Much evidence links mitochondrial dysfunction to the death of neurons in Parkinson disease (PD), and is particularly emphasized by our growing understanding of the function of genes linked to recessively inherited PD such as PINK1, parkin and DJ-1. Recent work has revealed an exciting link between the PINK1-Parkin pathway and the autophagic turnover of dysfunctional mitochondrial (mitophagy). We have recently shown that mitofusin is ubiquitinated by Parkin when it is recruited to dysfunctional mitochondria. Recent work also shows that regulated fission and fusion events help segregate dysfunctional mitochondria prior to mitophagy. Here we hypothesize how Parkin-mediated ubiquitination of Mfn may play a role in this mechanism
Parkin, an E3 ubiquitin ligase and a Parkinson's disease (PD) related gene, translocates to impaired...
AbstractAutosomal recessive early-onset Parkinson's disease is most often caused by mutations in the...
[eng] Parkinson's disease (PD) is a common neurodegenerative disorder of unknown cause. Some familia...
Much evidence links mitochondrial dysfunction to the death of neurons in Parkinson disease (PD), and...
peer reviewedPINK1 and Parkin mutations cause recessive Parkinson's disease (PD). In Drosophila and ...
Parkinson’s disease (PD) is characterized by massive degeneration of dopaminergic neurons in the sub...
Loss of the E3 ubiquitin ligase Parkin causes early onset Parkinson's disease, a neurodegenerative d...
Compelling evidence indicates that two autosomal recessive Parkinson's disease genes, PINK1 (PARK6) ...
Mitochondria are essential organelles that provide cellular energy and buffer cytoplasmic calcium. A...
The protein kinase PINK1 and ubiquitin ligase Parkin promote removal of damaged mitochondria via a f...
International audienceNeurons are specialized cells with complex and extended architecture and high ...
Phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1) and PARK2/Parkin mutations c...
peer reviewedMutations in the E3 ubiquitin ligase Parkin and the mitochondrial PTEN-induced putative...
Parkin is a ubiquitin E3 ligase that is implicated in familial Parkinson disease (PD). Previous stud...
Loss-of-function mutations in the PINK1 or parkin genes result in recessive heritable forms of parki...
Parkin, an E3 ubiquitin ligase and a Parkinson's disease (PD) related gene, translocates to impaired...
AbstractAutosomal recessive early-onset Parkinson's disease is most often caused by mutations in the...
[eng] Parkinson's disease (PD) is a common neurodegenerative disorder of unknown cause. Some familia...
Much evidence links mitochondrial dysfunction to the death of neurons in Parkinson disease (PD), and...
peer reviewedPINK1 and Parkin mutations cause recessive Parkinson's disease (PD). In Drosophila and ...
Parkinson’s disease (PD) is characterized by massive degeneration of dopaminergic neurons in the sub...
Loss of the E3 ubiquitin ligase Parkin causes early onset Parkinson's disease, a neurodegenerative d...
Compelling evidence indicates that two autosomal recessive Parkinson's disease genes, PINK1 (PARK6) ...
Mitochondria are essential organelles that provide cellular energy and buffer cytoplasmic calcium. A...
The protein kinase PINK1 and ubiquitin ligase Parkin promote removal of damaged mitochondria via a f...
International audienceNeurons are specialized cells with complex and extended architecture and high ...
Phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1) and PARK2/Parkin mutations c...
peer reviewedMutations in the E3 ubiquitin ligase Parkin and the mitochondrial PTEN-induced putative...
Parkin is a ubiquitin E3 ligase that is implicated in familial Parkinson disease (PD). Previous stud...
Loss-of-function mutations in the PINK1 or parkin genes result in recessive heritable forms of parki...
Parkin, an E3 ubiquitin ligase and a Parkinson's disease (PD) related gene, translocates to impaired...
AbstractAutosomal recessive early-onset Parkinson's disease is most often caused by mutations in the...
[eng] Parkinson's disease (PD) is a common neurodegenerative disorder of unknown cause. Some familia...