(Q49019318)

17 February 2018

title

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

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17 February 2018

author

Karl Kunzelmann

4

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17 February 2018

author name string

Mall M

1

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17 February 2018

Hipper A

2

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17 February 2018

Greger R

3

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17 February 2018

language of work or name

English

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publication date

1 February 1996

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17 February 2018

published in

FEBS Letters

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17 February 2018

volume

381

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17 February 2018

page(s)

47-52

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17 February 2018

issue

1-2

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17 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

Regulation of plasma membrane recycling by CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

Mutations in the putative pore-forming domain of CFTR do not change anion selectivity of the cAMP activated Cl- conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

Actin-dependent activation of ion conductances in bronchial epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

Forskolin and PMA pretreatment of HT29 cells alters their chloride conductance induced by cAMP, Ca2+ and hypotonic cell swelling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

The cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2896%2900079-8

10.1016/0014-5793(96)00079-8

21 January 2018

Identifiers

DOI

1 reference

17 February 2018

PubMed ID

8641437

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17 February 2018