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Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation

The transient receptor potential vanilloid 4 (TRPV4) cation channel, a member of the TRP vanilloid subfamily, is expressed in a broad range of tissues where it participates in the generation of Ca(2+) signals and/or depolarization of the membrane potential. Regulation of TRPV4 abundance at the cell...

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Autors principals: Kang, Sang Sun, Shin, Sung Hwa, Auh, Chung-Kyoon, Chun, Jaesun
Format: Artigo
Idioma:Inglês
Publicat: Korean Society for Biochemistry and Molecular Biology 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3538978/
https://ncbi.nlm.nih.gov/pubmed/23143559
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3858/emm.2012.44.12.080
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