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Life and death by death receptors
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-4141(199803)28:03<973::aid-immu973>3.0.co;2-topenalex-snapshot
Differential regulation of TRAIL and CD95 ligand in transformed cells of the T and B lymphocyte lineage
inferredcites →https://doi.org/10.1002/eji.200324786openalex-snapshot
CD95 death‐inducing signaling complex formation and internalization occur in lipid rafts of type I and type II cells
inferredcites →https://doi.org/10.1002/hep.1840360627openalex-snapshot
TRAIL-mediated apoptosis requires NF- k B inhibition and the mitochondrial permeability transition in human hepatoma cells
inferredcites →https://doi.org/10.1006/bbrc.1999.0493openalex-snapshot
Expression ofTRAILand Its Receptors in Human Brain Tumors
inferredcites →https://doi.org/10.1006/bbrc.2000.4044openalex-snapshot
Rapid Activation of Protein Kinase B/Akt Has a Key Role in Antiapoptotic Signaling during Liver Regeneration
inferredcites →https://doi.org/10.1007/s001090000112openalex-snapshot
Defining CD95 as a tumor suppressor gene
inferredcites →https://doi.org/10.1007/s004010050948openalex-snapshot
Human astrocytic brain tumors express APO2L/TRAIL
inferredcites →https://doi.org/10.1007/s004320100292openalex-snapshot
Expression of TNF-related apoptosis-inducing ligand (TRAIL) and its receptors in gastric carcinoma and tumor-infiltrating lymphocytes: a possible mechanism of immune evasion of the tumor
inferredcites →https://doi.org/10.1016/0092-8674(93)90134-copenalex-snapshot
Mice deficient for the 55 kd tumor necrosis factor receptor are resistant to endotoxic shock, yet succumb to L. monocytogenes infection
inferredcites →https://doi.org/10.1016/1074-7613(95)90057-8openalex-snapshot
Identification and characterization of a new member of the TNF family that induces apoptosis
inferredcites →https://doi.org/10.1016/j.bbcan.2005.01.001openalex-snapshot
Does CD95 have tumor promoting activities?
inferredcites →https://doi.org/10.1016/j.bbrc.2006.10.163openalex-snapshot
Acquired TRAIL resistance in human breast cancer cells are caused by the sustained cFLIPL and XIAP protein levels and ERK activation
inferredcites →https://doi.org/10.1016/j.biocel.2007.02.007openalex-snapshot
TRAIL signalling: Decisions between life and death
inferredcites →https://doi.org/10.1016/j.ccr.2007.08.029openalex-snapshot
Autocrine TNFα Signaling Renders Human Cancer Cells Susceptible to Smac-Mimetic-Induced Apoptosis
inferredcites →https://doi.org/10.1016/j.ccr.2008.02.003openalex-snapshot
Yes and PI3K Bind CD95 to Signal Invasion of Glioblastoma
inferredcites →https://doi.org/10.1016/j.cell.2006.01.021openalex-snapshot
The E3 Ubiquitin Ligase Itch Couples JNK Activation to TNFα-induced Cell Death by Inducing c-FLIPL Turnover
inferredcites →https://doi.org/10.1016/j.cell.2007.10.030openalex-snapshot
IAP Antagonists Induce Autoubiquitination of c-IAPs, NF-κB Activation, and TNFα-Dependent Apoptosis
inferredcites →https://doi.org/10.1016/j.cell.2008.03.036openalex-snapshot
TNF-α Induces Two Distinct Caspase-8 Activation Pathways
inferredcites →https://doi.org/10.1016/j.cub.2007.01.027openalex-snapshot
Ubiquitination of RIP1 regulates an NF-kappaB-independent cell-death switch in TNF signaling.
inferredcites →https://doi.org/10.1016/j.immuni.2004.08.017openalex-snapshot
Compartmentalization of TNF Receptor 1 Signaling
inferredcites →https://doi.org/10.1016/j.molcel.2006.03.026openalex-snapshot
Activation of IKK by TNFα Requires Site-Specific Ubiquitination of RIP1 and Polyubiquitin Binding by NEMO
inferredcites →https://doi.org/10.1016/j.molcel.2008.05.014openalex-snapshot
cIAP1 and cIAP2 Facilitate Cancer Cell Survival by Functioning as E3 Ligases that Promote RIP1 Ubiquitination
inferredcites →https://doi.org/10.1016/j.tibs.2005.01.003openalex-snapshot
The RIP kinases: crucial integrators of cellular stress
inferredcites →https://doi.org/10.1016/j.yexcr.2006.03.014openalex-snapshot
TNF-receptor I defective in internalization allows for cell death through activation of neutral sphingomyelinase
inferredcites →https://doi.org/10.1016/s0014-5793(03)00558-1openalex-snapshot
Actin dependent CD95 internalization is specific for Type I cells
inferredcites →https://doi.org/10.1016/s0092-8674(00)81589-5openalex-snapshot
Bid, a Bcl2 Interacting Protein, Mediates Cytochrome c Release from Mitochondria in Response to Activation of Cell Surface Death Receptors
inferredcites →https://doi.org/10.1016/s0092-8674(00)81590-1openalex-snapshot
Cleavage of BID by Caspase 8 Mediates the Mitochondrial Damage in the Fas Pathway of Apoptosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81874-7openalex-snapshot
Apoptosis by Death Factor
inferredcites →https://doi.org/10.1016/s0092-8674(01)00237-9openalex-snapshot
The TNF and TNF Receptor Superfamilies
inferredcites →https://doi.org/10.1016/s0092-8674(03)00521-xopenalex-snapshot
Induction of TNF Receptor I-Mediated Apoptosis via Two Sequential Signaling Complexes
inferredcites →https://doi.org/10.1016/s0952-7915(98)80223-9openalex-snapshot
Inhibition of Fas death signals by FLIPs
inferredcites →https://doi.org/10.1016/s0960-9822(00)00512-1openalex-snapshot
The caspase-8 inhibitor FLIP promotes activation of NF-κB and Erk signaling pathways
inferredcites →https://doi.org/10.1016/s0960-9822(06)90000-1openalex-snapshot
Cell death: TRAIL and its receptors
inferredcites →https://doi.org/10.1016/s1044-5323(03)00031-9openalex-snapshot
The CD95 Type I/Type II model
inferredcites →https://doi.org/10.1016/s1074-7613(00)00041-8openalex-snapshot
Signaling by the TNF Receptor Superfamily and T Cell Homeostasis
inferredcites →https://doi.org/10.1016/s1074-7613(00)80214-9openalex-snapshot
Requirement for Casper (c-FLIP) in Regulation of Death Receptor–Induced Apoptosis and Embryonic Development
inferredcites →https://doi.org/10.1016/s1074-7613(00)80399-4openalex-snapshot
The Novel Receptor TRAIL-R4 Induces NF-κB and Protects against TRAIL-Mediated Apoptosis, yet Retains an Incomplete Death Domain
inferredcites →https://doi.org/10.1016/s1074-7613(02)00502-2openalex-snapshot
Nature's TRAIL—On a Path to Cancer Immunotherapy
inferredcites →https://doi.org/10.1016/s1074-7613(03)00092-xopenalex-snapshot
Recruitment of TNF Receptor 1 to Lipid Rafts Is Essential for TNFα-Mediated NF-κB Activation
inferredcites →https://doi.org/10.1016/s1357-2725(00)00064-9openalex-snapshot
Tumor necrosis factor receptor-associated factor (TRAF) 2 and its role in TNF signaling
inferredcites →https://doi.org/10.1016/s1359-6101(02)00072-2openalex-snapshot
Non-apoptotic Fas signaling
inferredcites →https://doi.org/10.1038/35104568openalex-snapshot
Inhibition of JNK activation through NF-κB target genes
inferredcites →https://doi.org/10.1038/40657openalex-snapshot
Inhibition of death receptor signals by cellular FLIP
inferredcites →https://doi.org/10.1038/5517openalex-snapshot
Tumoricidal activity of tumor necrosis factor–related apoptosis–inducing ligand in vivo
inferredcites →https://doi.org/10.1038/78688openalex-snapshot
Fas engagement accelerates liver regeneration after partial hepatectomy
inferredcites →https://doi.org/10.1038/82732openalex-snapshot
Fas triggers an alternative, caspase-8–independent cell death pathway using the kinase RIP as effector molecule
inferredcites →https://doi.org/10.1038/86397openalex-snapshot
Differential hepatocyte toxicity of recombinant Apo2L/TRAIL versions
inferredcites →https://doi.org/10.1038/cdd.2008.115openalex-snapshot
The extracellular glycosphingolipid-binding motif of Fas defines its internalization route, mode and outcome of signals upon activation by ligand
inferredcites →https://doi.org/10.1038/nature03337openalex-snapshot
CD4+ T-cell help controls CD8+ T-cell memory via TRAIL-mediated activation-induced cell death
inferredcites →https://doi.org/10.1038/ncb916openalex-snapshot
Fas engagement induces neurite growth through ERK activation and p35 upregulation
inferredcites →https://doi.org/10.1038/nm1627openalex-snapshot
Death-receptor O-glycosylation controls tumor-cell sensitivity to the proapoptotic ligand Apo2L/TRAIL
inferredcites →https://doi.org/10.1038/sj.cdd.4400370openalex-snapshot
Cell death attenuation by `Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex
inferredcites →https://doi.org/10.1038/sj.cdd.4400783openalex-snapshot
Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c
inferredcites →https://doi.org/10.1038/sj.cdd.4401186openalex-snapshot
The CD95(APO-1/Fas) DISC and beyond
inferredcites →https://doi.org/10.1038/sj.cdd.4401189openalex-snapshot
Tumor necrosis factor signaling
inferredcites →https://doi.org/10.1038/sj.cdd.4402085openalex-snapshot
RIP1, a kinase on the crossroads of a cell's decision to live or die
inferredcites →https://doi.org/10.1038/sj.emboj.7600325openalex-snapshot
CD95 ligand induces motility and invasiveness of apoptosis‐resistant tumor cells
inferredcites →https://doi.org/10.1038/sj.emboj.7601016openalex-snapshot
The role of receptor internalization in CD95 signaling
inferredcites →https://doi.org/10.1038/sj.emboj.7601456openalex-snapshot
Palmitoylation is required for efficient Fas cell death signaling
inferredcites →https://doi.org/10.1038/sj.emboj.7601460openalex-snapshot
Palmitoylation of CD95 facilitates formation of SDS‐stable receptor aggregates that initiate apoptosis signaling
inferredcites →https://doi.org/10.1038/sj.embor.7400280openalex-snapshot
Induction of apoptosis and activation of NF‐κB by CD95 require different signalling thresholds
inferredcites →https://doi.org/10.1038/sj.embor.embor854openalex-snapshot
The role of the death‐domain kinase RIP in tumour‐necrosis‐factor‐induced activation of mitogen‐activated protein kinases
inferredcites →https://doi.org/10.1038/sj.onc.1204558openalex-snapshot
Differential activation of TRAIL-R1 and -2 by soluble and membrane TRAIL allows selective surface antigen-directed activation of TRAIL-R2 by a soluble TRAIL derivative
inferredcites →https://doi.org/10.1038/sj.onc.1209719openalex-snapshot
TRAIL promotes metastasis of human pancreatic ductal adenocarcinoma
inferredcites →https://doi.org/10.1042/0264-6021:3500505openalex-snapshot
Functional analysis of tumour necrosis factor-α-related apoptosis-inducing ligand (TRAIL): cysteine-230 plays a critical role in the homotrimerization and biological activity of this novel tumoricidal cytokine
inferredcites →https://doi.org/10.1046/j.1365-2141.1999.01630.xopenalex-snapshot
Functional expression of TRAIL by lymphoid and myeloid tumour cells
inferredcites →https://doi.org/10.1046/j.1523-1747.2003.12332.xopenalex-snapshot
TRAIL-Induced Apoptosis and Gene Induction in HaCaT Keratinocytes: Differential Contribution of TRAIL Receptors 1 and 2
inferredcites →https://doi.org/10.1053/j.gastro.2008.02.021openalex-snapshot
CD95 Ligand Is a Proliferative and Antiapoptotic Signal in Quiescent Hepatic Stellate Cells
inferredcites →https://doi.org/10.1053/jhep.2002.36942openalex-snapshot
TRAIL-mediated apoptosis requires NF-κB inhibition and the mitochondrial permeability transition in human hepatoma cells
inferredcites →https://doi.org/10.1073/pnas.0507329102openalex-snapshot
Preligand assembly domain-mediated ligand-independent association between TRAIL receptor 4 (TR4) and TR2 regulates TRAIL-induced apoptosis
inferredcites →https://doi.org/10.1073/pnas.95.2.570openalex-snapshot
The type 1 receptor (CD120a) is the high-affinity receptor for soluble tumor necrosis factor
inferredcites →https://doi.org/10.1073/pnas.96.20.10964openalex-snapshot
Caspase activation: The induced-proximity model
inferredcites →https://doi.org/10.1074/jbc.270.1.387openalex-snapshot
Self-association of the “Death Domains” of the p55 Tumor Necrosis Factor (TNF) Receptor and Fas/APO1 Prompts Signaling for TNF and Fas/APO1 Effects
inferredcites →https://doi.org/10.1074/jbc.271.22.12687openalex-snapshot
Induction of Apoptosis by Apo-2 Ligand, a New Member of the Tumor Necrosis Factor Cytokine Family
inferredcites →https://doi.org/10.1074/jbc.273.12.6921openalex-snapshot
Ceramide Formation Leads to Caspase-3 Activation during Hypoxic PC12 Cell Death
inferredcites →https://doi.org/10.1074/jbc.274.32.22532openalex-snapshot
Differential Modulation of Apoptosis Sensitivity in CD95 Type I and Type II Cells
inferredcites →https://doi.org/10.1074/jbc.274.43.30603openalex-snapshot
Tumor Necrosis Factor-related Apoptosis-inducing Ligand Receptors Signal NF-κB and JNK Activation and Apoptosis through Distinct Pathways
inferredcites →https://doi.org/10.1074/jbc.275.15.10838openalex-snapshot
Activation of NF-κB by FADD, Casper, and Caspase-8
inferredcites →https://doi.org/10.1074/jbc.c000284200openalex-snapshot
FADD Is Required for DR4- and DR5-mediated Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m010384200openalex-snapshot
MAPK/ERK Overrides the Apoptotic Signaling from Fas, TNF, and TRAIL Receptors
inferredcites →https://doi.org/10.1074/jbc.m206882200openalex-snapshot
The Long Form of FLIP Is an Activator of Caspase-8 at the Fas Death-inducing Signaling Complex
inferredcites →https://doi.org/10.1074/jbc.m303399200openalex-snapshot
Fas-associated Death Domain Protein and Caspase-8 Are Not Recruited to the Tumor Necrosis Factor Receptor 1 Signaling Complex during Tumor Necrosis Factor-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m404206200openalex-snapshot
The Kinase Activity of Rip1 Is Not Required for Tumor Necrosis Factor-α-induced IκB Kinase or p38 MAP Kinase Activation or for the Ubiquitination of Rip1 by Traf2
inferredcites →https://doi.org/10.1074/jbc.m410660200openalex-snapshot
Receptor-selective Mutants of Apoptosis-inducing Ligand 2/Tumor Necrosis Factor-related Apoptosis-inducing Ligand Reveal a Greater Contribution of Death Receptor (DR) 5 than DR4 to Apoptosis Signaling
inferredcites →https://doi.org/10.1074/jbc.m414358200openalex-snapshot
Caspase-10 Triggers Bid Cleavage and Caspase Cascade Activation in FasL-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m414425200openalex-snapshot
c-FLIPR, a New Regulator of Death Receptor-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m509560200openalex-snapshot
Molecular Determinants of Kinase Pathway Activation by Apo2 Ligand/Tumor Necrosis Factor-related Apoptosis-inducing Ligand
inferredcites →https://doi.org/10.1074/jbc.m600620200openalex-snapshot
Ubiquitination of RIP Is Required for Tumor Necrosis Factor α-induced NF-κB Activation
inferredcites →https://doi.org/10.1074/jbc.m700438200openalex-snapshot
Receptor-mediated Endocytosis Is Not Required for Tumor Necrosis Factor-related Apoptosis-inducing Ligand (TRAIL)-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m800823200openalex-snapshot
CD95 Stimulation Results in the Formation of a Novel Death Effector Domain Protein-containing Complex
inferredcites →https://doi.org/10.1074/jbc.m909721199openalex-snapshot
Cysteine 230 Is Essential for the Structure and Activity of the Cytotoxic Ligand TRAIL
inferredcites →https://doi.org/10.1074/jbc.m910438199openalex-snapshot
Temperature-sensitive Differential Affinity of TRAIL for Its Receptors
inferredcites →https://doi.org/10.1083/jcb.200501048openalex-snapshot
The extracellular domains of FasL and Fas are sufficient for the formation of supramolecular FasL-Fas clusters of high stability
inferredcites →https://doi.org/10.1084/jem.186.7.1165openalex-snapshot
Cloning and Characterization of TRAIL-R3, a Novel Member of the Emerging TRAIL Receptor Family
inferredcites →https://doi.org/10.1084/jem.187.8.1205openalex-snapshot
Conversion of Membrane-bound Fas(CD95) Ligand to Its Soluble Form Is Associated with Downregulation of Its Proapoptotic Activity and Loss of Liver Toxicity
inferredcites →https://doi.org/10.1084/jem.190.12.1891openalex-snapshot
Caspase Activation Is Required for T Cell Proliferation
inferredcites →https://doi.org/10.1093/embo-reports/kvf022openalex-snapshot
An essential role for membrane rafts in the initiation of Fas/CD95‐triggered cell death in mouse thymocytes
inferredcites →https://doi.org/10.1093/emboj/17.3.706openalex-snapshot
A dominant interfering mutant of FADD/MORT1 enhances deletion of autoreactive thymocytes and inhibits proliferation of mature T lymphocytes
inferredcites →https://doi.org/10.1093/emboj/17.6.1675openalex-snapshot
Two CD95 (APO‐1/Fas) signaling pathways
inferredcites →https://doi.org/10.1093/emboj/cdf356openalex-snapshot
c‐FLIPL is a dual function regulator for caspase‐8 activation and CD95‐mediated apoptosis
inferredcites →https://doi.org/10.1096/fasebj.10.4.8647340openalex-snapshot
Transcriptional control of liver regeneration
inferredcites →https://doi.org/10.1097/01.lab.0000027838.69455.39openalex-snapshot
Functional Expression of Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand in Human Colonic Adenocarcinoma Cells
inferredcites →https://doi.org/10.1101/gad.13.19.2514openalex-snapshot
Cleavage of the death domain kinase RIP by Caspase-8 prompts TNF-induced apoptosis
inferredcites →https://doi.org/10.1126/science.274.5288.787openalex-snapshot
Suppression of TNF-α-Induced Apoptosis by NF-κB
inferredcites →https://doi.org/10.1126/science.276.5309.111openalex-snapshot
The Receptor for the Cytotoxic Ligand TRAIL
inferredcites →https://doi.org/10.1126/science.277.5327.815openalex-snapshot
An Antagonist Decoy Receptor and a Death Domain-Containing Receptor for TRAIL
inferredcites →https://doi.org/10.1126/science.279.5358.1954openalex-snapshot
FADD: Essential for Embryo Development and Signaling from Some, But Not All, Inducers of Apoptosis
inferredcites →https://doi.org/10.1126/science.281.5381.1305openalex-snapshot
Death Receptors: Signaling and Modulation
inferredcites →https://doi.org/10.1126/science.281.5383.1680openalex-snapshot
NF-κB Antiapoptosis: Induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to Suppress Caspase-8 Activation
inferredcites →https://doi.org/10.1126/science.288.5475.2351openalex-snapshot
A Domain in TNF Receptors That Mediates Ligand-Independent Receptor Assembly and Signaling
inferredcites →https://doi.org/10.1126/science.288.5475.2354openalex-snapshot
Fas Preassociation Required for Apoptosis Signaling and Dominant Inhibition by Pathogenic Mutations
inferredcites →https://doi.org/10.1126/science.7510905openalex-snapshot
Protection from Fas-Mediated Apoptosis by a Soluble Form of the Fas Molecule
inferredcites →https://doi.org/10.1128/iai.68.3.1243-1251.2000openalex-snapshot
Tumor Necrosis Factor Receptor p55-Deficient Mice Respond to AcuteYersinia enterocoliticaInfection with Less Apoptosis and More Effective Host Resistance
inferredcites →https://doi.org/10.1128/mcb.00520-06openalex-snapshot
Differential Inhibition of TRAIL-Mediated DR5-DISC Formation by Decoy Receptors 1 and 2
inferredcites →https://doi.org/10.1128/mcb.21.24.8247-8254.2001openalex-snapshot
FLICE-Inhibitory Proteins: Regulators of Death Receptor-Mediated Apoptosis
inferredcites →https://doi.org/10.1128/mcb.22.1.207-220.2002openalex-snapshot
Molecular Ordering of the Initial Signaling Events of CD95
inferredcites →https://doi.org/10.1146/annurev.immunol.17.1.331openalex-snapshot
TUMOR NECROSIS FACTOR RECEPTOR AND Fas SIGNALING MECHANISMS
inferredcites →https://doi.org/10.1152/ajpgi.00062.2008openalex-snapshot
PI3K/Akt activation is critical for early hepatic regeneration after partial hepatectomy
inferredcites →https://doi.org/10.1152/ajpgi.00242.2005openalex-snapshot
Trail induces cell migration and invasion in apoptosis-resistant cholangiocarcinoma cells
inferredcites →https://doi.org/10.1152/ajpgi.00497.2006openalex-snapshot
cFLIPL prevents TRAIL-induced apoptosis of hepatocellular carcinoma cells by inhibiting the lysosomal pathway of apoptosis
inferredcites →https://doi.org/10.1158/0008-5472.can-08-0078openalex-snapshot
Metastasis Suppressor Function of Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand-R in Mice: Implications for TRAIL-Based Therapy in Humans?
inferredcites →https://doi.org/10.1158/1078-0432.ccr-05-2635openalex-snapshot
Preclinical Differentiation between Apparently Safe and Potentially Hepatotoxic Applications of TRAIL Either Alone or in Combination with Chemotherapeutic Drugs
inferredcites →https://doi.org/10.1172/jci23771openalex-snapshot
Inhibition of TNF receptor 1 internalization by adenovirus 14.7K as a novel immune escape mechanism
inferredcites →https://doi.org/10.1172/jci29900openalex-snapshot
TRAIL-R deficiency in mice promotes susceptibility to chronic inflammation and tumorigenesis
inferredcites →https://doi.org/10.1172/jci33061openalex-snapshot
TRAIL-R deficiency in mice enhances lymph node metastasis without affecting primary tumor development
inferredcites →https://doi.org/10.1172/jci34359openalex-snapshot
To kill a tumor cell: the potential of proapoptotic receptor agonists
inferredcites →https://doi.org/10.1172/jci6926openalex-snapshot
Safety and antitumor activity of recombinant soluble Apo2 ligand
inferredcites →https://doi.org/10.1182/blood.v98.1.194openalex-snapshot
The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis
inferredcites →https://doi.org/10.1371/journal.pbio.0030183openalex-snapshot
Engineering a Dimeric Caspase-9: A Re-evaluation of the Induced Proximity Model for Caspase Activation
inferredcites →https://doi.org/10.1593/neo.03421openalex-snapshot
Evidence for a Proangiogenic Activity of TNF-Related Apoptosis-Inducing Ligand
inferredcites →https://doi.org/10.4049/jimmunol.154.6.2706openalex-snapshot
Three functional soluble forms of the human apoptosis-inducing Fas molecule are produced by alternative splicing.
inferredcites →https://doi.org/10.4049/jimmunol.169.6.2851openalex-snapshot
Mitogen-Activated Protein Kinase/Extracellular Signal-Regulated Kinase Signaling in Activated T Cells Abrogates TRAIL-Induced Apoptosis Upstream of the Mitochondrial Amplification Loop and Caspase-8
inferredcites →https://doi.org/10.4049/jimmunol.172.1.123openalex-snapshot
NK Cell TRAIL Eliminates Immature Dendritic Cells In Vivo and Limits Dendritic Cell Vaccination Efficacy
inferredcites →https://doi.org/10.4049/jimmunol.175.1.311openalex-snapshot
Cellular FLIP Long Form Augments Caspase Activity and Death of T Cells through Heterodimerization with and Activation of Caspase-8
inferredcites →https://doi.org/10.4049/jimmunol.176.2.716openalex-snapshot
Cutting Edge: Modulation of Fas-Mediated Apoptosis by Lipid Rafts in T Lymphocytes
inferredcites →https://doi.org/10.4161/cc.3.10.1194openalex-snapshot
The relevance of NF-?B for CD95 Signaling in Tumor Cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Targeting cisplatin resistance in breast cancer using a combination of Thymoquinone and Silymarin: an in vitro and in vivo study
inferred← citeshttps://doi.org/10.1002/2211-5463.12492openalex-snapshot
Death receptor 6 promotes ovarian cancer cell migration through KIF 11
inferred← citeshttps://doi.org/10.1002/2211-5463.12786openalex-snapshot
Fluoride resistance in fibroblasts is conferred via reduced susceptibility to oxidative stress and apoptosis
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001150.pub2openalex-snapshot
Apoptosis: Molecular Mechanisms
inferred← citeshttps://doi.org/10.1002/9781118354599.ch17openalex-snapshot
Fusion Proteins with Toxic Activity
inferred← citeshttps://doi.org/10.1002/9781118355886.ch9openalex-snapshot
Oxidative Stress and Redox Signaling in Carcinogenesis
inferred← citeshttps://doi.org/10.1002/9781118696194.ch1.3openalex-snapshot
Cellular and Molecular Basis of Cancer
inferred← citeshttps://doi.org/10.1002/adma.201705673openalex-snapshot
Recent Advances in Magnetic‐Nanomaterial‐Based Mechanotransduction for Cell Fate Regulation
inferred← citeshttps://doi.org/10.1002/bit.70216openalex-snapshot
Engineering Murine Cross‐Reactivity Into an Affibody to Human Death Receptor 5
inferred← citeshttps://doi.org/10.1002/btpr.3007openalex-snapshot
A simplified method for the efficient purification and refolding of recombinant human TRAIL
inferred← citeshttps://doi.org/10.1002/cbin.11154openalex-snapshot
Soluble CXCL16 promotes TNF‐α‐induced apoptosis in DLBCL via the AMAD10‐NF‐κB regulatory feedback loop
inferred← citeshttps://doi.org/10.1002/cphc.201300755openalex-snapshot
Receptor–Ligand Interactions: Binding Affinities Studied by Single‐Molecule and Super‐Resolution Microscopy on Intact Cells
inferred← citeshttps://doi.org/10.1002/cphy.c120020openalex-snapshot
Apoptosis and Necrosis in the Liver
inferred← citeshttps://doi.org/10.1002/ddr.21527openalex-snapshot
Cristazine, a novel dioxopiperazine alkaloid, induces apoptosis via the death receptor pathway in A431 cells
inferred← citeshttps://doi.org/10.1002/dneu.20768openalex-snapshot
Understanding proneurotrophin actions: Recent advances and challenges
inferred← citeshttps://doi.org/10.1002/fsn3.3707openalex-snapshot
Phellinus merrillii extracts induce apoptosis of vascular smooth muscle cells via intrinsic and extrinsic pathways
inferred← citeshttps://doi.org/10.1002/fsn3.70555openalex-snapshot
The Beneficial Effects of Resveratrol on Hepatocellular Carcinoma and Nonalcoholic Fatty Liver Disease: Modulation of Apoptosis, Autophagy, Inflammation, and Oxidative Stress
inferred← citeshttps://doi.org/10.1002/hep.23729openalex-snapshot
A smac mimetic reduces TNF Related Apoptosis Inducing Ligand (TRAIL)‐induced invasion and metastasis of cholangiocarcinoma cells†
inferred← citeshttps://doi.org/10.1002/hep.24305openalex-snapshot
Delayed-onset caspase-dependent massive hepatocyte apoptosis upon fas activation in bak/bax-deficient mice
inferred← citeshttps://doi.org/10.1002/hep.26042openalex-snapshot
Beta-Catenin–NF-κB Interactions in Murine Hepatocytes: A Complex to Die for
inferred← citeshttps://doi.org/10.1002/hep.26082openalex-snapshot
Increased Apoptosis Induction in Hepatocellular Carcinoma by a Novel Tumor-Targeted TRAIL Fusion Protein Combined With Bortezomib
inferred← citeshttps://doi.org/10.1002/ijc.28076openalex-snapshot
Targeting the EP1 receptor reduces Fas ligand expression and increases the antitumor immune response in an in vivo model of colon cancer
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2013.tb00507.xopenalex-snapshot
Apoptosis and Necrosis in the Liver
inferred← citeshttps://doi.org/10.1002/jat.2822openalex-snapshot
Tributyltin and dibutyltin alter secretion of tumor necrosis factor alpha from human natural killer cells and a mixture of T cells and natural killer cells
inferred← citeshttps://doi.org/10.1002/jat.3658openalex-snapshot
In vitro assays and techniques utilized in anticancer drug discovery
inferred← citeshttps://doi.org/10.1002/jcp.22963openalex-snapshot
Arecoline‐induced death of human leukemia K562 cells is associated with surface up‐modulation of TNFR2
inferred← citeshttps://doi.org/10.1002/jcp.23034openalex-snapshot
The role of osteocyte apoptosis in cancer chemotherapy‐induced bone loss
inferred← citeshttps://doi.org/10.1002/jcp.25064openalex-snapshot
The Association Between p38 MAPK‐Mediated TNF‐α/TNFR2 up‐Regulation and 2‐(4‐Aminophenyl)‐7‐Methoxybenzothiazole‐Induced Apoptosis in Human Leukemia U937 Cells
inferred← citeshttps://doi.org/10.1002/jcp.27123openalex-snapshot
Antrodia salmonea‐induced oxidative stress abrogates HER‐2 signaling cascade and enhanced apoptosis in ovarian carcinoma cells
inferred← citeshttps://doi.org/10.1002/jcp.30132openalex-snapshot
Hsp70 in cancer: A double agent in the battle between survival and death
inferred← citeshttps://doi.org/10.1002/jmv.24964openalex-snapshot
Evaluation of trail receptor 1 (DR4) polymorphisms C626G and A683C as risk factors of hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1002/jsp2.1292openalex-snapshot
Targeted screening of inflammatory mediators in spontaneous degenerative disc disease in dogs reveals an upregulation of the tumor necrosis superfamily
inferred← citeshttps://doi.org/10.1002/prca.70002openalex-snapshot
Causal Effects From Kidney Function to Plasma Proteome: Integrated Observational and Mendelian Randomization Analysis With >50,000 UK Biobank Participants
inferred← citeshttps://doi.org/10.1002/prp2.70249openalex-snapshot
Damnacanthal Suppresses Breast Cancer Cells by Inducing Apoptosis and Cell Cycle Arrest via NF ‐ ĸB Signaling
inferred← citeshttps://doi.org/10.1002/smll.202101678openalex-snapshot
Nanoscale FasL Organization on DNA Origami to Decipher Apoptosis Signal Activation in Cells
inferred← citeshttps://doi.org/10.1007/16833_2024_310openalex-snapshot
Green and Blue Solutions: Natural Compounds from Plants and Marine Organisms Therapeutic Role in Induction of Cancer Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-4419-9533-9_9openalex-snapshot
Down-Regulation of Mast Cell Responses through ITIM Containing Inhibitory Receptors
inferred← citeshttps://doi.org/10.1007/978-1-4614-8051-8_7openalex-snapshot
Apoptosis Deregulation in CLL
inferred← citeshttps://doi.org/10.1007/978-1-4614-9302-0_3openalex-snapshot
Molecular Basis of Cell Death Programs in Mature T Cell Homeostasis
inferred← citeshttps://doi.org/10.1007/978-1-4614-9302-0_5openalex-snapshot
IAP Proteins and Their Therapeutic Potential
inferred← citeshttps://doi.org/10.1007/978-1-4614-9326-6_4openalex-snapshot
Cell-Death—Inducing Mechanisms of Cancer Chemopreventive Agents
inferred← citeshttps://doi.org/10.1007/978-1-4939-3588-8_6openalex-snapshot
A Low-Cost Method for Tracking the Induction of Apoptosis Using FRET-Based Activity Sensors in Suspension Cells
inferred← citeshttps://doi.org/10.1007/978-1-4939-7116-9_18openalex-snapshot
Analyzing Apoptosis Induction and Evasion in Ebola Virus-Infected Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-39855-2_16openalex-snapshot
Pro-apoptotic Properties of Chemopreventive Agents
inferred← citeshttps://doi.org/10.1007/978-3-030-43085-6_12openalex-snapshot
The Fas/FasL Signaling Pathway: Its Role in the Metastatic Process and as a Target for Treating Osteosarcoma Lung Metastases
inferred← citeshttps://doi.org/10.1007/978-3-031-63657-8_4openalex-snapshot
Lipid Storage, Lipolysis, and Lipotoxicity in Obesity
inferred← citeshttps://doi.org/10.1007/978-3-319-08831-0_64openalex-snapshot
Peeking into a Hidden Syndicate: Mitochondria of the Human Amniotic Membrane
inferred← citeshttps://doi.org/10.1007/978-3-319-13611-0_8openalex-snapshot
The Emerging Role of Protein S-Nitrosylation in Cancer Metastasis
inferred← citeshttps://doi.org/10.1007/978-3-319-25065-6_5openalex-snapshot
Molecular Mechanisms of Lipotoxicity in Nonalcoholic Fatty Liver Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-37076-7_64-1openalex-snapshot
Peeking into a Hidden Syndicate: Mitochondria of the Human Amniotic Membrane
inferred← citeshttps://doi.org/10.1007/978-3-319-39406-0_4openalex-snapshot
Apoptotic Caspases in Promoting Cancer: Implications from Their Roles in Development and Tissue Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-319-41319-8_10openalex-snapshot
Regulation of Apoptosis in Melanoma Cells: Critical Targets for Therapeutic Strategies
inferred← citeshttps://doi.org/10.1007/978-3-319-48382-5_6openalex-snapshot
Fat Cell and Fatty Acid Turnover in Obesity
inferred← citeshttps://doi.org/10.1007/978-3-319-53774-0_1openalex-snapshot
Cell Death in Drug-Induced Liver Injury
inferred← citeshttps://doi.org/10.1007/978-3-319-53774-0_5openalex-snapshot
Hepatocyte Lethal and Nonlethal Lipotoxic Injury
inferred← citeshttps://doi.org/10.1007/978-3-319-56805-8_6openalex-snapshot
Stem Cell Regulation by Death Ligands and Their Use in Cell Therapy
inferred← citeshttps://doi.org/10.1007/978-3-319-56805-8_9openalex-snapshot
Fas/CD95, Lipid Rafts, and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-58106-4_6openalex-snapshot
Beta-Catenin and the Survival of Hepatocytes
inferred← citeshttps://doi.org/10.1007/978-3-662-60266-9_51openalex-snapshot
Der programmierte Zelltod – Apoptose, Nekroptose, Ferroptose und Pyroptose
inferred← citeshttps://doi.org/10.1007/978-3-7091-0371-5_10openalex-snapshot
Regulation of Apoptosis in Melanoma Cells: Targets for Therapeutic Strategies
inferred← citeshttps://doi.org/10.1007/978-94-007-2869-1_18openalex-snapshot
Anthracyclines and Mitochondria
inferred← citeshttps://doi.org/10.1007/978-94-007-2869-1_7openalex-snapshot
The Mitochondrial Pathways of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-94-007-4917-7_9openalex-snapshot
Apoptotic Regulators and Its Clinical Implications in Mammary Carcinoma
inferred← citeshttps://doi.org/10.1007/978-981-99-7342-2_9openalex-snapshot
ROS, Redox Regulation, and Anticancer Therapy
inferred← citeshttps://doi.org/10.1007/s00018-013-1327-zopenalex-snapshot
Life in the Fas lane: differential outcomes of Fas signaling
inferred← citeshttps://doi.org/10.1007/s00044-025-03466-6openalex-snapshot
Silibinin: a natural flavonoid with multifaceted anticancer potential and therapeutic challenges
inferred← citeshttps://doi.org/10.1007/s00204-013-1078-5openalex-snapshot
Recent advances in 2D and 3D in vitro systems using primary hepatocytes, alternative hepatocyte sources and non-parenchymal liver cells and their use in investigating mechanisms of hepatotoxicity, cell signaling and ADME
inferred← citeshttps://doi.org/10.1007/s00204-018-2156-5openalex-snapshot
Flame retardants, hexabromocyclododecane (HCBD) and tetrabromobisphenol a (TBBPA), alter secretion of tumor necrosis factor alpha (TNFα) from human immune cells
inferred← citeshttps://doi.org/10.1007/s00210-020-02043-5openalex-snapshot
Inhibitory and ameliorative effect of heliomycin derived from actinomycete on induced hepatocellular carcinoma in rats
inferred← citeshttps://doi.org/10.1007/s00210-023-02645-9openalex-snapshot
Hispidulin: a promising anticancer agent and mechanistic breakthrough for targeted cancer therapy
inferred← citeshttps://doi.org/10.1007/s00210-025-04550-9openalex-snapshot
Molecular mechanisms underlying cyclophosphamide-induced ovarian injury and protective strategies
inferred← citeshttps://doi.org/10.1007/s00262-019-02368-yopenalex-snapshot
Interferon beta increases NK cell cytotoxicity against tumor cells in patients with nasopharyngeal carcinoma via tumor necrosis factor apoptosis-inducing ligand
inferred← citeshttps://doi.org/10.1007/s00264-023-05847-1openalex-snapshot
The role of apoptosis in the pathogenesis of osteoarthritis
inferred← citeshttps://doi.org/10.1007/s00281-013-0364-xopenalex-snapshot
Mechanisms regulating neutrophil survival and cell death
inferred← citeshttps://doi.org/10.1007/s00292-010-1372-4openalex-snapshot
Kutanes anaplastisches großzelliges Lymphom
inferred← citeshttps://doi.org/10.1007/s00441-015-2113-zopenalex-snapshot
Molecular basis of hair cell loss
inferred← citeshttps://doi.org/10.1007/s00701-025-06443-5openalex-snapshot
50 years of methylprednisolone application in spinal cord injury: a bibliometric analysis
inferred← citeshttps://doi.org/10.1007/s00726-015-2084-0openalex-snapshot
Intimacy and a deadly feud: the interplay of autophagy and apoptosis mediated by amino acids
inferred← citeshttps://doi.org/10.1007/s10059-010-0105-0openalex-snapshot
Reactive Oxygen Species in TNFα-Induced Signaling and Cell Death
inferred← citeshttps://doi.org/10.1007/s10495-010-0519-3openalex-snapshot
Identification of DELE, a novel DAP3-binding protein which is crucial for death receptor-mediated apoptosis induction
inferred← citeshttps://doi.org/10.1007/s10495-011-0662-5openalex-snapshot
Modulation of tumor necrosis factor related apoptosis-inducing ligand (TRAIL) receptors in a human osteoclast model in vitro
inferred← citeshttps://doi.org/10.1007/s10495-014-1068-yopenalex-snapshot
Hijacking of death receptor signaling by bacterial pathogen effectors
inferred← citeshttps://doi.org/10.1007/s10495-015-1104-6openalex-snapshot
Lipid rafts and raft-mediated supramolecular entities in the regulation of CD95 death receptor apoptotic signaling
inferred← citeshttps://doi.org/10.1007/s10495-017-1348-4openalex-snapshot
Surfactant protein D delays Fas- and TRAIL-mediated extrinsic pathway of apoptosis in T cells
inferred← citeshttps://doi.org/10.1007/s10495-018-1440-4openalex-snapshot
Negative regulators of cell death pathways in cancer: perspective on biomarkers and targeted therapies
inferred← citeshttps://doi.org/10.1007/s10495-022-01734-zopenalex-snapshot
XIAP as a multifaceted molecule in Cellular Signaling
inferred← citeshttps://doi.org/10.1007/s10534-026-00870-2openalex-snapshot
Concomitant induction of apoptosis and suppression of epithelial-mesenchymal transition (EMT) by a Cu(II)-flavonoid complex in colorectal cancer
inferred← citeshttps://doi.org/10.1007/s10930-015-9646-6openalex-snapshot
Structural Characterizations of the Fas Receptor and the Fas-Associated Protein with Death Domain Interactions
inferred← citeshttps://doi.org/10.1007/s11010-011-0716-6openalex-snapshot
Anti-tumor effects of dihydroartemisinin on human osteosarcoma
inferred← citeshttps://doi.org/10.1007/s11010-011-0756-yopenalex-snapshot
NF-κB mediates the induction of Fas receptor and Fas ligand by microcystin-LR in HepG2 cells
inferred← citeshttps://doi.org/10.1007/s11010-013-1740-5openalex-snapshot
Viability inhibition effect of gambogic acid combined with cisplatin on osteosarcoma cells via mitochondria-independent apoptotic pathway
inferred← citeshttps://doi.org/10.1007/s11010-013-1772-xopenalex-snapshot
Pronounced transcriptional regulation of apoptotic and TNF–NF-kappa-B signaling genes during the course of thymoquinone mediated apoptosis in HeLa cells
inferred← citeshttps://doi.org/10.1007/s11011-019-00508-yopenalex-snapshot
Effect of cholestasis and NeuroAid treatment on the expression of Bax, Bcl-2, Pgc-1α and Tfam genes involved in apoptosis and mitochondrial biogenesis in the striatum of male rats
inferred← citeshttps://doi.org/10.1007/s11033-019-05061-6openalex-snapshot
Newly isolated marine bacterial exopolysaccharides enhance antitumor activity in HepG2 cells via affecting key apoptotic factors and activating toll like receptors
inferred← citeshttps://doi.org/10.1007/s11596-021-2325-2openalex-snapshot
Knockdown of Microtubule Associated Serine/threonine Kinase Like Expression Inhibits Gastric Cancer Cell Growth and Induces Apoptosis by Activation of ERK1/2 and Inactivation of NF-κB Signaling
inferred← citeshttps://doi.org/10.1007/s11655-012-1206-8openalex-snapshot
Induction of apoptosis in human Hep3B hepatoma cells by norcantharidin through a p53 independent pathway via TRAIL/DR5 signal transduction
inferred← citeshttps://doi.org/10.1007/s11655-016-2251-5openalex-snapshot
Molecular Pathway of Psoralidin-Induced Apoptosis in HepG2 Cell Line
inferred← citeshttps://doi.org/10.1007/s12013-026-02070-8openalex-snapshot
Integrating Experimental Assays, Preclinical Models, and CRISPR-Based Functional Approaches for Cancer Drug Discovery
inferred← citeshttps://doi.org/10.1007/s12015-020-10096-5openalex-snapshot
Cardiomyocyte Death and Genome-Edited Stem Cell Therapy for Ischemic Heart Disease
inferred← citeshttps://doi.org/10.1007/s12032-011-9965-1openalex-snapshot
Soluble Fas and Fas ligand and prognosis in children with acute lymphoblastic leukemia
inferred← citeshttps://doi.org/10.1007/s12035-023-03813-xopenalex-snapshot
N6-Methyladenosine Methylation of mRNA in Cell Apoptosis
inferred← citeshttps://doi.org/10.1007/s12094-021-02770-yopenalex-snapshot
Resveratrol as a modulatory of apoptosis and autophagy in cancer therapy
inferred← citeshttps://doi.org/10.1007/s12291-024-01223-xopenalex-snapshot
Programmed Cell Death and its Implications for Skeletal Muscle Wasting
inferred← citeshttps://doi.org/10.1007/s12640-017-9861-3openalex-snapshot
Temporal Pattern and Crosstalk of Necroptosis Markers with Autophagy and Apoptosis Associated Proteins in Ischemic Hippocampus
inferred← citeshttps://doi.org/10.1007/s12672-025-02592-2openalex-snapshot
Specific signaling pathways mediated programmed cell death in tumor microenvironment and target therapies
inferred← citeshttps://doi.org/10.1007/s12975-017-0547-1openalex-snapshot
MicroRNA Changes in Preconditioning-Induced Neuroprotection
inferred← citeshttps://doi.org/10.1007/s13167-010-0042-1openalex-snapshot
“First do no harm” and the importance of prediction in oncology
inferred← citeshttps://doi.org/10.1007/s13238-015-0239-0openalex-snapshot
Death receptor 6 is a novel plasmacytoid dendritic cell-specific receptor and modulates type I interferon production
inferred← citeshttps://doi.org/10.1007/s13277-014-2447-2openalex-snapshot
Vascular marker expression during the development of various types of gynaecological malignancy
inferred← citeshttps://doi.org/10.1007/s13277-015-3634-5openalex-snapshot
Modulation of PKC signaling and induction of apoptosis through suppression of reactive oxygen species and tumor necrosis factor receptor 1 (TNFR1): key role of quercetin in cancer prevention
inferred← citeshttps://doi.org/10.1007/s13277-015-4307-0openalex-snapshot
The combination of thymoquinone and paclitaxel shows anti-tumor activity through the interplay with apoptosis network in triple-negative breast cancer
inferred← citeshttps://doi.org/10.1007/s13577-026-01351-xopenalex-snapshot
The interplay between circadian rhythm components and apoptosis in health and disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.11016-1openalex-snapshot
TNF Receptor Superfamily Signaling Pathways in Immune Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-374419-7.00001-9openalex-snapshot
Molecular Mechanisms of Cell Death
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.30046-3openalex-snapshot
Mitochondria in Cell Death Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-420128-6.00006-3openalex-snapshot
Developmental Pathways in Liver Regeneration-I
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64220-4openalex-snapshot
Cell Injury and Necrosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.99563-1openalex-snapshot
OBSOLETE: Transplant Arteriosclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-802761-5.00001-8openalex-snapshot
Molecular Mechanisms of Cell Death
inferred← citeshttps://doi.org/10.1016/b978-0-12-809405-1.00003-1openalex-snapshot
Neurite Development and Neurotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-809657-4.99563-2openalex-snapshot
Transplant Arteriosclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-813814-4.00002-xopenalex-snapshot
Hormones of Programmed Cell Death
inferred← citeshttps://doi.org/10.1016/b978-0-12-814208-0.00002-6openalex-snapshot
Molecular mechanisms of cell death
inferred← citeshttps://doi.org/10.1016/b978-0-12-815762-6.00003-2openalex-snapshot
Molecular pathways of apoptotic cell death
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00189-9openalex-snapshot
Mitochondria in Cell Death Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-824465-4.00161-7openalex-snapshot
TNF Receptor Superfamily Signaling Pathways in Immune Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-824465-4.00280-5openalex-snapshot
Cellular Cytotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-323-07155-0.00018-6openalex-snapshot
Cellular Growth Control and Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-323-90264-9.00036-2openalex-snapshot
Approaches and methods to study cell signaling: Linguistics of cellular communication
inferred← citeshttps://doi.org/10.1016/b978-0-323-95262-0.00009-7openalex-snapshot
Drug-induced liver injury
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00059-0openalex-snapshot
Cellular and Molecular Mechanisms of Tumor Promotion
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00265-5openalex-snapshot
Cell Death Mechanisms, Associated Toxicity and Therapeutic Applications
inferred← citeshttps://doi.org/10.1016/b978-0-443-15734-9.00037-6openalex-snapshot
Transplant Arteriosclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-443-18866-4.00010-9openalex-snapshot
Host- and genomics-based antiviral approaches
inferred← citeshttps://doi.org/10.1016/bs.acc.2015.12.003openalex-snapshot
Apoptosis Markers in Breast Cancer Therapy
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2021.01.003openalex-snapshot
Intrinsic and extrinsic pathways of apoptosis: Role in cancer development and prognosis
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2021.01.006openalex-snapshot
Cell death mechanisms and their roles in pregnancy related disorders
inferred← citeshttps://doi.org/10.1016/bs.apha.2019.01.006openalex-snapshot
Cell death in drug-induced liver injury
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2025.06.017openalex-snapshot
Cell death triad: Integrating apoptotic, autophagic, and necrotic cell death mechanisms
inferred← citeshttps://doi.org/10.1016/j.abb.2024.110245openalex-snapshot
New metal complexes of 1H-benzimidazole-2-yl hydrazones: Cytostatic, proapoptotic and modulatory activity on kinase signaling pathways
inferred← citeshttps://doi.org/10.1016/j.ajhg.2011.07.006openalex-snapshot
Microcephaly with Simplified Gyration, Epilepsy, and Infantile Diabetes Linked to Inappropriate Apoptosis of Neural Progenitors
inferred← citeshttps://doi.org/10.1016/j.ajpath.2012.03.040openalex-snapshot
Solid-Phase Immunoglobulins IgG and IgM Activate Macrophages with Solid-Phase IgM Acting via a Novel Scavenger Receptor A Pathway
inferred← citeshttps://doi.org/10.1016/j.ajpath.2019.07.014openalex-snapshot
Repression of Death Receptor–Mediated Apoptosis of Hepatocytes by Hepatitis B Virus e Antigen
inferred← citeshttps://doi.org/10.1016/j.ajpath.2024.06.014openalex-snapshot
Cell Death and Survival Mechanisms in Cholangiocarcinogenesis
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2018.09.012openalex-snapshot
Apoptosis and developmental capacity of vitrified parthenogenetic pig blastocysts
inferred← citeshttps://doi.org/10.1016/j.anl.2015.04.012openalex-snapshot
Possible role of apoptosis in pathogenesis of adenoid hypertrophy and chronic adenoiditis: Prospective case–control study
inferred← citeshttps://doi.org/10.1016/j.arcmed.2024.103122openalex-snapshot
Strong Correlation Between Double-Strand DNA Breaks and Total Sperm DNA Fragmentation in the Human Ejaculate
inferred← citeshttps://doi.org/10.1016/j.autrev.2011.08.011openalex-snapshot
The role of T cell apoptosis in nervous system autoimmunity
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.01.015openalex-snapshot
On the role of 4-hydroxynonenal in health and disease
inferred← citeshttps://doi.org/10.1016/j.bbagen.2015.02.002openalex-snapshot
Anti-angiogenic activities of snake venom CRISP isolated from Echis carinatus sochureki
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2015.07.016openalex-snapshot
NFκB- and AP-1-mediated DNA looping regulates matrix metalloproteinase-9 transcription in TNF-α-treated human leukemia U937 cells
inferred← citeshttps://doi.org/10.1016/j.bbalip.2014.06.009openalex-snapshot
Organization and functions of glycolipid-enriched microdomains in phagocytes
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119061openalex-snapshot
Cell death as a result of calcium signaling modulation: A cancer-centric prospective
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2024.119688openalex-snapshot
TRAIL-induced apoptosis and proteasomal activity – Mechanisms, signalling and interplay
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2026.120230openalex-snapshot
Coralyne enhances radiosensitivity of A549 cells by suppressing radiation-induced pro-survival transcriptional programs
inferred← citeshttps://doi.org/10.1016/j.bbcan.2012.03.007openalex-snapshot
CD95 signaling in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.bbcan.2020.188338openalex-snapshot
The emerging role of paraptosis in tumor cell biology: Perspectives for cancer prevention and therapy with natural compounds
inferred← citeshttps://doi.org/10.1016/j.bbcan.2020.188357openalex-snapshot
Caspase-8: The double-edged sword
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.02.059openalex-snapshot
Glutamine deprivation sensitizes human breast cancer MDA-MB-231 cells to TRIAL-mediated apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.153380openalex-snapshot
Deep learning predicts and in vitro experiments validates the synergistic anti-liver cancer effect of vincristine and lenvatinib: Mechanism involving apoptosis induction via the TNF-α/Caspase-8 pathway
inferred← citeshttps://doi.org/10.1016/j.bbrep.2025.102043openalex-snapshot
Fundamental mechanisms of cell death for polycystic ovary syndrome
inferred← citeshttps://doi.org/10.1016/j.bcp.2010.09.010openalex-snapshot
Sensitization of melanoma cells for death ligand-induced apoptosis by an indirubin derivative—Enhancement of both extrinsic and intrinsic apoptosis pathways
inferred← citeshttps://doi.org/10.1016/j.bcp.2012.06.007openalex-snapshot
Suppression of Akt/Foxp3-mediated miR-183 expression blocks Sp1-mediated ADAM17 expression and TNFα-mediated NFκB activation in piceatannol-treated human leukemia U937 cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.06.009openalex-snapshot
Hydroquinone-induced miR-122 down-regulation elicits ADAM17 up-regulation, leading to increased soluble TNF-α production in human leukemia cells with expressed Bcr/Abl
inferred← citeshttps://doi.org/10.1016/j.bcp.2018.10.019openalex-snapshot
C-27-carboxylated oleanane triterpenoids up-regulate TRAIL DISC assembly via p38 MAPK and CHOP-mediated DR5 expression in human glioblastoma cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2018.11.003openalex-snapshot
Non-mitotic effect of albendazole triggers apoptosis of human leukemia cells via SIRT3/ROS/p38 MAPK/TTP axis-mediated TNF-α upregulation
inferred← citeshttps://doi.org/10.1016/j.biocel.2011.08.004openalex-snapshot
Fas/FasL-dependent and -independent activation of caspase-8 in doxorubicin-treated human breast cancer MCF-7 cells: ADAM10 down-regulation activates Fas/FasL signaling pathway
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2010.03.023openalex-snapshot
The effect of carboxydextran-coated superparamagnetic iron oxide nanoparticles on c-Jun N-terminal kinase-mediated apoptosis in human macrophages
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.04.058openalex-snapshot
Tissue decellularization by activation of programmed cell death
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108388openalex-snapshot
Targeting anti-apoptotic mechanisms in tumour cells: Strategies for enhancing Cancer therapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.12.081openalex-snapshot
Erianin induces cell apoptosis through ERK pathway in human nasopharyngeal carcinoma
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.03.020openalex-snapshot
TNF-α renders macrophages resistant to a range of cancer chemotherapeutic agents through NF-κB-mediated antagonism of apoptosis signalling
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.05.014openalex-snapshot
Resveratrol enhances the expression of death receptor Fas/CD95 and induces differentiation and apoptosis in anaplastic large-cell lymphoma cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2024.216779openalex-snapshot
Molecular mechanisms in regulation of autophagy and apoptosis in view of epigenetic regulation of genes and involvement of liquid-liquid phase separation
inferred← citeshttps://doi.org/10.1016/j.cbi.2018.08.021openalex-snapshot
Sodium fluoride causes oxidative stress and apoptosis in cementoblasts
inferred← citeshttps://doi.org/10.1016/j.cellsig.2011.11.008openalex-snapshot
Peroxisome proliferator-activated receptor-γ cross-regulation of signaling events implicated in liver fibrogenesis
inferred← citeshttps://doi.org/10.1016/j.coi.2009.09.010openalex-snapshot
Are we ready to downregulate mast cells?
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2026.111832openalex-snapshot
Integrating experimental biology, computational methods, and artificial intelligence in anticancer drug discovery: Bridging the translational gap
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2022.103858openalex-snapshot
Targeting mitochondrial dysfunctions in pancreatic cancer evokes new therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.cyto.2010.03.009openalex-snapshot
Cytokine-induced tumor suppressors: A GRIM story
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2012.04.002openalex-snapshot
Emerging roles for TNIP1 in regulating post-receptor signaling
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2022.04.003openalex-snapshot
Crosstalk between lncRNAs in the apoptotic pathway and therapeutic targets in cancer
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110940openalex-snapshot
Chronic exposure of human glioblastoma tumors to low concentrations of a pesticide mixture induced multidrug resistance against chemotherapy agents
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118531openalex-snapshot
Exploring potential targets and mechanisms of PCB52-induced cardiotoxicity: Integration of network toxicology and zebrafish experimental evidence
inferred← citeshttps://doi.org/10.1016/j.ejbt.2020.07.006openalex-snapshot
The protective ability and cellular mechanism of Koelreuteria henryi Dummer flower extract against hydrogen peroxide-induced cellular oxidative damage
inferred← citeshttps://doi.org/10.1016/j.ejcb.2010.11.002openalex-snapshot
Subcellular compartmentalization of TNF receptor-1 and CD95 signaling pathways
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