Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/TRPV4> ?p ?o }
Showing triples 1 to 51 of
51
with 100 triples per page.
- TRPV4 abstract "Transient receptor potential cation channel subfamily V member 4 is an ion channel protein that in humans is encoded by the TRPV4 gene, co-discovered by, see also This gene encodes TRPV4, initially named vanilloid-receptor related osmotically activated channel (VR-OAC), and OSM9-like transient receptor potential channel, member 4 (OTRPC4), a member of the vanilloid subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that has been found involved in multiple physiologic functions, dysfunctions and also disease. It functions in the regulation of systemic osmotic pressure by the brain, in vascular function, in liver, intestinal, renal and bladder function, in skin barrier function and response of the skin to ultraviolet-B radiation, in growth and structural integrity of the skeleton, in function of joints, in airway- and lung function, in retinal and inner ear function, and in pain. The channel is activated by osmotic, mechanical and chemical cues. It also responds to thermal changes (warmth). Channel activation can be sensitized by inflammation and injury. Hereditary channelopathy mutations of TRPV4 lead to skeletal dysplasias, premature osteoarthritis, and neurological motor function disorders as a manifestation of a motor neuropathy or spinal muscle atrophy.".
- TRPV4 entrezgene "59341".
- TRPV4 wikiPageExternalLink NBK1285.
- TRPV4 wikiPageID "13530922".
- TRPV4 wikiPageLength "9280".
- TRPV4 wikiPageOutDegree "15".
- TRPV4 wikiPageRevisionID "677110840".
- TRPV4 wikiPageWikiLink Brachyolmia.
- TRPV4 wikiPageWikiLink Category:Ion_channels.
- TRPV4 wikiPageWikiLink Charcot–Marie–Tooth_disease.
- TRPV4 wikiPageWikiLink Congenital_distal_spinal_muscular_atrophy.
- TRPV4 wikiPageWikiLink Gene.
- TRPV4 wikiPageWikiLink Ion_channel.
- TRPV4 wikiPageWikiLink LYN.
- TRPV4 wikiPageWikiLink MAP7.
- TRPV4 wikiPageWikiLink Mutation.
- TRPV4 wikiPageWikiLink Protein-protein_interaction.
- TRPV4 wikiPageWikiLink Protein–protein_interaction.
- TRPV4 wikiPageWikiLink Scapuloperoneal_spinal_muscular_atrophy.
- TRPV4 wikiPageWikiLink TRPV.
- TRPV4 wikiPageWikiLink Transient_receptor_potential.
- TRPV4 wikiPageWikiLink Transient_receptor_potential_channel.
- TRPV4 wikiPageWikiLinkText "TRPV4".
- TRPV4 hasPhotoCollection TRPV4.
- TRPV4 wikiPageUsesTemplate Template:Ion_channels.
- TRPV4 wikiPageUsesTemplate Template:MeshName.
- TRPV4 wikiPageUsesTemplate Template:NLM_content.
- TRPV4 wikiPageUsesTemplate Template:PBB.
- TRPV4 wikiPageUsesTemplate Template:Reflist.
- TRPV4 subject Category:Ion_channels.
- TRPV4 hypernym Protein.
- TRPV4 type Article.
- TRPV4 type Biomolecule.
- TRPV4 type Protein.
- TRPV4 type Article.
- TRPV4 type Biophysic.
- TRPV4 type Channel.
- TRPV4 type Institute.
- TRPV4 type Source.
- TRPV4 type Thing.
- TRPV4 type Q206229.
- TRPV4 type Q8054.
- TRPV4 comment "Transient receptor potential cation channel subfamily V member 4 is an ion channel protein that in humans is encoded by the TRPV4 gene, co-discovered by, see also This gene encodes TRPV4, initially named vanilloid-receptor related osmotically activated channel (VR-OAC), and OSM9-like transient receptor potential channel, member 4 (OTRPC4), a member of the vanilloid subfamily in the transient receptor potential (TRP) superfamily of ion channels.".
- TRPV4 label "TRPV4".
- TRPV4 sameAs TRPV4.
- TRPV4 sameAs TRPV4.
- TRPV4 sameAs m.03c8h0p.
- TRPV4 sameAs Q7671500.
- TRPV4 sameAs Q7671500.
- TRPV4 wasDerivedFrom TRPV4?oldid=677110840.
- TRPV4 isPrimaryTopicOf TRPV4.