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Autophagy and signaling: their role in cell survival and cell death
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mcne.1999.0780openalex-snapshot
Autophagy Is Activated by Apoptotic Signalling in Sympathetic Neurons: An Alternative Mechanism of Death Execution
inferredcites →https://doi.org/10.1007/bf00174615openalex-snapshot
Developmental cell death: morphological diversity and multiple mechanisms
inferredcites →https://doi.org/10.1007/s00018-004-4297-yopenalex-snapshot
The role of insulin and IGF-1 signaling in longevity
inferredcites →https://doi.org/10.1016/0962-8924(94)90069-8openalex-snapshot
Autophagy and related mechanisms of lysosome-mediated protein degradation
inferredcites →https://doi.org/10.1016/j.bbrc.2003.07.012openalex-snapshot
Amino acid signalling and the integration of metabolism
inferredcites →https://doi.org/10.1016/j.biocel.2004.02.002openalex-snapshot
Regulation and role of autophagy in mammalian cells
inferredcites →https://doi.org/10.1016/j.biocel.2004.02.013openalex-snapshot
Mechanisms of chaperone-mediated autophagy
inferredcites →https://doi.org/10.1016/j.biocel.2004.04.009openalex-snapshot
Role of mitochondrial permeability transition pores in mitochondrial autophagy
inferredcites →https://doi.org/10.1016/j.biocel.2004.05.007openalex-snapshot
The role of macroautophagy in the ageing process, anti-ageing intervention and age-associated diseases
inferredcites →https://doi.org/10.1016/j.ceb.2004.09.011openalex-snapshot
Death by design: apoptosis, necrosis and autophagy
inferredcites →https://doi.org/10.1016/j.cell.2004.11.046openalex-snapshot
Growth Factor Regulation of Autophagy and Cell Survival in the Absence of Apoptosis
inferredcites →https://doi.org/10.1016/j.devcel.2004.07.005openalex-snapshot
Programmed Autophagy in the Drosophila Fat Body Is Induced by Ecdysone through Regulation of the PI3K Pathway
inferredcites →https://doi.org/10.1016/j.devcel.2004.07.009openalex-snapshot
Role and Regulation of Starvation-Induced Autophagy in the Drosophila Fat Body
inferredcites →https://doi.org/10.1016/j.tcb.2003.12.002openalex-snapshot
Autophagy: in sickness and in health
inferredcites →https://doi.org/10.1016/s0304-419x(03)00004-0openalex-snapshot
Autophagy: a barrier or an adaptive response to cancer
inferredcites →https://doi.org/10.1016/s0960-9822(03)00082-4openalex-snapshot
A SAGE Approach to Discovery of Genes Involved in Autophagic Cell Death
inferredcites →https://doi.org/10.1016/s0960-9822(03)00085-xopenalex-snapshot
Genome-Wide Analyses of Steroid- and Radiation-Triggered Programmed Cell Death in Drosophila
inferredcites →https://doi.org/10.1016/s1357-2725(02)00343-6openalex-snapshot
Role of the Apg12 conjugation system in mammalian autophagy
inferredcites →https://doi.org/10.1016/s1534-5807(03)00296-xopenalex-snapshot
A Unified Nomenclature for Yeast Autophagy-Related Genes
inferredcites →https://doi.org/10.1016/s1534-5807(04)00099-1openalex-snapshot
Development by Self-Digestion
inferredcites →https://doi.org/10.1038/45257openalex-snapshot
Induction of autophagy and inhibition of tumorigenesis by beclin 1
inferredcites →https://doi.org/10.1038/nature02866openalex-snapshot
Absence of S6K1 protects against age- and diet-induced obesity while enhancing insulin sensitivity
inferredcites →https://doi.org/10.1038/nature03029openalex-snapshot
The role of autophagy during the early neonatal starvation period
inferredcites →https://doi.org/10.1038/ncb1192openalex-snapshot
Role of Bcl-2 family proteins in a non-apoptotic programmed cell death dependent on autophagy genes
inferredcites →https://doi.org/10.1038/ng1494openalex-snapshot
Dysregulation of the TSC-mTOR pathway in human disease
inferredcites →https://doi.org/10.1038/nrm1018openalex-snapshot
TOR signalling in bugs, brain and brawn
inferredcites →https://doi.org/10.1038/nrm1660openalex-snapshot
Autophagy in metazoans: cell survival in the land of plenty
inferredcites →https://doi.org/10.1038/nrm1666openalex-snapshot
Autophagy: dual roles in life and death?
inferredcites →https://doi.org/10.1038/sj.cdd.4400759openalex-snapshot
Bcl-2 down-regulation causes autophagy in a caspase-independent manner in human leukemic HL60 cells
inferredcites →https://doi.org/10.1038/sj.cdd.4401246openalex-snapshot
HSpin1, a transmembrane protein interacting with Bcl-2/Bcl-xL, induces a caspase-independent autophagic cell death
inferredcites →https://doi.org/10.1038/sj.onc.1202538openalex-snapshot
Oncogenic Ras triggers cell suicide through the activation of a caspase-independent cell death program in human cancer cells
inferredcites →https://doi.org/10.1038/sj.onc.1207197openalex-snapshot
Phosphoinositide 3-kinase accelerates autophagic cell death during glucose deprivation in the rat cardiomyocyte-derived cell line H9c2
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/10.1042/0264-6021:3510545openalex-snapshot
Amino-acid-dependent signal transduction
inferredcites →https://doi.org/10.1042/bj20021266openalex-snapshot
Regulation of targets of mTOR (mammalian target of rapamycin) signalling by intracellular amino acid availability
inferredcites →https://doi.org/10.1042/bj20030826openalex-snapshot
Class III phosphoinositide 3-kinase–Beclin1 complex mediates the amino acid-dependent regulation of autophagy in C2C12 myotubes
inferredcites →https://doi.org/10.1046/j.1365-2141.1997.2623081.xopenalex-snapshot
Inhibition of autophagy abrogates tumour necrosis factor α induced apoptosis in human T‐lymphoblastic leukaemic cells
inferredcites →https://doi.org/10.1073/pnas.012485299openalex-snapshot
Regulation of starvation- and virus-induced autophagy by the eIF2α kinase signaling pathway
inferredcites →https://doi.org/10.1073/pnas.0400443101openalex-snapshot
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is required for induction of autophagy during lumen formation in vitro
inferredcites →https://doi.org/10.1074/jbc.270.5.2320openalex-snapshot
Phosphorylation of Ribosomal Protein S6 Is Inhibitory for Autophagy in Isolated Rat Hepatocytes
inferredcites →https://doi.org/10.1074/jbc.273.37.23758openalex-snapshot
Inhibition of Hepatocytic Autophagy by Adenosine, Aminoimidazole-4-carboxamide Riboside, and N 6-Mercaptopurine Riboside
inferredcites →https://doi.org/10.1074/jbc.275.2.992openalex-snapshot
Distinct Classes of Phosphatidylinositol 3′-Kinases Are Involved in Signaling Pathways That Control Macroautophagy in HT-29 Cells
inferredcites →https://doi.org/10.1074/jbc.c100319200openalex-snapshot
The Tumor Suppressor PTEN Positively Regulates Macroautophagy by Inhibiting the Phosphatidylinositol 3-Kinase/Protein Kinase B Pathway
inferredcites →https://doi.org/10.1074/jbc.c300534200openalex-snapshot
Thr2446 Is a Novel Mammalian Target of Rapamycin (mTOR) Phosphorylation Site Regulated by Nutrient Status
inferredcites →https://doi.org/10.1074/jbc.m003633200openalex-snapshot
Leucine Limitation Induces Autophagy and Activation of Lysosome-dependent Proteolysis in C2C12 Myotubes through a Mammalian Target of Rapamycin-independent Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.m103705200openalex-snapshot
Ganglioside GM3 Participates in the Pathological Conditions of Insulin Resistance
inferredcites →https://doi.org/10.1074/jbc.m104677200openalex-snapshot
Death-associated Protein (DAP) Kinase Plays a Central Role in Ceramide-induced Apoptosis in Cultured Hippocampal Neurons
inferredcites →https://doi.org/10.1074/jbc.m210699200openalex-snapshot
Involvement of Integrins in Osmosensing and Signaling toward Autophagic Proteolysis in Rat Liver
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.m306337200openalex-snapshot
Amino Acids and Insulin Control Autophagic Proteolysis through Different Signaling Pathways in Relation to mTOR in Isolated Rat Hepatocytes
inferredcites →https://doi.org/10.1074/jbc.m313561200openalex-snapshot
Ceramide-mediated Macroautophagy Involves Inhibition of Protein Kinase B and Up-regulation of Beclin 1
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.m413934200openalex-snapshot
Essential Roles of Atg5 and FADD in Autophagic Cell Death
inferredcites →https://doi.org/10.1074/jbc.m414499200openalex-snapshot
The Tuberous Sclerosis Protein TSC2 Is Not Required for the Regulation of the Mammalian Target of Rapamycin by Amino Acids and Certain Cellular Stresses
inferredcites →https://doi.org/10.1078/0171-9335-00433openalex-snapshot
Inhibition of autophagy with 3-methyladenine results in impaired turnover of lysosomes and accumulation of lipofuscin-like material
inferredcites →https://doi.org/10.1083/jcb.151.5.1025openalex-snapshot
Dissection of Autophagosome Biogenesis into Distinct Nucleation and Expansion Steps
inferredcites →https://doi.org/10.1083/jcb.152.3.519openalex-snapshot
Two Distinct Vps34 Phosphatidylinositol 3–Kinase Complexes Function in Autophagy and Carboxypeptidase Y Sorting in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1083/jcb.200109094openalex-snapshot
DAP kinase and DRP-1 mediate membrane blebbing and the formation of autophagic vesicles during programmed cell death
inferredcites →https://doi.org/10.1091/mbc.e03-09-0704openalex-snapshot
In Vivo Analysis of Autophagy in Response to Nutrient Starvation Using Transgenic Mice Expressing a Fluorescent Autophagosome Marker
inferredcites →https://doi.org/10.1091/mbc.e04-10-0906openalex-snapshot
Selective Inactivation of a Fas-associated Death Domain Protein (FADD)-dependent Apoptosis and Autophagy Pathway in Immortal Epithelial Cells
inferredcites →https://doi.org/10.1093/carcin/17.8.1595openalex-snapshot
Active cell death induced by the anti-estrogens tamoxifen and ICI 164 384 in human mammary carcinoma cells (MCF-7) in culture: the role of autophagy
inferredcites →https://doi.org/10.1093/embo-reports/kve061openalex-snapshot
Beclin–phosphatidylinositol 3‐kinase complex functions at the trans‐Golgi network
inferredcites →https://doi.org/10.1093/emboj/20.21.5971openalex-snapshot
The pre‐autophagosomal structure organized by concerted functions of APG genes is essential for autophagosome formation
inferredcites →https://doi.org/10.1093/toxsci/kfh273openalex-snapshot
Toxin-Induced Tail Phosphorylation of Hepatocellular S6 Kinase: Evidence for a Dual Involvement of the AMP-Activated Protein Kinase in S6 Kinase Regulation
inferredcites →https://doi.org/10.1096/fj.04-2284fjeopenalex-snapshot
Ceramide down‐regulates System A amino acid transport and protein synthesis in rat skeletal muscle cells
inferredcites →https://doi.org/10.1101/gad.1255404openalex-snapshot
The AMP-activated protein kinase AAK-2 links energy levels and insulin-like signals to lifespan in C. elegans
inferredcites →https://doi.org/10.1111/j.1432-1033.1993.tb18013.xopenalex-snapshot
Inhibition of hepatocytic autophagy by okadaic acid and other protein phosphatase inhibitors
inferredcites →https://doi.org/10.1111/j.1432-1033.1997.0240a.xopenalex-snapshot
The Phosphatidylinositol 3‐Kinase Inhibitors Wortmannin and LY294002 Inhibit Autophagy in Isolated Rat Hepatocytes
inferredcites →https://doi.org/10.1126/science.1063518openalex-snapshot
Mammalian TOR: A Homeostatic ATP Sensor
inferredcites →https://doi.org/10.1126/science.1082889openalex-snapshot
Mitochondrial Dysfunction in the Elderly: Possible Role in Insulin Resistance
inferredcites →https://doi.org/10.1126/science.1087782openalex-snapshot
Autophagy Genes Are Essential for Dauer Development and Life-Span Extension in C. elegans
inferredcites →https://doi.org/10.1126/science.1096645openalex-snapshot
Regulation of an ATG7 - beclin 1 Program of Autophagic Cell Death by Caspase-8
inferredcites →https://doi.org/10.1126/science.1099993openalex-snapshot
Autophagy in Health and Disease: A Double-Edged Sword
inferredcites →https://doi.org/10.1126/science.1106148openalex-snapshot
Phosphorylation and Regulation of Akt/PKB by the Rictor-mTOR Complex
inferredcites →https://doi.org/10.1126/science.289.5482.1150openalex-snapshot
Mitochondria--the Death Signal Integrators
inferredcites →https://doi.org/10.1128/jvi.72.11.8586-8596.1998openalex-snapshot
Protection against Fatal Sindbis Virus Encephalitis by Beclin, a Novel Bcl-2-Interacting Protein
inferredcites →https://doi.org/10.1128/mcb.21.17.5742-5752.2001openalex-snapshot
Antagonistic Controls of Autophagy and Glycogen Accumulation by Snf1p, the Yeast Homolog of AMP-Activated Protein Kinase, and the Cyclin-Dependent Kinase Pho85p
inferredcites →https://doi.org/10.1128/mcb.22.15.5575-5584.2002openalex-snapshot
The Immunosuppressant Rapamycin Mimics a Starvation-Like Signal Distinct from Amino Acid and Glucose Deprivation
inferredcites →https://doi.org/10.1128/mcb.25.3.1025-1040.2005openalex-snapshot
Inhibition of Macroautophagy Triggers Apoptosis
inferredcites →https://doi.org/10.1146/annurev.med.50.1.57openalex-snapshot
The Ubiquitin-Proteasome Pathway and Pathogenesis of Human Diseases
inferredcites →https://doi.org/10.1146/annurev.ph.28.030166.002251openalex-snapshot
Functions of Lysosomes
inferredcites →https://doi.org/10.1172/jci0214571openalex-snapshot
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy
inferredcites →https://doi.org/10.1172/jci14571openalex-snapshot
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy
inferredcites →https://doi.org/10.1210/en.2003-0982openalex-snapshot
Minireview: The AMP-Activated Protein Kinase Cascade: The Key Sensor of Cellular Energy Status
inferredcites →https://doi.org/10.1210/en.2004-0921openalex-snapshot
Increased Activation of the Mammalian Target of Rapamycin Pathway in Liver and Skeletal Muscle of Obese Rats: Possible Involvement in Obesity-Linked Insulin Resistance
inferredcites →https://doi.org/10.1210/er.2001-0039openalex-snapshot
Oxidative Stress and Stress-Activated Signaling Pathways: A Unifying Hypothesis of Type 2 Diabetes
inferredcites →https://doi.org/10.4161/auto.1.1.1270openalex-snapshot
Maturation of Autophagic Vacuoles in Mammalian Cells
inferredcites →https://doi.org/10.4161/auto.1.2.1738openalex-snapshot
Does Autophagy Contribute To Cell Death?
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3906/zoo-1905-21zenodo-depositor-declared
Vertebrate insulin alters the expression profile of steroid hormone ecdysone receptor complex components and autophagy-related genes in the pupal fat body of the silkworm, Bombyxmori
inferred← citeshttps://doi.org/10.1002/9781118500354.ch9openalex-snapshot
Marine toxins as modulators of apoptosis
inferred← citeshttps://doi.org/10.1002/adfm.202100738openalex-snapshot
Nanoagent‐Promoted Mild‐Temperature Photothermal Therapy for Cancer Treatment
inferred← citeshttps://doi.org/10.1002/adfm.202102832openalex-snapshot
Intracellular Nanoparticle Formation and Hydroxychloroquine Release for Autophagy‐Inhibited Mild‐Temperature Photothermal Therapy for Tumors
inferred← citeshttps://doi.org/10.1002/adhm.201300294openalex-snapshot
Autophagy‐Sensitized Cytotoxicity of Quantum Dots in PC12 Cells
inferred← citeshttps://doi.org/10.1002/adhm.202300410openalex-snapshot
Multifaceted Roles of Copper Ions in Anticancer Nanomedicine
inferred← citeshttps://doi.org/10.1002/advs.201700897openalex-snapshot
Brain Delivery of Multifunctional Dendrimer Protein Bioconjugates
inferred← citeshttps://doi.org/10.1002/art.27305openalex-snapshot
Autophagy is a protective mechanism in normal cartilage, and its aging‐related loss is linked with cell death and osteoarthritis
inferred← citeshttps://doi.org/10.1002/bies.202300211openalex-snapshot
Contrasting views on the role of AMPK in autophagy
inferred← citeshttps://doi.org/10.1002/biof.101openalex-snapshot
Role of mitochondrial ion channels in cell death
inferred← citeshttps://doi.org/10.1002/bit.23282openalex-snapshot
A review of the mammalian unfolded protein response
inferred← citeshttps://doi.org/10.1002/cam4.1418openalex-snapshot
Inhibition of breast cancer cell growth by methyl pyropheophenylchlorin photodynamic therapy is mediated though endoplasmic reticulum stress‐induced autophagy in vitro and vivo
inferred← citeshttps://doi.org/10.1002/cbin.11076openalex-snapshot
Bufalin induces protective autophagy by Cbl‐b regulating mTOR and ERK signaling pathways in gastric cancer cells
inferred← citeshttps://doi.org/10.1002/cbin.11967openalex-snapshot
Epithelial‐to‐mesenchymal transition as a learning paradigm of cell biology
inferred← citeshttps://doi.org/10.1002/cbin.70071openalex-snapshot
Targeting mTOR and Its Associated Signaling to Induce Cell Death in Breast Cancer Stem Cells
inferred← citeshttps://doi.org/10.1002/ijc.24076openalex-snapshot
HAMLET (human α‐lactalbumin made lethal to tumor cells) triggers autophagic tumor cell death
inferred← citeshttps://doi.org/10.1002/ijc.24402openalex-snapshot
The induction of autophagy by γ‐radiation contributes to the radioresistance of glioma stem cells
inferred← citeshttps://doi.org/10.1002/ijc.24500openalex-snapshot
Autophagy—A double‐edged sword in oncology
inferred← citeshttps://doi.org/10.1002/jat.3999openalex-snapshot
The role of protein kinase C alpha in tri‐ortho‐cresyl phosphate‐induced autophagy in human neuroblastoma SK‐N‐SH cells
inferred← citeshttps://doi.org/10.1002/jat.4205openalex-snapshot
Hydrogen sulfide alleviates apoptosis and autophagy induced by beryllium sulfate in 16HBE cells
inferred← citeshttps://doi.org/10.1002/jbt.22161openalex-snapshot
Fumonisin B1 actuates oxidative stress‐associated colonic damage via apoptosis and autophagy activation in murine model
inferred← citeshttps://doi.org/10.1002/jbt.70425openalex-snapshot
Integrated Transcriptomic and Metabolomic Analyses in Characterizing the Anti‐Prostate Cancer Effects of Hederagenin
inferred← citeshttps://doi.org/10.1002/jcb.21295openalex-snapshot
Akt2, but not Akt1 or Akt3 mediates pressure‐stimulated serum‐opsonized latex bead phagocytosis through activating mTOR and p70 S6 kinase
inferred← citeshttps://doi.org/10.1002/jcb.23399openalex-snapshot
AMPK promotes skeletal muscle autophagy through activation of forkhead FoxO3a and interaction with Ulk1
inferred← citeshttps://doi.org/10.1002/jcb.24356openalex-snapshot
Mitochondrial accumulation under oxidative stress is due to defects in autophagy
inferred← citeshttps://doi.org/10.1002/jcb.24494openalex-snapshot
Bovine herpesvirus type 4 infection modulates autophagy in a permissive cell line
inferred← citeshttps://doi.org/10.1002/jcb.26180openalex-snapshot
LRWD1 Regulates Microtubule Nucleation and Proper Cell Cycle Progression in the Human Testicular Embryonic Carcinoma Cells
inferred← citeshttps://doi.org/10.1002/jcb.30311openalex-snapshot
Rhein induces changes in the lysosomal compartment of HeLa cells
inferred← citeshttps://doi.org/10.1002/jcp.24351openalex-snapshot
mTOR signaling for biological control and cancer
inferred← citeshttps://doi.org/10.1002/jcp.26015openalex-snapshot
S‐Adenosylmethionine‐mediated apoptosis is potentiated by autophagy inhibition induced by chloroquine in human breast cancer cells
inferred← citeshttps://doi.org/10.1002/jcp.27034openalex-snapshot
Antioxidant effect of human placenta hydrolysate against oxidative stress on muscle atrophy
inferred← citeshttps://doi.org/10.1002/jcp.27979openalex-snapshot
Rapamycin enhances growth inhibition on urothelial carcinoma cells through LKB1 deficiency‐mediated mitochondrial dysregulation
inferred← citeshttps://doi.org/10.1002/jcp.29433openalex-snapshot
Autophagy protects PC12 cells against deoxynivalenol toxicity via the Class III PI3K/beclin 1/Bcl‐2 pathway
inferred← citeshttps://doi.org/10.1002/jlb.1hi1017-396rropenalex-snapshot
Frontline Science: IL-18 primes murine NK cells for proliferation by promoting protein synthesis, survival, and autophagy
inferred← citeshttps://doi.org/10.1002/jnr.21760openalex-snapshot
Okadaic acid increases autophagosomes in rat neurons: Implications for Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/jnr.22168openalex-snapshot
Apoptosis and autophagy in rat cerebellar granule neuron death: Role of reactive oxygen species
inferred← citeshttps://doi.org/10.1002/jnr.23066openalex-snapshot
Cooperative action of JNK and AKT/mTOR in 1‐methyl‐4‐phenylpyridinium‐induced autophagy of neuronal PC12 cells
inferred← citeshttps://doi.org/10.1002/lsm.20911openalex-snapshot
Protective effect of autophagy in laser‐induced glioma cell death in vitro
inferred← citeshttps://doi.org/10.1002/lsm.21088openalex-snapshot
RIP3 expression induces a death profile change in U2OS osteosarcoma cells after 5-ALA-PDT
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/mc.22933openalex-snapshot
Interleukin 7 receptor activates PI3K/Akt/mTOR signaling pathway via downregulation of Beclin‐1 in lung cancer
inferred← citeshttps://doi.org/10.1002/mds.29298openalex-snapshot
Type 2 Diabetes and Parkinson's Disease: A Focused Review of Current Concepts
inferred← citeshttps://doi.org/10.1002/med.21398openalex-snapshot
Targeting Programmed Cell Death Using Small‐Molecule Compounds to Improve Potential Cancer Therapy
inferred← citeshttps://doi.org/10.1002/mus.21423openalex-snapshot
Autophagy, lithium, and amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1002/mus.25511openalex-snapshot
N‐methyl‐D‐aspartate (NMDA) impairs myogenesis in C2C12 cells
inferred← citeshttps://doi.org/10.1002/npp2.70055openalex-snapshot
Advances in research on autophagy in the maintenance of insect–microbe symbiosis
inferred← citeshttps://doi.org/10.1002/pros.20707openalex-snapshot
Expression of BNIP3 correlates with hypoxia‐inducible factor (HIF)‐1α, HIF‐2α and the androgen receptor in prostate cancer and is regulated directly by hypoxia but not androgens in cell lines
inferred← citeshttps://doi.org/10.1002/pros.23161openalex-snapshot
Coordinated induction of cell survival signaling in the inflamed microenvironment of the prostate
inferred← citeshttps://doi.org/10.1002/prp2.248openalex-snapshot
Fibromyalgia syndrome: metabolic and autophagic processes in intermittent cold stress mice
inferred← citeshttps://doi.org/10.1002/ptr.6482openalex-snapshot
Stem Cell Therapy: Curcumin Does the Trick
inferred← citeshttps://doi.org/10.1002/rmv.1973openalex-snapshot
Autophagy: The multi‐purpose bridge in viral infections and host cells
inferred← citeshttps://doi.org/10.1002/rmv.2292openalex-snapshot
Cell death mechanisms involved in cell injury caused by SARS‐CoV‐2
inferred← citeshttps://doi.org/10.1002/smll.201201363openalex-snapshot
Exposure to Titanium Dioxide Nanoparticles Induces Autophagy in Primary Human Keratinocytes
inferred← citeshttps://doi.org/10.1002/tox.22503openalex-snapshot
Methylisothiazolinone may induce cell death and inflammatory response through DNA damage in human liver epithelium cells
inferred← citeshttps://doi.org/10.1002/tox.23020openalex-snapshot
Quercetin induces autophagy in myelodysplastic bone marrow including hematopoietic stem/progenitor compartment
inferred← citeshttps://doi.org/10.1002/tox.23445openalex-snapshot
Apoptosis, rather than neurogenesis, induces significant hippocampal‐dependent learning and memory impairment in chronic low Cd2+ exposure
inferred← citeshttps://doi.org/10.1007/112_2008_802openalex-snapshot
Lipid homeostasis in macrophages – Implications for atherosclerosis
inferred← citeshttps://doi.org/10.1007/400_2008_25openalex-snapshot
Autophagy in Cancer and Chemotherapy
inferred← citeshttps://doi.org/10.1007/978-0-387-73226-8_17openalex-snapshot
Activation of Caspase-Independent Programmed Pathways in Seizure-Induced Neuronal Necrosis
inferred← citeshttps://doi.org/10.1007/978-0-387-85498-4_13openalex-snapshot
Biological Activity of Defence-Related Plant Secondary Metabolites
inferred← citeshttps://doi.org/10.1007/978-0-387-89445-4_3openalex-snapshot
The Role of Autophagy and Apoptosis in the Drug Resistance of Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4020-8833-9_13openalex-snapshot
Acute-phase reaction of the pancreas
inferred← citeshttps://doi.org/10.1007/978-1-4419-7002-2_8openalex-snapshot
Protein Metabolism and Lifespan in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1007/978-1-4614-0730-0_3openalex-snapshot
Targeting Argininosuccinate Synthetase in Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-1-4614-5441-0_22openalex-snapshot
The Pancreatic β Cells in Human Type 2 Diabetes
inferred← citeshttps://doi.org/10.1007/978-1-4614-6280-4_11openalex-snapshot
Stress Induced Mutagenesis, Genetic Diversification, and Cell Survival via Anastasis, the Reversal of Late Stage Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-4899-7606-2_15openalex-snapshot
Potential Mechanisms of PTA: Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-4939-1176-9_16openalex-snapshot
Co-targeting Adaptive Survival Pathways
inferred← citeshttps://doi.org/10.1007/978-1-4939-8769-6_11openalex-snapshot
Determining the Impact of Metabolic Nutrients on Autophagy
inferred← citeshttps://doi.org/10.1007/978-1-59745-157-4_12openalex-snapshot
Molecular Links Between Autophagy and Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-59745-157-4_3openalex-snapshot
Methods for Assessing Autophagy and Autophagic Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-59745-157-4_5openalex-snapshot
Amino Acid Regulation of Autophagosome Formation
inferred← citeshttps://doi.org/10.1007/978-1-59745-221-2_5openalex-snapshot
Autophagy and Autophagic Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-59745-564-0_21openalex-snapshot
The Mammalian Target of Rapamycin and Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-60327-271-1_9openalex-snapshot
Downstream Targets of mTORC1
inferred← citeshttps://doi.org/10.1007/978-1-60761-857-7_9openalex-snapshot
Reactive Oxygen and Nitrogen Species, Oxidative and Nitrosative Stress, and Their Role in the Pathogenesis of Acute Kidney Injury
inferred← citeshttps://doi.org/10.1007/978-3-031-07634-3_5openalex-snapshot
Autophagy in Cancer: A Metabolic Perspective
inferred← citeshttps://doi.org/10.1007/978-3-319-77495-4_11openalex-snapshot
Activation of Caspase-Independent Programmed Pathways in Seizure-Induced Neuronal Necrosis
inferred← citeshttps://doi.org/10.1007/978-3-642-00152-9_2openalex-snapshot
Cellular Stress in Acute Pancreatitis
inferred← citeshttps://doi.org/10.1007/978-3-642-00302-8_2openalex-snapshot
Macroautophagy Signaling and Regulation
inferred← citeshttps://doi.org/10.1007/978-3-642-00302-8_4openalex-snapshot
Autophagy and Lymphocyte Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-7091-1824-5_9openalex-snapshot
Contribution of pH Alterations to the Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/978-94-007-4575-9_15openalex-snapshot
Plant-Derived Isoprenoids Mediate Regulation of mTOR Signaling in Tumor Cells
inferred← citeshttps://doi.org/10.1007/978-94-017-8984-4_2openalex-snapshot
Exploiting BH3 Mimetics for Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-981-15-0602-4_9openalex-snapshot
Oxidative Stress and Autophagy
inferred← citeshttps://doi.org/10.1007/978-981-15-4272-5_7openalex-snapshot
Autophagy and Ischemic Stroke
inferred← citeshttps://doi.org/10.1007/bf02977326openalex-snapshot
Magnolol-lnduced H460 cells deathvia autophagy but not apoptosis
inferred← citeshttps://doi.org/10.1007/s00011-020-01400-7openalex-snapshot
Cellular and molecular events of inflammation induced transdifferentiation (EMT) and regeneration (MET) in mesenteric mesothelial cells
inferred← citeshttps://doi.org/10.1007/s00018-009-0080-9openalex-snapshot
A small GTPase, human Rab32, is required for the formation of autophagic vacuoles under basal conditions
inferred← citeshttps://doi.org/10.1007/s00018-012-1032-3openalex-snapshot
Tightrope act: autophagy in stem cell renewal, differentiation, proliferation, and aging
inferred← citeshttps://doi.org/10.1007/s00018-012-1195-yopenalex-snapshot
Control of cell growth: Rag GTPases in activation of TORC1
inferred← citeshttps://doi.org/10.1007/s00018-013-1533-8openalex-snapshot
Reduced syncytin-1 expression in choriocarcinoma BeWo cells activates the calpain1–AIF-mediated apoptosis, implication for preeclampsia
inferred← citeshttps://doi.org/10.1007/s00109-007-0173-6openalex-snapshot
Involvement of autophagy in viral infections: antiviral function and subversion by viruses
inferred← citeshttps://doi.org/10.1007/s00109-021-02127-6openalex-snapshot
Progranulin associates with Rab2 and is involved in autophagosome-lysosome fusion in Gaucher disease
inferred← citeshttps://doi.org/10.1007/s00125-016-4058-5openalex-snapshot
Survival or death: a dual role for autophagy in stress-induced pericyte loss in diabetic retinopathy
inferred← citeshttps://doi.org/10.1007/s00204-014-1386-4openalex-snapshot
Resveratrol and its oligomers: modulation of sphingolipid metabolism and signaling in disease
inferred← citeshttps://doi.org/10.1007/s00204-018-2266-0openalex-snapshot
Perfluoroalkyl acid exposure induces protective mitochondrial and endoplasmic reticulum autophagy in lung cells
inferred← citeshttps://doi.org/10.1007/s00213-025-06995-5openalex-snapshot
3-Methyladenine administration alleviates cognitive and memory dysfunction in attention-deficit/hyperactivity disorder by modulating autophagy
inferred← citeshttps://doi.org/10.1007/s00221-022-06392-wopenalex-snapshot
H19 silencing decreases kainic acid-induced hippocampus neuron injury via activating the PI3K/AKT pathway via the H19/miR-206 axis
inferred← citeshttps://doi.org/10.1007/s00253-013-4971-1openalex-snapshot
Autophagy promotes survival in aging submerged cultures of the filamentous fungus Aspergillus niger
inferred← citeshttps://doi.org/10.1007/s00253-014-5721-8openalex-snapshot
Role of autophagy and its significance in cellular homeostasis
inferred← citeshttps://doi.org/10.1007/s00277-011-1315-zopenalex-snapshot
The time-dependent autophagy protects against apoptosis with possible involvement of Sirt1 protein in multiple myeloma under nutrient depletion
inferred← citeshttps://doi.org/10.1007/s00280-013-2363-yopenalex-snapshot
Autophagy, a novel target for chemotherapeutic intervention of thyroid cancer
inferred← citeshttps://doi.org/10.1007/s00280-014-2451-7openalex-snapshot
Bortezomib induces protective autophagy through AMP-activated protein kinase activation in cultured pancreatic and colorectal cancer cells
inferred← citeshttps://doi.org/10.1007/s00280-017-3298-5openalex-snapshot
Up-regulation of autophagy is a mechanism of resistance to chemotherapy and can be inhibited by pantoprazole to increase drug sensitivity
inferred← citeshttps://doi.org/10.1007/s00394-015-0930-1openalex-snapshot
Sensitization of estrogen receptor-positive breast cancer cell lines to 4-hydroxytamoxifen by isothiocyanates present in cruciferous plants
inferred← citeshttps://doi.org/10.1007/s00395-014-0416-yopenalex-snapshot
Mitochondrial KATP channel involvement in angiotensin II-induced autophagy in vascular smooth muscle cells
inferred← citeshttps://doi.org/10.1007/s00403-014-1521-3openalex-snapshot
Oxidative stress and substance P mediate psychological stress-induced autophagy and delay of hair growth in mice
inferred← citeshttps://doi.org/10.1007/s00404-018-4841-2openalex-snapshot
Orlistat induces apoptosis and protective autophagy in ovarian cancer cells: involvement of Akt-mTOR-mediated signaling pathway
inferred← citeshttps://doi.org/10.1007/s00408-016-9936-6openalex-snapshot
Gemcitabine-Induced Autophagy Protects Human Lung Cancer Cells from Apoptotic Death
inferred← citeshttps://doi.org/10.1007/s00417-013-2542-xopenalex-snapshot
Acute exposure to thimerosal induces antiproliferative properties, apoptosis, and autophagy activation in human Chang conjunctival cells
inferred← citeshttps://doi.org/10.1007/s00432-016-2317-yopenalex-snapshot
BRAF V600E-dependent role of autophagy in uveal melanoma
inferred← citeshttps://doi.org/10.1007/s00705-012-1270-6openalex-snapshot
Newcastle disease virus triggers autophagy in U251 glioma cells to enhance virus replication
inferred← citeshttps://doi.org/10.1007/s00726-014-1785-0openalex-snapshot
l-Glutamine deprivation induces autophagy and alters the mTOR and MAPK signaling pathways in porcine intestinal epithelial cells
inferred← citeshttps://doi.org/10.1007/s10142-019-00714-yopenalex-snapshot
Membrane proteomic analysis reveals the intestinal development is deteriorated by intrauterine growth restriction in piglets
inferred← citeshttps://doi.org/10.1007/s10157-009-0254-7openalex-snapshot
Cisplatin-induced macroautophagy occurs prior to apoptosis in proximal tubules in vivo
inferred← citeshttps://doi.org/10.1007/s10495-008-0307-5openalex-snapshot
The paradox of autophagy and its implication in cancer etiology and therapy
inferred← citeshttps://doi.org/10.1007/s10495-013-0805-yopenalex-snapshot
Tiron and trolox potentiate the autophagic cell death induced by magnolol analog Ery5 by activation of Bax in HL-60 cells
inferred← citeshttps://doi.org/10.1007/s10495-013-0809-7openalex-snapshot
Differential autophagic cell death under stress with ectopic cytoplasmic and mitochondrial-specific PPP2R2B in human neuroblastoma cells
inferred← citeshttps://doi.org/10.1007/s10495-013-0936-1openalex-snapshot
Post-translational regulation of the cellular levels of DAPK
inferred← citeshttps://doi.org/10.1007/s10495-014-1074-0openalex-snapshot
Lysophosphatidic acid rescues bone mesenchymal stem cells from hydrogen peroxide-induced apoptosis
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/s10495-015-1176-3openalex-snapshot
AMBRA1 and SQSTM1 expression pattern in prostate cancer
inferred← citeshttps://doi.org/10.1007/s10495-016-1335-1openalex-snapshot
Natural products as modulator of autophagy with potential clinical prospects
inferred← citeshttps://doi.org/10.1007/s10495-018-1497-0openalex-snapshot
Molecular mechanisms of apoptosis and autophagy elicited by combined treatment with oridonin and cetuximab in laryngeal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1007/s10545-007-0772-yopenalex-snapshot
Interpretation of plasma amino acids in the follow‐up of patients: The impact of compartmentation
inferred← citeshttps://doi.org/10.1007/s10545-013-9613-3openalex-snapshot
Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation and adaptive immunity
inferred← citeshttps://doi.org/10.1007/s10557-006-0583-7openalex-snapshot
The Interplay between Pro-Death and Pro-Survival Signaling Pathways in Myocardial Ischemia/Reperfusion Injury: Apoptosis Meets Autophagy
inferred← citeshttps://doi.org/10.1007/s10571-011-9706-1openalex-snapshot
p65/RelA-Ser529 NF-κB Subunit Phosphorylation Induces Autophagic Astroglial Death (Clasmatodendrosis) Following Status Epilepticus
inferred← citeshttps://doi.org/10.1007/s10571-015-0227-1openalex-snapshot
Traumatic Brain Injury-Induced Neuronal Apoptosis is Reduced Through Modulation of PI3K and Autophagy Pathways in Mouse by FTY720
inferred← citeshttps://doi.org/10.1007/s10585-015-9743-0openalex-snapshot
Skeletal metastases from breast cancer: pathogenesis of bone tropism and treatment strategy
inferred← citeshttps://doi.org/10.1007/s10856-022-06710-2openalex-snapshot
Reconstruction of rabbit mandibular bone defects using carbonate apatite honeycomb blocks with an interconnected porous structure
inferred← citeshttps://doi.org/10.1007/s11010-013-1608-8openalex-snapshot
AMP-activated protein kinase (AMPK)/Ulk1-dependent autophagic pathway contributes to C6 ceramide-induced cytotoxic effects in cultured colorectal cancer HT-29 cells
inferred← citeshttps://doi.org/10.1007/s11033-009-9451-4openalex-snapshot
Induction of macroautophagy by heat
inferred← citeshttps://doi.org/10.1007/s11033-021-06667-5openalex-snapshot
Toxoplasma gondii profilin and tachyzoites RH strain may manipulate autophagy via downregulating Atg5 and Atg12 and upregulating Atg7
inferred← citeshttps://doi.org/10.1007/s11033-022-07756-9openalex-snapshot
The role of autophagy and apoptosis in early brain injury after subarachnoid hemorrhage: an updated review
inferred← citeshttps://doi.org/10.1007/s11033-023-08641-9openalex-snapshot
Role of apoptosis and autophagy in mediating tramadol-induced neurodegeneration in the rat hippocampus
inferred← citeshttps://doi.org/10.1007/s11064-018-2692-7openalex-snapshot
Quercetin Might Promote Autophagy in a Middle Cerebral Artery Occlusion-Mediated Ischemia Model: Comments on Fawad-Ali Shah et al.
inferred← citeshttps://doi.org/10.1007/s11357-011-9307-4openalex-snapshot
Survival features of EBV-stabilized cells from centenarians: morpho-functional and transcriptomic analyses
inferred← citeshttps://doi.org/10.1007/s11357-015-9764-2openalex-snapshot
Cellular senescence: from growth arrest to immunogenic conversion
inferred← citeshttps://doi.org/10.1007/s12017-017-8458-6openalex-snapshot
VEGF-Mediated Cognitive and Synaptic Improvement in Chronic Cerebral Hypoperfusion Rats Involves Autophagy Process
inferred← citeshttps://doi.org/10.1007/s12020-012-9826-5openalex-snapshot
Rosiglitazone protects against palmitate-induced pancreatic beta-cell death by activation of autophagy via 5′-AMP-activated protein kinase modulation
inferred← citeshttps://doi.org/10.1007/s12035-014-8921-4openalex-snapshot
Mechanism and Regulation of Autophagy and Its Role in Neuronal Diseases
inferred← citeshttps://doi.org/10.1007/s12035-018-0892-4openalex-snapshot
The Interplay Between Apolipoprotein E4 and the Autophagic–Endocytic–Lysosomal Axis
inferred← citeshttps://doi.org/10.1007/s12192-019-01010-1openalex-snapshot
Cadmium stress effects indicating marine pollution in different species of sea urchin employed as environmental bioindicators
inferred← citeshttps://doi.org/10.1007/s12264-020-00513-7openalex-snapshot
Blockade of HCN2 Channels Provides Neuroprotection Against Ischemic Injury via Accelerating Autophagic Degradation in Hippocampal Neurons
inferred← citeshttps://doi.org/10.1007/s12282-019-01012-yopenalex-snapshot
Vitamin K2 induces non-apoptotic cell death along with autophagosome formation in breast cancer cell lines
inferred← citeshttps://doi.org/10.1007/s13238-010-0048-4openalex-snapshot
Beclin 1 cleavage by caspase-3 inactivates autophagy and promotes apoptosis
inferred← citeshttps://doi.org/10.1007/s13238-013-0002-3openalex-snapshot
Targeting tissue-specific metabolic signaling pathways in aging: the promise and limitations
inferred← citeshttps://doi.org/10.1007/s13238-013-3077-yopenalex-snapshot
Targeting tissue-specific metabolic signaling pathways in aging: the promise and limitations
inferred← citeshttps://doi.org/10.1007/s13273-015-0004-8openalex-snapshot
Curcumin derivative HBC induces autophagy through activating AMPK signal in A549 cancer cells
inferred← citeshttps://doi.org/10.1007/s13277-015-3425-zopenalex-snapshot
The role of hypoxia-inducible factor-1α in radiation-induced autophagic cell death in breast cancer cells
inferred← citeshttps://doi.org/10.1007/s13410-018-0681-7openalex-snapshot
Dietary zinc reduces endoplasmic reticulum stress and autophagy to protect against diabetic renal damage in streptozotocin-induced diabetic rats
inferred← citeshttps://doi.org/10.1007/s42995-026-00414-0openalex-snapshot
Genetic selection response and genomic basis of resistance to Cryptocaryon irritans in large yellow croaker (Larimichthys crocea)
inferred← citeshttps://doi.org/10.1016/b978-0-08-046884-6.01106-4openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-08-100601-6.02137-2openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-12-374145-5.00306-5openalex-snapshot
Signaling in Autophagy Related Pathways
inferred← citeshttps://doi.org/10.1016/b978-0-12-801033-4.00003-5openalex-snapshot
Inhibition of ErbB Receptors and Autophagy in Cancer Therapy
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.02137-1openalex-snapshot
The Sertoli Cell as a Target for Toxicants ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-805253-2.00014-6openalex-snapshot
The Role of Autophagy in Vascular Biology and Atherosclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-805420-8.00015-9openalex-snapshot
Intestinal Autophagy Defends Against Salmonella Infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-816388-7.00005-xopenalex-snapshot
Mechanisms of Cell Death
inferred← citeshttps://doi.org/10.1016/b978-0-12-817868-3.00013-5openalex-snapshot
Autophagy in head and neck cancer therapy
inferred← citeshttps://doi.org/10.1016/b978-0-12-819609-0.00006-7openalex-snapshot
Complement factors-mediated modulation of autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-819937-4.00006-6openalex-snapshot
Chemo-sensitizing agents from natural origin for colorectal cancer: Pharmacodynamic and cellular pharmacokinetics approaches
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00102-9openalex-snapshot
Toxicity of Airborne Metals
inferred← citeshttps://doi.org/10.1016/b978-1-4557-0737-9.00024-2openalex-snapshot
Cell Death, Apoptosis, and Autophagy in Retinal Injury
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2018.05.006openalex-snapshot
Mitochondria and Reactive Oxygen Species in Aging and Age-Related Diseases
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2019.12.004openalex-snapshot
The interplay of autophagy and non-apoptotic cell death pathways
inferred← citeshttps://doi.org/10.1016/j.aanat.2021.151781openalex-snapshot
Autophagy-related proteases accompany the transition of pre-chondrogenic cells into chondroblasts
inferred← citeshttps://doi.org/10.1016/j.abb.2019.01.002openalex-snapshot
Mitochondrial regulation of airway smooth muscle functions in health and pulmonary diseases
inferred← citeshttps://doi.org/10.1016/j.addr.2021.114022openalex-snapshot
Mechanisms of immune response to inorganic nanoparticles and their degradation products
inferred← citeshttps://doi.org/10.1016/j.ajog.2020.05.015openalex-snapshot
Deficiency of the oxidative stress–responsive kinase p70S6K1 restores autophagy and ameliorates neural tube defects in diabetic embryopathy
inferred← citeshttps://doi.org/10.1016/j.ajoms.2025.07.016openalex-snapshot
Influence of parallel holes in bone regenerative material for vertical bone augmentation
inferred← citeshttps://doi.org/10.1016/j.apsb.2014.12.010openalex-snapshot
DMH1 (4-[6-(4-isopropoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl]quinoline) inhibits chemotherapeutic drug-induced autophagy
inferred← citeshttps://doi.org/10.1016/j.apsb.2020.10.018openalex-snapshot
Natural compounds modulate the autophagy with potential implication of stroke
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.01.006openalex-snapshot
Natural compounds in the regulation of proteostatic pathways: An invincible artillery against stress, ageing, and diseases
inferred← citeshttps://doi.org/10.1016/j.aquatox.2018.05.021openalex-snapshot
Genome-wide identification of 99 autophagy-related (Atg) genes in the monogonont rotifer Brachionus spp. and transcriptional modulation in response to cadmium
inferred← citeshttps://doi.org/10.1016/j.arr.2009.01.001openalex-snapshot
Heat shock proteins as gatekeepers of proteolytic pathways—Implications for age-related macular degeneration (AMD)
inferred← citeshttps://doi.org/10.1016/j.arr.2018.08.004openalex-snapshot
The effect of fasting or calorie restriction on autophagy induction: A review of the literature
inferred← citeshttps://doi.org/10.1016/j.arr.2023.102085openalex-snapshot
TDP-43 as a therapeutic target in neurodegenerative diseases: Focusing on motor neuron disease and frontotemporal dementia
inferred← citeshttps://doi.org/10.1016/j.arr.2024.102428openalex-snapshot
Autophagy in aging-related diseases and cancer: Principles, regulatory mechanisms and therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.09.001openalex-snapshot
A novel proteolysis-resistant cyclic helix B peptide ameliorates kidney ischemia reperfusion injury
inferred← citeshttps://doi.org/10.1016/j.bbagen.2023.130330openalex-snapshot
Cancer metabolism within tumor microenvironments
inferred← citeshttps://doi.org/10.1016/j.bbalip.2008.12.007openalex-snapshot
Endolysosomal phospholipidosis and cytosolic lipid droplet storage and release in macrophages
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.07.014openalex-snapshot
Autophagy: A lysosomal degradation pathway with a central role in health and disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.12.010openalex-snapshot
Autophagy in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.09.016openalex-snapshot
Involvement of caspase-9 in autophagy-mediated cell survival pathway
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119041openalex-snapshot
Interactions between reactive oxygen species and autophagy
inferred← citeshttps://doi.org/10.1016/j.bbapap.2009.12.001openalex-snapshot
Dissecting the role of mTOR: Lessons from mTOR inhibitors
inferred← citeshttps://doi.org/10.1016/j.bbapap.2013.02.041openalex-snapshot
The biological activities of protein/oleic acid complexes reside in the fatty acid
inferred← citeshttps://doi.org/10.1016/j.bbcan.2005.11.003openalex-snapshot
Lysosomes and lysosomal proteins in cancer cell death (new players of an old struggle)
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.12.167openalex-snapshot
HAMLET, protein folding, and tumor cell death
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.02.126openalex-snapshot
Role of AMP-activated protein kinase in autophagy and proteasome function
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.12.178openalex-snapshot
Autophagy is upregulated in rats with status epilepticus and partly inhibited by Vitamin E
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.08.007openalex-snapshot
Activation of autophagy during glutamate-induced HT22 cell death
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.07.097openalex-snapshot
Epigallocatechin-gallate (EGCG) regulates autophagy in human retinal pigment epithelial cells: A potential role for reducing UVB light-induced retinal damage
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