scholarly article | Q13442814 |
P2093 | author name string | Peter J Hollenbeck | |
Alex Liu | |||
Swathi Devireddy | |||
Taylor Lampe | |||
P2860 | cites work | PINK1 is selectively stabilized on impaired mitochondria to activate Parkin | Q21145802 |
Parkinson's disease-associated kinase PINK1 regulates Miro protein level and axonal transport of mitochondria | Q21563375 | ||
PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease | Q24294809 | ||
PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility | Q24296955 | ||
The axonal transport of mitochondria | Q27007553 | ||
The pathways of mitophagy for quality control and clearance of mitochondria | Q27009206 | ||
Mechanisms of mitophagy | Q27310261 | ||
The yeast complex I equivalent NADH dehydrogenase rescues pink1 mutants | Q27335187 | ||
Disruption of fast axonal transport is a pathogenic mechanism for intraneuronal amyloid beta | Q28239322 | ||
TANGO: a generic tool for high-throughput 3D image analysis for studying nuclear organization | Q28364897 | ||
Inhibition of fast axonal transport by pathogenic SOD1 involves activation of p38 MAP kinase | Q28533850 | ||
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 | ||
A guided tour into subcellular colocalization analysis in light microscopy | Q29547199 | ||
Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin | Q29547423 | ||
A pyramid approach to subpixel registration based on intensity | Q29614713 | ||
Drosophila parkin requires PINK1 for mitochondrial translocation and ubiquitinates mitofusin | Q29615625 | ||
The PINK1/Parkin pathway regulates mitochondrial morphology | Q29615641 | ||
Mitochondrial dynamics--fusion, fission, movement, and mitophagy--in neurodegenerative diseases | Q29615646 | ||
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin | Q29615684 | ||
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy | Q29616005 | ||
Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions | Q29617065 | ||
Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin | Q30273805 | ||
Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons | Q30425491 | ||
Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons | Q30477062 | ||
Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin | Q30490028 | ||
Bioenergetics of neurons inhibit the translocation response of Parkin following rapid mitochondrial depolarization. | Q30498087 | ||
Transcellular degradation of axonal mitochondria. | Q30583027 | ||
The mitochondrial fusion-promoting factor mitofusin is a substrate of the PINK1/parkin pathway | Q33552320 | ||
Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex | Q33779586 | ||
Evidence that myosin activity opposes microtubule-based axonal transport of mitochondria | Q33998992 | ||
Defects in mitochondrial axonal transport and membrane potential without increased reactive oxygen species production in a Drosophila model of Friedreich ataxia | Q34143936 | ||
Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations | Q34600251 | ||
Mitochondrial movement and positioning in axons: the role of growth factor signaling | Q35131142 | ||
Spatial parkin translocation and degradation of damaged mitochondria via mitophagy in live cortical neurons | Q35855944 | ||
Silent information regulator 2 (Sir2) and Forkhead box O (FOXO) complement mitochondrial dysfunction and dopaminergic neuron loss in Drosophila PTEN-induced kinase 1 (PINK1) null mutant | Q35921597 | ||
Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function | Q36042047 | ||
Mitochondria and neurotransmission: evacuating the synapse | Q36213274 | ||
The axonal transport of mitochondria. | Q36321480 | ||
Mitochondrial trafficking and morphology in healthy and injured neurons | Q36692390 | ||
The PINK1-Parkin pathway promotes both mitophagy and selective respiratory chain turnover in vivo | Q36782133 | ||
Mitochondrial biogenesis in the axons of vertebrate peripheral neurons | Q36883274 | ||
TRAP1 rescues PINK1 loss-of-function phenotypes | Q36950677 | ||
Mitochondrial membrane potential in axons increases with local nerve growth factor or semaphorin signaling | Q37003099 | ||
Bcl-x L increases mitochondrial fission, fusion, and biomass in neurons | Q37202353 | ||
Mitochondrial quality control: a matter of life and death for neurons | Q37987023 | ||
Effects of imaging conditions on mitochondrial transport and length in larval motor axons of Drosophila | Q40068903 | ||
Measurement of mitochondrial membrane potential using fluorescent rhodamine derivatives | Q40223888 | ||
Drosophila Trap1 protects against mitochondrial dysfunction in a PINK1/parkin model of Parkinson's disease. | Q41892915 | ||
Effects of the uncoupling agents FCCP and CCCP on the saltatory movements of cytoplasmic organelles | Q42816519 | ||
Drosophila Miro is required for both anterograde and retrograde axonal mitochondrial transport. | Q43099615 | ||
Glutamate decreases mitochondrial size and movement in primary forebrain neurons. | Q44566043 | ||
Principles of the mitochondrial fusion and fission cycle in neurons | Q44593503 | ||
Axonal mitochondrial transport and potential are correlated | Q44901240 | ||
Analysis of mitochondrial traffic in Drosophila | Q46811563 | ||
Nerve growth factor signaling regulates motility and docking of axonal mitochondria. | Q51642532 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 25 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | quality control | Q827792 |
P304 | page(s) | 9391-9401 | |
P577 | publication date | 2015-06-01 | |
P1433 | published in | Journal of Neuroscience | Q1709864 |
P1476 | title | The Organization of Mitochondrial Quality Control and Life Cycle in the Nervous System In Vivo in the Absence of PINK1. | |
P478 | volume | 35 |
Q34530501 | A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix Saguenay |
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Q83224626 | Degradation of engulfed mitochondria is rate-limiting in Optineurin-mediated mitophagy in neurons |
Q42120365 | Drosophila PINK1 and parkin loss-of-function mutants display a range of non-motor Parkinson's disease phenotypes |
Q61799073 | Emerging Concepts and Functions of Autophagy as a Regulator of Synaptic Components and Plasticity |
Q37364126 | Impaired Mitochondrial Dynamics and Mitophagy in Neuronal Models of Tuberous Sclerosis Complex |
Q41628799 | In vivo imaging reveals mitophagy independence in the maintenance of axonal mitochondria during normal aging |
Q38838388 | Live imaging of mitochondrial dynamics in CNS dopaminergic neurons in vivo demonstrates early reversal of mitochondrial transport following MPP(+) exposure. |
Q38796472 | Mechanisms of neuronal homeostasis: Autophagy in the axon |
Q39201676 | Methodological advances in imaging intravital axonal transport |
Q37346842 | Miro phosphorylation sites regulate Parkin recruitment and mitochondrial motility |
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Q92633565 | Mitophagy in Alzheimer's Disease and Other Age-Related Neurodegenerative Diseases |
Q47449361 | Mitostasis in Neurons: Maintaining Mitochondria in an Extended Cellular Architecture |
Q92602431 | Mul1 restrains Parkin-mediated mitophagy in mature neurons by maintaining ER-mitochondrial contacts |
Q64973813 | Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo. |
Q90310268 | PINK1 and Parkin mitochondrial quality control: a source of regional vulnerability in Parkinson's disease |
Q36380626 | ROS regulation of axonal mitochondrial transport is mediated by Ca2+ and JNK in Drosophila |
Q58716523 | Reduction of PINK1 or DJ-1 impair mitochondrial motility in neurites and alter ER-mitochondria contacts |
Q51019981 | Releasing Syntaphilin Removes Stressed Mitochondria from Axons Independent of Mitophagy under Pathophysiological Conditions. |
Q26744483 | Roles of PTEN with DNA Repair in Parkinson's Disease |
Q37490393 | Seeking an In Vivo Neuronal Context for the PINK1/Parkin Pathway. |
Q47994216 | Shedding light on mitophagy in neurons: what is the evidence for PINK1/Parkin mitophagy in vivo? |
Q93064904 | Somatic autophagy of axonal mitochondria in ischemic neurons |
Q26778641 | The associations between Parkinson's disease and cancer: the plot thickens |
Q54114653 | δ-Opioid Receptor Activation Attenuates Hypoxia/MPP+-Induced Downregulation of PINK1: a Novel Mechanism of Neuroprotection Against Parkinsonian Injury. |