Cargando…
Behavioral Phenotyping in a Murine Model of GBA1-Associated Parkinson Disease
Mutations in GBA1, the gene encoding glucocerebrosidase, are common genetic risk factors for Parkinson disease (PD). While the mechanism underlying this relationship is unclear, patients with GBA1-associated PD often have an earlier onset and faster progression than idiopathic PD. Previously, we mod...
Autores principales: | Do, Jenny, Perez, Gani, Berhe, Bahafta, Tayebi, Nahid, Sidransky, Ellen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267726/ https://www.ncbi.nlm.nih.gov/pubmed/34202076 http://dx.doi.org/10.3390/ijms22136826 |
Ejemplares similares
-
Is Gauchian genotyping of GBA1 variants reliable?
por: Tayebi, Nahid, et al.
Publicado: (2023) -
Longitudinal evaluation of olfactory function in individuals with Gaucher disease and GBA1 mutation carriers with and without Parkinson's disease
por: Lopez, Grisel J., et al.
Publicado: (2022) -
Next-Generation Sequencing Analysis of GBA1: The Challenge of Detecting Complex Recombinant Alleles
por: Woo, Elizabeth G., et al.
Publicado: (2021) -
Small Molecule Chaperones for the Treatment of Gaucher Disease and GBA1-Associated Parkinson Disease
por: Han, Tae-Un, et al.
Publicado: (2020) -
GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis
por: Mallett, Victoria, et al.
Publicado: (2016)