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Lisa Ebihara

Showing results (11-20 of 21) with videos related to

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The Journal of Biological Chemistry|October 6, 2005
An aberrant sequence in a connexin46 mutant underlies congenital cataractsPeter J Minogue, Xiaoqin Liu, Lisa Ebihara, et al.
The Journal of Membrane Biology|November 19, 2014
The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gatingJun-Jie Tong, Peter J Minogue, Matthew Kobeszko, et al.
American Journal of Physiology. Cell Physiology|January 11, 2013
Properties of two cataract-associated mutations located in the NH2 terminus of connexin 46Jun-Jie Tong, Bonnie C H Sohn, Anh Lam, et al.
European Journal of Cell Biology|June 13, 2003
Loss of function and impaired degradation of a cataract-associated mutant connexin50Viviana M Berthoud, Peter J Minogue, Jun Guo, et al.
The Journal of Biological Chemistry|February 5, 2022
Cataract-linked serine mutations in the gap junction protein connexin50 expose a sorting signal that promotes its lysosomal degradationPeter J Minogue, Jun-Jie Tong, Kelly Wichmann, et al.
American Journal of Physiology. Cell Physiology|January 14, 2011
Different consequences of cataract-associated mutations at adjacent positions in the first extracellular boundary of connexin50Jun-Jie Tong, Peter J Minogue, Wenji Guo, 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.
Experimental Eye Research|January 16, 2007
Transgenic overexpression of connexin50 induces cataractsJune Chung, Viviana M Berthoud, Layne Novak, 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.
Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|October 6, 2005
An aberrant sequence in a connexin46 mutant underlies congenital cataractsPeter J Minogue, Xiaoqin Liu, Lisa Ebihara, et al.
The Journal of Membrane Biology|November 19, 2014
The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gatingJun-Jie Tong, Peter J Minogue, Matthew Kobeszko, et al.
American Journal of Physiology. Cell Physiology|January 11, 2013
Properties of two cataract-associated mutations located in the NH2 terminus of connexin 46Jun-Jie Tong, Bonnie C H Sohn, Anh Lam, et al.
European Journal of Cell Biology|June 13, 2003
Loss of function and impaired degradation of a cataract-associated mutant connexin50Viviana M Berthoud, Peter J Minogue, Jun Guo, et al.
The Journal of Biological Chemistry|February 5, 2022
Cataract-linked serine mutations in the gap junction protein connexin50 expose a sorting signal that promotes its lysosomal degradationPeter J Minogue, Jun-Jie Tong, Kelly Wichmann, et al.
American Journal of Physiology. Cell Physiology|January 14, 2011
Different consequences of cataract-associated mutations at adjacent positions in the first extracellular boundary of connexin50Jun-Jie Tong, Peter J Minogue, Wenji Guo, 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.
Experimental Eye Research|January 16, 2007
Transgenic overexpression of connexin50 induces cataractsJune Chung, Viviana M Berthoud, Layne Novak, 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.
Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Pageof 3