Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations

por Aypek, Hande, Bay, Veysel, Meşe, Gülistan
Publicado 2016

Connexin26 mutations causing palmoplantar keratoderma and deafness interact with connexin43, modifying gap junction and hemichannel properties

por Shuja, Zunaira, Li, Leping, Gupta, Shashank, Meşe, Gülistan, White, Thomas W.
Publicado 2016

Differentially altered Ca(2+) regulation and Ca(2+) permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome

por Sánchez, Helmuth A., Meşe, Gülistan, Srinivas, Miduturu, White, Thomas W., Verselis, Vytas K.
Publicado 2010

Gap Junction Channels Exhibit Connexin-specific Permeability to Cyclic Nucleotides

por Kanaporis, Giedrius, Mese, Gulistan, Valiuniene, Laima, White, Thomas W., Brink, Peter R., Valiunas, Virginijus
Publicado 2008

Altered conductance and permeability of Cx40 mutations associated with atrial fibrillation

por Santa Cruz, Ana, Meşe, Gülistan, Valiuniene, Laima, Brink, Peter R., White, Thomas W., Valiunas, Virginijus
Publicado 2015

Biofabrication of in situ Self Assembled 3D Cell Cultures in a Weightlessness Environment Generated using Magnetic Levitation

por Anil-Inevi, Muge, Yaman, Sena, Yildiz, Ahu Arslan, Mese, Gulistan, Yalcin-Ozuysal, Ozden, Tekin, H. Cumhur, Ozcivici, Engin
Publicado 2018

The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome

por Mese, Gulistan, Sellitto, Caterina, Li, Leping, Wang, Hong-Zhan, Valiunas, Virginijus, Richard, Gabriele, Brink, Peter R., White, Thomas W.
Publicado 2011

SEMA6D Differentially Regulates Proliferation, Migration, and Invasion of Breast Cell Lines

por Gunyuz, Zehra Elif, Sahi-Ilhan, Ece, Kucukkose, Cansu, Ipekgil, Dogac, Tok, Gunes, Mese, Gulistan, Ozcivici, Engin, Yalcin-Ozuysal, Ozden
Publicado 2022