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Eric C Beyer

Showing results (71-80 of 88) with videos related to

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Frontiers in Physiology|June 15, 2017
Mono-Heteromeric Configurations of Gap Junction Channels Formed by Connexin43 and Connexin45 Reduce Unitary Conductance and Determine both Voltage Gating and Metabolic Flux AsymmetryGuoqiang Zhong, Nazem Akoum, Daniel A Appadurai, et al.
Plos One|August 23, 2017
Characterization of a variant of gap junction protein α8 identified in a family with hereditary cataractDebbie S Kuo, Jared T Sokol, Peter J Minogue, et al.
Experimental Eye Research|April 4, 2016
Connexin23 deletion does not affect lens transparencyViviana M Berthoud, Peter J Minogue, Joseph I Snabb, et al.
Biophysical Journal|November 11, 2021
Molecular mechanisms underlying enhanced hemichannel function of a cataract-associated Cx50 mutantJun-Jie Tong, Umair Khan, Bassam G Haddad, et al.
Journal of Cell Science|July 31, 2008
An intact connexin N-terminus is required for function but not gap junction formationJohn W Kyle, Peter J Minogue, Bettina C Thomas, et al.
The Journal of Biological Chemistry|June 18, 2023
A crystallin mutant cataract with mineral depositsPeter J Minogue, Junyuan Gao, Richard T Mathias, et al.
Experimental Eye Research|January 16, 2007
Transgenic overexpression of connexin50 induces cataractsJune Chung, Viviana M Berthoud, Layne Novak, et al.
Biochemical and Biophysical Research Communications|June 28, 2005
Connexin43 with a cytoplasmic loop deletion inhibits the function of several connexinsMin Wang, Agustín D Martínez, Viviana M Berthoud, et al.
Experimental Eye Research|November 3, 2012
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataractG Senthil Kumar, John W Kyle, Peter J Minogue, et al.
Molecular Vision|September 17, 2009
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutationJochen Graw, Werner Schmidt, Peter J Minogue, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Frontiers in Physiology|June 15, 2017
Mono-Heteromeric Configurations of Gap Junction Channels Formed by Connexin43 and Connexin45 Reduce Unitary Conductance and Determine both Voltage Gating and Metabolic Flux AsymmetryGuoqiang Zhong, Nazem Akoum, Daniel A Appadurai, et al.
Plos One|August 23, 2017
Characterization of a variant of gap junction protein α8 identified in a family with hereditary cataractDebbie S Kuo, Jared T Sokol, Peter J Minogue, et al.
Experimental Eye Research|April 4, 2016
Connexin23 deletion does not affect lens transparencyViviana M Berthoud, Peter J Minogue, Joseph I Snabb, et al.
Biophysical Journal|November 11, 2021
Molecular mechanisms underlying enhanced hemichannel function of a cataract-associated Cx50 mutantJun-Jie Tong, Umair Khan, Bassam G Haddad, et al.
Journal of Cell Science|July 31, 2008
An intact connexin N-terminus is required for function but not gap junction formationJohn W Kyle, Peter J Minogue, Bettina C Thomas, et al.
The Journal of Biological Chemistry|June 18, 2023
A crystallin mutant cataract with mineral depositsPeter J Minogue, Junyuan Gao, Richard T Mathias, et al.
Experimental Eye Research|January 16, 2007
Transgenic overexpression of connexin50 induces cataractsJune Chung, Viviana M Berthoud, Layne Novak, et al.
Biochemical and Biophysical Research Communications|June 28, 2005
Connexin43 with a cytoplasmic loop deletion inhibits the function of several connexinsMin Wang, Agustín D Martínez, Viviana M Berthoud, et al.
Experimental Eye Research|November 3, 2012
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataractG Senthil Kumar, John W Kyle, Peter J Minogue, et al.
Molecular Vision|September 17, 2009
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutationJochen Graw, Werner Schmidt, Peter J Minogue, et al.
Pageof 9