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Mitophagy mechanisms and role in human diseases
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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/embj.201385902openalex-snapshot
Parkin and PINK1 function in a vesicular trafficking pathway regulating mitochondrial quality control
inferredcites →https://doi.org/10.1007/s00415-013-7003-2openalex-snapshot
Recent advances in Parkinson’s disease genetics
inferredcites →https://doi.org/10.1007/s12265-010-9174-xopenalex-snapshot
Mitochondrial Pruning by Nix and BNip3: An Essential Function for Cardiac-Expressed Death Factors
inferredcites →https://doi.org/10.1016/j.bbrc.2012.10.041openalex-snapshot
Mitochondrial hexokinase HKI is a novel substrate of the Parkin ubiquitin ligase
inferredcites →https://doi.org/10.1016/j.cmet.2011.04.008openalex-snapshot
High-Mobility Group Box 1 Is Essential for Mitochondrial Quality Control
inferredcites →https://doi.org/10.1016/j.cmet.2013.03.014openalex-snapshot
Rheb Regulates Mitophagy Induced by Mitochondrial Energetic Status
inferredcites →https://doi.org/10.1016/j.cub.2012.02.005openalex-snapshot
Spatial Parkin Translocation and Degradation of Damaged Mitochondria via Mitophagy in Live Cortical Neurons
inferredcites →https://doi.org/10.1016/j.devcel.2009.06.013openalex-snapshot
Mitochondria-Anchored Receptor Atg32 Mediates Degradation of Mitochondria via Selective Autophagy
inferredcites →https://doi.org/10.1016/j.devcel.2009.06.014openalex-snapshot
Atg32 Is a Mitochondrial Protein that Confers Selectivity during Mitophagy
inferredcites →https://doi.org/10.1016/j.devcel.2013.05.024openalex-snapshot
The Scaffold Protein Atg11 Recruits Fission Machinery to Drive Selective Mitochondria Degradation by Autophagy
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2013.05.014openalex-snapshot
Cellular metabolic and autophagic pathways: Traffic control by redox signaling
inferredcites →https://doi.org/10.1016/j.humpath.2010.05.016openalex-snapshot
PINK1 displays tissue-specific subcellular location and regulates apoptosis and cell growth in breast cancer cells
inferredcites →https://doi.org/10.1016/j.redox.2012.11.008openalex-snapshot
Autophagy and mitophagy in cellular damage control
inferredcites →https://doi.org/10.1016/j.redox.2013.08.005openalex-snapshot
Zonated induction of autophagy and mitochondrial spheroids limits acetaminophen-induced necrosis in the liver
inferredcites →https://doi.org/10.1016/j.yjmcc.2011.10.008openalex-snapshot
p53-TIGAR axis attenuates mitophagy to exacerbate cardiac damage after ischemia
inferredcites →https://doi.org/10.1016/s1534-5807(01)00055-7openalex-snapshot
The Role of Dynamin-Related Protein 1, a Mediator of Mitochondrial Fission, in Apoptosis
inferredcites →https://doi.org/10.1038/cdd.2009.200openalex-snapshot
The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy
inferredcites →https://doi.org/10.1038/cddis.2014.51openalex-snapshot
Phosphorylated AKT inhibits the apoptosis induced by DRAM-mediated mitophagy in hepatocellular carcinoma by preventing the translocation of DRAM to mitochondria
inferredcites →https://doi.org/10.1038/embor.2009.256openalex-snapshot
Nix is a selective autophagy receptor for mitochondrial clearance
inferredcites →https://doi.org/10.1038/embor.2013.114openalex-snapshot
Casein kinase 2 is essential for mitophagy
inferredcites →https://doi.org/10.1038/embor.2013.168openalex-snapshot
Loss of iron triggers PINK1/Parkin‐independent mitophagy
inferredcites →https://doi.org/10.1038/nature07006openalex-snapshot
Essential role for Nix in autophagic maturation of erythroid cells
inferredcites →https://doi.org/10.1038/nature10546openalex-snapshot
Image-based genome-wide siRNA screen identifies selective autophagy factors
inferredcites →https://doi.org/10.1038/nature10992openalex-snapshot
Mitochondrial DNA that escapes from autophagy causes inflammation and heart failure
inferredcites →https://doi.org/10.1038/nature12043openalex-snapshot
Landscape of the PARKIN-dependent ubiquitylome in response to mitochondrial depolarization
inferredcites →https://doi.org/10.1038/nature12748openalex-snapshot
High-content genome-wide RNAi screens identify regulators of parkin upstream of mitophagy
inferredcites →https://doi.org/10.1038/ncb2012openalex-snapshot
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
inferredcites →https://doi.org/10.1038/ncb2422openalex-snapshot
Mitochondrial outer-membrane protein FUNDC1 mediates hypoxia-induced mitophagy in mammalian cells
inferredcites →https://doi.org/10.1038/ncb2837openalex-snapshot
Cardiolipin externalization to the outer mitochondrial membrane acts as an elimination signal for mitophagy in neuronal cells
inferredcites →https://doi.org/10.1038/ncomms3308openalex-snapshot
Cytosolic p53 inhibits Parkin-mediated mitophagy and promotes mitochondrial dysfunction in the mouse heart
inferredcites →https://doi.org/10.1038/ng.491openalex-snapshot
Somatic mutations of the Parkinson's disease–associated gene PARK2 in glioblastoma and other human malignancies
inferredcites →https://doi.org/10.1038/nm1574openalex-snapshot
The role of autophagy in cardiomyocytes in the basal state and in response to hemodynamic stress
inferredcites →https://doi.org/10.1038/nn.3489openalex-snapshot
The Parkinson's disease–linked proteins Fbxo7 and Parkin interact to mediate mitophagy
inferredcites →https://doi.org/10.1038/nrneurol.2013.132openalex-snapshot
Advances in the genetics of Parkinson disease
inferredcites →https://doi.org/10.1038/onc.2008.199openalex-snapshot
Parkin as a tumor suppressor gene for hepatocellular carcinoma
inferredcites →https://doi.org/10.1038/onc.2012.494openalex-snapshot
Mitochondrial dynamics regulates migration and invasion of breast cancer cells
inferredcites →https://doi.org/10.1038/sj.bjc.6605568openalex-snapshot
High expression of gabarapl1 is associated with a better outcome for patients with lymph node-positive breast cancer
inferredcites →https://doi.org/10.1038/sj.emboj.7601963openalex-snapshot
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
inferredcites →https://doi.org/10.1038/sj.onc.1208642openalex-snapshot
Loss of BNIP3 expression is a late event in pancreatic cancer contributing to chemoresistance and worsened prognosis
inferredcites →https://doi.org/10.1038/sj.onc.1209772openalex-snapshot
Correlated break at PARK2/FRA6E and loss of AF-6/Afadin protein expression are associated with poor outcome in breast cancer
inferredcites →https://doi.org/10.1042/bj20081386openalex-snapshot
How mitochondria produce reactive oxygen species
inferredcites →https://doi.org/10.1042/bj20111451openalex-snapshot
Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling
inferredcites →https://doi.org/10.1042/bst20120231openalex-snapshot
Convergent mechanisms for dysregulation of mitochondrial quality control in metabolic disease: implications for mitochondrial therapeutics
inferredcites →https://doi.org/10.1073/pnas.0911187107openalex-snapshot
PINK1-dependent recruitment of Parkin to mitochondria in mitophagy
inferredcites →https://doi.org/10.1073/pnas.0913485107openalex-snapshot
Drosophila Parkin requires PINK1 for mitochondrial translocation and ubiquitinates Mitofusin
inferredcites →https://doi.org/10.1073/pnas.1009941107openalex-snapshot
PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant mice
inferredcites →https://doi.org/10.1073/pnas.1106291108openalex-snapshot
PTEN-inducible kinase 1 (PINK1)/Park6 is indispensable for normal heart function
inferredcites →https://doi.org/10.1073/pnas.1107402108openalex-snapshot
Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation
inferredcites →https://doi.org/10.1074/jbc.c200677200openalex-snapshot
Loss of OPA1 Perturbates the Mitochondrial Inner Membrane Structure and Integrity, Leading to Cytochrome c Release and Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m110.209338openalex-snapshot
Parkin Mediates Proteasome-dependent Protein Degradation and Rupture of the Outer Mitochondrial Membrane
inferredcites →https://doi.org/10.1074/jbc.m112.391680openalex-snapshot
Phosphatase and Tensin Homolog (PTEN)-induced Putative Kinase 1 (PINK1)-dependent Ubiquitination of Endogenous Parkin Attenuates Mitophagy
inferredcites →https://doi.org/10.1074/jbc.m112.411363openalex-snapshot
Parkin Protein Deficiency Exacerbates Cardiac Injury and Reduces Survival following Myocardial Infarction
inferredcites →https://doi.org/10.1074/jbc.m406960200openalex-snapshot
Uth1p Is Involved in the Autophagic Degradation of Mitochondria
inferredcites →https://doi.org/10.1074/jbc.m605940200openalex-snapshot
Aup1p, a Yeast Mitochondrial Protein Phosphatase Homolog, Is Required for Efficient Stationary Phase Mitophagy and Cell Survival
inferredcites →https://doi.org/10.1074/jbc.m606059200openalex-snapshot
Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology
inferredcites →https://doi.org/10.1074/jbc.m800102200openalex-snapshot
Mitochondrial Autophagy Is an HIF-1-dependent Adaptive Metabolic Response to Hypoxia
inferredcites →https://doi.org/10.1083/jcb.200809125openalex-snapshot
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
inferredcites →https://doi.org/10.1083/jcb.201001039openalex-snapshot
Disease-causing mutations in Parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy
inferredcites →https://doi.org/10.1083/jcb.201007013openalex-snapshot
Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin
inferredcites →https://doi.org/10.1083/jcb.201008084openalex-snapshot
Mitochondrial membrane potential regulates PINK1 import and proteolytic destabilization by PARL
inferredcites →https://doi.org/10.1089/ars.2010.3779openalex-snapshot
The Interplay Between Mitochondrial Dynamics and Mitophagy
inferredcites →https://doi.org/10.1089/ars.2013.5416openalex-snapshot
Mitophagy Is Required for Acute Cardioprotection by Simvastatin
inferredcites →https://doi.org/10.1089/rej.2005.8.3openalex-snapshot
Selective Mitochondrial Autophagy, or Mitophagy, as a Targeted Defense Against Oxidative Stress, Mitochondrial Dysfunction, and Aging
inferredcites →https://doi.org/10.1091/mbc.e11-02-0145openalex-snapshot
Phosphorylation of Serine 114 on Atg32 mediates mitophagy
inferredcites →https://doi.org/10.1091/mbc.e13-01-0016openalex-snapshot
SARM1 and TRAF6 bind to and stabilize PINK1 on depolarized mitochondria
inferredcites →https://doi.org/10.1091/mbc.e13-09-0525openalex-snapshot
Mutations in Fis1 disrupt orderly disposal of defective mitochondria
inferredcites →https://doi.org/10.1093/hmg/ddq215openalex-snapshot
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients
inferredcites →https://doi.org/10.1093/hmg/ddq288openalex-snapshot
Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics
inferredcites →https://doi.org/10.1093/hmg/ddq419openalex-snapshot
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy
inferredcites →https://doi.org/10.1093/hmg/ddq430openalex-snapshot
DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy
inferredcites →https://doi.org/10.1093/hmg/ddq531openalex-snapshot
Bioenergetics of neurons inhibit the translocation response of Parkin following rapid mitochondrial depolarization
inferredcites →https://doi.org/10.1093/hmg/ddr048openalex-snapshot
Broad activation of the ubiquitin–proteasome system by Parkin is critical for mitophagy
inferredcites →https://doi.org/10.1093/hmg/ddr529openalex-snapshot
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition
inferredcites →https://doi.org/10.1093/hmg/dds325openalex-snapshot
ROS-dependent regulation of Parkin and DJ-1 localization during oxidative stress in neurons
inferredcites →https://doi.org/10.1093/hmg/ddt058openalex-snapshot
AF-6 is a positive modulator of the PINK1/parkin pathway and is deficient in Parkinson's disease
inferredcites →https://doi.org/10.1096/fj.01-0206fjeopenalex-snapshot
The mitochondrial permeability transition initiates autophagy in rat hepatocytes
inferredcites →https://doi.org/10.1096/fj.11-196543openalex-snapshot
Inhibition of mitochondrial fission prevents cell cycle progression in lung cancer
inferredcites →https://doi.org/10.1126/science.1231031openalex-snapshot
PINK1-Phosphorylated Mitofusin 2 Is a Parkin Receptor for Culling Damaged Mitochondria
inferredcites →https://doi.org/10.1128/mcb.00167-12openalex-snapshot
BNip3 Regulates Mitochondrial Function and Lipid Metabolism in the Liver
inferredcites →https://doi.org/10.1152/ajpcell.00056.2010openalex-snapshot
Mitochondrial degradation by autophagy (mitophagy) in GFP-LC3 transgenic hepatocytes during nutrient deprivation
inferredcites →https://doi.org/10.1152/ajpendo.00093.2013openalex-snapshot
Dysfunctional mitochondrial bioenergetics and oxidative stress in Akita+/Ins2-derived β-cells
inferredcites →https://doi.org/10.1152/ajpheart.00584.2011openalex-snapshot
Hemin causes mitochondrial dysfunction in endothelial cells through promoting lipid peroxidation: the protective role of autophagy
inferredcites →https://doi.org/10.1158/0008-5472.can-04-0089openalex-snapshot
Silencing of the Hypoxia-Inducible Cell Death Protein BNIP3 in Pancreatic Cancer
inferredcites →https://doi.org/10.1159/000346388openalex-snapshot
Autophagy and Viruses: Adversaries or Allies?
inferredcites →https://doi.org/10.1159/000479441openalex-snapshot
Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy
inferredcites →https://doi.org/10.1161/circresaha.111.246108openalex-snapshot
Contribution of Impaired Mitochondrial Autophagy to Cardiac Aging
inferredcites →https://doi.org/10.1172/jci31457openalex-snapshot
Mechanistic and prognostic significance of aberrant methylation in the molecular pathogenesis of human hepatocellular carcinoma
inferredcites →https://doi.org/10.1186/1756-6606-5-35openalex-snapshot
Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue
inferredcites →https://doi.org/10.1200/jco.2008.18.5678openalex-snapshot
Gene Expression Profiling Reveals a New Classification of Adrenocortical Tumors and Identifies Molecular Predictors of Malignancy and Survival
inferredcites →https://doi.org/10.1242/jcs.131300openalex-snapshot
Restricted mitochondrial protein acetylation initiates mitochondrial autophagy
inferredcites →https://doi.org/10.1289/ehp.1002839openalex-snapshot
Rotenone, Paraquat, and Parkinson’s Disease
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.0010054openalex-snapshot
The Mitochondrial Fusion-Promoting Factor Mitofusin Is a Substrate of the PINK1/Parkin Pathway
inferredcites →https://doi.org/10.1371/journal.pone.0016746openalex-snapshot
Mutations in PINK1 and Parkin Impair Ubiquitination of Mitofusins in Human Fibroblasts
inferredcites →https://doi.org/10.1371/journal.pone.0020975openalex-snapshot
Preconditioning Involves Selective Mitophagy Mediated by Parkin and p62/SQSTM1
inferredcites →https://doi.org/10.1371/journal.pone.0025622openalex-snapshot
Bioenergetic Consequences of PINK1 Mutations in Parkinson Disease
inferredcites →https://doi.org/10.1371/journal.pone.0045319openalex-snapshot
Defects in Mitochondrial Fission Protein Dynamin-Related Protein 1 Are Linked to Apoptotic Resistance and Autophagy in a Lung Cancer Model
inferredcites →https://doi.org/10.1515/hsz-2012-0198openalex-snapshot
Integration of cellular bioenergetics with mitochondrial quality control and autophagy
inferredcites →https://doi.org/10.1523/jneurosci.1917-11.2011openalex-snapshot
Parkin Interacts with Ambra1 to Induce Mitophagy
inferredcites →https://doi.org/10.1530/eje-11-0806openalex-snapshot
Combined expression of BUB1B, DLGAP5, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients
inferredcites →https://doi.org/10.2353/ajpath.2007.060524openalex-snapshot
Regulation of Autophagy by Extracellular Signal-Regulated Protein Kinases During 1-Methyl-4-Phenylpyridinium-Induced Cell Death
inferredcites →https://doi.org/10.4161/auto.25413openalex-snapshot
Genome-wide RNAi screen identifies ATPase inhibitory factor 1 (ATPIF1) as essential for PARK2 recruitment and mitophagy
inferredcites →https://doi.org/10.4161/auto.25665openalex-snapshot
Dynamin 1-like-dependent mitochondrial fission initiates overactive mitophagy in the hepatotoxicity of cadmium
inferredcites →https://doi.org/10.4161/auto.26122openalex-snapshot
The accumulation of misfolded proteins in the mitochondrial matrix is sensed by PINK1 to induce PARK2/Parkin-mediated mitophagy of polarized mitochondria
inferredcites →https://doi.org/10.4161/auto.26281openalex-snapshot
Proteolytic processing of Atg32 by the mitochondrial i-AAA protease Yme1 regulates mitophagy
inferredcites →https://doi.org/10.4161/auto.6.4.11819openalex-snapshot
GABARAPL1 (GEC1) associates with autophagic vesicles
inferredcites →https://doi.org/10.4161/auto.6.7.13286openalex-snapshot
The PINK1/Parkin-mediated mitophagy is compromised by PD-associated mutations
inferredcites →https://doi.org/10.4161/auto.6.8.13426openalex-snapshot
p62/SQSTM1 is required for Parkin-induced mitochondrial clustering but not mitophagy; VDAC1 is dispensable for both
inferredcites →https://doi.org/10.4161/auto.7.10.15904openalex-snapshot
GABARAPL1 (GEC1): Original or copycat?
inferredcites →https://doi.org/10.4161/auto.7.5.14684openalex-snapshot
DJ-1 regulation of mitochondrial function and autophagy through oxidative stress
inferredcites →https://doi.org/10.4161/cc.23722openalex-snapshot
Cigarette smoke metabolically promotes cancer, via autophagy and premature aging in the host stromal microenvironment
inferredcites →https://doi.org/10.4161/cc.24215openalex-snapshot
Parkin deficiency contributes to pancreatic tumorigenesis by inducing spindle multipolarity and misorientation
inferredcites →https://doi.org/10.7554/elife.01612openalex-snapshot
Mitochondrial Rab GAPs govern autophagosome biogenesis during mitophagy
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.4794612openalex-extracted
Molecular Mechanism of 4-Hydroxynonenal Induced Cell Death
inferred← citeshttps://doi.org/10.1002/9781118952108.ch6openalex-snapshot
Biological Consequences of Protein Moonlighting
inferred← citeshttps://doi.org/10.1002/ddr.21258openalex-snapshot
Bioprotective Carnitinoids: Lipoic Acid, Butyrate, and Mitochondria‐Targeting to Treat Radiation Injury: Mitochondrial Drugs Come of Age
inferred← citeshttps://doi.org/10.1002/ddr.21294openalex-snapshot
Epigenetic Treatment of Neurodegenerative Disorders: Alzheimer and Parkinson Diseases
inferred← citeshttps://doi.org/10.1002/jcp.25215openalex-snapshot
Acetylcholine Attenuates Hypoxia/Reoxygenation Injury by Inducing Mitophagy Through PINK1/Parkin Signal Pathway in H9c2 Cells
inferred← citeshttps://doi.org/10.1002/jcp.28117openalex-snapshot
Nix/BNIP3L‐dependent mitophagy accounts for airway epithelial cell injury induced by cigarette smoke
inferred← citeshttps://doi.org/10.1002/mco2.70326openalex-snapshot
Mitochondrial Dysfunction in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1002/mco2.70385openalex-snapshot
Mitochondrial Diseases: Molecular Pathogenesis and Therapeutic Advances
inferred← citeshttps://doi.org/10.1002/ptr.8156openalex-snapshot
Regulation of mitophagy and mitochondrial function: Natural compounds as potential therapeutic strategies for Parkinson's disease
inferred← citeshttps://doi.org/10.1007/978-3-319-26587-2_171-1openalex-snapshot
Mitochondrial Biology in Hepatobiliary Tumors: Changes of the Cellular Energy Factory
inferred← citeshttps://doi.org/10.1007/978-3-319-26956-6_171openalex-snapshot
Mitochondrial Biology in Hepatobiliary Tumors: Changes of the Cellular Energy Factory
inferred← citeshttps://doi.org/10.1007/s00018-018-2973-yopenalex-snapshot
Targeting autophagy using metallic nanoparticles: a promising strategy for cancer treatment
inferred← citeshttps://doi.org/10.1007/s00401-014-1361-4openalex-snapshot
Autophagy in neuronal cells: general principles and physiological and pathological functions
inferred← citeshttps://doi.org/10.1007/s00709-020-01540-xopenalex-snapshot
Cytoplasmic inheritance of mitochondria and chloroplasts in the anisogamous brown alga Mutimo cylindricus (Phaeophyceae)
inferred← citeshttps://doi.org/10.1007/s10571-017-0492-2openalex-snapshot
Mitophagy in Refractory Temporal Lobe Epilepsy Patients with Hippocampal Sclerosis
inferred← citeshttps://doi.org/10.1007/s10815-021-02218-wopenalex-snapshot
Effect of oxygen and glucose availability during in vitro maturation of bovine oocytes on development and gene expression
inferred← citeshttps://doi.org/10.1007/s11033-022-07738-xopenalex-snapshot
Role of Mitophagy in neurodegenerative Diseases and potential tagarts for Therapy
inferred← citeshttps://doi.org/10.1007/s11357-021-00414-1openalex-snapshot
University of Alabama at Birmingham Nathan Shock Center: comparative energetics of aging
inferred← citeshttps://doi.org/10.1007/s13679-019-00360-2openalex-snapshot
The Role of Adipose Tissue and Adipokines in Sepsis: Inflammatory and Metabolic Considerations, and the Obesity Paradox
inferred← citeshttps://doi.org/10.1016/b978-0-323-99879-6.00009-2openalex-snapshot
Mitophagy in cancer and cancer stem cells: a role in metabolic reprogramming
inferred← citeshttps://doi.org/10.1016/j.actbio.2025.07.059openalex-snapshot
Nanotechnology-targeted modulation of mitophagy in cancer therapy: Progress and challenges
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.06.014openalex-snapshot
Targeting whole body metabolism and mitochondrial bioenergetics in the drug development for Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.apsb.2025.11.030openalex-snapshot
Transmitophagy in the heart: An overview of molecular mechanisms and implications for pathophysiology
inferred← citeshttps://doi.org/10.1016/j.arr.2014.12.010openalex-snapshot
Mitochondrial proteases and protein quality control in ageing and longevity
inferred← citeshttps://doi.org/10.1016/j.bbabio.2016.12.008openalex-snapshot
Dysregulation of mitophagy in carcinogenesis and tumor progression
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.11.019openalex-snapshot
TNF-α regulates miRNA targeting mitochondrial complex-I and induces cell death in dopaminergic cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.02.170openalex-snapshot
PINK1/Parkin mediated mitophagy ameliorates palmitic acid-induced apoptosis through reducing mitochondrial ROS production in podocytes
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.04.032openalex-snapshot
DUSP1 overexpression attenuates renal tubular mitochondrial dysfunction by restoring Parkin-mediated mitophagy in diabetic nephropathy
inferred← citeshttps://doi.org/10.1016/j.biocel.2016.10.006openalex-snapshot
Autophagy deficient melanocytes display a senescence associated secretory phenotype that includes oxidized lipid mediators
inferred← citeshttps://doi.org/10.1016/j.bj.2015.10.002openalex-snapshot
Metabolic, autophagic, and mitophagic activities in cancer initiation and progression
inferred← citeshttps://doi.org/10.1016/j.ccmp.2023.100103openalex-snapshot
Electroacupuncture Alleviates HIF1-α-mediated Early Mitophagy in Spinal Cord Injury
inferred← citeshttps://doi.org/10.1016/j.ccr.2017.11.026openalex-snapshot
Bright lights down under: Metal ion complexes turning the spotlight on metabolic processes at the cellular level
inferred← citeshttps://doi.org/10.1016/j.cell.2016.11.042openalex-snapshot
Prohibitin 2 Is an Inner Mitochondrial Membrane Mitophagy Receptor
inferred← citeshttps://doi.org/10.1016/j.cellsig.2014.09.004openalex-snapshot
Mulan E3 ubiquitin ligase interacts with multiple E2 conjugating enzymes and participates in mitophagy by recruiting GABARAP
inferred← citeshttps://doi.org/10.1016/j.cotox.2016.08.002openalex-snapshot
Development of Keap1-interactive small molecules that regulate Nrf2 transcriptional activity
inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.175136openalex-snapshot
MitoTEMPO protects against podocyte injury by inhibiting NLRP3 inflammasome via PINK1/Parkin pathway-mediated mitophagy
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2019.09.020openalex-snapshot
Glucose starvation-induced oxidative stress causes mitochondrial dysfunction and apoptosis via Prohibitin 1 upregulation in human breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.fsi.2023.109037openalex-snapshot
NEDD4 activates mitophagy by interacting with LC3 to restrain reactive oxygen species and apoptosis in Apostichopus japonicus challenged with Vibrio splendidus
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e30568openalex-snapshot
SIRT3 and RORα are two prospective targets against mitophagy during simulated ischemia/reperfusion injury in H9c2 cells
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.03.052openalex-snapshot
Genipin protects rats against lipopolysaccharide-induced acute lung injury by reinforcing autophagy
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110739openalex-snapshot
The ubiquitin-binding protein ANKRD13A mediates VCP-dependent mitochondrial outer membrane rupture during PINK1/Parkin-mediated mitophagy
inferred← citeshttps://doi.org/10.1016/j.jep.2019.03.033openalex-snapshot
Mitochondrial dynamics modulation as a critical contribution for Shenmai injection in attenuating hypoxia/reoxygenation injury
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2019.110976openalex-snapshot
Synthesis, photophysical and anticancer properties of mitochondria-targeted phosphorescent cyclometalated iridium(III) N-heterocyclic carbene complexes
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2023.112427openalex-snapshot
Cyclometalated iridium(III) complexes as anti-breast cancer and anti-metastasis agents via STAT3 inhibition
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2024.112986openalex-snapshot
Dynamic insights into mitochondrial function: Monitoring viscosity and SO2 levels in living cells
inferred← citeshttps://doi.org/10.1016/j.livres.2018.08.001openalex-snapshot
Tumor-suppressing effects of autophagy on hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2016.06.004openalex-snapshot
Emerging Mitochondrial Therapeutic Targets in Optic Neuropathies
inferred← citeshttps://doi.org/10.1016/j.phrs.2024.107394openalex-snapshot
Investigating the interplay between mitophagy and diabetic neuropathy: Uncovering the hidden secrets of the disease pathology
inferred← citeshttps://doi.org/10.1016/j.redox.2015.01.003openalex-snapshot
Teaching the basics of autophagy and mitophagy to redox biologists—Mechanisms and experimental approaches
inferred← citeshttps://doi.org/10.1016/j.redox.2016.11.004openalex-snapshot
Inhibition of autophagy with bafilomycin and chloroquine decreases mitochondrial quality and bioenergetic function in primary neurons
inferred← citeshttps://doi.org/10.1016/j.redox.2018.04.005openalex-snapshot
Methods for assessing mitochondrial quality control mechanisms and cellular consequences in cell culture
inferred← citeshttps://doi.org/10.1016/j.redox.2018.07.025openalex-snapshot
Artesunate-induced mitophagy alters cellular redox status
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.136953openalex-snapshot
6‴-Feruloylspinosin alleviated beta-amyloid induced toxicity by promoting mitophagy in Caenorhabditis elegans (GMC101) and PC12 cells
inferred← citeshttps://doi.org/10.1016/j.tiv.2016.04.006openalex-snapshot
PINK1/Parkin-mediated mitophagy play a protective role in manganese induced apoptosis in SH-SY5Y cells
inferred← citeshttps://doi.org/10.1016/j.toxlet.2022.11.004openalex-snapshot
Dasatinib causes keratinocyte apoptosis via inhibiting high mobility group Box 1-mediated mitophagy
inferred← citeshttps://doi.org/10.1016/j.tranon.2024.101886openalex-snapshot
Identification of HSPD1 as a novel invasive biomarker associated with mitophagy in pituitary adenomas
inferred← citeshttps://doi.org/10.1016/j.yexcr.2015.04.016openalex-snapshot
ABT737 enhances cholangiocarcinoma sensitivity to cisplatin through regulation of mitochondrial dynamics
inferred← citeshttps://doi.org/10.1016/j.yexcr.2018.04.016openalex-snapshot
Hepatitis B Virus X protein elevates Parkin-mediated mitophagy through Lon Peptidase in starvation
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c05935openalex-snapshot
SLC25A39: A Guardian against Cadmium-Induced Pleiotropic Disruption of Mitochondrial Homeostasis in Rat Neuronal Cells
inferred← citeshttps://doi.org/10.1021/acs.langmuir.5c04928openalex-snapshot
Biointerface Behavior of Layered Double Hydroxides: Dispersibility and Toxicity Assessment Using Experimental and Computational Models
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.6b00405openalex-snapshot
Iron Oxide Nanoparticles Induce Autophagosome Accumulation through Multiple Mechanisms: Lysosome Impairment, Mitochondrial Damage, and ER Stress
inferred← citeshttps://doi.org/10.1021/acsami.7b01735openalex-snapshot
Light-Up Mitophagy in Live Cells with Dual-Functional Theranostic Phosphorescent Iridium(III) Complexes
inferred← citeshttps://doi.org/10.1038/cddis.2017.380openalex-snapshot
Exogenous H2S facilitating ubiquitin aggregates clearance via autophagy attenuates type 2 diabetes-induced cardiomyopathy
inferred← citeshttps://doi.org/10.1038/nchembio.2287openalex-snapshot
The pharmacological regulation of cellular mitophagy
inferred← citeshttps://doi.org/10.1038/s12276-018-0199-6openalex-snapshot
The role of the apoptosis-related protein BCL-B in the regulation of mitophagy in hepatic stellate cells during the regression of liver fibrosis
inferred← citeshttps://doi.org/10.1038/s41401-018-0193-5openalex-snapshot
Sulfuretin protects hepatic cells through regulation of ROS levels and autophagic flux
inferred← citeshttps://doi.org/10.1038/s41418-019-0292-yopenalex-snapshot
Autophagy and cancer stem cells: molecular mechanisms and therapeutic applications
inferred← citeshttps://doi.org/10.1038/s41467-025-63040-xopenalex-snapshot
Dual-key cooperatively activated DNA regulator for controlling mitochondria-lysosome interactions
inferred← citeshttps://doi.org/10.1038/s41556-018-0037-zopenalex-snapshot
Cargo recognition and degradation by selective autophagy
inferred← citeshttps://doi.org/10.1038/s41598-018-26949-6openalex-snapshot
AKT signalling selectively regulates PINK1 mitophagy in SHSY5Y cells and human iPSC-derived neurons
inferred← citeshttps://doi.org/10.1038/s41598-023-49018-zopenalex-snapshot
The interplay between sex, time of day, fasting status, and their impact on cardiac mitochondrial structure, function, and dynamics
inferred← citeshttps://doi.org/10.1042/bj20150568openalex-snapshot
KEAP1–NRF2 signalling and autophagy in protection against oxidative and reductive proteotoxicity
inferred← citeshttps://doi.org/10.1080/15548627.2015.1061849openalex-snapshot
Thyroid hormone induction of mitochondrial activity is coupled to mitophagy via ROS-AMPK-ULK1 signaling
inferred← citeshttps://doi.org/10.1080/15548627.2017.1356948openalex-snapshot
Regulation of autophagy, mitochondrial dynamics, and cellular bioenergetics by 4-hydroxynonenal in primary neurons
inferred← citeshttps://doi.org/10.1080/15548627.2019.1628520openalex-snapshot
PHB2 (prohibitin 2) promotes PINK1-PRKN/Parkin-dependent mitophagy by the PARL-PGAM5-PINK1 axis
inferred← citeshttps://doi.org/10.1080/15548627.2021.2020979openalex-snapshot
Restoration of mitophagy ameliorates cardiomyopathy in Barth syndrome
inferred← citeshttps://doi.org/10.1080/23723556.2017.1405142openalex-snapshot
Autophagy and mitophagy in hepatocarcinogenesis
inferred← citeshttps://doi.org/10.1089/ars.2014.6223openalex-snapshot
Mitochondria-Associated Membranes: Composition, Molecular Mechanisms, and Physiopathological Implications
inferred← citeshttps://doi.org/10.1111/acer.13877openalex-snapshot
A Unifying Hypothesis Linking Hepatic Adaptations for Ethanol Metabolism to the Proinflammatory and Profibrotic Events of Alcoholic Liver Disease
inferred← citeshttps://doi.org/10.1111/iej.13055openalex-snapshot
Simvastatin alleviates bone resorption in apical periodontitis possibly by inhibition of mitophagy‐related osteoblast apoptosis
inferred← citeshttps://doi.org/10.1111/jcmm.17917openalex-snapshot
Acid ground nano‐realgar processed product inhibits breast cancer by inducing mitophagy via the p53/ BNIP3 / NIX pathway
inferred← citeshttps://doi.org/10.1111/jnc.12844openalex-snapshot
Bioenergetic adaptation in response to autophagy regulators during rotenone exposure
inferred← citeshttps://doi.org/10.1111/jnc.14308openalex-snapshot
Mitochondrial function and autophagy: integrating proteotoxic, redox, and metabolic stress in Parkinson's disease
inferred← citeshttps://doi.org/10.1136/jclinpath-2016-203926openalex-snapshot
Elevated levels of autophagy-related marker ULK1 and mitochondrion-associated autophagy inhibitor LRPPRC are associated with biochemical progression and overall survival after androgen deprivation therapy in patients with metastatic prostate cancer
inferred← citeshttps://doi.org/10.1152/ajplung.00128.2016openalex-snapshot
Differential regulation of autophagy and mitophagy in pulmonary diseases
inferred← citeshttps://doi.org/10.1155/2017/8495160openalex-snapshot
The Interrelation between Reactive Oxygen Species and Autophagy in Neurological Disorders
inferred← citeshttps://doi.org/10.1155/2019/1283075openalex-snapshot
Sestrins at the Interface of ROS Control and Autophagy Regulation in Health and Disease
inferred← citeshttps://doi.org/10.1155/2020/5820245openalex-snapshot
Drp-1 as Potential Therapeutic Target for Lipopolysaccharide-Induced Vascular Hyperpermeability
inferred← citeshttps://doi.org/10.1155/2021/6617256openalex-snapshot
The Role of Mitophagy in Regulating Cell Death
inferred← citeshttps://doi.org/10.1155/2021/6621232openalex-snapshot
[Retracted] S‐Nitroso‐L‐Cysteine Ameliorated Pulmonary Hypertension in the MCT‐Induced Rats through Anti‐ROS and Anti‐Inflammatory Pathways
inferred← citeshttps://doi.org/10.1159/000381510openalex-snapshot
Mitophagy: Basic Mechanism and Potential Role in Kidney Diseases
inferred← citeshttps://doi.org/10.1159/000491070openalex-snapshot
Persistence and Transcription of Paternal mtDNA Dependent on the Delivery Strategy Rather than Mitochondria Source in Fish Embryos
inferred← citeshttps://doi.org/10.1186/s12929-018-0487-4openalex-snapshot
Mitophagy, a potential therapeutic target for stroke
inferred← citeshttps://doi.org/10.1186/s12967-020-02283-2openalex-snapshot
Role of Parkin-mediated mitophagy in the protective effect of polydatin in sepsis-induced acute kidney injury
inferred← citeshttps://doi.org/10.1186/s12967-025-06283-yopenalex-snapshot
Human neural stem cell-derived exosomes activate PINK1/Parkin pathway to protect against oxidative stress-induced neuronal injury in ischemic stroke
inferred← citeshttps://doi.org/10.1186/s13041-025-01201-1openalex-snapshot
Role of autophagy in neurotoxic protein’s clearance following post-ischemic stroke: where we are and what we know?
inferred← citeshttps://doi.org/10.1242/jcs.247379openalex-snapshot
Mitochondrial survivin reduces oxidative phosphorylation in cancer cells by inhibiting mitophagy
inferred← citeshttps://doi.org/10.1248/bpb.b15-00096openalex-snapshot
Choose Delicately and Reuse Adequately: The Newly Revealed Process of Autophagy
inferred← citeshttps://doi.org/10.1371/journal.pone.0140906openalex-snapshot
Disrupted Renal Mitochondrial Homeostasis after Liver Transplantation in Rats
inferred← citeshttps://doi.org/10.14336/ad.2020.0913openalex-snapshot
Delineating the Role of Mitophagy Inducers for Alzheimer Disease Patients
inferred← citeshttps://doi.org/10.14814/phy2.15686openalex-snapshot
Cardiomyocyte ZKSCAN3 regulates remodeling following pressure‐overload
inferred← citeshttps://doi.org/10.1515/biol-2022-0958openalex-snapshot
The role of rapamycin in the PINK1/Parkin signaling pathway in mitophagy in podocytes
inferred← citeshttps://doi.org/10.1515/hsz-2019-0268openalex-snapshot
Bioenergetics and translational metabolism: implications for genetics, physiology and precision medicine
inferred← citeshttps://doi.org/10.2119/molmed.2014.00057openalex-snapshot
Reduction of Cardiac Cell Death after Helium Postconditioning in Rats: Transcriptional Analysis of Cell Death and Survival Pathways
inferred← citeshttps://doi.org/10.2147/dddt.s248628openalex-snapshot
Melatonin Attenuates Anoxia/Reoxygenation Injury by Inhibiting Excessive Mitophagy Through the MT2/SIRT3/FoxO3a Signaling Pathway in H9c2 Cells
inferred← citeshttps://doi.org/10.2147/vhrm.s264130openalex-snapshot
Targeting Cardiac Metabolic Pathways: A Role in Ischemic Management
inferred← citeshttps://doi.org/10.2174/1381612826666200107144810openalex-snapshot
Emerging Role of Mitophagy in Inflammatory Diseases: Cellular and Molecular Episodes
inferred← citeshttps://doi.org/10.2174/1381612826666200826165735openalex-snapshot
Mitochondrial-induced Epigenetic Modifications: From Biology to Clinical Translation
inferred← citeshttps://doi.org/10.2174/1570159x21666230314140528openalex-snapshot
Pharmacological Progress of Mitophagy Regulation
inferred← citeshttps://doi.org/10.21873/anticanres.12266openalex-snapshot
Dual Role of Mitophagy in Cancer Drug Resistance
inferred← citeshttps://doi.org/10.3168/jds.2024-24800openalex-snapshot
Targeting PHB2-mediated mitophagy alleviates nonesterified fatty acid-induced mitochondrial dysfunction in bovine mammary epithelial cells
inferred← citeshttps://doi.org/10.32657/10356/72655openalex-snapshot
Molecular mechanisms underlying selective clearance of protein aggregates and mitochondria by autophagy
inferred← citeshttps://doi.org/10.3389/fcell.2020.610516openalex-snapshot
Sex Hormone Regulation of Proteins Modulating Mitochondrial Metabolism, Dynamics and Inter-Organellar Cross Talk in Cardiovascular Disease
inferred← citeshttps://doi.org/10.3389/fimmu.2021.624117openalex-snapshot
Comprehensive Integration of Genome-Wide Association and Gene Expression Studies Reveals Novel Gene Signatures and Potential Therapeutic Targets for Helicobacter pylori-Induced Gastric Disease
inferred← citeshttps://doi.org/10.3389/fnagi.2022.986849openalex-snapshot
Exploring therapeutic potential of mitophagy modulators using Drosophila models of Parkinson’s disease
inferred← citeshttps://doi.org/10.3389/fnins.2020.00245openalex-snapshot
Nix Plays a Neuroprotective Role in Early Brain Injury After Experimental Subarachnoid Hemorrhage in Rats
inferred← citeshttps://doi.org/10.3389/fonc.2017.00081openalex-snapshot
The Close Interconnection between Mitochondrial Dynamics and Mitophagy in Cancer
inferred← citeshttps://doi.org/10.3389/fphar.2014.00244openalex-snapshot
Emerging role of selective autophagy in human diseases
inferred← citeshttps://doi.org/10.3389/fragi.2020.610406openalex-snapshot
The Promise of a Golden Era for Exploring the Frontiers of Aging, Metabolism and Redox Biology
inferred← citeshttps://doi.org/10.3389/fragi.2022.812810openalex-snapshot
Differential Effects of 2-Deoxyglucose and Glucose Deprivation on 4-Hydroxynonenal Dependent Mitochondrial Dysfunction in Primary Neurons
inferred← citeshttps://doi.org/10.3390/ijms160920704openalex-snapshot
Mitochondria: A Therapeutic Target for Parkinson’s Disease?
inferred← citeshttps://doi.org/10.3390/nu9111176openalex-snapshot
The Role of Mammalian Target of Rapamycin (mTOR) in Insulin Signaling
inferred← citeshttps://doi.org/10.37349/emed.2023.00157openalex-snapshot
Autophagy in ischemic stroke: role of circular RNAs
inferred← citeshttps://doi.org/10.3791/53657openalex-snapshot
Time-Lapse Video Microscopy for Assessment of EYFP-Parkin Aggregation as a Marker for Cellular Mitophagy
inferred← citeshttps://doi.org/10.3892/mmr.2019.10413openalex-snapshot
NME4 may enhance non‑small cell lung cancer progression by overcoming cell cycle arrest and promoting cellular proliferation
inferred← citeshttps://doi.org/10.4081/ejtm.2018.7687openalex-snapshot
Increasing autophagy does not affect neurogenic muscle atrophy
inferred← citeshttps://doi.org/10.5734/jgm.2022.19.2.49openalex-snapshot
Mitophagy stimulation as a novel strategy for the treatment of mitochondrial diseases
inferred← citeshttps://doi.org/10.70675/5453e14cz1debz499cza93cz316d9cc9d155openalex-snapshot
Rôle de la dynamique mitochondriale à la phase aigue de l'infarctus du myocarde
inferred← citeshttps://doi.org/10.70675/c8145e7bz8153z43acz8532z3ea5954dd01copenalex-snapshot
Mechanisms and function of mitophagy in adaptation to heat stress during development of C. elegans
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