(Q46717210)

24 December 2017

title

Mouse model of type II Bartter's syndrome. II. Altered expression of renal sodium- and water-transporting proteins (English)

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24 December 2017

author

Francois Verrey

8

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author name string

Carsten A Wagner

1

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Dominique Loffing-Cueni

2

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Qingshang Yan

3

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Nicole Schulz

4

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Panagiotis Fakitsas

5

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Monique Carrel

6

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Tong Wang

7

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John P Geibel

9

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Gerhard Giebisch

10

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Steven C Hebert

11

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Johannes Loffing

12

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publication date

5 March 2008

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24 December 2017

American Journal of Physiology - Renal Physiology

published in

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24 December 2017

volume

294

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issue

6

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page(s)

F1373-80

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24 December 2017

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

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Mouse model of type II Bartter's syndrome. I. Upregulation of thiazide-sensitive Na-Cl cotransport activity

21 January 2018

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Axial flow modulates proximal tubule NHE3 and H-ATPase activities by changing microvillus bending moments

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Adaptation of the distal convoluted tubule of the rat. Structural and functional effects of dietary salt intake and chronic diuretic infusion

21 January 2018

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Salt handling in the distal nephron: lessons learned from inherited human disorders.

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Apical localization of the Na-K-Cl cotransporter, rBSC1, on rat thick ascending limbs

21 January 2018

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Sodium and calcium transport pathways along the mammalian distal nephron: from rabbit to human

21 January 2018

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Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.

21 January 2018

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Impaired renal NaCl absorption in mice lacking the ROMK potassium channel, a model for type II Bartter's syndrome

21 January 2018

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Aldosterone-mediated regulation of ENaC alpha, beta, and gamma subunit proteins in rat kidney

21 January 2018

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Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome

21 January 2018

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Collecting duct-specific gene inactivation of alphaENaC in the mouse kidney does not impair sodium and potassium balance.

21 January 2018

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Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

21 January 2018

1 reference

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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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Association between activating mutations of calcium-sensing receptor and Bartter's syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

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24 December 2017

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24 December 2017