(Q35054035)

6 August 2017

title

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

1 reference

6 August 2017

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M Oblatt-Montal

1

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6 August 2017

G L Reddy

2

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6 August 2017

T Iwamoto

3

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6 August 2017

J M Tomich

4

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6 August 2017

M Montal

5

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6 August 2017

language of work or name

English

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publication date

1 February 1994

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6 August 2017

number of pages

5

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Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

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6 August 2017

volume

91

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6 August 2017

issue

4

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6 August 2017

page(s)

1495-1499

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The detection and classification of membrane-spanning proteins.

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Amino acid preferences for specific locations at the ends of alpha helices

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Kinetic analysis of channel gating. Application to the cholinergic receptor channel and the chloride channel from Torpedo californica

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

M2 delta, a candidate for the structure lining the ionic channel of the nicotinic cholinergic receptor

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Molecular anatomy and molecular design of channel proteins

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Cystic fibrosis: molecular biology and therapeutic implications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

ABC Transporters: From Microorganisms to Man

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

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

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43186

Bundles of amphipathic transmembrane alpha-helices as a structural motif for ion-conducting channel proteins: studies on sodium channels and acetylcholine receptors

9 December 2018

1 reference

12 December 2020

Effect of Deleting the R Domain on CFTR-Generated Chloride Channels

1 reference

12 December 2020

Synthetic peptides and proteins as models for pore-forming structure of channel proteins

1 reference

12 December 2020

Nicotinic acetylcholine receptor at 9 A resolution.

1 reference

12 December 2020

Single-channel recordings from purified acetylcholine receptors reconstituted in bilayers formed at the tip of patch pipets

1 reference

12 December 2020

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.91.4.1495

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6 August 2017

0 references

1 reference

6 August 2017

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