## Abstract Mutations in parkin are the second most common known cause of Parkinson's disease (PD). Parkin is an ubiquitin E3 ligase that monoubiquitinates and polyubiquitinates proteins to regulate a variety of cellular processes. Loss of parkin's E3 ligase activity is thought to play a pathogenic
β¦ LIBER β¦
The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease
β Scribed by O. Bandmann; M.B. Davis; C.D. Mrasden; N.W. Wood
- Book ID
- 116129371
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 251 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0306-4522
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The role of parkin in familial and spora
β
Ted M. Dawson; Valina L. Dawson
π
Article
π
2010
π
John Wiley and Sons
π
English
β 122 KB
π 1 views
The role of inflammation in sporadic and
β
Deleidi, Michela; Gasser, Thomas
π
Article
π
2013
π
Springer
π
English
β 583 KB
Do polymorphisms in the familial Parkins
β
Greg T. Sutherland; Glenda M. Halliday; Peter A. Silburn; Frank L. Mastaglia; Do
π
Article
π
2009
π
John Wiley and Sons
π
English
β 74 KB
## Abstract Recent whole genome association studies provided little evidence that polymorphisms at the familial Parkinsonism loci influence the risk for Parkinson's disease (PD). However, these studies are not designed to detect the types of subtle effects that common variants may impose. Here, we
Analysis of the parkin deletion in spora
β
R. KrΓΌger; A. M. M. Vieira-SΓ€cker; W. Kuhn; T. MΓΌller; D. Woitalla; L. SchΓΆls; H
π
Article
π
1999
π
Springer
π
English
β 68 KB
Protein aggregation in the pathogenesis
β
Kevin St. P. McNaught; C. Warren Olanow
π
Article
π
2006
π
Elsevier Science
π
English
β 395 KB
Analysis of the GIGYF2 gene in familial
β
L. Samaranch; E. Lorenzo; M. A. Pastor; M. Riverol; M. R. Luquin; M. C. RodrΓgue
π
Article
π
2009
π
John Wiley and Sons
π
English
β 119 KB