(Q40939810)

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

scientific article published on July 1999

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 September 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

cystic fibrosis

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transmembrane protein

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Gergely L Lukacs

5

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

author name string

Haardt M

1

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Benharouga M

2

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Lechardeur D

3

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Kartner N

4

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Europe PubMed Central

PubMed publication ID

25 September 2017

language of work or name

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publication date

1 July 1999

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Europe PubMed Central

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25 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

25 September 2017

274

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Europe PubMed Central

PubMed publication ID

25 September 2017

31

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Europe PubMed Central

PubMed publication ID

25 September 2017

21873-21877

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Europe PubMed Central

PubMed publication ID

25 September 2017

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

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.274.31.21873

21 January 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Cystic fibrosis: genotypic and phenotypic variations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

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.274.31.21873

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.274.31.21873

21 January 2018

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

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.274.31.21873

21 January 2018

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Protein targeting by tyrosine- and di-leucine-based signals: evidence for distinct saturable components

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

Ubiquitin-dependent protein degradation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

21 January 2018

The ubiquitin system

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

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.274.31.21873

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.274.31.21873

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.274.31.21873

21 January 2018

Regulation of CFTR channel gating

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.31.21873

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.274.31.21873

21 January 2018

Identifiers

10.1074/JBC.274.31.21873

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

ResearchGate publication ID

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