(Q38313574)

2 September 2017

title

Identification of the cystic fibrosis transmembrane conductance regulator domains that are important for interactions with ROMK2. (English)

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2 September 2017

main subject

transmembrane protein

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cystic fibrosis

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author name string

Cahill P

1

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2 September 2017

Nason MW Jr

2

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2 September 2017

Ambrose C

3

1 reference

2 September 2017

Yao TY

4

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2 September 2017

Thomas P

5

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2 September 2017

Egan ME

6

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2 September 2017

language of work or name

English

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publication date

1 June 2000

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Journal of Biological Chemistry

2 September 2017

number of pages

5

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based on heuristic

inferred from page(s)

published in

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2 September 2017

volume

275

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2 September 2017

issue

22

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2 September 2017

page(s)

16697-16701

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

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

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.M910205199

CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Wild type but not deltaF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

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.M910205199

Rapid and efficient site-specific mutagenesis without phenotypic selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Cloning and expression of an inwardly rectifying ATP-regulated potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

The second half of the cystic fibrosis transmembrane conductance regulator forms a functional chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

The amino-terminal portion of CFTR forms a regulated Cl- channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Membrane topology distinguishes a subfamily of the ATP-binding cassette (ABC) transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Promiscuous coupling between the sulphonylurea receptor and inwardly rectifying potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Stimulation of CFTR activity by its phosphorylated R domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Separation of drug transport and chloride channel functions of the human multidrug resistance P-glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M910205199

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.M910205199

21 January 2018

Identifiers

DOI

10.1074/JBC.M910205199

1 reference

2 September 2017

1 reference