Cargando…
Molecular dynamics and protein frustration analysis of human fused in Sarcoma protein variants in Amyotrophic Lateral Sclerosis type 6: An In Silico approach
Amyotrophic lateral sclerosis (ALS) is the most frequent adult-onset motor neuron disorder. The disease is characterized by degeneration of upper and lower motor neurons, leading to death usually within five years after the onset of symptoms. While most cases are sporadic, 5%-10% of cases can be ass...
Autores principales: | Bonet, L. F. S., Loureiro, J. P., Pereira, G. R. C., Da Silva, A. N. R., De Mesquita, J. F. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480726/ https://www.ncbi.nlm.nih.gov/pubmed/34587215 http://dx.doi.org/10.1371/journal.pone.0258061 |
Ejemplares similares
-
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis
por: Grassano, Maurizio, et al.
Publicado: (2022) -
Autophagy dysregulation by mutant fused in sarcoma—implications for amyotrophic lateral sclerosis
por: Soo, K Y, et al.
Publicado: (2015) -
In silico analysis of PFN1 related to amyotrophic lateral sclerosis
por: Pereira, Gabriel Rodrigues Coutinho, et al.
Publicado: (2019) -
Protein disulphide isomerase (PDI) is protective against amyotrophic lateral sclerosis (ALS)-related mutant Fused in Sarcoma (FUS) in in vitro models
por: Parakh, S., et al.
Publicado: (2021) -
Clinical and Genetic Features of Patients with Juvenile Amyotrophic Lateral Sclerosis with Fused in Sarcoma (FUS) Mutation
por: Yu, Xiaolong, et al.
Publicado: (2018)