International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sensor for mitochondrial damage. Its best understood role involves phosphorylating ubiquitin and the E3 ligase Parkin (PRKN) to trigger a ubiquitylation cascade that results in selective clearance of damaged mitochondria through mitophagy. Here we focus on other physiological roles of PINK1. Some of these also lie upstream of Parkin but others represent autonomous functions, for which alternative substrates have been identified. We argue that PINK1 orchestrates a multi-arm response to mitochondrial damage that impacts on mitochondrial architecture and biogenesis, calcium handling, transcription and translation. We further discuss a role for PINK...
<div><p>Loss-of-function mutations in <i>PINK1</i>, which encodes a mitochondrially targeted serine/...
Mutations in the PINK1 gene cause early-onset recessive Parkinson disease. PINK1 is a mitochondriall...
AbstractMutations in PTEN-induced putative kinase 1 (PINK1) cause recessive form of Parkinson’s dise...
International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sen...
International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sen...
International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sen...
PTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sensor for mitochondrial ...
Mitochondrial dysfunction plays a significant role in the pathogenesis of Parkinson’s disease (PD). ...
Mutations in phosphatase and tensin homologue-induced kinase 1 (PINK1) cause recessively inherited P...
The gene PINK1 [phosphatase and tensin homologue (PTEN)-induced putative kinase 1] encodes a serine/...
Loss-of-function mutations in PINK1 and Parkin cause parkinsonism in humans and mitochondrial dysfun...
SummaryMutations in the mitochondrial kinase PINK1 and the cytosolic E3 ligase Parkin can cause Park...
The gene PINK1 [phosphatase and tensin homologue (PTEN)-induced putative kinase 1] encodes a serine/...
Abstract Insights from inherited forms of parkinsonism suggest that insufficient mitophagy may be on...
PINK1 mutations that disrupt its kinase activity cause autosomal recessive early onset Parkinson's d...
<div><p>Loss-of-function mutations in <i>PINK1</i>, which encodes a mitochondrially targeted serine/...
Mutations in the PINK1 gene cause early-onset recessive Parkinson disease. PINK1 is a mitochondriall...
AbstractMutations in PTEN-induced putative kinase 1 (PINK1) cause recessive form of Parkinson’s dise...
International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sen...
International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sen...
International audiencePTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sen...
PTEN-induced kinase 1 (PINK1) is a Parkinson's disease gene that acts as a sensor for mitochondrial ...
Mitochondrial dysfunction plays a significant role in the pathogenesis of Parkinson’s disease (PD). ...
Mutations in phosphatase and tensin homologue-induced kinase 1 (PINK1) cause recessively inherited P...
The gene PINK1 [phosphatase and tensin homologue (PTEN)-induced putative kinase 1] encodes a serine/...
Loss-of-function mutations in PINK1 and Parkin cause parkinsonism in humans and mitochondrial dysfun...
SummaryMutations in the mitochondrial kinase PINK1 and the cytosolic E3 ligase Parkin can cause Park...
The gene PINK1 [phosphatase and tensin homologue (PTEN)-induced putative kinase 1] encodes a serine/...
Abstract Insights from inherited forms of parkinsonism suggest that insufficient mitophagy may be on...
PINK1 mutations that disrupt its kinase activity cause autosomal recessive early onset Parkinson's d...
<div><p>Loss-of-function mutations in <i>PINK1</i>, which encodes a mitochondrially targeted serine/...
Mutations in the PINK1 gene cause early-onset recessive Parkinson disease. PINK1 is a mitochondriall...
AbstractMutations in PTEN-induced putative kinase 1 (PINK1) cause recessive form of Parkinson’s dise...