Parkin and Parkinsonʼs disease

Yoshikuni Mizuno(Juntendo University), Keiji Tanaka(Kyushu University), Nobutaka Hattori(Juntendo University Hospital), Toshiaki Suzuki(Rakuten (Japan)), Hideo Mori(Juntendo University)

Current Opinion in Neurology

August 1, 2001

10.1097/00019052-200108000-00008

Cited by 122

Related Papers

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

|Nature|1998|5.2k

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

|Nature Genetics|2000|2k

PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy

|The Journal of Cell Biology|2010|1.9k

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

|Nature Genetics|2009|1.3k

Ubiquitination of a New Form of α-Synuclein by Parkin from Human Brain: Implications for Parkinson's Disease

|Science|2001|1.1k