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Mammalian autophagy: core molecular machinery and signaling regulation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-642-00302-8_1openalex-snapshot
An Overview of the Molecular Mechanism of Autophagy
inferredcites →https://doi.org/10.1016/j.cell.2005.02.031openalex-snapshot
Phosphorylation and Functional Inactivation of TSC2 by Erk
inferredcites →https://doi.org/10.1016/j.cell.2006.05.034openalex-snapshot
DRAM, a p53-Induced Modulator of Autophagy, Is Critical for Apoptosis
inferredcites →https://doi.org/10.1016/j.cmet.2007.11.001openalex-snapshot
FoxO3 Controls Autophagy in Skeletal Muscle In Vivo
inferredcites →https://doi.org/10.1016/j.molcel.2006.12.009openalex-snapshot
Control of Macroautophagy by Calcium, Calmodulin-Dependent Kinase Kinase-β, and Bcl-2
inferredcites →https://doi.org/10.1016/j.molcel.2008.03.003openalex-snapshot
AMPK Phosphorylation of Raptor Mediates a Metabolic Checkpoint
inferredcites →https://doi.org/10.1016/j.molcel.2008.06.001openalex-snapshot
JNK1-Mediated Phosphorylation of Bcl-2 Regulates Starvation-Induced Autophagy
inferredcites →https://doi.org/10.1016/s0070-2153(05)73007-6openalex-snapshot
Chaperone‐Mediated Autophagy in Aging and Disease
inferredcites →https://doi.org/10.1016/s1534-5807(03)00402-7openalex-snapshot
The Atg1-Atg13 Complex Regulates Atg9 and Atg23 Retrieval Transport from the Pre-Autophagosomal Structure
inferredcites →https://doi.org/10.1038/cdd.2008.84openalex-snapshot
Hypoxia signals autophagy in tumor cells via AMPK activity, independent of HIF-1, BNIP3, and BNIP3L
inferredcites →https://doi.org/10.1038/cdd.2009.19openalex-snapshot
Bif-1/Endophilin B1: a candidate for crescent driving force in autophagy
inferredcites →https://doi.org/10.1038/emboj.2009.8openalex-snapshot
TAK1 activates AMPK‐dependent cytoprotective autophagy in TRAIL‐treated epithelial cells
inferredcites →https://doi.org/10.1038/embor.2008.246openalex-snapshot
DAP‐kinase‐mediated phosphorylation on the BH3 domain of beclin 1 promotes dissociation of beclin 1 from Bcl‐XL and induction of autophagy
inferredcites →https://doi.org/10.1038/nature05925openalex-snapshot
Ambra1 regulates autophagy and development of the nervous system
inferredcites →https://doi.org/10.1038/nature06639openalex-snapshot
Autophagy fights disease through cellular self-digestion
inferredcites →https://doi.org/10.1038/ncb1007-1102openalex-snapshot
Autophagosome formation: core machinery and adaptations
inferredcites →https://doi.org/10.1038/ncb1426openalex-snapshot
Autophagic and tumour suppressor activity of a novel Beclin1-binding protein UVRAG
inferredcites →https://doi.org/10.1038/ncb1537openalex-snapshot
The energy sensing LKB1–AMPK pathway regulates p27kip1 phosphorylation mediating the decision to enter autophagy or apoptosis
inferredcites →https://doi.org/10.1038/ncb1634openalex-snapshot
Bif-1 interacts with Beclin 1 through UVRAG and regulates autophagy and tumorigenesis
inferredcites →https://doi.org/10.1038/ncb1730openalex-snapshot
Regulation of autophagy by cytoplasmic p53
inferredcites →https://doi.org/10.1038/ncb1740openalex-snapshot
Beclin1-binding UVRAG targets the class C Vps complex to coordinate autophagosome maturation and endocytic trafficking
inferredcites →https://doi.org/10.1038/ncb1846openalex-snapshot
Two Beclin 1-binding proteins, Atg14L and Rubicon, reciprocally regulate autophagy at different stages
inferredcites →https://doi.org/10.1038/ncb1854openalex-snapshot
Distinct regulation of autophagic activity by Atg14L and Rubicon associated with Beclin 1–phosphatidylinositol-3-kinase complex
inferredcites →https://doi.org/10.1038/ncb839openalex-snapshot
TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling
inferredcites →https://doi.org/10.1038/sj.cdd.4401751openalex-snapshot
Autophagy and signaling: their role in cell survival and cell death
inferredcites →https://doi.org/10.1038/sj.emboj.7601689openalex-snapshot
Functional and physical interaction between Bcl‐XL and a BH3‐like domain in Beclin‐1
inferredcites →https://doi.org/10.1038/sj.onc.1207539openalex-snapshot
Ras is involved in the negative control of autophagy through the class I PI3-kinase
inferredcites →https://doi.org/10.1073/pnas.0502857102openalex-snapshot
The coordinate regulation of the p53 and mTOR pathways in cells
inferredcites →https://doi.org/10.1073/pnas.0810452105openalex-snapshot
Identification of Barkor as a mammalian autophagy-specific factor for Beclin 1 and class III phosphatidylinositol 3-kinase
inferredcites →https://doi.org/10.1074/jbc.c700195200openalex-snapshot
The Atg12-Atg5 Conjugate Has a Novel E3-like Activity for Protein Lipidation in Autophagy
inferredcites →https://doi.org/10.1074/jbc.m210998200openalex-snapshot
Amino Acids Interfere with the ERK1/2-dependent Control of Macroautophagy by Controlling the Activation of Raf-1 in Human Colon Cancer HT-29 Cells
inferredcites →https://doi.org/10.1074/jbc.m706956200openalex-snapshot
The Pancreatitis-induced Vacuole Membrane Protein 1 Triggers Autophagy in Mammalian Cells
inferredcites →https://doi.org/10.1074/jbc.m900301200openalex-snapshot
An ATP-competitive Mammalian Target of Rapamycin Inhibitor Reveals Rapamycin-resistant Functions of mTORC1
inferredcites →https://doi.org/10.1074/jbc.m900573200openalex-snapshot
ULK1·ATG13·FIP200 Complex Mediates mTOR Signaling and Is Essential for Autophagy
inferredcites →https://doi.org/10.1083/jcb.150.6.1507openalex-snapshot
Tor-Mediated Induction of Autophagy via an Apg1 Protein Kinase Complex
inferredcites →https://doi.org/10.1083/jcb.200712064openalex-snapshot
FIP200, a ULK-interacting protein, is required for autophagosome formation in mammalian cells
inferredcites →https://doi.org/10.1091/mbc.e07-12-1257openalex-snapshot
The Atg16L Complex Specifies the Site of LC3 Lipidation for Membrane Biogenesis in Autophagy
inferredcites →https://doi.org/10.1091/mbc.e08-01-0075openalex-snapshot
Vacuole Membrane Protein 1 Is an Endoplasmic Reticulum Protein Required for Organelle Biogenesis, Protein Secretion, and Development
inferredcites →https://doi.org/10.1091/mbc.e08-01-0080openalex-snapshot
Beclin 1 Forms Two Distinct Phosphatidylinositol 3-Kinase Complexes with Mammalian Atg14 and UVRAG
inferredcites →https://doi.org/10.1091/mbc.e08-03-0309openalex-snapshot
The Atg8 Conjugation System Is Indispensable for Proper Development of Autophagic Isolation Membranes in Mice
inferredcites →https://doi.org/10.1091/mbc.e08-03-0312openalex-snapshot
An Atg4B Mutant Hampers the Lipidation of LC3 Paralogues and Causes Defects in Autophagosome Closure
inferredcites →https://doi.org/10.1091/mbc.e08-07-0671openalex-snapshot
The TP53INP2 Protein Is Required for Autophagy in Mammalian Cells
inferredcites →https://doi.org/10.1091/mbc.e08-12-1248openalex-snapshot
Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy
inferredcites →https://doi.org/10.1091/mbc.e08-12-1249openalex-snapshot
ULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery
inferredcites →https://doi.org/10.1101/gad.519709openalex-snapshot
Autophagy mediates the mitotic senescence transition
inferredcites →https://doi.org/10.1126/science.1106148openalex-snapshot
Phosphorylation and Regulation of Akt/PKB by the Rictor-mTOR Complex
inferredcites →https://doi.org/10.1158/0008-5472.can-07-6163openalex-snapshot
Mammalian Target of Rapamycin and S6 Kinase 1 Positively Regulate 6-thioguanine-Induced Autophagy
inferredcites →https://doi.org/10.1182/blood-2008-02-137398openalex-snapshot
Ulk1 plays a critical role in the autophagic clearance of mitochondria and ribosomes during reticulocyte maturation
inferredcites →https://doi.org/10.1242/jcs.01620openalex-snapshot
The molecular machinery of autophagy: unanswered questions
inferredcites →https://doi.org/10.1242/jcs.03172openalex-snapshot
Starvation and ULK1-dependent cycling of mammalian Atg9 between the TGN and endosomes
inferredcites →https://doi.org/10.4161/auto.5.5.8249openalex-snapshot
A novel, human Atg13 binding protein, Atg101, interacts with ULK1 and is essential for macroautophagy
inferredcites →https://doi.org/10.4161/auto.6260openalex-snapshot
Bcl-2 family members: Dual regulators of apoptosis and autophagy
inferredcites →https://doi.org/10.4161/cc.7.19.6751openalex-snapshot
Mutant p53 protein localized in the cytoplasm inhibits autophagy
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Paeonol Ameliorated Hyperlipidemia in Mice by Regulating Ampk/Mtor Pathways and Autophagy Via Nrf2
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Lipid droplets and fatty acid‐induced lipotoxicity: in a nutshell
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Microbiome−host proteostasis crosstalk—An emerging perspective on mechanisms and interventions toward healthy longevity
inferred← citeshttps://doi.org/10.1002/1878-0261.12567openalex-snapshot
Emerging roles of HECT‐type E3 ubiquitin ligases in autophagy regulation
inferred← citeshttps://doi.org/10.1002/2211-5463.13307openalex-snapshot
A brief overview of BNIP3L/NIX receptor‐mediated mitophagy
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.201100039openalex-snapshot
Protein Abundance Variation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0006165.pub2openalex-snapshot
Mitochondrial DNA : Fate of the Paternal Mitochondrial Genome
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Mitochondrial DNA : Fate of the Paternal Mitochondrial Genome
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Exoerythrocytic development ofPlasmodiumparasites
inferred← citeshttps://doi.org/10.1002/9781118677551.ch7openalex-snapshot
Autophagy: A Home Remodeler for Hepatitis C Virus
inferred← citeshttps://doi.org/10.1002/9781118978320.ch2openalex-snapshot
Lysosome Biogenesis and Autophagy
inferred← citeshttps://doi.org/10.1002/9781119017127.ch12openalex-snapshot
A Get‐Together to Tear It Apart
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Epigenotoxicity of Titanium Dioxide Nanoparticles
inferred← citeshttps://doi.org/10.1002/adbi.201800259openalex-snapshot
Crosstalk between Autophagy and Nanomaterials: Internalization, Activation, Termination
inferred← citeshttps://doi.org/10.1002/advs.202205483openalex-snapshot
Targeting the Lysosomal Degradation of Rab22a‐NeoF1 Fusion Protein for Osteosarcoma Lung Metastasis
inferred← citeshttps://doi.org/10.1002/ajmg.c.31317openalex-snapshot
Autophagy and mitochondria in Pompe disease: Nothing is so new as what has long been forgotten
inferred← citeshttps://doi.org/10.1002/biof.101openalex-snapshot
Role of mitochondrial ion channels in cell death
inferred← citeshttps://doi.org/10.1002/biof.1079openalex-snapshot
Curcumin, a component of turmeric: From farm to pharmacy
inferred← citeshttps://doi.org/10.1002/bit.24393openalex-snapshot
Inhibition of glutamine‐dependent autophagy increases t‐PA production in CHO Cell fed‐batch processes
inferred← citeshttps://doi.org/10.1002/brb3.2376openalex-snapshot
Protective mechanism of FoxO1 against early brain injury after subarachnoid hemorrhage by regulating autophagy
inferred← citeshttps://doi.org/10.1002/cbf.3402openalex-snapshot
Roles for VEGF‐C/NRP–2 axis in regulating renal tubular epithelial cell survival and autophagy during serum deprivation
inferred← citeshttps://doi.org/10.1002/cbf.3740openalex-snapshot
ATG5: A central autophagy regulator implicated in various human diseases
inferred← citeshttps://doi.org/10.1002/cbf.70072openalex-snapshot
Estrogen G‐Protein Coupled Receptor Antagonist G15 Promotes Tau Clearance in 2D and 3D Tauopathy Models
inferred← citeshttps://doi.org/10.1002/cbin.10497openalex-snapshot
Depletion of p18/LAMTOR1 promotes cell survival via activation of p27kip1‐dependent autophagy under starvation
inferred← citeshttps://doi.org/10.1002/cbin.11208openalex-snapshot
Insulin secretion impairment induced by rosuvastatin partly though autophagy in INS‐1E cells
inferred← citeshttps://doi.org/10.1002/cbin.12081openalex-snapshot
Autophagy‐targeted nanoparticles in breast carcinoma: A systematic review
inferred← citeshttps://doi.org/10.1002/cbin.12114openalex-snapshot
Lipid droplets, autophagy, and ER stress as key (survival) pathways during ischemia‐reperfusion of transplanted grafts
inferred← citeshttps://doi.org/10.1002/cjoc.202300639openalex-snapshot
A High‐Contrast Autolysosome Probe for Detecting Interaction between Autophagosomes and Autolysosomes in Mitophagy†
inferred← citeshttps://doi.org/10.1002/ctm2.1445openalex-snapshot
H1Innovative approaches to combat anti‐cancer drug resistance: Targeting lncRNA and autophagy
inferred← citeshttps://doi.org/10.1002/eji.201242835openalex-snapshot
A bacterial protein promotes the recognition of the Legionella pneumophila vacuole by autophagy
inferred← citeshttps://doi.org/10.1002/emmm.201202176openalex-snapshot
Transcription factor EB (TFEB) is a new therapeutic target for Pompe disease
inferred← citeshttps://doi.org/10.1002/epi4.12386openalex-snapshot
Neurodegenerative pathways as targets for acquired epilepsy therapy development
inferred← citeshttps://doi.org/10.1002/exp.20240112openalex-snapshot
Autophagy‐Targeting Nanomedicine: Strike at the Heart of the Cancer via Precise Modulation of Autophagy
inferred← citeshttps://doi.org/10.1002/fsn3.70632openalex-snapshot
Proteostasis Disruption by Proteasome Inhibitor MG132 and Propolin G Induces ER Stress‐ and Autophagy‐Mediated Apoptosis in Breast Cancer
inferred← citeshttps://doi.org/10.1002/ijc.27935openalex-snapshot
The dual PI3K/mTOR inhibitor NVP‐BEZ235 and chloroquine synergize to trigger apoptosis via mitochondrial‐lysosomal cross‐talk
inferred← citeshttps://doi.org/10.1002/ijc.31398openalex-snapshot
Targeting EGFR‐mediated autophagy as a potential strategy for cancer therapy
inferred← citeshttps://doi.org/10.1002/jat.3049openalex-snapshot
Carnosic acid induces autophagic cell death through inhibition of the Akt/mTOR pathway in human hepatoma cells
inferred← citeshttps://doi.org/10.1002/jat.3114openalex-snapshot
The relationship between Cd‐induced autophagy and lysosomal activation in WRL‐68 cells
inferred← citeshttps://doi.org/10.1002/jat.3393openalex-snapshot
Autophagy function and its relationship to pathology, clinical applications, drug metabolism and toxicity
inferred← citeshttps://doi.org/10.1002/jbmr.3530openalex-snapshot
Tsc1 Regulates the Balance Between Osteoblast and Adipocyte Differentiation Through Autophagy/Notch1/β-Catenin Cascade
inferred← citeshttps://doi.org/10.1002/jbt.23211openalex-snapshot
Retracted: Britannin mediates apoptosis and glycolysis of T‐cell lymphoblastic lymphoma cells by AMPK‐dependent autophagy
inferred← citeshttps://doi.org/10.1002/jcb.27467openalex-snapshot
Association of single nucleotide autophagy‐related protein 5 gene polymorphism rs2245214 with susceptibility to non–small cell lung cancer
inferred← citeshttps://doi.org/10.1002/jcb.29669openalex-snapshot
The functional interplay of lncRNA EGOT and HuR regulates hypoxia‐induced autophagy in renal tubular cells
inferred← citeshttps://doi.org/10.1002/jcb.30405openalex-snapshot
Identification of potential selective autophagy receptors from protein‐content profiling of autophagosomes
inferred← citeshttps://doi.org/10.1002/jcp.22769openalex-snapshot
The roles of integrin β4 in Vascular Endothelial Cells
inferred← citeshttps://doi.org/10.1002/jcp.26538openalex-snapshot
RETRACTED: Phytosomal curcumin inhibits tumor growth in colitis‐associated colorectal cancer
inferred← citeshttps://doi.org/10.1002/jcp.27502openalex-snapshot
RNA‐binding protein, human antigen R regulates hypoxia‐induced autophagy by targeting ATG7/ATG16L1 expressions and autophagosome formation
inferred← citeshttps://doi.org/10.1002/jcp.29069openalex-snapshot
Retracted: EZH2 regulates H2B phosphorylation and elevates colon cancer cell autophagy
inferred← citeshttps://doi.org/10.1002/jcp.30217openalex-snapshot
Dectin‐1–mediated suppression of RANKL‐induced osteoclastogenesis by glucan from baker's yeast
inferred← citeshttps://doi.org/10.1002/jcp.30354openalex-snapshot
The ERK1/2–ATG13–FIP200 signaling cascade is required for autophagy induction to protect renal cells from hypoglycemia‐induced cell death
inferred← citeshttps://doi.org/10.1002/jez.b.22936openalex-snapshot
Detection and analysis of autophagy in the American alligator (Alligator mississippiensis)
inferred← citeshttps://doi.org/10.1002/jper.19-0510openalex-snapshot
Calcitriol decreases live Porphyromonas gingivalis internalized into epithelial cells and monocytes by promoting autophagy
inferred← citeshttps://doi.org/10.1002/kjm2.12462openalex-snapshot
Diosmetin inhibits apoptosis and activates AMPK ‐induced autophagy in myocardial damage under hypoxia environment
inferred← citeshttps://doi.org/10.1002/mc.22212openalex-snapshot
Oroxylin A induces autophagy in human malignant glioma cells via the mTOR‐STAT3‐Notch signaling pathway
inferred← citeshttps://doi.org/10.1002/mco2.70024openalex-snapshot
Programmed cell death: molecular mechanisms, biological functions, diseases, and therapeutic targets
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Targeting the Enhanced Sensitivity of Radiotherapy in Cancer: Mechanisms, Applications, and Challenges
inferred← citeshttps://doi.org/10.1002/mco2.70244openalex-snapshot
Mitochondria as Regulators of Nonapoptotic Cell Death in Cancer
inferred← citeshttps://doi.org/10.1002/mco2.83openalex-snapshot
Lomerizine 2HCl inhibits cell proliferation and induces protective autophagy in colorectal cancer via the PI3K/Akt/mTOR signaling pathway
inferred← citeshttps://doi.org/10.1002/mds.26477openalex-snapshot
Autophagy and A lpha‐ S ynuclein: R elevance to P arkinson's D isease and R elated S ynucleopathies
inferred← citeshttps://doi.org/10.1002/med.21303openalex-snapshot
The Role and Therapeutic Potential of Autophagy Modulation in Controlling Virus‐Induced Cell Death
inferred← citeshttps://doi.org/10.1002/med.21662openalex-snapshot
How autophagy can restore proteostasis defects in multiple diseases?
inferred← citeshttps://doi.org/10.1002/mnfr.201700610openalex-snapshot
Resveratrol Potently Counteracts Quercetin Starvation‐Induced Autophagy and Sensitizes HepG2 Cancer Cells to Apoptosis
inferred← citeshttps://doi.org/10.1002/ntls.20220067openalex-snapshot
Autophagy dark genes: Can we find them with machine learning?
inferred← citeshttps://doi.org/10.1002/pro.3866openalex-snapshot
Atg3 promotes Atg8 lipidation via altering lipid diffusion and rearrangement
inferred← citeshttps://doi.org/10.1002/ps.70032openalex-snapshot
The autophagy pathway participates in resistance to Candidatus Liberibacter asiaticus infection in Diaphorina citri
inferred← citeshttps://doi.org/10.1002/ptr.5834openalex-snapshot
Neuroprotective Natural Products for the Treatment of Parkinson's Disease by Targeting the Autophagy-Lysosome Pathway: A Systematic Review
inferred← citeshttps://doi.org/10.1002/ptr.6422openalex-snapshot
Molecular mechanisms of natural compounds in cell death induction and sensitization to chemotherapeutic drugs in lung cancer
inferred← citeshttps://doi.org/10.1002/ptr.7551openalex-snapshot
Targeting autophagy and neuroinflammation pathways with plant‐derived natural compounds as potential antidepressant agents
inferred← citeshttps://doi.org/10.1002/ptr.8214openalex-snapshot
Diosmetin as a promising natural therapeutic agent: In vivo, in vitro mechanisms, and clinical studies
inferred← citeshttps://doi.org/10.1002/ptr.8386openalex-snapshot
Platycodin D2 Mediates Incomplete Autophagy and Ferroptosis in Breast Cancer Cells by Regulating Mitochondrial ROS
inferred← citeshttps://doi.org/10.1002/smll.202507517openalex-snapshot
Nanoparticle‐Mediated Modulation of Bulk and Selective Autophagy: From Mechanistic Activation to Clinical Perspectives
inferred← citeshttps://doi.org/10.1002/smsc.202400607openalex-snapshot
Nanomedicine Approaches for Autophagy Modulation in Cancer Therapy
inferred← citeshttps://doi.org/10.1002/tox.22506openalex-snapshot
Cigarette smoke extract and isoprene resulted in the induction of apoptosis and autophagy in human placenta choriocarcinoma JEG‐3 cells
inferred← citeshttps://doi.org/10.1002/tox.23677openalex-snapshot
Excessive fluoride impairs autophagy flux in ameloblasts which is prevented by the autophagy activator rapamycin
inferred← citeshttps://doi.org/10.1002/tox.23935openalex-snapshot
Principle active metabolites of Pinus morrisonicola Hayata synergistically inhibit cell proliferation and autophagy to elevate apoptosis in hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1002/tox.24195openalex-snapshot
RETRACTED: Pachymic acid activates TP53INP2 / TRAF6 /caspase‐8 pathway to promote apoptosis in renal cell carcinoma cells
inferred← citeshttps://doi.org/10.1002/wsbm.1505openalex-snapshot
Dynamic organization of intracellular organelle networks
inferred← citeshttps://doi.org/10.1007/5584_2022_715openalex-snapshot
Virus, Exosome, and MicroRNA: New Insights into Autophagy
inferred← citeshttps://doi.org/10.1007/978-1-0716-1589-8_10openalex-snapshot
Correlative Light and Electron Microscopy (CLEM): Bringing Together the Best of Both Worlds to Study Neuronal Autophagy
inferred← citeshttps://doi.org/10.1007/978-1-4614-1680-7_11openalex-snapshot
Autophagy and Self-Defense
inferred← citeshttps://doi.org/10.1007/978-1-4614-6561-4_12openalex-snapshot
Autophagy and Cancer Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-1-4614-6561-4_5openalex-snapshot
Role of Autophagy in Tumorigenesis
inferred← citeshttps://doi.org/10.1007/978-1-4614-7855-3_13openalex-snapshot
Glycogen Metabolism and Lafora Disease
inferred← citeshttps://doi.org/10.1007/978-1-4614-8220-8_12openalex-snapshot
Autophagic Cell Death: A Real Killer, an Accomplice, or an Innocent Bystander?
inferred← citeshttps://doi.org/10.1007/978-1-4614-8220-8_13openalex-snapshot
Autophagy in Necrosis: A Force for Survival
inferred← citeshttps://doi.org/10.1007/978-1-4614-9545-1_6openalex-snapshot
Modulating Autophagy and the “Reverse Warburg Effect”
inferred← citeshttps://doi.org/10.1007/978-1-4939-1176-9_16openalex-snapshot
Co-targeting Adaptive Survival Pathways
inferred← citeshttps://doi.org/10.1007/978-1-4939-8873-0_26openalex-snapshot
In Vitro Screening Platforms for Identifying Autophagy Modulators in Mammalian Cells
inferred← citeshttps://doi.org/10.1007/978-1-4939-9450-2_25openalex-snapshot
Monitoring Antigen Processing for MHC Presentation via Macroautophagy
inferred← citeshttps://doi.org/10.1007/978-1-62703-218-6_35openalex-snapshot
Antigen Processing for MHC Presentation via Macroautophagy
inferred← citeshttps://doi.org/10.1007/978-1-62703-302-2_26openalex-snapshot
Monitoring Autophagy in Dictyostelium
inferred← citeshttps://doi.org/10.1007/978-1-62703-456-2_10openalex-snapshot
Modulation of Autophagy as a Novel Cancer Therapeutic Strategy
inferred← citeshttps://doi.org/10.1007/978-1-62703-770-9_9openalex-snapshot
Autophagy in White Adipose Tissue
inferred← citeshttps://doi.org/10.1007/978-3-030-53868-2_4openalex-snapshot
The Growing Clinical Relevance of Cellular Stress Responses and Regulated Cell Death
inferred← citeshttps://doi.org/10.1007/978-3-030-74180-8_4openalex-snapshot
Amino Acids in Autophagy: Regulation and Function
inferred← citeshttps://doi.org/10.1007/978-3-031-07634-3_5openalex-snapshot
Autophagy in Cancer: A Metabolic Perspective
inferred← citeshttps://doi.org/10.1007/978-3-031-47375-3_24openalex-snapshot
Intraosseous Administration of Molecular Hydrogen: A Novel Technique—From Molecular Effects to Tissue Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-031-66421-2_5openalex-snapshot
Autophagy and Multidrug Resistance in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-12253-3_19openalex-snapshot
Role of Inositol Triphosphate Receptor in Cancer and Its Targeting Through Autophagy
inferred← citeshttps://doi.org/10.1007/978-3-319-17807-3_6openalex-snapshot
Hypoxia: A Formidable Saboteur of the Anti-tumor Response
inferred← citeshttps://doi.org/10.1007/978-3-319-28637-2_12openalex-snapshot
The Deleterious Duo of Neurodegeneration: Lysosomes and Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-319-30079-5_5openalex-snapshot
What Is the Pathobiology of Inflammation to Cell Death? Apoptosis, Necrosis, Necroptosis, Autophagic Cell Death, Pyroptosis, and NETosis
inferred← citeshttps://doi.org/10.1007/978-3-319-41457-7_10openalex-snapshot
Cardiac Autophagy and Its Regulation by Reversible Protein Acetylation
inferred← citeshttps://doi.org/10.1007/978-3-319-78655-1_18openalex-snapshot
Cell-Autonomous (Cell-Intrinsic) Stress Responses
inferred← citeshttps://doi.org/10.1007/978-3-642-27928-7_5openalex-snapshot
Selective autophagy in cellular quality control
inferred← citeshttps://doi.org/10.1007/978-3-642-38487-5_1openalex-snapshot
Dictyostelium discoideum as a Model in Biomedical Research
inferred← citeshttps://doi.org/10.1007/978-3-642-45179-9_3openalex-snapshot
Theories and Mechanisms of Aging
inferred← citeshttps://doi.org/10.1007/978-3-662-48250-6_3openalex-snapshot
Theorien und Mechanismen des Alterns
inferred← citeshttps://doi.org/10.1007/978-3-7091-0885-7_5openalex-snapshot
Limited and Degradative Proteolysis in the Context of Posttranslational Regulatory Networks: Current Technical and Conceptional Advances
inferred← citeshttps://doi.org/10.1007/978-3-7091-1431-5_5openalex-snapshot
Autophagy in Glioma Cells
inferred← citeshttps://doi.org/10.1007/978-4-431-55825-5_8openalex-snapshot
The Role of Transglutaminase Type 2 in the Regulation of Autophagy
inferred← citeshttps://doi.org/10.1007/978-94-007-1291-1_3openalex-snapshot
Mitochondrial Dynamics and Autophagy
inferred← citeshttps://doi.org/10.1007/978-94-007-6211-4_14openalex-snapshot
Autophagy, Cell Death, and Cancer
inferred← citeshttps://doi.org/10.1007/978-981-10-3162-5_14openalex-snapshot
Autophagic Proteases: Functional and Pathophysiological Aspects
inferred← citeshttps://doi.org/10.1007/978-981-13-8871-2_28openalex-snapshot
Cell Apoptosis and Autophagy in Renal Fibrosis
inferred← citeshttps://doi.org/10.1007/978-981-15-4272-5_13openalex-snapshot
Autophagy and Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-981-16-2830-6_2openalex-snapshot
Autophagosomal Membrane Origin and Formation
inferred← citeshttps://doi.org/10.1007/978-981-16-4525-9_1openalex-snapshot
Molecular Processes and Regulation of Autophagy
inferred← citeshttps://doi.org/10.1007/978-981-95-0233-2_5openalex-snapshot
Melanin Clearance Mechanism in the Skin
inferred← citeshttps://doi.org/10.1007/978-981-96-6202-9_17openalex-snapshot
Degradation of Misfolded Proteins in Neurodegenerative Diseases: Therapeutic Targets and Strategies
inferred← citeshttps://doi.org/10.1007/s00018-011-0748-9openalex-snapshot
Involvement of members of the Rab family and related small GTPases in autophagosome formation and maturation
inferred← citeshttps://doi.org/10.1007/s00018-013-1355-8openalex-snapshot
Bacterial serine proteases secreted by the autotransporter pathway: classification, specificity, and role in virulence
inferred← citeshttps://doi.org/10.1007/s00018-014-1829-3openalex-snapshot
Autophagy and cell reprogramming
inferred← citeshttps://doi.org/10.1007/s00018-016-2403-yopenalex-snapshot
The cellular autophagy/apoptosis checkpoint during inflammation
inferred← citeshttps://doi.org/10.1007/s00018-018-2843-7openalex-snapshot
Mitochondrial quality control in AMD: does mitophagy play a pivotal role?
inferred← citeshttps://doi.org/10.1007/s00109-014-1241-3openalex-snapshot
Protective role of autophagy and autophagy-related protein 5 in early tumorigenesis
inferred← citeshttps://doi.org/10.1007/s00109-015-1254-6openalex-snapshot
Mitophagy and heart failure
inferred← citeshttps://doi.org/10.1007/s00109-015-1282-2openalex-snapshot
miR-26a enhances autophagy to protect against ethanol-induced acute liver injury
inferred← citeshttps://doi.org/10.1007/s00109-016-1387-2openalex-snapshot
Exosomal transfer of miR-30a between cardiomyocytes regulates autophagy after hypoxia
inferred← citeshttps://doi.org/10.1007/s00109-016-1461-9openalex-snapshot
Autophagy core machinery: overcoming spatial barriers in neurons
inferred← citeshttps://doi.org/10.1007/s00203-020-01945-5openalex-snapshot
Curcuma longa L. (turmeric), Rosmarinus officinalis L. (rosemary), and Thymus vulgaris L. (thyme) extracts aid murine macrophages (RAW 264.7) to fight Streptococcus mutans during in vitro infection
inferred← citeshttps://doi.org/10.1007/s00204-013-1110-9openalex-snapshot
Cadmium and cellular signaling cascades: interactions between cell death and survival pathways
inferred← citeshttps://doi.org/10.1007/s00204-014-1263-1openalex-snapshot
Metformin aggravates immune-mediated liver injury in mice
inferred← citeshttps://doi.org/10.1007/s00204-016-1864-yopenalex-snapshot
Oxidative stress and gene expression profiling of cell death pathways in alpha-cypermethrin-treated SH-SY5Y cells
inferred← citeshttps://doi.org/10.1007/s00232-016-9874-5openalex-snapshot
Nutrient Starvation Decreases Cx43 Levels and Limits Intercellular Communication in Primary Bovine Corneal Endothelial Cells
inferred← citeshttps://doi.org/10.1007/s00262-013-1487-6openalex-snapshot
Emerging role of tumor-associated macrophages as therapeutic targets in patients with metastatic renal cell carcinoma
inferred← citeshttps://doi.org/10.1007/s00277-024-06089-wopenalex-snapshot
All-trans retinoic acid potentiates cell death induced by quizartinib in acute myeloid leukemia with FLT3-ITD mutations
inferred← citeshttps://doi.org/10.1007/s00280-018-3669-6openalex-snapshot
Autophagy modulation: a prudent approach in cancer treatment?
inferred← citeshttps://doi.org/10.1007/s00403-024-03559-zopenalex-snapshot
Imperatorin promotes melanin degradation in keratinocytes through facilitating autophagy via the PI3K/Akt signaling pathway
inferred← citeshttps://doi.org/10.1007/s00418-011-0869-0openalex-snapshot
Proteasome inhibition by quercetin triggers macroautophagy and blocks mTOR activity
inferred← citeshttps://doi.org/10.1007/s00418-012-1057-6openalex-snapshot
Interactions between autophagic and endo-lysosomal markers in endothelial cells
inferred← citeshttps://doi.org/10.1007/s00418-018-1751-0openalex-snapshot
The role of autophagy in morphogenesis and stem cell maintenance
inferred← citeshttps://doi.org/10.1007/s00430-014-0340-7openalex-snapshot
Rubella virus perturbs autophagy
inferred← citeshttps://doi.org/10.1007/s00432-017-2487-2openalex-snapshot
Role of autophagy in regulating the radiosensitivity of tumor cells
inferred← citeshttps://doi.org/10.1007/s00432-024-05782-7openalex-snapshot
MARCH5 promotes hepatocellular carcinoma progression by inducing p53 ubiquitination degradation
inferred← citeshttps://doi.org/10.1007/s00441-019-03111-wopenalex-snapshot
Autophagy as a consequence of seasonal functions of testis and epididymis in adult male European bison (Bison bonasus, Linnaeus 1758)
inferred← citeshttps://doi.org/10.1007/s00508-014-0592-7openalex-snapshot
Biological pathways involved in the development of inflammatory bowel disease
inferred← citeshttps://doi.org/10.1007/s00709-010-0190-0openalex-snapshot
From signal transduction to autophagy of plant cell organelles: lessons from yeast and mammals and plant-specific features
inferred← citeshttps://doi.org/10.1007/s00709-017-1169-xopenalex-snapshot
Cubic membrane formation supports cell survival of amoeba Chaos under starvation-induced stress
inferred← citeshttps://doi.org/10.1007/s10059-012-0098-yopenalex-snapshot
Genes for Plant Autophagy: Functions and Interactions
inferred← citeshttps://doi.org/10.1007/s10059-013-0140-8openalex-snapshot
Autophagy: A Critical Regulator of Cellular Metabolism and Homeostasis
inferred← citeshttps://doi.org/10.1007/s10143-024-02879-yopenalex-snapshot
Transcription factor EB (TFEB) promotes autophagy in early brain injury after subarachnoid hemorrhage in rats
inferred← citeshttps://doi.org/10.1007/s10495-011-0658-1openalex-snapshot
Mammalian target of rapamycin regulates isoliquiritigenin-induced autophagic and apoptotic cell death in adenoid cystic carcinoma cells
inferred← citeshttps://doi.org/10.1007/s10495-014-0981-4openalex-snapshot
The roles of autophagy in development and stress responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10495-015-1108-2openalex-snapshot
Autophagy in the light of sphingolipid metabolism
inferred← citeshttps://doi.org/10.1007/s10495-015-1112-6openalex-snapshot
Sphingolipids as cell fate regulators in lung development and disease
inferred← citeshttps://doi.org/10.1007/s10495-018-1480-9openalex-snapshot
Targeting autophagy for combating chemoresistance and radioresistance in glioblastoma
inferred← citeshttps://doi.org/10.1007/s10522-011-9331-xopenalex-snapshot
Selective autophagy in the maintenance of cellular homeostasis in aging organisms
inferred← citeshttps://doi.org/10.1007/s10528-025-11125-zopenalex-snapshot
Autophagy Process in Parkinson’s Disease Depends on Mutations in the GBA1 and LRRK2 Genes
inferred← citeshttps://doi.org/10.1007/s10529-013-1276-5openalex-snapshot
Autophagy and its implication in Chinese hamster ovary cell culture
inferred← citeshttps://doi.org/10.1007/s10549-018-5023-4openalex-snapshot
Resistance to endocrine therapy in breast cancer: molecular mechanisms and future goals
inferred← citeshttps://doi.org/10.1007/s10549-020-05795-zopenalex-snapshot
Differential expression and prognostic relevance of autophagy-related markers ATG4B, GABARAP, and LC3B in breast cancer
inferred← citeshttps://doi.org/10.1007/s10565-013-9261-2openalex-snapshot
Dopamine- and zinc-induced autophagosome formation facilitates PC12 cell survival
inferred← citeshttps://doi.org/10.1007/s10565-016-9371-8openalex-snapshot
Autophagy regulates death of retinal pigment epithelium cells in age-related macular degeneration
inferred← citeshttps://doi.org/10.1007/s10565-021-09629-6openalex-snapshot
Vitamin D3 decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy
inferred← citeshttps://doi.org/10.1007/s10571-014-0125-yopenalex-snapshot
15d-Prostaglandin J2 Protects Cortical Neurons Against Oxygen–Glucose Deprivation/Reoxygenation Injury: Involvement of Inhibiting Autophagy Through Upregulation of Bcl-2
inferred← citeshttps://doi.org/10.1007/s10571-023-01336-6openalex-snapshot
Crosstalk Between Autophagy and Inflammation in Chronic Cerebral Ischaemia
inferred← citeshttps://doi.org/10.1007/s10735-018-9808-xopenalex-snapshot
Autophagy promotes hepatic differentiation of hepatic progenitor cells by regulating the Wnt/β-catenin signaling pathway
inferred← citeshttps://doi.org/10.1007/s10735-020-09953-xopenalex-snapshot
Immunoexpression pattern of autophagy mediators in alveolar bone osteoclasts following estrogen withdrawal in female rats
inferred← citeshttps://doi.org/10.1007/s10741-012-9350-yopenalex-snapshot
Cardiomyocyte autophagy: metabolic profit and loss
inferred← citeshttps://doi.org/10.1007/s10753-021-01523-xopenalex-snapshot
Stellate Ganglion Block Improves the Proliferation and Function of Splenic CD4 + T Cells Through Inhibition of Posthemorrhagic Shock Mesenteric Lymph–Mediated Autophagy
inferred← citeshttps://doi.org/10.1007/s10787-023-01187-zopenalex-snapshot
Brain insulin resistance linked Alzheimer’s and Parkinson’s disease pathology: An undying implication of epigenetic and autophagy modulation
inferred← citeshttps://doi.org/10.1007/s10863-017-9719-7openalex-snapshot
Mitochondria and FOXO3 in stem cell homeostasis, a window into hematopoietic stem cell fate determination
inferred← citeshttps://doi.org/10.1007/s11010-016-2749-3openalex-snapshot
Salidroside protects cortical neurons against glutamate-induced cytotoxicity by inhibiting autophagy
inferred← citeshttps://doi.org/10.1007/s11010-016-2853-4openalex-snapshot
Akt/AMPK/mTOR pathway was involved in the autophagy induced by vitamin E succinate in human gastric cancer SGC-7901 cells
inferred← citeshttps://doi.org/10.1007/s11010-016-2868-xopenalex-snapshot
Induction of autophagy by salidroside through the AMPK-mTOR pathway protects vascular endothelial cells from oxidative stress-induced apoptosis
inferred← citeshttps://doi.org/10.1007/s11011-018-0214-6openalex-snapshot
Autophagy stimulation as a promising approach in treatment of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s11033-021-06334-9openalex-snapshot
Interplay of autophagy and cancer stem cells in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s11064-015-1564-7openalex-snapshot
mTOR and Erk1/2 Signaling in the Cerebrospinal Fluid-Contacting Nucleus is Involved in Neuropathic Pain
inferred← citeshttps://doi.org/10.1007/s11064-019-02802-8openalex-snapshot
Quercetin and Sodium Butyrate Synergistically Increase Apoptosis in Rat C6 and Human T98G Glioblastoma Cells Through Inhibition of Autophagy
inferred← citeshttps://doi.org/10.1007/s11064-024-04266-xopenalex-snapshot
Chaperone-Mediated Autophagy Alleviates Cerebral Ischemia–Reperfusion Injury by Inhibiting P53-Mediated Mitochondria-Associated Apoptosis
inferred← citeshttps://doi.org/10.1007/s11356-020-07914-1openalex-snapshot
The impact of proteostasis dysfunction secondary to environmental and genetic causes on neurodegenerative diseases progression and potential therapeutic intervention
inferred← citeshttps://doi.org/10.1007/s11427-014-4607-4openalex-snapshot
Increased leptin by hypoxic-preconditioning promotes autophagy of mesenchymal stem cells and protects them from apoptosis
inferred← citeshttps://doi.org/10.1007/s11427-024-2905-5openalex-snapshot
The mechanisms and functions of mitochondria-encapsulating extracellular vesicles
inferred← citeshttps://doi.org/10.1007/s11481-012-9431-7openalex-snapshot
Curcumin Ameliorates the Neurodegenerative Pathology in A53T α-synuclein Cell Model of Parkinson’s Disease Through the Downregulation of mTOR/p70S6K Signaling and the Recovery of Macroautophagy
inferred← citeshttps://doi.org/10.1007/s11481-013-9519-8openalex-snapshot
Sorting Through the Roles of Beclin 1 in Microglia and Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s11626-019-00327-6openalex-snapshot
HSP90 inhibitor DPB induces autophagy and more effectively apoptosis in A549 cells combined with autophagy inhibitors
inferred← citeshttps://doi.org/10.1007/s11626-019-00381-0openalex-snapshot
Small molecules re-establish neural cell fate of human fibroblasts via autophagy activation
inferred← citeshttps://doi.org/10.1007/s11655-018-2847-zopenalex-snapshot
Triptolide, A Potential Autophagy Modulator
inferred← citeshttps://doi.org/10.1007/s11655-022-3540-9openalex-snapshot
Emodin Ameliorates High Glucose-Induced Podocyte Apoptosis via Regulating AMPK/mTOR-Mediated Autophagy Signaling Pathway
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