(Q40816688)

English

Disease-associated mutations in the extracytoplasmic loops of cystic fibrosis transmembrane conductance regulator do not impede biosynthetic processing but impair chloride channel stability

scientific article published on 6 February 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Disease-associated mutations in the extracytoplasmic loops of cystic fibrosis transmembrane conductance regulator do not impede biosynthetic processing but impair chloride channel stability (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

cystic fibrosis

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transmembrane protein

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author name string

Hämmerle MM

1

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Aleksandrov AA

2

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Riordan JR

3

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

language of work or name

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publication date

6 February 2001

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

24 September 2017

276

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

14848-14854

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

21 January 2018

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

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.M011017200

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.M011017200

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.M011017200

21 January 2018

Regulation of CFTR ion channel gating by MgATP.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

21 January 2018

Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

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.M011017200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

21 January 2018

A conserved region of the R domain of cystic fibrosis transmembrane conductance regulator is important in processing and function

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

21 January 2018

Structure of the multidrug resistance P-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M011017200

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.M011017200

21 January 2018

Identifiers

10.1074/JBC.M011017200

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

ResearchGate publication ID

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