Associated Papers
PINK1-dependent NFKB signaling contributes to amyloid pathology in Alzheimer disease.
Du F et al.
Autophagy, 2025
A positive feedback loop between SMAD3 and PINK1 in regulation of mitophagy.
Tang M et al.
Cell Discovery, 2025
PINK1 controls RTN3L-mediated ER autophagy by regulating peripheral tubule junctions.
Chidambaram R et al.
The Journal of Cell Biology, 2024
PINK1 and Parkin regulate IP3R-mediated ER calcium release.
Ham SJ et al.
Nature Communications, 2023
Substitution of PINK1 Gly411 modulates substrate receptivity and turnover.
Fiesel FC et al.
Autophagy, 2023
PINK1 drives production of mtDNA-containing extracellular vesicles to promote invasiveness.
Rabas N et al.
The Journal of Cell Biology, 2021
Decision between mitophagy and apoptosis by Parkin via VDAC1 ubiquitination.
Ham SJ et al.
Proceedings of the National Academy of Sciences of the United States of America, 2020
The Parkinson's disease gene PINK1 activates Akt via PINK1 kinase-dependent regulation of the phospholipid PI(3,4,5)P3.
Furlong RM et al.
Journal of Cell Science, 2019
PINK1 signalling rescues amyloid pathology and mitochondrial dysfunction in Alzheimer's disease.
Du F et al.
Brain : a Journal of Neurology, 2017
Mitophagy Controls the Activities of Tumor Suppressor p53 to Regulate Hepatic Cancer Stem Cells.
Liu K et al.
Molecular Cell, 2017
Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation.
Sheng XJ et al.
Plos One, 2017
Covalent ISG15 conjugation positively regulates the ubiquitin E3 ligase activity of parkin.
Im E et al.
Open Biology, 2016
Interaction between RING1 (R1) and the Ubiquitin-like (UBL) Domains Is Critical for the Regulation of Parkin Activity.
Ham SJ et al.
The Journal of Biological Chemistry, 2016
In Vitro Comparison of the Activity Requirements and Substrate Specificity of Human and Triboleum castaneum PINK1 Orthologues.
Aerts L et al.
Plos One, 2016
PINK1 phosphorylates transglutaminase 2 and blocks its proteasomal degradation.
Min B et al.
Journal of Neuroscience Research, 2015
The Parkinson's gene PINK1 regulates cell cycle progression and promotes cancer-associated phenotypes.
O'Flanagan CH et al.
Oncogene, 2015
PINK1 kinase catalytic activity is regulated by phosphorylation on serines 228 and 402.
Aerts L et al.
The Journal of Biological Chemistry, 2015
Phosphorylation of mitochondrial polyubiquitin by PINK1 promotes Parkin mitochondrial tethering.
Shiba-Fukushima K et al.
Plos Genetics, 2014
Mutant PINK1 upregulates tyrosine hydroxylase and dopamine levels, leading to vulnerability of dopaminergic neurons.
Zhou ZD et al.
Free Radical Biology & Medicine, 2014
A dimeric PINK1-containing complex on depolarized mitochondria stimulates Parkin recruitment.
Okatsu K et al.
The Journal of Biological Chemistry, 2013
SARM1 and TRAF6 bind to and stabilize PINK1 on depolarized mitochondria.
Murata H et al.
Molecular Biology of the Cell, 2013
A neo-substrate that amplifies catalytic activity of parkinson's-disease-related kinase PINK1.
Hertz NT et al.
Cell, 2013
Parkin-catalyzed ubiquitin-ester transfer is triggered by PINK1-dependent phosphorylation.
Iguchi M et al.
The Journal of Biological Chemistry, 2013
PINK1 protects against cell death induced by mitochondrial depolarization, by phosphorylating Bcl-xL and impairing its pro-apoptotic cleavage.
Arena G et al.
Cell Death and Differentiation, 2013
PINK1 and Parkin complementarily protect dopaminergic neurons in vertebrates.
Matsui H et al.
Human Molecular Genetics, 2013
PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria.
Chen Y et al.
Science (new York, N.y.), 2013
Characterization of PINK1 (PTEN-induced putative kinase 1) mutations associated with Parkinson disease in mammalian cells and Drosophila.
Song S et al.
The Journal of Biological Chemistry, 2013
PINK1 positively regulates IL-1β-mediated signaling through Tollip and IRAK1 modulation.
Lee HJ et al.
Journal of Neuroinflammation, 2012
PINK1 stimulates interleukin-1β-mediated inflammatory signaling via the positive regulation of TRAF6 and TAK1.
Lee HJ et al.
Cellular and Molecular Life Sciences : Cmls, 2012
[Role of mitophagy in hereditary Parkinson's disease].
Matsuda N et al.
Brain and Nerve = Shinkei Kenkyu No Shinpo, 2012
PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria.
Okatsu K et al.
Nature Communications, 2012
PINK1-mediated phosphorylation of the Parkin ubiquitin-like domain primes mitochondrial translocation of Parkin and regulates mitophagy.
Shiba-Fukushima K et al.
Scientific Reports, 2012
Genetic mutations and functions of PINK1.
Kawajiri S et al.
Trends in Pharmacological Sciences, 2011
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy.
Matsuda N et al.
The Journal of Cell Biology, 2010
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1.
Geisler S et al.
Nature Cell Biology, 2010
Phosphorylation of parkin by Parkinson disease-linked kinase PINK1 activates parkin E3 ligase function and NF-kappaB signaling.
Sha D et al.
Human Molecular Genetics, 2010
Molecular interaction between parkin and PINK1 in mammalian neuronal cells.
Um JW et al.
Molecular and Cellular Neurosciences, 2009
Pink1 Parkinson mutations, the Cdc37/Hsp90 chaperones and Parkin all influence the maturation or subcellular distribution of Pink1.
Weihofen A et al.
Human Molecular Genetics, 2008
PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1.
Pridgeon JW et al.
Plos Biology, 2007
Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability.
Beilina A et al.
Proceedings of the National Academy of Sciences of the United States of America, 2005