962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00232-007-9056-6

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/17673962

ResearchGate publication ID

0 references

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