TRPP2 and TRPV4 form an EGF-activated calcium permeable channel at the apical membrane of renal collecting duct cells. - Wikidata - awgldk - TriplyDB

TRPP2 and TRPV4 form an EGF-activated calcium permeable channel at the apical membrane of renal collecting duct cells.

TRPP2 and TRPV4 form an EGF-activated calcium permeable channel at the apical membrane of renal collecting duct cells.

http://www.wikidata.org/entity/Q34974223

about

OFD1 and flotillins are integral components of a ciliary signaling protein complex organized by polycystins in renal epithelia and odontoblasts The native TRPP2-dependent channel of murine renal primary cilia The cAMP Signaling Pathway and Direct Protein Kinase A Phosphorylation Regulate Polycystin-2 (TRPP2) Channel Function ADAM17 promotes proliferation of collecting duct kidney epithelial cells through ERK activation and increased glycolysis in polycystic kidney disease.TRPV4 activation mediates flow-induced nitric oxide production in the rat thick ascending limb.Epidermal growth factor-induced proliferation of collecting duct cells from Oak Ridge polycystic kidney mice involves activation of Na+/H+ exchanger.Impaired epithelial Na+ channel activity contributes to cystogenesis and development of autosomal recessive polycystic kidney disease in PCK rats.Deciphering physiological role of the mechanosensitive TRPV4 channel in the distal nephron.Flow regulation of endothelin-1 production in the inner medullary collecting duct Molecular pathways and therapies in autosomal-dominant polycystic kidney disease The polycystin complex mediates Wnt/Ca(2+) signalling.Progress in ciliary ion channel physiology.Primary cilia regulate the osmotic stress response of renal epithelial cells through TRPM3.Hydrogen peroxide suppresses TRPM4 trafficking to the apical membrane in mouse cortical collecting duct principal cells.Calcium channels in primary cilia.Renoprotection: focus on TRPV1, TRPV4, TRPC6 and TRPM2.Primary Cilia in Cystic Kidney Disease.Polycystin and calcium signaling in cell death and survival.The Sorting Nexin 3 Retromer Pathway Regulates the Cell Surface Localization and Activity of a Wnt-Activated Polycystin Channel Complex.TRPV4 Regulates Tight Junctions and Affects Differentiation in a Cell Culture Model of the Corneal Epithelium.Mechanotransduction of the endothelial glycocalyx mediates nitric oxide production through activation of TRP channels.Deficient transient receptor potential vanilloid type 4 function contributes to compromised [Ca2+]i homeostasis in human autosomal-dominant polycystic kidney disease cells.

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TRPP2 and TRPV4 form an EGF-activated calcium permeable channel at the apical membrane of renal collecting duct cells.

http://www.wikidata.org/entity/Q34974223

description

2013 nî lūn-bûn

@nan

2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

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TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@en

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@nl

type

label

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@ast

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@en

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@nl

prefLabel

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@ast

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@en

TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@nl

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JOURNAL.PONE.0073424

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TRPP2 and TRPV4 form an EGF-ac ...... f renal collecting duct cells.

@en

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Aleksander Baldys

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

Binlin Song

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

Chang-Jiang Yu

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

Jia-Ning Zhang

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Monika Gooz

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P Darwin Bell

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

Pal Gooz

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

Shuai Jiang

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

Stacy Steele

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

Wen-Feng Chu

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

P2860

Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel

Endothelial cell surface F1-F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin

Frequent somatic mutations of GNAQ in uveal melanoma and blue naevi

Functional characterization of homo- and heteromeric channel kinases TRPM6 and TRPM7

Cloning and functional expression of a human Ca2+-permeable cation channel activated by calcium store depletion

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

Transient receptor potential cation channels in disease

A diacylglycerol-gated cation channel in vomeronasal neuron dendrites is impaired in TRPC2 mutant mice: mechanism of pheromone transduction

Atomic force microscopy reveals the alternating subunit arrangement of the TRPP2-TRPV4 heterotetramer.

Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator.

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e73424

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scholarly article

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10.1371/JOURNAL.PONE.0073424

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P433

8

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8

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Grzegorz Owsianik

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2013-08-16T00:00:00Z

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256102850

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23977387

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3745395

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