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Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/mds.22798openalex-snapshot
The role of parkin in familial and sporadic Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.26695openalex-snapshot
Apoptosis‐inducing factor in nigral dopamine neurons: Higher levels in primates than in mice
inferredcites →https://doi.org/10.1016/j.cell.2011.02.010openalex-snapshot
PARIS (ZNF746) Repression of PGC-1α Contributes to Neurodegeneration in Parkinson's Disease
inferredcites →https://doi.org/10.1016/j.celrep.2014.10.046openalex-snapshot
Parkin Sensitizes toward Apoptosis Induced by Mitochondrial Depolarization through Promoting Degradation of Mcl-1
inferredcites →https://doi.org/10.1016/j.cub.2014.07.014openalex-snapshot
PINK1 Triggers Autocatalytic Activation of Parkin to Specify Cell Fate Decisions
inferredcites →https://doi.org/10.1016/j.expneurol.2009.04.013openalex-snapshot
Mitochondrial μ-calpain is not involved in the processing of apoptosis-inducing factor
inferredcites →https://doi.org/10.1016/j.molcel.2005.02.003openalex-snapshot
BH3 Domains of BH3-Only Proteins Differentially Regulate Bax-Mediated Mitochondrial Membrane Permeabilization Both Directly and Indirectly
inferredcites →https://doi.org/10.1016/j.molcel.2013.01.036openalex-snapshot
The E3 Ligase Parkin Maintains Mitochondrial Integrity by Increasing Linear Ubiquitination of NEMO
inferredcites →https://doi.org/10.1016/j.nbd.2010.09.005openalex-snapshot
Apoptosis-inducing factor mediates dopaminergic cell death in response to LPS-induced inflammatory stimulus
inferredcites →https://doi.org/10.1016/j.neulet.2016.01.029openalex-snapshot
Expression changes of genes associated with apoptosis and survival processes in Parkinson’s disease
inferredcites →https://doi.org/10.1016/j.stemcr.2016.08.012openalex-snapshot
Parkin and PINK1 Patient iPSC-Derived Midbrain Dopamine Neurons Exhibit Mitochondrial Dysfunction and α-Synuclein Accumulation
inferredcites →https://doi.org/10.1016/j.ymthe.2006.06.009openalex-snapshot
Parkin Protects against Neurotoxicity in the 6-Hydroxydopamine Rat Model for Parkinson's Disease
inferredcites →https://doi.org/10.1016/s1097-2765(02)00583-xopenalex-snapshot
CHIP Is Associated with Parkin, a Gene Responsible for Familial Parkinson's Disease, and Enhances Its Ubiquitin Ligase Activity
inferredcites →https://doi.org/10.1038/17135openalex-snapshot
Molecular characterization of mitochondrial apoptosis-inducing factor
inferredcites →https://doi.org/10.1038/cdd.2010.142openalex-snapshot
Parkin is transcriptionally regulated by ATF4: evidence for an interconnection between mitochondrial stress and ER stress
inferredcites →https://doi.org/10.1038/cddis.2014.278openalex-snapshot
Inhibition of apoptotic Bax translocation to the mitochondria is a central function of parkin
inferredcites →https://doi.org/10.1038/cddis.2016.72openalex-snapshot
Parp mutations protect against mitochondrial dysfunction and neurodegeneration in a PARKIN model of Parkinson’s disease
inferredcites →https://doi.org/10.1038/nature14879openalex-snapshot
Mechanism of phospho-ubiquitin-induced PARKIN activation
inferredcites →https://doi.org/10.1038/nn.3500openalex-snapshot
Parthanatos mediates AIMP2-activated age-dependent dopaminergic neuronal loss
inferredcites →https://doi.org/10.1038/s41586-018-0224-xopenalex-snapshot
Mechanism of parkin activation by PINK1
inferredcites →https://doi.org/10.1038/s41594-018-0088-7openalex-snapshot
Mechanism of parkin activation by phosphorylation
inferredcites →https://doi.org/10.1038/sj.emboj.7600614openalex-snapshot
Export of mitochondrial AIF in response to proapoptotic stimuli depends on processing at the intermembrane space
inferredcites →https://doi.org/10.1038/sj.emboj.7601276openalex-snapshot
Dissociating the dual roles of apoptosis‐inducing factor in maintaining mitochondrial structure and apoptosis
inferredcites →https://doi.org/10.1038/sj.onc.1204436openalex-snapshot
Staurosporine induces apoptosis through both caspase-dependent and caspase-independent mechanisms
inferredcites →https://doi.org/10.1042/an20090046openalex-snapshot
Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
inferredcites →https://doi.org/10.1046/j.1471-4159.2002.00975.xopenalex-snapshot
Intranuclear localization of apoptosis‐inducing factor (AIF) and large scale dna fragmentation after traumatic brain injury in rats and in neuronal cultures exposed to peroxynitrite
inferredcites →https://doi.org/10.1073/pnas.0501078102openalex-snapshot
Increased glutathione S -transferase activity rescues dopaminergic neuron loss in a Drosophila model of Parkinson's disease
inferredcites →https://doi.org/10.1073/pnas.0508052102openalex-snapshot
Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration
inferredcites →https://doi.org/10.1074/jbc.c000447200openalex-snapshot
Parkin Suppresses Unfolded Protein Stress-induced Cell Death through Its E3 Ubiquitin-protein Ligase Activity
inferredcites →https://doi.org/10.1074/jbc.m109806200openalex-snapshot
Parkin and CASK/LIN-2 Associate via a PDZ-mediated Interaction and Are Co-localized in Lipid Rafts and Postsynaptic Densities in Brain
inferredcites →https://doi.org/10.1083/jcb.200809125openalex-snapshot
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
inferredcites →https://doi.org/10.1093/hmg/12.5.517openalex-snapshot
Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death
inferredcites →https://doi.org/10.1093/hmg/ddh180openalex-snapshot
Parkin protects human dopaminergic neuroblastoma cells against dopamine-induced apoptosis
inferredcites →https://doi.org/10.1093/hmg/ddp327openalex-snapshot
Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair
inferredcites →https://doi.org/10.1093/hmg/ddx132openalex-snapshot
SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons andDrosophila
inferredcites →https://doi.org/10.1096/fasebj.14.5.729openalex-snapshot
Mitochondrio‐nuclear translocation of AIF in apoptosis and necrosis
inferredcites →https://doi.org/10.1097/01.wcb.0000087090.01171.e7openalex-snapshot
Translocation of Apoptosis-Inducing Factor in Vulnerable Neurons after Transient Cerebral Ischemia and in Neuronal Cultures after Oxygen-Glucose Deprivation
inferredcites →https://doi.org/10.1097/wco.0b013e3281e6692bopenalex-snapshot
Impact of recent genetic findings in Parkinson??s disease
inferredcites →https://doi.org/10.1111/bph.12416openalex-snapshot
Parthanatos: mitochondrial‐linked mechanisms and therapeutic opportunities
inferredcites →https://doi.org/10.1111/j.1471-4159.2005.03329.xopenalex-snapshot
Apoptosis inducing factor mediates caspase‐independent 1‐methyl‐4‐phenylpyridinium toxicity in dopaminergic cells
inferredcites →https://doi.org/10.1126/science.aad6872openalex-snapshot
A nuclease that mediates cell death induced by DNA damage and poly(ADP-ribose) polymerase-1
inferredcites →https://doi.org/10.1126/scisignal.2000902openalex-snapshot
Poly(ADP-Ribose) (PAR) Binding to Apoptosis-Inducing Factor Is Critical for PAR Polymerase-1–Dependent Cell Death (Parthanatos)
inferredcites →https://doi.org/10.1128/mcb.02141-06openalex-snapshot
Sequential Activation of Poly(ADP-Ribose) Polymerase 1, Calpains, and Bax Is Essential in Apoptosis-Inducing Factor-Mediated Programmed Necrosis
inferredcites →https://doi.org/10.1159/000354307openalex-snapshot
Parkin Plays a Role in Sporadic Parkinson's Disease
inferredcites →https://doi.org/10.1196/annals.1427.014openalex-snapshot
Mitochondrial and Nuclear Cross Talk in Cell Death
inferredcites →https://doi.org/10.1371/journal.pbio.1000298openalex-snapshot
PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin
inferredcites →https://doi.org/10.1371/journal.pone.0078648openalex-snapshot
Profiling of Parkin-Binding Partners Using Tandem Affinity Purification
inferredcites →https://doi.org/10.3389/fncel.2018.00081openalex-snapshot
Cryopreservation of Primary Mouse Neurons: The Benefit of Neurostore Cryoprotective Medium
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4781335openalex-extracted
The Abl1 Tyrosine Kinase and p53 are Key Players in Doxorubicin-Induced Cardiomyopathy and Their Cell Death Signaling Differs in Atrial and Ventricular Cardiomyocytes
inferred← citeshttps://doi.org/10.1007/s10571-020-00914-2openalex-snapshot
Parkin, an E3 Ubiquitin Ligase, Plays an Essential Role in Mitochondrial Quality Control in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s10695-020-00907-4openalex-snapshot
Molecular characterization and functional analysis of apoptosis-inducing factor (AIF) in palmitic acid-induced apoptosis in Ctenopharyngodon idellus kidney (CIK) cells
inferred← citeshttps://doi.org/10.1007/s12035-023-03372-1openalex-snapshot
Apoptotic Factors and Mitochondrial Complexes Assist Determination of Strain-Specific Susceptibility of Mice to Parkinsonian Neurotoxin MPTP
inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109491openalex-snapshot
Apoptosis-inducing factor 1 mediates Vibrio splendidus-induced coelomocyte apoptosis via importin β dependent nuclear translocation in Apostichopus japonicus
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2025.112984openalex-snapshot
Proteomic profiling of parthanatos and the neuroprotective potential of sodium perborate tetrahydrate
inferred← citeshttps://doi.org/10.1016/j.nbd.2023.106314openalex-snapshot
Poly (ADP-Ribose) polymerase 1 and parthanatos in neurological diseases: From pathogenesis to therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.nbd.2025.106889openalex-snapshot
α-Synuclein pathology and mitochondrial dysfunction: Toxic partners in Parkinson's disease
inferred← citeshttps://doi.org/10.1038/s41537-025-00559-4openalex-snapshot
Exploring genetic associations and drug targets for mitochondrial proteins and schizophrenia risk
inferred← citeshttps://doi.org/10.1186/s12967-024-05623-8openalex-snapshot
The Abl1 tyrosine kinase is a key player in doxorubicin-induced cardiomyopathy and its p53/p73 cell death mediated signaling differs in atrial and ventricular cardiomyocytes
inferred← citeshttps://doi.org/10.1515/hsz-2020-0254openalex-snapshot
Apoptosis inducing factor and mitochondrial NADH dehydrogenases: redox-controlled gear boxes to switch between mitochondrial biogenesis and cell death
inferred← citeshttps://doi.org/10.3389/fncel.2025.1623747openalex-snapshot
SFXN2 contributes mitochondrial dysfunction-induced apoptosis as a substrate of Parkin
inferred← citeshttps://doi.org/10.3389/fphar.2023.1138128openalex-snapshot
Traditional Chinese medicine in treating ischemic stroke by modulating mitochondria: A comprehensive overview of experimental studies
inferred← citeshttps://doi.org/10.3390/ijms241713656openalex-snapshot
Mitochondrial Factors in the Cell Nucleus
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