Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice. - Test2 - elhamkhani - TriplyDB

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

http://www.wikidata.org/entity/Q30599895

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Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice

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P2860

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

http://www.wikidata.org/entity/Q30599895

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@ast

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@en

type

label

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@ast

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@en

prefLabel

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@ast

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@en

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S12929-014-0068-0

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Journal of Biomedical Science

P1476

Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.

@en

P2093

Andreas Zimmer

http://www.w3.org/2001/XMLSchema#string

Anja Schrewe

http://www.w3.org/2001/XMLSchema#string

Birgit Rathkolb

http://www.w3.org/2001/XMLSchema#string

Boris Ivandic

http://www.w3.org/2001/XMLSchema#string

Dirk H Busch

http://www.w3.org/2001/XMLSchema#string

Helmut Fuchs

http://www.w3.org/2001/XMLSchema#string

Holger Schulz

http://www.w3.org/2001/XMLSchema#string

Ildikó Rácz

http://www.w3.org/2001/XMLSchema#string

Ines Bolle

http://www.w3.org/2001/XMLSchema#string

Jack Favor

http://www.w3.org/2001/XMLSchema#string

P2860

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

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Molecular regulation of NKCC2 in the thick ascending limb

Rare mutations in SLC12A1 and SLC12A3 protect against hypertension by reducing the activity of renal salt cotransporters

Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models

Uncompensated polyuria in a mouse model of Bartter's syndrome

Mouse phenotyping.

Innovations in phenotyping of mouse models in the German Mouse Clinic.

Rare mutations in renal sodium and potassium transporter genes exhibit impaired transport function.

Differential regulation of the bumetanide-sensitive cotransporter (NKCC2) by ovarian hormones.

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s12929-014-0068-0

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68

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scholarly article

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10.1186/S12929-014-0068-0

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21

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Martin Hrabě de Angelis

Valérie Gailus-Durner

Elisabeth Kemter

Bernhard Aigner

Svetoslav Kalaydjiev

P577

2014-08-02T00:00:00Z

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264431200

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1021645907

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25084970

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4237776

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