CHOP is dispensable for lens transparency in wild-type and connexin50 mutant mice

por Minogue, Peter J., Beyer, Eric C., Berthoud, Viviana M.
Publicado 2019

Do Connexin Mutants Cause Cataracts by Perturbing Glutathione Levels and Redox Metabolism in the Lens?

por Jara, Oscar, Minogue, Peter J., Berthoud, Viviana M., Beyer, Eric C.
Publicado 2020

Levels and Modifications of Both Lens Fiber Cell Connexins Are Affected in Connexin Mutant Mice

por Jara, Oscar, Minogue, Peter J., Berthoud, Viviana M., Beyer, Eric C.
Publicado 2022

p62/Sequestosome 1 levels increase and phosphorylation is altered in Cx50D47A lenses, but deletion of p62/sequestosome 1 does not improve transparency

por Jara, Oscar, Mysliwiec, Hubert, Minogue, Peter J., Berthoud, Viviana M., Beyer, Eric C.
Publicado 2020

The Connexin50D47A Mutant Causes Cataracts by Calcium Precipitation

por Berthoud, Viviana M., Gao, Junyuan, Minogue, Peter J., Jara, Oscar, Mathias, Richard T., Beyer, Eric C.
Publicado 2019

Connexin Mutants Compromise the Lens Circulation and Cause Cataracts through Biomineralization

por Berthoud, Viviana M., Gao, Junyuan, Minogue, Peter J., Jara, Oscar, Mathias, Richard T., Beyer, Eric C.
Publicado 2020

The Connexin46 Mutant, Cx46T19M, Causes Loss of Gap Junction Function and Alters Hemi-channel Gating

por Tong, Jun-Jie, Minogue, Peter J., Kobeszko, Matthew, Beyer, Eric C., Berthoud, Viviana M., Ebihara, Lisa
Publicado 2014

Cataract-linked serine mutations in the gap junction protein connexin50 expose a sorting signal that promotes its lysosomal degradation

por Minogue, Peter J., Tong, Jun-Jie, Wichmann, Kelly, Mysliwiec, Hubert, Ebihara, Lisa, Beyer, Eric C., Berthoud, Viviana M.
Publicado 2022

Connexin Mutants Cause Cataracts Through Deposition of Apatite

por Minogue, Peter J., Sommer, Andre J., Williams, James C., Bledsoe, Sharon B., Beyer, Eric C., Berthoud, Viviana M.
Publicado 2022

Physiological and Optical Alterations Precede the Appearance of Cataracts in Cx46fs380 Mice

por Minogue, Peter J., Gao, Junyuan, Zoltoski, Rebecca K., Novak, Layne A., Mathias, Richard T., Beyer, Eric C., Berthoud, Viviana M.
Publicado 2017

Characterization of a variant of gap junction protein α8 identified in a family with hereditary cataract

por Kuo, Debbie S., Sokol, Jared T., Minogue, Peter J., Berthoud, Viviana M., Slavotinek, Anne M., Beyer, Eric C., Gould, Douglas B.
Publicado 2017

A crystallin mutant cataract with mineral deposits

por Minogue, Peter J., Gao, Junyuan, Mathias, Richard T., Williams, James C., Bledsoe, Sharon B., Sommer, Andre J., Beyer, Eric C., Berthoud, Viviana M.
Publicado 2023

The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation

por Graw, Jochen, Schmidt, Werner, Minogue, Peter J., Rodriguez, Jessica, Tong, Jun-Jie, Klopp, Norman, Illig, Thomas, Ebihara, Lisa, Berthoud, Viviana M., Beyer, Eric C.
Publicado 2009