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Gülistan Meşe

Showing results (1-10 of 7) with videos related to

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BMC Cell Biology|February 3, 2016
Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutationsHande Aypek, Veysel Bay, Gülistan Meşe
The Journal of Investigative Dermatology|October 16, 2007
Gap junctions: basic structure and functionGülistan Meşe, Gabriele Richard, Thomas W White
American Journal of Physiology. Cell Physiology|August 8, 2008
Connexin26 deafness associated mutations show altered permeability to large cationic moleculesGülistan Meşe, Virginijus Valiunas, Peter R Brink, et al.
The Journal of Investigative Dermatology|January 15, 2016
Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel PropertiesZunaira Shuja, Leping Li, Shashank Gupta, et al.
Human Genetics|July 9, 2004
Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing lossGülistan Meşe, Eric Londin, Rickie Mui, et al.
The Journal of General Physiology|October 28, 2015
Altered conductance and permeability of Cx40 mutations associated with atrial fibrillationAna Santa Cruz, Gülistan Meşe, Laima Valiuniene, et al.
Experimental Cell Research|April 1, 2009
The cataract causing Cx50-S50P mutant inhibits Cx43 and intercellular communication in the lens epitheliumAdam M DeRosa, Gülistan Meşe, Leping Li, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
BMC Cell Biology|February 3, 2016
Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutationsHande Aypek, Veysel Bay, Gülistan Meşe
The Journal of Investigative Dermatology|October 16, 2007
Gap junctions: basic structure and functionGülistan Meşe, Gabriele Richard, Thomas W White
American Journal of Physiology. Cell Physiology|August 8, 2008
Connexin26 deafness associated mutations show altered permeability to large cationic moleculesGülistan Meşe, Virginijus Valiunas, Peter R Brink, et al.
The Journal of Investigative Dermatology|January 15, 2016
Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel PropertiesZunaira Shuja, Leping Li, Shashank Gupta, et al.
Human Genetics|July 9, 2004
Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing lossGülistan Meşe, Eric Londin, Rickie Mui, et al.
The Journal of General Physiology|October 28, 2015
Altered conductance and permeability of Cx40 mutations associated with atrial fibrillationAna Santa Cruz, Gülistan Meşe, Laima Valiuniene, et al.
Experimental Cell Research|April 1, 2009
The cataract causing Cx50-S50P mutant inhibits Cx43 and intercellular communication in the lens epitheliumAdam M DeRosa, Gülistan Meşe, Leping Li, et al.
Pageof 1