Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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TRPV4 as a therapeutic target for joint diseases.Pleiotropic function of TRPV4 ion channels in the central nervous system.Microtubules tune mechanotransduction through NOX2 and TRPV4 to decrease sclerostin abundance in osteocytes.

P2860

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P2860

Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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http://www.wikidata.org/entity/Q36584629

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2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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2014年论文

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2014年论文

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name

Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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type

Item

label

Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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prefLabel

Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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P1476

Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

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P2093

Amy L McNulty

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

Farshid Guilak

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

Holly A Leddy

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

Wolfgang Liedtke

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

P2860

An orally active TRPV4 channel blocker prevents and resolves pulmonary edema induced by heart failure

Abnormal osmotic regulation in trpv4-/- mice.

Temporomandibular joint pain: a critical role for Trpv4 in the trigeminal ganglion.

The puzzle of TRPV4 channelopathies.

Follistatin in chondrocytes: the link between TRPV4 channelopathies and skeletal malformations.

Patient-derived skeletal dysplasia induced pluripotent stem cells display abnormal chondrogenic marker expression and regulation by BMP2 and TGFβ1

Increased basal activity is a key determinant in the severity of human skeletal dysplasia caused by TRPV4 mutations

Mice expressing mutant Trpv4 recapitulate the human TRPV4 disorders

Calcium regulation of neuronal gene expression

TRPV4-associated skeletal dysplasias.

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e962971

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scholarly article

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10.4161/2167549X.2014.962971

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2014-10-30T00:00:00Z

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26942100

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Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

about

P2860

P2860

Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias.

description

name

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P1433

P1476

P2093

P2860

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P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

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P433

P478

P577

P698

P932