Cargando…
A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene
Parkinson's disease (PD) is characterized by a great clinical heterogeneity. Nevertheless, the biological drivers of this heterogeneity have not been completely elucidated and are likely to be complex, arising from interactions between genetic, epigenetic, and environmental factors. Despite thi...
Autores principales: | Vinagre-Aragón, Ana, Campo-Caballero, David, Mondragón-Rezola, Elisabet, Pardina-Vilella, Lara, Hernandez Eguiazu, Haizea, Gorostidi, Ana, Croitoru, Ioana, Bergareche, Alberto, Ruiz-Martinez, Javier |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982912/ https://www.ncbi.nlm.nih.gov/pubmed/33763016 http://dx.doi.org/10.3389/fneur.2021.635396 |
Ejemplares similares
-
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
por: Fan, Ying, et al.
Publicado: (2021) -
Elevated urine BMP phospholipids in LRRK2 and VPS35 mutation carriers with and without Parkinson’s disease
por: Gomes, Sara, et al.
Publicado: (2023) -
LRRK2 R1441G mice are more liable to dopamine depletion and locomotor inactivity
por: Liu, Hui-Fang, et al.
Publicado: (2014) -
Mitochondrial dysfunction and mitophagy defects in LRRK2-R1441C Parkinson’s disease models
por: Williamson, Matthew G, et al.
Publicado: (2023) -
Efficient Allele-Specific Targeting of LRRK2 R1441 Mutations Mediated by RNAi
por: de Yñigo-Mojado, Laura, et al.
Publicado: (2011)