(Q28369080)

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Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

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title

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange (English)

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main subject

African clawed frog

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Xenopus laevis oocyte

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D A Scott

1

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L P Karniski

series ordinal

2

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language of work or name

English

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publication date

January 2000

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published in

American Journal of Physiology - Cell Physiology

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volume

278

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issue

1

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page(s)

C207-11

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cites work

Mechanisms of chloride transport in the proximal tubule

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reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Iodide transport in the thyroid gland

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Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Cloning and characterization of the thyroid iodide transporter

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Chloride/formate exchange with formic acid recycling: a mechanism of active chloride transport across epithelial membranes

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

A mutation in PDS causes non-syndromic recessive deafness

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Association of congenital deafness with goitre; the nature of the thyroid defect

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

DEAF-MUTISM AND GOITRE

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reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Pendred syndrome--100 years of underascertainment?

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Effect of formate on volume reabsorption in the rabbit proximal tubule

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

The Pendred syndrome gene encodes a chloride-iodide transport protein

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1152%2FAJPCELL.2000.278.1.C207

retrieved

21 January 2018

Identifiers

DOI

10.1152/AJPCELL.2000.278.1.C207

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PubMed publication ID

10644529

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(Q28369080)

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

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