review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Ji-Soo Kim | |
Ji-Young Han | |||
Jin H Son | |||
P2860 | cites work | Mitochondrial BCL-2 inhibits AMBRA1-induced autophagy | Q24294358 |
PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease | Q24294809 | ||
Ubiquitin is phosphorylated by PINK1 to activate parkin | Q24296532 | ||
PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility | Q24296955 | ||
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1 | Q24297155 | ||
Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA | Q24299860 | ||
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy | Q24300975 | ||
Parkin interacts with Ambra1 to induce mitophagy | Q24313512 | ||
Mitochondrial complex I deficiency in Parkinson's disease | Q69370277 | ||
Mitochondrial dysfunction in Parkinson's disease | Q80228162 | ||
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy | Q24317471 | ||
Broad activation of the ubiquitin-proteasome system by Parkin is critical for mitophagy | Q24339224 | ||
Mitochondrial biology and Parkinson's disease | Q26824090 | ||
Peroxisome proliferator-activated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism | Q28266830 | ||
Regulation of intracellular accumulation of mutant Huntingtin by Beclin 1 | Q28300820 | ||
Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial Parkinsonism-linked gene DJ-1 | Q28506681 | ||
The autophagy-related protein beclin 1 shows reduced expression in early Alzheimer disease and regulates amyloid beta accumulation in mice | Q28591283 | ||
PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria | Q28592217 | ||
Loss of PINK1 causes mitochondrial functional defects and increased sensitivity to oxidative stress | Q28592727 | ||
PINK1 loss-of-function mutations affect mitochondrial complex I activity via NdufA10 ubiquinone uncoupling | Q28593164 | ||
Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress. | Q28593258 | ||
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice | Q28593859 | ||
Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants | Q29615627 | ||
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin | Q29615684 | ||
Metabolic control through the PGC-1 family of transcription coactivators | Q29616509 | ||
PINK1 phosphorylates ubiquitin to activate Parkin E3 ubiquitin ligase activity | Q29617292 | ||
PINK1 is activated by mitochondrial membrane potential depolarization and stimulates Parkin E3 ligase activity by phosphorylating Serine 65 | Q29622844 | ||
p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria | Q34269257 | ||
Voltage-dependent anion channels (VDACs) recruit Parkin to defective mitochondria to promote mitochondrial autophagy | Q34305642 | ||
Role of PINK1 binding to the TOM complex and alternate intracellular membranes in recruitment and activation of the E3 ligase Parkin | Q35783335 | ||
Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function | Q36042047 | ||
PINK1-mediated phosphorylation of the Parkin ubiquitin-like domain primes mitochondrial translocation of Parkin and regulates mitophagy | Q36476931 | ||
Rescue of PINK1 protein null-specific mitochondrial complex IV deficits by ginsenoside Re activation of nitric oxide signaling | Q36492752 | ||
A novel PGC-1α isoform in brain localizes to mitochondria and associates with PINK1 and VDAC. | Q37069425 | ||
The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy | Q39754547 | ||
Synergistic activation of the human MnSOD promoter by DJ-1 and PGC-1alpha: regulation by SUMOylation and oxidation | Q39952558 | ||
Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6. | Q40201823 | ||
Parkin enhances mitochondrial biogenesis in proliferating cells | Q40322753 | ||
Parkin mediates proteasome-dependent protein degradation and rupture of the outer mitochondrial membrane | Q42235376 | ||
How could Parkin-mediated ubiquitination of mitofusin promote mitophagy? | Q42943868 | ||
The antioxidant Trolox helps recovery from the familial Parkinson's disease-specific mitochondrial deficits caused by PINK1- and DJ-1-deficiency in dopaminergic neuronal cells | Q43965888 | ||
Effect of coenzyme Q10 on the mitochondrial function of skin fibroblasts from Parkinson patients | Q44894243 | ||
Mitochondrial complex I and II activities of lymphocytes and platelets in Parkinson's disease | Q48595004 | ||
Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's disease | Q48673461 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P921 | main subject | Parkinson's disease | Q11085 |
P304 | page(s) | 345-351 | |
P577 | publication date | 2014-12-12 | |
P1433 | published in | Experimental neurobiology | Q26842060 |
P1476 | title | Mitochondrial homeostasis molecules: regulation by a trio of recessive Parkinson's disease genes | |
P478 | volume | 23 |
Q26740364 | Chaperone-Mediated Autophagy and Mitochondrial Homeostasis in Parkinson's Disease |
Q38649157 | Does PGC1α/FNDC5/BDNF Elicit the Beneficial Effects of Exercise on Neurodegenerative Disorders? |
Q48271930 | Effects of eldepryl on glial cell proliferation and activation in the substantia nigra and striatum in a rat model of Parkinson's disease |
Q38811976 | Fire and water: Tumor cell adaptation to metabolic conditions |
Q53453128 | Mitochondrial Dysfunction in Parkinson's Disease. |
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