Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease (Q28255135)

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26 December 2019

title

Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease (English)

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26 December 2019

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Gerardo Gamba

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26 December 2019

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Ernesto Sabath

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26 December 2019

Patricia Meade

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26 December 2019

Jennifer Berkman

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26 December 2019

Paola de los Heros

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26 December 2019

Erika Moreno

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26 December 2019

Norma A Bobadilla

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26 December 2019

Norma Vázquez

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language of work or name

English

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publication date

6 April 2004

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American Journal of Physiology - Renal Physiology

26 December 2019

published in

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26 December 2019

volume

287

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26 December 2019

issue

2

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26 December 2019

page(s)

F195-203

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Specific regions of heteromeric subunits involved in enhancement of G protein-gated K+ channel activity

26 December 2019

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Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome

21 January 2018

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The structural unit of the thiazide-sensitive NaCl cotransporter is a homodimer.

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21 January 2018

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N-Glycosylation at two sites critically alters thiazide binding and activity of the rat thiazide-sensitive Na(+):Cl(-) cotransporter.

21 January 2018

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The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum

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Clarification of the site of action of chlorothiazide in the rat nephron

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Molecular pathogenesis of Bartter's and Gitelman's syndromes.

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cAMP-dependent activation of the renal-specific Na+-K+-2Cl- cotransporter is mediated by regulation of cotransporter trafficking

21 January 2018

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Characterization of the thiazide-sensitive Na(+)-Cl(-) cotransporter: a new model for ions and diuretics interaction

21 January 2018

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Functional properties of the apical Na+-K+-2Cl- cotransporter isoforms

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Localization of the thiazide sensitive Na-Cl cotransporter, rTSC1 in the rat kidney

21 January 2018

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Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

21 January 2018

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Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

21 January 2018

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Mutations in the human Na-K-2Cl cotransporter (NKCC2) identified in Bartter syndrome type I consistently result in nonfunctional transporters

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Na transport proteins are expressed by rat alveolar epithelial type I cells

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The renal thiazide-sensitive Na-Cl cotransporter as mediator of the aldosterone-escape phenomenon

21 January 2018

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Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4

21 January 2018

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