Cargando…
Degradation of Tyrosine Hydroxylase by the Ubiquitin-Proteasome System in the Pathogenesis of Parkinson’s Disease and Dopa-Responsive Dystonia
Nigrostriatal dopaminergic systems govern physiological functions related to locomotion, and their dysfunction leads to movement disorders, such as Parkinson’s disease and dopa-responsive dystonia (Segawa disease). Previous studies revealed that expression of the gene encoding nigrostriatal tyrosine...
Autores principales: | Kawahata, Ichiro, Fukunaga, Kohji |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312529/ https://www.ncbi.nlm.nih.gov/pubmed/32471089 http://dx.doi.org/10.3390/ijms21113779 |
Ejemplares similares
-
Dopa-responsive dystonia caused by tyrosine hydroxylase deficiency: Three cases report and literature review
por: Dong, Han-Yu, et al.
Publicado: (2020) -
Personalized Medicine to Improve Treatment of Dopa-Responsive Dystonia—A Focus on Tyrosine Hydroxylase Deficiency
por: Nygaard, Gyrid, et al.
Publicado: (2021) -
GTP Cyclohydrolase I and Tyrosine Hydroxylase Gene Mutations in Familial and Sporadic Dopa-Responsive Dystonia Patients
por: Cai, Chunyou, et al.
Publicado: (2013) -
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?
por: Bally, Julien F., et al.
Publicado: (2020) -
Functional Studies of Tyrosine Hydroxylase Missense Variants Reveal Distinct Patterns of Molecular Defects in Dopa-Responsive Dystonia
por: Fossbakk, Agnete, et al.
Publicado: (2014)