(Q40677468)

English

A mutation in the cystic fibrosis transmembrane conductance regulator generates a novel internalization sequence and enhances endocytic rates

scientific article published on 15 January 2003

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scholarly article

1 reference

Europe PubMed Central

22 September 2017

A mutation in the cystic fibrosis transmembrane conductance regulator generates a novel internalization sequence and enhances endocytic rates (English)

1 reference

Europe PubMed Central

22 September 2017

cystic fibrosis

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transmembrane protein

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author name string

Mark R Silvis

1

1 reference

Europe PubMed Central

22 September 2017

John A Picciano

2

1 reference

Europe PubMed Central

22 September 2017

Carol Bertrand

3

1 reference

Europe PubMed Central

22 September 2017

Kelly Weixel

4

1 reference

Europe PubMed Central

22 September 2017

Robert J Bridges

5

1 reference

Europe PubMed Central

22 September 2017

Neil A Bradbury

6

1 reference

Europe PubMed Central

22 September 2017

language of work or name

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publication date

15 January 2003

1 reference

Europe PubMed Central

22 September 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

22 September 2017

278

1 reference

Europe PubMed Central

22 September 2017

11554-11560

1 reference

Europe PubMed Central

22 September 2017

13

1 reference

Europe PubMed Central

22 September 2017

Traffic jam: a compendium of human diseases that affect intracellular transport processes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

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.M212843200

21 January 2018

Immunocytochemical localization of the cystic fibrosis gene product CFTR

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Linking cargo to vesicle formation: receptor tail interactions with coat proteins.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

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.M212843200

21 January 2018

Mu 2 binding directs the cystic fibrosis transmembrane conductance regulator to the clathrin-mediated endocytic pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

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.M212843200

21 January 2018

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Cystic fibrosis: genotypic and phenotypic variations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Identification of a non-canonical tyrosine-based endocytic motif in an ionotropic receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Analysis of a mutant strain of human fibroblasts with a defect in the internalization of receptor-bound low density lipoprotein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

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.M212843200

21 January 2018

Disease-Associated Mutations in Cytoplasmic Loops 1 and 2 of Cystic Fibrosis Transmembrane Conductance Regulator Impede Processing or Opening of the Channel†

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patients

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M212843200

21 January 2018

Identifiers

10.1074/JBC.M212843200

1 reference

Europe PubMed Central

22 September 2017

1 reference

Europe PubMed Central

22 September 2017

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