Cargando…
Variation in optineurin (OPTN) allele frequencies between and within populations
PURPOSE: To evaluate the extent to which mutations in the optineurin (OPTN) glaucoma gene play a role in glaucoma in different populations. METHODS: Case-controlled study of OPTN sequence variants in individuals with or without glaucoma in populations of different ancestral origins and evaluate prev...
Autores principales: | Ayala-Lugo, Rosa M., Pawar, Hemant, Reed, David M., Lichter, Paul R., Moroi, Sayoko E., Page, Michael, Eadie, James, Azocar, Veronica, Maul, Eugenio, Ntim-Amponsah, Christine, Bromley, William, Obeng-Nyarkoh, Ebenezer, Johnson, A. Tim, Kijek, Theresa Guckian, Downs, Catherine A., Johnson, Jenae M., Perez-Grossmann, Rodolfo A., Guevara-Fujita, Maria-Luisa, Fujita, Ricardo, Wallace, Margaret R., Richards, Julia E. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533035/ https://www.ncbi.nlm.nih.gov/pubmed/17293779 |
Ejemplares similares
-
Absence of optineurin (OPTN) gene mutations in Taiwanese patients with juvenile-onset open-angle glaucoma
por: Yen, Yung-Chang, et al.
Publicado: (2008) -
Deciphering the mitophagy receptor network identifies a crucial role for OPTN (optineurin) in acute myeloid leukemia
por: Meyer, Laura M., et al.
Publicado: (2023) -
ALS-Associated E478G Mutation in Human OPTN (Optineurin) Promotes Inflammation and Induces Neuronal Cell Death
por: Liu, Zhengzhao, et al.
Publicado: (2018) -
Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP
por: Nolan, Matthew, et al.
Publicado: (2021) -
Optineurin Functions for Optimal Immunity
por: Slowicka, Karolina, et al.
Publicado: (2018)