Loss of FBXO7 (PARK15) results in reduced proteasome activity and models a parkinsonism-like phenotype in mice
Mutations in the FBXO7 (PARK15) gene have been implicated in a juvenile form of parkinsonism termed parkinsonian pyramidal syndrome (PPS), characterized by Parkinsonian symptoms and pyramidal tract signs. FBXO7 (F-box protein only 7) is a subunit of the SCF (SKP1/cullin-1/F-box protein) E3 ubiquitin...
Main Authors: | Vingill, S, Brockelt, D, Lancelin, C, Tatenhorst, L, Dontcheva, G, Preisinger, C, Schwedhelm-Domeyer, N, Joseph, S, Mitkovski, M, Goebbels, S, Nave, K, Schulz, J, Marquardt, T, Lingor, P, Stegmüller, J |
---|---|
格式: | Journal article |
語言: | English |
出版: |
EMBO Press
2016
|
相似書籍
-
The centrosomal E3 ubiquitin ligase FBXO31-SCF regulates neuronal morphogenesis and migration.
由: Mayur Vadhvani, et al.
出版: (2013-01-01) -
Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect
由: Marta Correa‐Vela, et al.
出版: (2020-08-01) -
p250GAP is a novel player in the Cdh1-APC/Smurf1 pathway of axon growth regulation.
由: Madhuvanthi Kannan, et al.
出版: (2012-01-01) -
Loss of nuclear activity of the FBXO7 protein in patients with parkinsonian-pyramidal syndrome (PARK15).
由: Tianna Zhao, et al.
出版: (2011-02-01) -
Glypican-4 serum levels are associated with cognitive dysfunction and vascular risk factors in Parkinson’s disease
由: Lars Tatenhorst, et al.
出版: (2024-02-01)