Pages that link to "Q29615684"
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The following pages link to Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin (Q29615684):
Displaying 50 items.
- PINK1 is selectively stabilized on impaired mitochondria to activate Parkin (Q21145802) (← links)
- The phosphorylation-dependent regulation of mitochondrial proteins in stress responses (Q21285141) (← links)
- Parkinson's disease-associated kinase PINK1 regulates Miro protein level and axonal transport of mitochondria (Q21563375) (← links)
- Parkinson's Disease: Genetics and Pathogenesis (Q22242000) (← links)
- How do changes in the mtDNA and mitochondrial dysfunction influence cancer and cancer therapy? Challenges, opportunities and models (Q22252348) (← links)
- Transgenic rodent models of Parkinson’s disease (Q22252835) (← links)
- Sleep and brain energy levels: ATP changes during sleep (Q23761106) (← links)
- Correlation between the biochemical pathways altered by mutated Parkinson-related genes and chronic exposure to manganese (Q23914777) (← links)
- Parkin is activated by PINK1-dependent phosphorylation of ubiquitin at Ser65 (Q24292901) (← links)
- Ubiquitin is phosphorylated by PINK1 to activate parkin (Q24296532) (← links)
- PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility (Q24296955) (← links)
- PARK13 regulates PINK1 and subcellular relocation patterns under oxidative stress in neurons (Q24297072) (← links)
- PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1 (Q24297155) (← links)
- The mitochondrial deubiquitinase USP30 opposes parkin-mediated mitophagy (Q24298748) (← links)
- MUL1 acts in parallel to the PINK1/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin (Q24298771) (← links)
- PINK1 is recruited to mitochondria with parkin and associates with LC3 in mitophagy (Q24299149) (← links)
- Mitochondrial Parkin recruitment is impaired in neurons derived from mutant PINK1 induced pluripotent stem cells (Q24300095) (← links)
- Identification of new kinase clusters required for neurite outgrowth and retraction by a loss-of-function RNA interference screen (Q24300657) (← links)
- Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy (Q24300975) (← links)
- Short mitochondrial ARF triggers Parkin/PINK1-dependent mitophagy (Q24303986) (← links)
- Phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1)-dependent ubiquitination of endogenous Parkin attenuates mitophagy: study in human primary fibroblasts and induced pluripotent stem cell-derived neurons (Q24305292) (← links)
- CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins (Q24306257) (← links)
- Biochemical aspects of the neuroprotective mechanism of PTEN-induced kinase-1 (PINK1) (Q24307730) (← links)
- The role of oxidative stress in Parkinson's disease (Q24307946) (← links)
- Proteomic analysis of increased Parkin expression and its interactants provides evidence for a role in modulation of mitochondrial function (Q24312050) (← links)
- PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1 (Q24312106) (← links)
- Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation (Q24312713) (← links)
- RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathways (Q24313263) (← links)
- Phosphorylation of parkin by Parkinson disease-linked kinase PINK1 activates parkin E3 ligase function and NF-kappaB signaling (Q24313304) (← links)
- Parkin interacts with Ambra1 to induce mitophagy (Q24313512) (← links)
- Inactivation of Pink1 gene in vivo sensitizes dopamine-producing neurons to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and can be rescued by autosomal recessive Parkinson disease genes, Parkin or DJ-1 (Q24315046) (← links)
- The Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagy (Q24316726) (← links)
- Parkin is recruited selectively to impaired mitochondria and promotes their autophagy (Q24317471) (← links)
- Hexokinase activity is required for recruitment of parkin to depolarized mitochondria (Q24318901) (← links)
- Loss of PINK1 function promotes mitophagy through effects on oxidative stress and mitochondrial fission (Q24320327) (← links)
- The kinase domain of mitochondrial PINK1 faces the cytoplasm (Q24321709) (← links)
- Genome-wide RNAi screen identifies ATPase inhibitory factor 1 (ATPIF1) as essential for PARK2 recruitment and mitophagy (Q24322579) (← links)
- PINK1 is necessary for long term survival and mitochondrial function in human dopaminergic neurons (Q24322788) (← links)
- Loss of PINK1 attenuates HIF-1α induction by preventing 4E-BP1-dependent switch in protein translation under hypoxia (Q24337840) (← links)
- Broad activation of the ubiquitin-proteasome system by Parkin is critical for mitophagy (Q24339224) (← links)
- Structure and Function of Parkin, PINK1, and DJ-1, the Three Musketeers of Neuroprotection (Q24339442) (← links)
- PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease (Q24597726) (← links)
- Oxidative stress, mitochondrial dysfunction, and aging (Q24635310) (← links)
- Mitochondria, calcium and cell death: a deadly triad in neurodegeneration (Q24646020) (← links)
- Mitochondrial dysfunction in Parkinson's disease (Q26741872) (← links)
- Parkinson's Disease: The Mitochondria-Iron Link (Q26746899) (← links)
- Neuroprotective and Therapeutic Strategies against Parkinson's Disease: Recent Perspectives (Q26747508) (← links)
- Ubiquitin phosphorylation in Parkinson's disease: Implications for pathogenesis and treatment (Q26770342) (← links)
- Mitochondrial Quality Control and Muscle Mass Maintenance (Q26770420) (← links)
- Parkin Regulation and Neurodegenerative Disorders (Q26770443) (← links)