Understanding the role of the protein UCH1 in Parkinson’s disease
Although the cause(s) of Parkinson’s is currently unknown, most researchers believe that multiple factors play a contributory role in causing Parkinson’s and it is likely to be caused by a combination of both genetic and environmental factors. We know that genetics play an important role in the development of Parkinson’s. Nine genes are associated with the rare familial/inherited form of Parkinson’s. One of them, PARK5, is responsible for producing the protein known as UCH-L1, which is involved in the cell machinery that breaks down unwanted proteins in the nervous system. This gene was originally identified by this group of researchers in 1987 and has been linked with susceptibility to familial Parkinson’s. There may also be genetic factors that make people more susceptible to the non-inherited form of Parkinson’s. The genetic basis of Parkinson’s is therefore complex.
Similar entries
- Analysis of the role of parkin in familial and non-familial Parkinson’s disease
- Identifying and understanding the genetic causes of Parkinson’s disease and parkinsonian syndromes
- Identification of genes that predispose to the development of Parkinson’s disease
- PINK1 mutation heterozygosity and the risk of Parkinson’s disease
- Investigating the involvement of glycine receptors in the development of Parkinson’s disease
- Involvement of glial cells in the development and progression of Parkinson’s disease
- Calculating Gene And Protein Connections In A Parkinson's Disease Model
- Family History Of Melanoma Linked To Parkinson's Disease
- Pesticide Parkinson's link strong
- Spring 2008 edition of Parkinson's News



