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The apoptosis/autophagy paradox: autophagic vacuolization before apoptotic death
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.biocel.2004.04.009openalex-snapshot
Role of mitochondrial permeability transition pores in mitochondrial autophagy
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/s0022-1759(02)00069-8openalex-snapshot
Quantitation of mitochondrial alterations associated with apoptosis
inferredcites →https://doi.org/10.1016/s0960-9822(01)00100-2openalex-snapshot
Mitochondria are selectively eliminated from eukaryotic cells after blockade of caspases during apoptosis
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/10.1038/35022595openalex-snapshot
Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice
inferredcites →https://doi.org/10.1038/35022604openalex-snapshot
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
inferredcites →https://doi.org/10.1038/35080097openalex-snapshot
Programmed cell death and apoptosis: origins of the theory
inferredcites →https://doi.org/10.1038/35085008openalex-snapshot
Four deaths and a funeral: from caspases to alternative mechanisms
inferredcites →https://doi.org/10.1038/nature03029openalex-snapshot
The role of autophagy during the early neonatal starvation period
inferredcites →https://doi.org/10.1038/ncb1101-e255openalex-snapshot
Organelle-specific initiation of cell death pathways
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/sj.cdd.4400852openalex-snapshot
The autophagosomal–lysosomal compartment in programmed cell death
inferredcites →https://doi.org/10.1038/sj.cdd.4401006openalex-snapshot
Endoplasmic reticulum stress-induced cell death requires mitochondrial membrane permeabilization
inferredcites →https://doi.org/10.1038/sj.cdd.4401359openalex-snapshot
Role of autophagy in temozolomide-induced cytotoxicity for malignant glioma cells
inferredcites →https://doi.org/10.1038/sj.cdd.4401445openalex-snapshot
Autophagy in human tumors: cell survival or death?
inferredcites →https://doi.org/10.1038/sj.onc.1204575openalex-snapshot
The adenine nucleotide translocator: a target of nitric oxide, peroxynitrite, and 4-hydroxynonenal
inferredcites →https://doi.org/10.1038/sj.onc.1204953openalex-snapshot
Adenine nucleotide translocator mediates the mitochondrial membrane permeabilization induced by lonidamine, arsenite and CD437
inferredcites →https://doi.org/10.1038/sj.onc.1206622openalex-snapshot
Mitochondrial membrane permeabilization is a critical step of lysosome-initiated apoptosis induced by hydroxychloroquine
inferredcites →https://doi.org/10.1038/sj.onc.1206827openalex-snapshot
The chemopreventive agent N-(4-hydroxyphenyl)retinamide induces apoptosis through a mitochondrial pathway regulated by proteins from the Bcl-2 family
inferredcites →https://doi.org/10.1038/sj.onc.1207572openalex-snapshot
Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy
inferredcites →https://doi.org/10.1073/pnas.0401897101openalex-snapshot
Cytomegalovirus cell death suppressor vMIA blocks Bax- but not Bak-mediated apoptosis by binding and sequestering Bax at mitochondria
inferredcites →https://doi.org/10.1073/pnas.2436255100openalex-snapshot
Beclin 1, an autophagy gene essential for early embryonic development, is a haploinsufficient tumor suppressor
inferredcites →https://doi.org/10.1073/pnas.96.22.12536openalex-snapshot
A cytomegalovirus-encoded mitochondria-localized inhibitor of apoptosis structurally unrelated to Bcl-2
inferredcites →https://doi.org/10.1074/jbc.274.18.12692openalex-snapshot
Normal Lysosomal Morphology and Function in LAMP-1-deficient Mice
inferredcites →https://doi.org/10.1074/jbc.m300550200openalex-snapshot
The Mouse APG10 Homologue, an E2-like Enzyme for Apg12p Conjugation, Facilitates MAP-LC3 Modification
inferredcites →https://doi.org/10.1074/jbc.m308408200openalex-snapshot
An Anti-apoptotic Viral Protein That Recruits Bax to Mitochondria
inferredcites →https://doi.org/10.1074/jbc.m406411200openalex-snapshot
Preapoptotic Chromatin Condensation Upstream of the Mitochondrial Checkpoint
inferredcites →https://doi.org/10.1083/jcb.148.6.1141openalex-snapshot
Synaptotagmin VII Regulates Ca2+-Dependent Exocytosis of Lysosomes in Fibroblasts
inferredcites →https://doi.org/10.1083/jcb.152.4.657openalex-snapshot
Dissection of Autophagosome Formation Using Apg5-Deficient Mouse Embryonic Stem Cells
inferredcites →https://doi.org/10.1083/jcb.200302109openalex-snapshot
Alternating metabolic pathways in NGF-deprived sympathetic neurons affect caspase-independent death
inferredcites →https://doi.org/10.1084/jem.181.5.1661openalex-snapshot
Reduction in mitochondrial potential constitutes an early irreversible step of programmed lymphocyte death in vivo.
inferredcites →https://doi.org/10.1084/jem.194.8.1097openalex-snapshot
Human Immunodeficiency Virus 1 Envelope Glycoprotein Complex-Induced Apoptosis Involves Mammalian Target of Rapamycin/Fkbp12-Rapamycin–Associated Protein–Mediated P53 Phosphorylation
inferredcites →https://doi.org/10.1084/jem.20021952openalex-snapshot
Lysosomal Membrane Permeabilization Induces Cell Death in a Mitochondrion-dependent Fashion
inferredcites →https://doi.org/10.1091/mbc.e02-02-0114openalex-snapshot
Role of LAMP-2 in Lysosome Biogenesis and Autophagy
inferredcites →https://doi.org/10.1091/mbc.e04-02-0103openalex-snapshot
Disturbed Cholesterol Traffic but Normal Proteolytic Function in LAMP-1/LAMP-2 Double-deficient Fibroblasts
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/19.21.5720openalex-snapshot
LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing
inferredcites →https://doi.org/10.1093/emboj/cdf391openalex-snapshot
Sequential involvement of Cdk1, mTOR and p53 in apoptosis induced by the HIV‐1 envelope
inferredcites →https://doi.org/10.1101/gad.1126903openalex-snapshot
Ways of dying: multiple pathways to apoptosis
inferredcites →https://doi.org/10.1101/gad.1199904openalex-snapshot
Alkylating DNA damage stimulates a regulated form of necrotic cell death
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.1099320openalex-snapshot
The Pathophysiology of Mitochondrial Cell Death
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.1103966openalex-snapshot
Autophagy Defends Cells Against Invading Group A Streptococcus
inferredcites →https://doi.org/10.1128/mcb.25.3.1025-1040.2005openalex-snapshot
Inhibition of Macroautophagy Triggers Apoptosis
inferredcites →https://doi.org/10.1152/ajpgi.00175.2003openalex-snapshot
Mitochondrial autophagy and injury in the liver in α 1 -antitrypsin deficiency
inferredcites →https://doi.org/10.1158/0008-5472.can-03-2404openalex-snapshot
Resveratrol-induced Autophagocytosis in Ovarian Cancer Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-03-3084openalex-snapshot
Pivotal Role of the Cell Death Factor BNIP3 in Ceramide-Induced Autophagic Cell Death in Malignant Glioma Cells
inferredcites →https://doi.org/10.1172/jci20039openalex-snapshot
Promotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene
inferredcites →https://doi.org/10.1242/dev.00933openalex-snapshot
Caspases function in autophagic programmed cell death inDrosophila
inferredcites →https://doi.org/10.1242/dev.128.8.1443openalex-snapshot
Steroid regulation of autophagic programmed cell death during development
inferredcites →https://doi.org/10.1242/jcs.114.24.4557openalex-snapshot
Identification of essential genes in cultured mammalian cells using small interfering RNAs
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.4767642openalex-extracted
FUT2-Dependent Fucosylation of LAMP1 Promotes Apoptosis of Colorectal Cancer Cells by Regulating Autophagy-Lysosomal Pathway
inferred← citeshttps://doi.org/10.1002/2211-5463.12080openalex-snapshot
AC ‐1001 H3 CDR peptide induces apoptosis and signs of autophagy in vitro and exhibits antimetastatic activity in a syngeneic melanoma model
inferred← citeshttps://doi.org/10.1002/9781118105771.ch5openalex-snapshot
Transglutaminase 2 at the Crossroads between Cell Death and Survival
inferred← citeshttps://doi.org/10.1002/adma.202312352openalex-snapshot
Molecular Motor‐Driven Light‐Controlled Logic‐Gated K+ Channel for Cancer Cell Apoptosis
inferred← citeshttps://doi.org/10.1002/adom.71303openalex-snapshot
Chiral Diazafluorene‐Based Re(I) Emitters Showing Circularly Polarized Photo‐/Electroluminescence and Enantiomer‐Dependent Cytotoxicity
inferred← citeshttps://doi.org/10.1002/biof.121openalex-snapshot
Pineapple bromelain induces autophagy, facilitating apoptotic response in mammary carcinoma cells
inferred← citeshttps://doi.org/10.1002/cjp2.20openalex-snapshot
Regulation of macroautophagy in amiodarone‐induced pulmonary fibrosis
inferred← citeshttps://doi.org/10.1002/emmm.201302771openalex-snapshot
Tyrosine kinase inhibition increases functional parkin‐Beclin‐1 interaction and enhances amyloid clearance and cognitive performance
inferred← citeshttps://doi.org/10.1002/glia.20785openalex-snapshot
TNF‐α‐ and TRAIL‐resistant glioma cells undergo autophagy‐dependent cell death induced by activated microglia
inferred← citeshttps://doi.org/10.1002/ijc.24500openalex-snapshot
Autophagy—A double‐edged sword in oncology
inferred← citeshttps://doi.org/10.1002/jcb.24977openalex-snapshot
The Effects of Pyrrolo[1,2-b][1,2,5]Benzothiadiazepines in MEC1 Cells
inferred← citeshttps://doi.org/10.1002/jcb.29889openalex-snapshot
Lipid droplets and autophagy—links and regulations from yeast to humans
inferred← citeshttps://doi.org/10.1002/jcp.22137openalex-snapshot
Inhibitive effects of Photofrin on cellular autophagy
inferred← citeshttps://doi.org/10.1002/jcp.22609openalex-snapshot
Role of Excitatory Amino Acid Transporter‐2 (EAAT2) and glutamate in neurodegeneration: Opportunities for developing novel therapeutics
inferred← citeshttps://doi.org/10.1002/jcp.25912openalex-snapshot
Knockout of ATG5 leads to malignant cell transformation and resistance to Src family kinase inhibitor PP2
inferred← citeshttps://doi.org/10.1002/jemt.20986openalex-snapshot
An electron microscopic analysis on the ultra structural abnormalities in sperm of the common carp Cyprinus carpio L. inhabiting a polluted lake, Umiam (Meghalaya, India)
inferred← citeshttps://doi.org/10.1002/jemt.21006openalex-snapshot
Programmed neuronal cell death induced by HIV‐1 tat and methamphetamine
inferred← citeshttps://doi.org/10.1002/jhet.4285openalex-snapshot
Discovery of 4H ‐thieno[3,2‐b]pyrrole derivatives as potential anticancer agents
inferred← citeshttps://doi.org/10.1002/jobm.201200273openalex-snapshot
Galleria mellonella hemocytes destruction after infection with Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1002/mabi.202300102openalex-snapshot
Current Status and Trends in Nucleic Acids for Cancer Therapy: A Focus on Polysaccharide‐Based Nanomedicines
inferred← citeshttps://doi.org/10.1002/mc.23096openalex-snapshot
Cardiac glycoside sensitized hepatocellular carcinoma cells to TRAIL via ROS generation, p38MAPK, mitochondrial transition, and autophagy mediation
inferred← citeshttps://doi.org/10.1002/ptr.2286openalex-snapshot
Treatment of PC‐3 and DU145 prostate cancer cells by prenylflavonoids from hop (Humulus lupulus L.) induces a caspase‐independent form of cell death
inferred← citeshttps://doi.org/10.1002/tox.22216openalex-snapshot
m TOR inhibition by rapamycin protects against deltamethrin‐induced apoptosis in PC 12 Cells
inferred← citeshttps://doi.org/10.1007/8904_2013_277openalex-snapshot
Danon Disease Due to a Novel LAMP2 Microduplication
inferred← citeshttps://doi.org/10.1007/978-0-387-74087-4_8openalex-snapshot
Apoptosis and Tumor Cell Death in Response to HAMLET (Human α-Lactalbumin Made Lethal to Tumor Cells)
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/10.1007/978-1-4020-9293-0_1openalex-snapshot
Molecular Pathways of Different Types of Cell Death: Many Roads to Death
inferred← citeshttps://doi.org/10.1007/978-1-4020-9597-9openalex-snapshot
Apoptosis in carcinogenesis and chemotherapy : apoptosis in cancer
inferred← citeshttps://doi.org/10.1007/978-1-4020-9597-9_2openalex-snapshot
Anti-Cancer Strategy of Transitional Cell Carcinoma of Bladder Based on Induction of Different Types of Programmed Cell Deaths
inferred← citeshttps://doi.org/10.1007/978-1-4939-7211-1_8openalex-snapshot
Cell Death and Autophagy in Prion Diseases
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/10.1007/978-1-61779-430-8_9openalex-snapshot
Evaluation of rapamycin-induced cell death.
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/10.1007/978-3-030-05067-2_10openalex-snapshot
Autophagy in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-30845-2_18openalex-snapshot
Endoplasmic Reticulum Stress and Autophagy in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-26666-4_9openalex-snapshot
Methods for Studying Autophagy Within the Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/978-3-319-42740-9_7openalex-snapshot
Role of Autophagy in Tumor Progression and Regression
inferred← citeshttps://doi.org/10.1007/978-3-540-36832-8_4openalex-snapshot
Extranuclear Inheritance: Genetics and Biogenesis of Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-642-00302-8_15openalex-snapshot
Autophagy in HIV-Induced T Cell Death
inferred← citeshttps://doi.org/10.1007/978-3-642-60458-4_16openalex-snapshot
Extranuclear Inheritance: Genetics and Biogenesis of Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-662-44006-3_14openalex-snapshot
Autophagy and Necroptosis in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-662-56111-9_6openalex-snapshot
Zellvitalität, Apoptose und Nekrose, Autophagie
inferred← citeshttps://doi.org/10.1007/978-3-7091-1431-5_5openalex-snapshot
Autophagy in Glioma Cells
inferred← citeshttps://doi.org/10.1007/978-981-15-6930-2_13openalex-snapshot
Mechanistic Insights into Autophagosome–Lysosome Fusion in Cancer Therapeutics
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/s00244-015-0207-yopenalex-snapshot
Effects of Methylmercury on Harbour Seal Peripheral Blood Leucocytes In Vitro Studied by Electron Microscopy
inferred← citeshttps://doi.org/10.1007/s00418-006-0235-9openalex-snapshot
Enzyme-assisted photosensitization with rose Bengal acetate induces structural and functional alteration of mitochondria in HeLa cells
inferred← citeshttps://doi.org/10.1007/s00435-007-0050-4openalex-snapshot
Natural cyclic degeneration by a sequence of programmed cell death modes in Semibalanus balanoides (Linnaeus, 1767) (Crustacea, Cirripedia Thoracica)
inferred← citeshttps://doi.org/10.1007/s00535-014-0995-2openalex-snapshot
Indomethacin suppresses LAMP-2 expression and induces lipophagy and lipoapoptosis in rat enterocytes via the ER stress pathway
inferred← citeshttps://doi.org/10.1007/s00702-009-0240-yopenalex-snapshot
Recent advances in our understanding of neurodegeneration
inferred← citeshttps://doi.org/10.1007/s00726-015-2071-5openalex-snapshot
Excessive l-cysteine induces vacuole-like cell death by activating endoplasmic reticulum stress and mitogen-activated protein kinase signaling in intestinal porcine epithelial cells
inferred← citeshttps://doi.org/10.1007/s10340-023-01642-4openalex-snapshot
Abamectin induces mortality, inhibits food consumption, and causes histological changes in the midgut of the velvetbean caterpillar Anticarsia gemmatalis (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1007/s10452-024-10132-3openalex-snapshot
Deciphering the transcriptional regulatory networks of FOX genes in nitrite-induced spleen injury in largemouth bass
inferred← citeshttps://doi.org/10.1007/s10495-006-6712-8openalex-snapshot
Apoptosis effector mechanisms: A requiem performed in different keys
inferred← citeshttps://doi.org/10.1007/s10495-007-0154-9openalex-snapshot
Apoptosis and autophagy: regulatory connections between two supposedly different processes
inferred← citeshttps://doi.org/10.1007/s10495-008-0292-8openalex-snapshot
Apoptosis, autophagy and cell cycle arrest following photodamage to mitochondrial interior
inferred← citeshttps://doi.org/10.1007/s10495-008-0303-9openalex-snapshot
Immunogenic cell death modalities and their impact on cancer treatment
inferred← citeshttps://doi.org/10.1007/s10495-009-0445-4openalex-snapshot
Autophagy and apoptosis in planarians
inferred← citeshttps://doi.org/10.1007/s10495-010-0481-0openalex-snapshot
Molecular and cellular mechanisms of excitotoxic neuronal death
inferred← citeshttps://doi.org/10.1007/s10495-011-0589-xopenalex-snapshot
Conversation between apoptosis and autophagy: “Is it your turn or mine?”
inferred← citeshttps://doi.org/10.1007/s10495-011-0626-9openalex-snapshot
Follicular atresia in the prepubertal spiny mouse (Acomys cahirinus) ovary
inferred← citeshttps://doi.org/10.1007/s10495-021-01687-9openalex-snapshot
Mechanism of interaction between autophagy and apoptosis in cancer
inferred← citeshttps://doi.org/10.1007/s10522-006-9029-7openalex-snapshot
Increased resistance of lipofuscin-loaded prematurely senescent fibroblasts to starvation-induced programmed cell death
inferred← citeshttps://doi.org/10.1007/s10549-007-9873-4openalex-snapshot
Macroautophagy inhibition sensitizes tamoxifen-resistant breast cancer cells and enhances mitochondrial depolarization
inferred← citeshttps://doi.org/10.1007/s10616-007-9080-5openalex-snapshot
Influence of glucose starvation on the pathway of death in insect cell line Sl: apoptosis follows autophagy
inferred← citeshttps://doi.org/10.1007/s10616-017-0154-8openalex-snapshot
The investigation of ceranib-2 on apoptosis and drug interaction with carboplatin in human non small cell lung cancer cells in vitro
inferred← citeshttps://doi.org/10.1007/s10637-014-0108-3openalex-snapshot
The combination of RAF265, SB590885, ZSTK474 on thyroid cancer cell lines deeply impact on proliferation and MAPK and PI3K/Akt signaling pathways
inferred← citeshttps://doi.org/10.1007/s10637-019-00827-yopenalex-snapshot
In vivo and in vitro inhibition of osteosarcoma growth by the pan Bcl-2 inhibitor AT-101
inferred← citeshttps://doi.org/10.1007/s11010-013-1806-4openalex-snapshot
LAMP2 as a marker of EBV-mediated B lymphocyte transformation in the study of lysosomal storage diseases
inferred← citeshttps://doi.org/10.1007/s11010-014-2102-7openalex-snapshot
Crosstalk between protective autophagy and NF-κB signal in high glucose-induced podocytes
inferred← citeshttps://doi.org/10.1007/s11302-023-09975-6openalex-snapshot
Preclinical evaluation of bozepinib in bladder cancer cell lines: modulation of the NPP1 enzyme
inferred← citeshttps://doi.org/10.1007/s11356-012-1410-2openalex-snapshot
Flow cytometry detection of lysosomal presence and lysosomal membrane integrity in the three-spined stickleback (Gasterosteus aculeatus L.) immune cells: applications in environmental aquatic immunotoxicology.
inferred← citeshttps://doi.org/10.1007/s11684-010-0096-4openalex-snapshot
Autoimmune regulator regulates autophagy in THP-1 human monocytes
inferred← citeshttps://doi.org/10.1007/s12010-018-2721-7openalex-snapshot
Synthetic Dibenzoxanthene Derivatives Induce Apoptosis Through Mitochondrial Pathway in Human Hepatocellular Cancer Cells
inferred← citeshttps://doi.org/10.1007/s12011-025-04599-wopenalex-snapshot
Long-Term Impact of Cr(VI) Exposure in Swiss Albino Mice: ROS-Driven Modulation of Autophagy and Cellular Fate
inferred← citeshttps://doi.org/10.1007/s12013-012-9504-5openalex-snapshot
Rapamycin Induces Apoptosis When Autophagy is Inhibited in T-47D Mammary Cells and Both Processes are Regulated by Phlda1
inferred← citeshttps://doi.org/10.1007/s12038-007-0058-4openalex-snapshot
Heat shock transcription factors regulate heat induced cell death in a rat histiocytoma
inferred← citeshttps://doi.org/10.1007/s12079-016-0364-4openalex-snapshot
Autophagy is a regulator of TRAIL-induced apoptosis in NSCLC A549 cells
inferred← citeshttps://doi.org/10.1007/s12192-019-01029-4openalex-snapshot
Co-enzyme Q10 protects primary chicken myocardial cells from heat stress by upregulating autophagy and suppressing the PI3K/AKT/mTOR pathway
inferred← citeshttps://doi.org/10.1007/s12253-015-9981-0openalex-snapshot
Expression of LC3, LAMP2, KEAP1 and NRF2 in Salivary Adenoid Cystic Carcinoma
inferred← citeshttps://doi.org/10.1007/s12274-024-6595-4openalex-snapshot
Enhanced population of excited single state strategy: irradiation and ultrasound dual-response and host tumor-driven nano-sensitizers construction in triple synergistic therapy
inferred← citeshttps://doi.org/10.1007/s12603-023-2005-yopenalex-snapshot
Dietary Tyrosine Intake (FFQ) Is Associated with Locus Coeruleus, Attention and Grey Matter Maintenance: An MRI Structural Study on 398 Healthy Individuals of the Berlin Aging Study-II
inferred← citeshttps://doi.org/10.1007/s12640-009-9065-6openalex-snapshot
Nitric Oxide-Mediated Toxicity in Paraquat-Exposed SH-SY5Y Cells: A Protective Role of 7-Nitroindazole
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/s40259-016-0160-yopenalex-snapshot
Combination Therapy with AKT3 and PI3KCA siRNA Enhances the Antitumor Effect of Temozolomide and Carmustine in T98G Glioblastoma Multiforme Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-800148-6.00012-2openalex-snapshot
Polycation-Mediated Integrated Cell Death Processes
inferred← citeshttps://doi.org/10.1016/b978-0-12-805420-8.00009-3openalex-snapshot
Methods for Measuring Autophagy Levels in Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-812005-7.00006-0openalex-snapshot
Autophagy and Novel Therapeutic Strategies in Neuroblastoma
inferred← citeshttps://doi.org/10.1016/b978-0-12-812146-7.00008-1openalex-snapshot
Role of the Transcription Factor Interferon Regulatory Factor-1 in Regulating Autophagy in Lipopolysaccharide-Stimulated Macrophages
inferred← citeshttps://doi.org/10.1016/b978-0-12-812146-7.00020-2openalex-snapshot
Silibinin Protects Ultraviolet B–Irradiated Skin by Balancing Apoptosis and Autophagy in Epidermis and Dermis
inferred← citeshttps://doi.org/10.1016/b978-0-12-820595-2.00013-8openalex-snapshot
Cell signaling and apoptosis in animals
inferred← citeshttps://doi.org/10.1016/b978-0-323-89906-2.00008-3openalex-snapshot
Autophagy in Lewy body diseases and multiple system atrophy
inferred← citeshttps://doi.org/10.1016/b978-044452809-4/50142-3openalex-snapshot
Advances in our Understanding of Neurodegeneration
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2019.02.004openalex-snapshot
Voices from the dead: The complex vocabulary and intricate grammar of dead cells
inferred← citeshttps://doi.org/10.1016/j.addr.2015.10.012openalex-snapshot
Endostatin and endorepellin: A common route of action for similar angiostatic cancer avengers
inferred← citeshttps://doi.org/10.1016/j.antiviral.2015.09.016openalex-snapshot
Enterovirus 71 induces autophagy by regulating has-miR-30a expression to promote viral replication
inferred← citeshttps://doi.org/10.1016/j.apcatb.2017.11.018openalex-snapshot
Antimicrobial activity of photocatalysts: Fundamentals, mechanisms, kinetics and recent advances
inferred← citeshttps://doi.org/10.1016/j.aqrep.2022.101457openalex-snapshot
The effect of chloroquine on large yellow croaker (Larimichthys crocea): From autophagy, inflammation, to apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.05.005openalex-snapshot
Autophagy and oxidative stress in cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.06.012openalex-snapshot
Autophagy is not uniformly cytoprotective: a personalized medicine approach for autophagy inhibition as a therapeutic strategy in non-small cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.bbagen.2020.129625openalex-snapshot
NDRG1 suppresses basal and hypoxia-induced autophagy at both the initiation and degradation stages and sensitizes pancreatic cancer cells to lysosomal membrane permeabilization
inferred← citeshttps://doi.org/10.1016/j.bbalip.2023.159444openalex-snapshot
Ceramide regulation of autophagy: A biophysical approach
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.2008.07.027openalex-snapshot
Role of the proteolytic hierarchy between cathepsin L, cathepsin D and caspase-3 in regulation of cellular susceptibility to apoptosis and autophagy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.12.008openalex-snapshot
Molecular and cellular basis of lysosomal transmembrane protein dysfunction
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2009.01.006openalex-snapshot
Anti- and pro-tumor functions of autophagy
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.2013.06.072openalex-snapshot
Knockdown of TIGAR by RNA interference induces apoptosis and autophagy in HepG2 hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.05.148openalex-snapshot
Metformin preconditioning provide neuroprotection through enhancement of autophagy and suppression of inflammation and apoptosis after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.02.015openalex-snapshot
EGCG stimulates autophagy and reduces cytoplasmic HMGB1 levels in endotoxin-stimulated macrophages
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.05.023openalex-snapshot
Killing of tumor cells: A drama in two acts
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.09.017openalex-snapshot
MG-2477, a new tubulin inhibitor, induces autophagy through inhibition of the Akt/mTOR pathway and delayed apoptosis in A549 cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2012.08.007openalex-snapshot
Rottlerin induces autophagy which leads to apoptotic cell death through inhibition of PI3K/Akt/mTOR pathway in human pancreatic cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2017.06.133openalex-snapshot
Eriocalyxin B, a novel autophagy inducer, exerts anti-tumor activity through the suppression of Akt/mTOR/p70S6K signaling pathway in breast cancer
inferred← citeshttps://doi.org/10.1016/j.biocel.2018.06.006openalex-snapshot
Telmisartan generates ROS-dependent upregulation of death receptor 5 to sensitize TRAIL in lung cancer via inhibition of autophagy flux
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2012.10.034openalex-snapshot
Rapamycin encapsulated in dual-responsive micelles for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2014.02.044openalex-snapshot
The effect of gamma keratose on cell viability in vitro after thermal stress and the regulation of cell death pathway-specific gene expression
inferred← citeshttps://doi.org/10.1016/j.biopha.2016.05.043openalex-snapshot
Hemolin triggers cell survival on fibroblasts in response to serum deprivation by inhibition of apoptosis
inferred← citeshttps://doi.org/10.1016/j.brainres.2018.07.007openalex-snapshot
The recovery from transient cognitive dysfunction induced by propofol was associated with enhanced autophagic flux in normal healthy adult mice
inferred← citeshttps://doi.org/10.1016/j.canlet.2010.10.001openalex-snapshot
Targeting apoptotic and autophagic pathways for cancer therapeutics
inferred← citeshttps://doi.org/10.1016/j.canlet.2010.12.007openalex-snapshot
Induction of autophagy-dependent apoptosis by the survivin suppressant YM155 in prostate cancer cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2025.217643openalex-snapshot
FUT2-dependent fucosylation of LAMP1 promotes the apoptosis of colorectal cancer cells by regulating the autophagy-lysosomal pathway
inferred← citeshttps://doi.org/10.1016/j.carpath.2008.02.004openalex-snapshot
Cardiomyocyte death and renewal in the normal and diseased heart
inferred← citeshttps://doi.org/10.1016/j.cca.2014.05.003openalex-snapshot
Human DExD/H RNA helicases: Emerging roles in stress survival regulation
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.08.008openalex-snapshot
Cellular and nuclear degradation during apoptosis
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.09.009openalex-snapshot
Glucose metabolism and programmed cell death: an evolutionary and mechanistic perspective
inferred← citeshttps://doi.org/10.1016/j.cellsig.2014.06.014openalex-snapshot
miR-let-7f-1 regulates SPARC mediated cisplatin resistance in medulloblastoma cells
inferred← citeshttps://doi.org/10.1016/j.cjca.2017.01.002openalex-snapshot
Autophagy, Metabolic Disease, and Pathogenesis of Heart Dysfunction
inferred← citeshttps://doi.org/10.1016/j.copbio.2008.07.007openalex-snapshot
Feast or famine: autophagy control and engineering in eukaryotic cell culture
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.02.053openalex-snapshot
Measurement of the 100 MHz EMF radiation in vivo effects on zebrafish D. rerio embryonic development: A multidisciplinary study
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116984openalex-snapshot
Hepatic inflammation, ballooning, and pyknosis caused by LED light exposure in a mouse model, with differential effects by age and gender
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116204openalex-snapshot
Design, synthesis and biological evaluation of CDC20 inhibitors for treatment of triple-negative breast cancer
inferred← citeshttps://doi.org/10.1016/j.ejpb.2022.09.020openalex-snapshot
Pitavastatin loaded nanoparticles: A suitable ophthalmic treatment for Acanthamoeba Keratitis inducing cell death and autophagy in Acanthamoeba polyphaga
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.114534openalex-snapshot
PDGFRα/β-PI3K-Akt pathway response to the interplay of mitochondrial dysfunction and DNA damage in Aroclor 1254-exposed porcine granulosa cells
inferred← citeshttps://doi.org/10.1016/j.exger.2009.11.002openalex-snapshot
Skeletal muscle autophagy and apoptosis during aging: Effects of calorie restriction and life-long exercise
inferred← citeshttps://doi.org/10.1016/j.exger.2017.11.022openalex-snapshot
Skeletal muscle from aged American Quarter Horses shows impairments in mitochondrial biogenesis and expression of autophagy markers
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.115007openalex-snapshot
Optineurin regulates motor and learning behaviors by affecting dopaminergic neuron survival in mice
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2010.06.006openalex-snapshot
Induction of apoptotic cell death via accumulation of autophagosomes in rat granulosa cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.02.024openalex-snapshot
Activation of apoptosis signal-regulating kinase 1 is a key factor in paraquat-induced cell death: Modulation by the Nrf2/Trx axis
inferred← citeshttps://doi.org/10.1016/j.gene.2006.12.039openalex-snapshot
Characterization of a novel alternatively spliced human transcript encoding an N-terminally truncated Vps24 protein that suppresses the effects of Bax in an ESCRT independent manner in yeast
inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2018.03.021openalex-snapshot
Primary evidence of the mechanisms of action of HIV aspartyl peptidase inhibitors on Trypanosoma cruzi trypomastigote forms
inferred← citeshttps://doi.org/10.1016/j.isci.2025.113878openalex-snapshot
PKA orchestrates long-range lysosomal vesicle transport during synaptic maintenance
inferred← citeshttps://doi.org/10.1016/j.jep.2023.116547openalex-snapshot
Combined Epimedii Folium and Ligustri Lucidi Fructus with dexamethasone alleviate the proliferation of airway smooth muscle cells by regulating apoptosis/autophagy
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2011.09.090openalex-snapshot
Multi-walled carbon nanotubes (MWCNT): Induction of DNA damage in plant and mammalian cells
inferred← citeshttps://doi.org/10.1016/j.jip.2026.108669openalex-snapshot
Intramolluscan alterations of sporocysts induced by sublethal concentrations of Bauhinia monandra protein fraction in the Biomphalaria glabrata–Schistosoma mansoni interaction
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2015.01.012openalex-snapshot
Suppression of murine experimental autoimmune encephalomyelitis development by 1,25-dihydroxyvitamin D3 with autophagy modulation
inferred← citeshttps://doi.org/10.1016/j.mam.2006.08.005openalex-snapshot
Roles of LAMP-1 and LAMP-2 in lysosome biogenesis and autophagy
inferred← citeshttps://doi.org/10.1016/j.mam.2021.101038openalex-snapshot
New insights into the role of autophagy in retinal and eye diseases
inferred← citeshttps://doi.org/10.1016/j.mex.2014.10.003openalex-snapshot
Reducing background cytokine expression in epithelial cells without serum starvation
inferred← citeshttps://doi.org/10.1016/j.molmet.2017.05.005openalex-snapshot
Mitochondrial transcription factor B2 is essential for mitochondrial and cellular function in pancreatic β-cells
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2012.08.007openalex-snapshot
In vitro and in vivo genotoxicity of silver nanoparticles
inferred← citeshttps://doi.org/10.1016/j.nbd.2014.10.011openalex-snapshot
Lysosomal enzyme cathepsin B enhances the aggregate forming activity of exogenous α-synuclein fibrils
inferred← citeshttps://doi.org/10.1016/j.neuint.2012.01.020openalex-snapshot
Hypoxic stress activates chaperone-mediated autophagy and modulates neuronal cell survival
inferred← citeshttps://doi.org/10.1016/j.neuint.2012.10.014openalex-snapshot
Retinoic acid protects against proteasome inhibition associated cell death in SH-SY5Y cells via the AKT pathway
inferred← citeshttps://doi.org/10.1016/j.neulet.2009.03.027openalex-snapshot
Role of autophagy and proteasome degradation pathways in apoptosis of PC12 cells overexpressing human α-synuclein
inferred← citeshttps://doi.org/10.1016/j.neuro.2011.04.006openalex-snapshot
Fipronil is a powerful uncoupler of oxidative phosphorylation that triggers apoptosis in human neuronal cell line SHSY5Y
inferred← citeshttps://doi.org/10.1016/j.neuro.2025.03.003openalex-snapshot
Neuronal degeneration, mitochondrial dysfunction, and disturbance of movements induced by rotenone in the ascidian Styela plicata
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2010.10.065openalex-snapshot
Mesenchymal stem cells support dorsal root ganglion neurons survival by inhibiting the metalloproteinase pathway
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2012.03.004openalex-snapshot
Methamphetamine-induced neurotoxicity linked to ubiquitin-proteasome system dysfunction and autophagy-related changes that can be modulated by protein kinase C delta in dopaminergic neuronal cells
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2012.12.018openalex-snapshot
Decreased parkin solubility is associated with impairment of autophagy in the nigrostriatum of sporadic Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.niox.2020.04.005openalex-snapshot
Isolation and culture of murine bone marrow-derived macrophages for nitric oxide and redox biology
inferred← citeshttps://doi.org/10.1016/j.npep.2023.102367openalex-snapshot
FGF-18 alleviates memory impairments and neuropathological changes in a rat model of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.omto.2022.02.002openalex-snapshot
Potential for reversing miR-634-mediated cytoprotective processes to improve efficacy of chemotherapy against oral squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.pharep.2015.04.012openalex-snapshot
Knockdown of AKT3 and PI3KCA by RNA interference changes the expression of the genes that are related to apoptosis and autophagy in T98G glioblastoma multiforme cells
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.06.007openalex-snapshot
Chloroquine and nanoparticle drug delivery: A promising combination
inferred← citeshttps://doi.org/10.1016/j.phrs.2024.107099openalex-snapshot
Natural products for combating multidrug resistance in cancer
inferred← citeshttps://doi.org/10.1016/j.placenta.2008.09.001openalex-snapshot
Autophagic and Apoptotic Cell Death in Amniotic Epithelial Cells
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2016.08.001openalex-snapshot
Autophagy in the eye: Development, degeneration, and aging
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.152847openalex-snapshot
Acute oral exposure to imidacloprid induces apoptosis and autophagy in the midgut of honey bee Apis mellifera workers
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170543openalex-snapshot
Advances in polychlorinated biphenyls-induced female reproductive toxicity
inferred← citeshttps://doi.org/10.1016/j.semcancer.2013.08.008openalex-snapshot
Autophagy contributes to modulating the cytotoxicities of Bcl-2 homology domain-3 mimetics
inferred← citeshttps://doi.org/10.1016/j.semcancer.2019.10.013openalex-snapshot
The role of cell signaling in the crosstalk between autophagy and apoptosis in the regulation of tumor cell survival in response to sorafenib and neratinib
inferred← citeshttps://doi.org/10.1016/j.taap.2013.01.013openalex-snapshot
Autophagy regulates chlorpyrifos-induced apoptosis in SH-SY5Y cells
inferred← citeshttps://doi.org/10.1016/j.taap.2013.05.009openalex-snapshot
Scrambled and fried: Cigarette smoke exposure causes antral follicle destruction and oocyte dysfunction through oxidative stress
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.12.019openalex-snapshot
Hydrogel encapsulation as a handling and vitrification tool for zebrafish ovarian tissue
inferred← citeshttps://doi.org/10.1016/j.tiv.2006.09.007openalex-snapshot
Autophagy-mediated chemosensitizing effect of the plant alkaloid voacamine on multidrug resistant cells
inferred← citeshttps://doi.org/10.1016/j.toxlet.2010.04.013openalex-snapshot
Mitochondria, reactive oxygen species and cadmium toxicity in the kidney
inferred← citeshttps://doi.org/10.1016/j.toxrep.2014.07.018openalex-snapshot
A novel quinazolinone derivative induces cytochrome c interdependent apoptosis and autophagy in human leukemia MOLT-4 cells
inferred← citeshttps://doi.org/10.1016/j.virusres.2018.08.014openalex-snapshot
The effect of human herpesvirus 6B infection on the MAPK pathway
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.02.008openalex-snapshot
Basis of lethality in C. elegans lacking CUP-5, the Mucolipidosis Type IV orthologue
inferred← citeshttps://doi.org/10.1016/j.yexcr.2009.11.005openalex-snapshot
Bortezomib induces autophagic death in proliferating human endothelial cells
inferred← citeshttps://doi.org/10.1016/j.yexcr.2014.05.013openalex-snapshot
Degradation of AF1Q by chaperone-mediated autophagy
inferred← citeshttps://doi.org/10.1016/j.yexcr.2018.04.022openalex-snapshot
Antihypertensive drug-candesartan attenuates TRAIL resistance in human lung cancer via AMPK-mediated inhibition of autophagy flux
inferred← citeshttps://doi.org/10.1016/j.yexcr.2023.113600openalex-snapshot
Berberine attenuates liver fibrosis by autophagy inhibition triggering apoptosis via the miR-30a-5p/ATG5 axis
inferred← citeshttps://doi.org/10.1016/j.ymeth.2015.01.008openalex-snapshot
Autophagic flux determination in vivo and ex vivo
inferred← citeshttps://doi.org/10.1016/s0076-6879(08)03627-6openalex-snapshot
Chapter 27 Physiological Autophagy in the Syrian Hamster Harderian Gland
inferred← citeshttps://doi.org/10.1016/s0076-6879(08)04014-7openalex-snapshot
Chapter 14 Autophagy in Lung Cancer
inferred← citeshttps://doi.org/10.1016/s0076-6879(08)04021-4openalex-snapshot
Chapter 21 Monitoring Autophagy in Lysosomal Storage Disorders
inferred← citeshttps://doi.org/10.1016/s1937-6448(07)66005-5openalex-snapshot
New Insights into the Mechanisms of Macroautophagy in Mammalian Cells
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.1c00489openalex-snapshot
Discovery and Early Clinical Development of LY3202626, a Low-Dose, CNS-Penetrant BACE Inhibitor
inferred← citeshttps://doi.org/10.1021/acsami.9b15577openalex-snapshot
AIE-Based Theranostic Agent: In Situ Tracking Mitophagy Prior to Late Apoptosis To Guide the Photodynamic Therapy
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.8b00068openalex-snapshot
Toxicity of Nanomaterials: Exposure, Pathways, Assessment, and Recent Advances
inferred← citeshttps://doi.org/10.1021/jf105003nopenalex-snapshot
Identification and Anti-human Glioblastoma Activity of Tagitinin C from Tithonia diversifolia Methanolic Extract
inferred← citeshttps://doi.org/10.1021/jf5054063openalex-snapshot
Thymoquinone Induces Caspase-Independent, Autophagic Cell Death in CPT-11-Resistant LoVo Colon Cancer via Mitochondrial Dysfunction and Activation of JNK and p38
inferred← citeshttps://doi.org/10.1038/aps.2013.29openalex-snapshot
Crosstalk between the proteasome system and autophagy in the clearance of α-synuclein
inferred← citeshttps://doi.org/10.1038/cdd.2008.150openalex-snapshot
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009
inferred← citeshttps://doi.org/10.1038/cdd.2009.34openalex-snapshot
The inositol 1,4,5-trisphosphate receptor regulates autophagy through its interaction with Beclin 1
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