Results 61 to 70 of about 23,205 (164)

PINK1 phosphorylates ubiquitin predominantly in astrocytes [PDF]

open access: yesnpj Parkinson's Disease, 2019
AbstractLoss-of-function mutations in PINK1 are causally linked to recessively inherited Parkinson’s disease (PD), with marked loss of dopaminergic neurons in the substantia nigra that are required for normal movement. PINK1 is a nuclear-encoded mitochondrial-targeted kinase that phosphorylates a conserved serine at amino acid 65 (pS65) in ubiquitin as
Sandeep K. Barodia   +5 more
openaire   +2 more sources

PINK1 and Parkin to control mitochondria remodeling [PDF]

open access: yesAnatomy & Cell Biology, 2010
Parkinson's disease (PD), one of the most common neurodegenerative diseases, is characterized by movement disorders and a loss of dopaminergic (DA) neurons. PD mainly occurs sporadically, but may also result from genetic mutations in several PD-linked genes.
Koh, Hyongjong, Chung, Jongkyeong
openaire   +2 more sources

PINK1 import regulation at a crossroad of mitochondrial fate: the molecular mechanisms of PINK1 import [PDF]

open access: yesThe Journal of Biochemistry, 2019
Abstract PTEN-induced kinase 1 (PINK1) is a mitochondrial kinase whose activity is tightly regulated by the mitochondrial health status. In response to mitochondrial damage, activated PINK1 can promote mitophagy, an autophagic elimination of damaged mitochondria, by cooperating with Parkin ubiquitin ligase.
openaire   +2 more sources

The yeast complex I equivalent NADH dehydrogenase rescues pink1 mutants.

open access: yesPLoS Genetics, 2012
Pink1 is a mitochondrial kinase involved in Parkinson's disease, and loss of Pink1 function affects mitochondrial morphology via a pathway involving Parkin and components of the mitochondrial remodeling machinery.
Sven Vilain   +9 more
doaj   +1 more source

Increased cysteine metabolism in PINK1 models of Parkinson's disease

open access: yesDisease Models & Mechanisms, 2023
Marco Travaglio   +6 more
doaj   +1 more source

NRF2 Regulates PINK1 Expression under Oxidative Stress Conditions.

open access: yesPLoS ONE, 2015
Mutations of the PTEN-induced putative kinase 1 (PINK1) gene are a cause of autosomal recessive forms of Parkinson's disease. Recent studies have revealed that PINK1 is an essential factor for controlling mitochondrial quality, and that it protects cells
Hitoshi Murata   +5 more
doaj   +1 more source

A positive feedback loop between SMAD3 and PINK1 in regulation of mitophagy

open access: yesCell Discovery
PTEN-induced kinase-1 (PINK1) is a crucial player in selective clearance of damaged mitochondria via the autophagy-lysosome pathway, a process termed mitophagy.
Mingzhu Tang   +13 more
doaj   +1 more source

Increased mitochondrial calcium sensitivity and abnormal expression of innate immunity genes precede dopaminergic defects in Pink1-deficient mice.

open access: yesPLoS ONE, 2011
BackgroundPTEN-induced kinase 1 (PINK1) is linked to recessive Parkinsonism (EOPD). Pink1 deletion results in impaired dopamine (DA) release and decreased mitochondrial respiration in the striatum of mice. To reveal additional mechanisms of Pink1-related
Ravi S Akundi   +7 more
doaj   +1 more source

The Roles of PINK1 and Parkin in Parkinson's Disease

open access: yesPLoS Biology, 2010
​ResearchResearch into the causes of both sporadic and familial Parkinson's disease have led to the idea that a key risk factor might be mitochondrial dysfunction. The neurons of the substantia nigra, which are specifically lost in Parkinson's disease, seem to be especially vulnerable to the effects of mitochondrial damage.
openaire   +4 more sources

PINK1 modulates Prdx2 to reduce lipotoxicity‐induced apoptosis and attenuate cardiac dysfunction in heart failure mice with a preserved ejection fraction

open access: yesClinical and Translational Medicine
Introduction Heart failure with preserved ejection fraction (HFpEF) is a complex condition characterized by metabolic dysfunction and myocardial lipotoxicity.
Hao Zhang   +10 more
doaj   +1 more source

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