04.03. Department of Molecular Biology and Genetics
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Issue Date | Title | Author(s) | |
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1 | Feb-2016 | Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations | Aypek, Hande; Bay, Veysel; Meşe, Gülistan |
2 | Jan-2016 | Connexin26 mutations causing palmoplantar keratoderma and deafness interact with connexin43, modifying gap junction and hemichannel properties | Shuja, Zunaira; Li, Leping; Gupta, Shashank; Meşe, Gülistan ; White, Thomas W. |