(Q41281567)

29 September 2017

Effects of lovastatin on trafficking of cystic fibrosis transmembrane conductance regulator in human tracheal epithelium (English)

1 reference

29 September 2017

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transmembrane protein

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author name string

Shen BQ

series ordinal

1

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29 September 2017

Widdicombe JH

series ordinal

2

1 reference

29 September 2017

Mrsny RJ

series ordinal

3

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29 September 2017

language of work or name

English

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publication date

1 October 1995

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Journal of Biological Chemistry

29 September 2017

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29 September 2017

270

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29 September 2017

25102-25106

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29 September 2017

42

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

29 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

The spectrum of cystic fibrosis mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Distinct transport vesicles mediate the delivery of plasma membrane proteins to the apical and basolateral domains of MDCK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Regulation of the mevalonate pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Ultrastructural localization of variant forms of cystic fibrosis transmembrane conductance regulator in human bronchial epithelial of xenografts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Altered protein folding may be the molecular basis of most cases of cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Prenyl proteins in eukaryotic cells: a new type of membrane anchor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

Antisense oligodeoxynucleotides to the cystic fibrosis transmembrane conductance regulator inhibit cAMP-activated but not calcium-activated chloride currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.42.25102

21 January 2018

Identifiers

DOI

10.1074/JBC.270.42.25102

1 reference

29 September 2017

1 reference