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- W2058094511 endingPage "170" @default.
- W2058094511 startingPage "159" @default.
- W2058094511 abstract "Gap junctions provide coupled cells with a direct pathway for sharing ions, nutrients, and small metabolites, thus helping to maintain homeostasis in various tissues. Abnormal function and/or expression of specific connexin genes has been linked to several diseases, including genetic deafness, skin disease, peripheral neuropathies, and cataracts. Research has provided significant insight into the function of gap junction proteins in both in vitro and in vivo models; however, questions regarding the exact mechanisms by which connexin related diseases occur in mammalian systems remain. Here, we discuss the disease states that are related to three human connexin genes, Cx26 (GJB2), Cx46 (GJA3) and Cx50 (GJA8), and recent scientific evidence characterizing those diseases in various experimental models." @default.
- W2058094511 created "2016-06-24" @default.
- W2058094511 creator A5004077716 @default.
- W2058094511 creator A5044719208 @default.
- W2058094511 date "2004-03-01" @default.
- W2058094511 modified "2023-09-26" @default.
- W2058094511 title "Connexin disorders of the ear, skin, and lens" @default.
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