(Q28505870)

24 January 2017

title

SLC26A7 is a Cl- channel regulated by intracellular pH (English)

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Solute carrier family 26, member 7

24 January 2017

main subject

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GOA release 2020-03-11

author name string

Kil Hwan Kim

1

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24 January 2017

Nikolay Shcheynikov

2

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24 January 2017

Youxue Wang

3

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24 January 2017

Shmuel Muallem

4

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24 January 2017

language of work or name

English

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publication date

25 February 2005

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Journal of Biological Chemistry

24 January 2017

published in

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24 January 2017

volume

280

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24 January 2017

issue

8

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24 January 2017

page(s)

6463–6470

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The SLC26 gene family of multifunctional anion exchangers

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Prestin is the motor protein of cochlear outer hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Gating of CFTR by the STAS domain of SLC26 transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

The mouse sulfate anion transporter gene Sat1 (Slc26a1): cloning, tissue distribution, gene structure, functional characterization, and transcriptional regulation thyroid hormone

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Identification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Dynamic control of cystic fibrosis transmembrane conductance regulator Cl(-)/HCO3(-) selectivity by external Cl(-)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

Membrane-specific Regulation of Cl−Channels by Purinergic Receptors in Rat Submandibular Gland Acinar and Duct Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M409162200

21 January 2018

Identifiers

DOI

10.1074/JBC.M409162200

0 references

1 reference