(Q40850802)

English

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

scientific article

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scholarly article

1 reference

Europe PubMed Central

24 September 2017

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

1 reference

Europe PubMed Central

24 September 2017

transmembrane protein

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cystic fibrosis

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author name string

Gentzsch M

1

1 reference

Europe PubMed Central

24 September 2017

Riordan JR

2

1 reference

Europe PubMed Central

24 September 2017

language of work or name

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publication date

1 January 2001

1 reference

Europe PubMed Central

24 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

24 September 2017

276

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Europe PubMed Central

24 September 2017

1291-1298

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Europe PubMed Central

24 September 2017

2

1 reference

Europe PubMed Central

24 September 2017

Cystic fibrosis: channel, catalytic, and folding properties of the CFTR protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Cystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

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.M003672200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

CFTR chloride channel regulation by an interdomain interaction.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Efficient expression of CFTR function with adeno-associated virus vectors that carry shortened CFTR genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

PDZ domains bind carboxy-terminal sequences of target proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Recognition of unique carboxyl-terminal motifs by distinct PDZ domains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

A PDZ-interacting domain in CFTR is an apical membrane polarization signal

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

PDZ domains: fundamental building blocks in the organization of protein complexes at the plasma membrane

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Cystic fibrosis transmembrane conductance regulator has an altered structure when its maturation is inhibited

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Covalent modification of the active site threonine of proteasomal beta subunits and the Escherichia coli homolog HslV by a new class of inhibitors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

The carboxyl terminus of the cystic fibrosis transmembrane conductance regulator binds to AP-2 clathrin adaptors.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

The C terminus of SUR1 is required for trafficking of KATP channels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

The structural era of endocytosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Removal of multiple arginine-framed trafficking signals overcomes misprocessing of delta F508 CFTR present in most patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Limited proteolysis as a probe for arrested conformational maturation of delta F508 CFTR

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Efficient endocytosis of the cystic fibrosis transmembrane conductance regulator requires a tyrosine-based signal

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M003672200

21 January 2018

Identifiers

10.1074/JBC.M003672200

1 reference

Europe PubMed Central

24 September 2017

1 reference

Europe PubMed Central

24 September 2017

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