(Q42675378)

4 November 2017

title

Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator (English)

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4 November 2017

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transmembrane protein

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7

Guggino WB

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4 November 2017

Carroll TP

1

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4 November 2017

Morales MM

2

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4 November 2017

Fulmer SB

3

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4 November 2017

Allen SS

4

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4 November 2017

Flotte TR

5

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4 November 2017

Cutting GR

6

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4 November 2017

language of work or name

English

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publication date

1 May 1995

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Journal of Biological Chemistry

4 November 2017

published in

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4 November 2017

volume

270

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4 November 2017

issue

20

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4 November 2017

page(s)

11941-11946

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

4 November 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

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.270.20.11941

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

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.270.20.11941

Identification of an ion channel-forming motif in the primary structure of CFTR, the cystic fibrosis chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Novel pore-lining residues in CFTR that govern permeation and open-channel block

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Rapid and efficient site-specific mutagenesis without phenotypic selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

An analysis of vertebrate mRNA sequences: intimations of translational control

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Transmembrane Mutations Alter the Channel Characteristics of the Cystic Fibrosis Transmembrane Conductance Regulator Expressed in Xenopus Oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

Multi-ion pore behaviour in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11941

21 January 2018

Identifiers

DOI

10.1074/JBC.270.20.11941

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4 November 2017

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