(Q43684821)

English

Cysteine substitutions reveal dual functions of the amino-terminal tail in cystic fibrosis transmembrane conductance regulator channel gating

scientific article published on 23 July 2001

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 November 2017

Cysteine substitutions reveal dual functions of the amino-terminal tail in cystic fibrosis transmembrane conductance regulator channel gating (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

cystic fibrosis

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transmembrane protein

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author name string

Fu J

1

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Kirk KL

2

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

language of work or name

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publication date

23 July 2001

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

25 November 2017

276

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

38

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

35660-35668

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Cystic Fibrosis Heterozygote Resistance to Cholera Toxin in the Cystic Fibrosis Mouse Model

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator)

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Regulation of CFTR Cl- channel gating by ATP binding and hydrolysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Expression and characterization of the NBD1-R domain region of CFTR: evidence for subunit-subunit interactions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

CFTR chloride channel regulation by an interdomain interaction.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Severed molecules functionally define the boundaries of the cystic fibrosis transmembrane conductance regulator's NH(2)-terminal nucleotide binding domain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Preservation and staining of myelinated nerve fibers.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Redox reagents and divalent cations alter the kinetics of cystic fibrosis transmembrane conductance regulator channel gating

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Cystic fibrosis transmembrane conductance regulator: the purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105079200

21 January 2018

Identifiers

10.1074/JBC.M105079200

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

ResearchGate publication ID

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