Cargando…
Posttranslational Modifications, Localization, and Protein Interactions of Optineurin, the Product of a Glaucoma Gene
BACKGROUND: Glaucoma is a major blinding disease. The most common form of this disease, primary open angle glaucoma (POAG), is genetically heterogeneous. One of the candidate genes, optineurin, is linked principally to normal tension glaucoma, a subtype of POAG. The present study was undertaken to i...
Autores principales: | Ying, Hongyu, Shen, Xiang, Park, BumChan, Yue, Beatrice Y. J. T. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820081/ https://www.ncbi.nlm.nih.gov/pubmed/20161783 http://dx.doi.org/10.1371/journal.pone.0009168 |
Ejemplares similares
-
Impairment of Protein Trafficking upon Overexpression and Mutation of Optineurin
por: Park, BumChan, et al.
Publicado: (2010) -
Effects of mutations and deletions in the human optineurin gene
por: Turturro, Sanja, et al.
Publicado: (2014) -
Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
por: Swarup, Ghanshyam, et al.
Publicado: (2018) -
Dysfunction of Optineurin in Amyotrophic Lateral Sclerosis and Glaucoma
por: Toth, Reka P., et al.
Publicado: (2018) -
Induction of autophagy in rats upon overexpression of wild-type and mutant optineurin gene
por: Ying, Hongyu, et al.
Publicado: (2015)