Cargando…
ALS-Associated E478G Mutation in Human OPTN (Optineurin) Promotes Inflammation and Induces Neuronal Cell Death
Amyotrophic Lateral Sclerosis (ALS) is a group of neurodegenerative disorders that featured with the death of motor neurons, which leads to loss of voluntary control on muscles. The etiologies vary among different subtypes of ALS, and no effective management or medication could be provided to the pa...
Autores principales: | Liu, Zhengzhao, Li, Hongming, Hong, Chungu, Chen, Menglu, Yue, Tao, Chen, Chunyuan, Wang, Zhenxing, You, Qing, Li, Chuanyin, Weng, Qinjie, Xie, Hui, Hu, Ronggui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251386/ https://www.ncbi.nlm.nih.gov/pubmed/30519240 http://dx.doi.org/10.3389/fimmu.2018.02647 |
Ejemplares similares
-
Variation in optineurin (OPTN) allele frequencies between and within populations
por: Ayala-Lugo, Rosa M., et al.
Publicado: (2007) -
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) -
Neutralizing peripheral circulating IL1β slows the progression of ALS in a lentivirus‐infected OPTN(E478G)
mouse model
por: Hu, Wen‐Bao, et al.
Publicado: (2022) -
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)