Cargando…
Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson Disease
BACKGROUND: Homozygous and compound heterozygous variants in glucocerebrosidase (GBA) can cause Gaucher disease (GD), whereas heterozygous variants increase the risk of developing Parkinson's disease (PD). GD patients display altered peripheral immune proteins. However, it is unknown if these a...
Autores principales: | Galper, Jasmin, Balwani, Manisha, Fahn, Stanley, Waters, Cheryl, Krohn, Lynne, Gan‐Or, Ziv, Dzamko, Nicolas, Alcalay, Roy N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248172/ https://www.ncbi.nlm.nih.gov/pubmed/33570220 http://dx.doi.org/10.1002/mds.28525 |
Ejemplares similares
-
Plasma Glucosylsphingosine in
GBA1
Mutation Carriers with and without Parkinson's Disease
por: Surface, Matthew, et al.
Publicado: (2021) -
SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease
por: Alcalay, Roy N, et al.
Publicado: (2016) -
Chaperoning glucocerebrosidase: a therapeutic strategy for both Gaucher disease and Parkinsonism
por: McMahon, Benjamin, et al.
Publicado: (2016) -
Evaluation of Strategies for Measuring Lysosomal Glucocerebrosidase Activity
por: Ysselstein, Daniel, et al.
Publicado: (2021) -
Brain Microglial Activation Increased in Glucocerebrosidase (GBA) Mutation Carriers without Parkinson's disease
por: Mullin, Stephen, et al.
Publicado: (2020)