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Tumor necrosis factor signaling

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inferredcites →https://doi.org/10.1002/(sici)1521-4141(199906)29:06<1785::aid-immu1785>3.0.co;2-uopenalex-snapshot
TWEAK can induce cell death via endogenous TNF and TNF receptor 1
inferredcites →https://doi.org/10.1002/1521-1878(200007)22:7<637::aid-bies6>3.0.co;2-eopenalex-snapshot
p38 MAPK signalling cascades: ancient roles and new functions
inferredcites →https://doi.org/10.1002/1521-4141(200002)30:2<652::aid-immu652>3.0.co;2-lopenalex-snapshot
A crucial role for p80 TNF-R2 in amplifying p60 TNF-R1 apoptosis signals in T lymphocytes
inferredcites →https://doi.org/10.1002/1529-0131(200001)43:1<38::aid-anr6>3.0.co;2-lopenalex-snapshot
Reduction of chemokine levels and leukocyte traffic to joints by tumor necrosis factor α blockade in patients with rheumatoid arthritis
inferredcites →https://doi.org/10.1002/eji.1830241139openalex-snapshot
Involvement of the tumor necrosis factor receptor p75 in mediating cytotoxicity and gene regulating activities
inferredcites →https://doi.org/10.1002/eji.1830270719openalex-snapshot
Crucial role of tumor necrosis factor (TNF) receptor 2 and membrane‐bound TNF in experimental cerebral malaria
inferredcites →https://doi.org/10.1002/hep.510250125openalex-snapshot
Induction of Early–Immediate Genes by Tumor Necrosis Factor α Contribute to Liver Repair Following Chemical–Induced Hepatotoxicity
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05978.xopenalex-snapshot
Depletion of the mitochondrial electron transport abrogates the cytotoxic and gene‐inductive effects of TNF.
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06780.xopenalex-snapshot
Divergent signalling via APO‐1/Fas and the TNF receptor, two homologous molecules involved in physiological cell death.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00542.xopenalex-snapshot
The p38/RK mitogen‐activated protein kinase pathway regulates interleukin‐6 synthesis response to tumor necrosis factor.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00760.xopenalex-snapshot
Cathepsin D protease mediates programmed cell death induced by interferon‐gamma, Fas/APO‐1 and TNF‐alpha.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb01007.xopenalex-snapshot
RIP mediates tumor necrosis factor receptor 1 activation of NF‐kappaB but not Fas/APO‐1‐initiated apoptosis.
inferredcites →https://doi.org/10.1006/bbrc.1998.8113openalex-snapshot
Inhibitors of ADP-Ribosylation Impair Inducible Nitric Oxide Synthase Gene Transcription through Inhibition of NF Kappa B Activation
inferredcites →https://doi.org/10.1006/bbrc.2000.3173openalex-snapshot
Activation of ERK1/2 and cPLA2 by the p55 TNF Receptor Occurs Independently of FAN
inferredcites →https://doi.org/10.1006/cyto.1995.0063openalex-snapshot
Cytotoxicity in L929 murine fibrosarcoma cells after triggering of transfected human p75 tumour necrosis factor (TNF) receptor is mediated by endogenous murine TNF
inferredcites →https://doi.org/10.1006/cyto.2001.0921openalex-snapshot
A20 INHIBITS NF-κB ACTIVATION DOWNSTREAM OF MULTIPLE MAP3 KINASES AND INTERACTS WITH THE IκB SIGNALOSOME
inferredcites →https://doi.org/10.1007/978-94-015-8070-0_48openalex-snapshot
Soluble and cell surface receptors for tumor necrosis factor
inferredcites →https://doi.org/10.1007/bf02786481openalex-snapshot
Lymphoid neoorganogenesis
inferredcites →https://doi.org/10.1007/s11912-001-0090-8openalex-snapshot
Isolated limb perfusion for extremity soft-tissue sarcomas, in-transit metastases, and other unresectable tumors: Credits, debits, and future perspectives
inferredcites →https://doi.org/10.1016/0014-5793(95)00534-gopenalex-snapshot
A protein related to a proteasomal subunit binds to the intracellular domain of the p55 TNF receptor upstream to its ‘death domain’
inferredcites →https://doi.org/10.1016/0092-8674(88)90486-2openalex-snapshot
A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: Ramifications for the complex physiology of TNF
inferredcites →https://doi.org/10.1016/0092-8674(89)90944-6openalex-snapshot
Manganous superoxide dismutase is essential for cellular resistance to cytotoxicity of tumor necrosis factor
inferredcites →https://doi.org/10.1016/0092-8674(92)90532-hopenalex-snapshot
The p70 tumor necrosis factor receptor mediates cytotoxicity
inferredcites →https://doi.org/10.1016/0092-8674(93)90132-aopenalex-snapshot
Crystal structure of the soluble human 55 kd TNF receptor-human TNFβ complex: Implications for TNF receptor activation
inferredcites →https://doi.org/10.1016/0092-8674(93)90222-copenalex-snapshot
Tumor necrosis factor's cytotoxic activity is signaled by the p55 TNF receptor
inferredcites →https://doi.org/10.1016/0092-8674(93)90464-2openalex-snapshot
A novel domain within the 55 kd TNF receptor signals cell death
inferredcites →https://doi.org/10.1016/0092-8674(94)90275-5openalex-snapshot
Functional dichotomy of neutral and acidic sphingomyelinases in tumor necrosis factor signaling
inferredcites →https://doi.org/10.1016/0092-8674(95)90070-5openalex-snapshot
The TNF receptor 1-associated protein TRADD signals cell death and NF-κB activation
inferredcites →https://doi.org/10.1016/0092-8674(95)90071-3openalex-snapshot
FADD, a novel death domain-containing protein, interacts with the death domain of fas and initiates apoptosis
inferredcites →https://doi.org/10.1016/0092-8674(95)90149-3openalex-snapshot
The TNFR2-TRAF signaling complex contains two novel proteins related to baculoviral inhibitor of apoptosis proteins
inferredcites →https://doi.org/10.1016/0092-8674(95)90192-2openalex-snapshot
The transmembrane form of tumor necrosis factor is the prime activating ligand of the 80 kDa tumor necrosis factor receptor
inferredcites →https://doi.org/10.1016/0960-9822(93)90009-dopenalex-snapshot
Emerging families of cytokines and receptors
inferredcites →https://doi.org/10.1016/1074-7613(95)90001-2openalex-snapshot
Tumor necrosis factor-α is required in the protective immune response against mycobacterium tuberculosis in mice
inferredcites →https://doi.org/10.1016/s0002-9270(01)02494-7openalex-snapshot
Integrating anti–tumor necrosis factor therapy in inflammatory bowel disease: current and future perspectives
inferredcites →https://doi.org/10.1016/s0002-9343(01)01035-xopenalex-snapshot
Exacerbation of mycobacterium tuberculosis enteritis masquerading as crohn’s disease after treatment with a tumor necrosis factor-α inhibitor
inferredcites →https://doi.org/10.1016/s0002-9440(10)63056-8openalex-snapshot
Cathepsin B Knockout Mice Are Resistant to Tumor Necrosis Factor-α-Mediated Hepatocyte Apoptosis and Liver Injury
inferredcites →https://doi.org/10.1016/s0009-3084(99)00079-1openalex-snapshot
Functional analysis of acid and neutral sphingomyelinases in vitro and in vivo
inferredcites →https://doi.org/10.1016/s0014-5793(00)01206-0openalex-snapshot
Caspase‐induced inactivation of the anti‐apoptotic TRAF1 during Fas ligand‐mediated apoptosis
inferredcites →https://doi.org/10.1016/s0014-5793(00)01212-6openalex-snapshot
Activation of a pro‐apoptotic amplification loop through inhibition of NF‐κB‐dependent survival signals by caspase‐mediated inactivation of RIP
inferredcites →https://doi.org/10.1016/s0014-5793(98)00226-9openalex-snapshot
TRAF2 plays a dual role in NF‐κB‐dependent gene activation by mediating the TNF‐induced activation of p38 MAPK and IκB kinase pathways
inferredcites →https://doi.org/10.1016/s0021-9258(17)46725-1openalex-snapshot
Tumor necrosis factor-induced activation and increased tyrosine phosphorylation of mitogen-activated protein (MAP) kinase in human fibroblasts.
inferredcites →https://doi.org/10.1016/s0021-9258(18)35695-3openalex-snapshot
Tumor necrosis factor stimulates multiple serine/threonine protein kinases in Swiss 3T3 and L929 cells. Implication of casein kinase-2 and extracellular signal-regulated kinases in the tumor necrosis factor signal transduction pathway.
inferredcites →https://doi.org/10.1016/s0021-9258(18)42768-8openalex-snapshot
Cytotoxic activity of tumor necrosis factor is mediated by early damage of mitochondrial functions. Evidence for the involvement of mitochondrial radical generation.
inferredcites →https://doi.org/10.1016/s0021-9258(18)98383-3openalex-snapshot
Tumor necrosis factor-alpha induces expression of monocyte chemoattractant JE via fos and jun genes in clonal osteoblastic MC3T3-E1 cells
inferredcites →https://doi.org/10.1016/s0021-9258(19)61427-4openalex-snapshot
The Inhibitor of Apoptosis, cIAP2, Functions as a Ubiquitin-Protein Ligase and Promotes in VitroMonoubiquitination of Caspases 3 and 7
inferredcites →https://doi.org/10.1016/s0092-8674(00)00009-xopenalex-snapshot
Identification of DIABLO, a Mammalian Protein that Promotes Apoptosis by Binding to and Antagonizing IAP Proteins
inferredcites →https://doi.org/10.1016/s0092-8674(00)80169-5openalex-snapshot
FAN, a Novel WD-Repeat Protein, Couples the p55 TNF-Receptor to Neutral Sphingomyelinase
inferredcites →https://doi.org/10.1016/s0092-8674(00)80222-6openalex-snapshot
The Transcriptional Activity of NF-κB Is Regulated by the IκB-Associated PKAc Subunit through a Cyclic AMP–Independent Mechanism
inferredcites →https://doi.org/10.1016/s0092-8674(00)80406-7openalex-snapshot
The IκB Kinase Complex (IKK) Contains Two Kinase Subunits, IKKα and IKKβ, Necessary for IκB Phosphorylation and NF-κB Activation
inferredcites →https://doi.org/10.1016/s0092-8674(00)80595-4openalex-snapshot
Akt Promotes Cell Survival by Phosphorylating and Inhibiting a Forkhead Transcription Factor
inferredcites →https://doi.org/10.1016/s0092-8674(00)80721-7openalex-snapshot
Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes
inferredcites →https://doi.org/10.1016/s0092-8674(00)80984-8openalex-snapshot
TRADD–TRAF2 and TRADD–FADD Interactions Define Two Distinct TNF Receptor 1 Signal Transduction Pathways
inferredcites →https://doi.org/10.1016/s0092-8674(00)81265-9openalex-snapshot
Involvement of MACH, a Novel MORT1/FADD-Interacting Protease, in Fas/APO-1- and TNF Receptor–Induced Cell Death
inferredcites →https://doi.org/10.1016/s0092-8674(00)81266-0openalex-snapshot
FLICE, A Novel FADD-Homologous ICE/CED-3–like Protease, Is Recruited to the CD95 (Fas/APO-1) Death-Inducing Signaling Complex
inferredcites →https://doi.org/10.1016/s0092-8674(00)81375-6openalex-snapshot
Dissection of TNF Receptor 1 Effector Functions: JNK Activation Is Not Linked to Apoptosis While NF-κB Activation Prevents Cell Death
inferredcites →https://doi.org/10.1016/s0092-8674(00)81466-xopenalex-snapshot
Complementation Cloning of NEMO, a Component of the IκB Kinase Complex Essential for NF-κB Activation
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(01)00237-9openalex-snapshot
The TNF and TNF Receptor Superfamilies
inferredcites →https://doi.org/10.1016/s0304-3835(00)00694-7openalex-snapshot
Poly(APD-ribosyl)ation, a DNA damage-driven protein modification and regulator of genomic instability
inferredcites →https://doi.org/10.1016/s0896-6273(00)80716-3openalex-snapshot
Caspase-8 Is Required for Cell Death Induced by Expanded Polyglutamine Repeats
inferredcites →https://doi.org/10.1016/s0896-6273(00)80727-8openalex-snapshot
The Jnk1 and Jnk2 Protein Kinases Are Required for Regional Specific Apoptosis during Early Brain Development
inferredcites →https://doi.org/10.1016/s0898-6568(01)00160-7openalex-snapshot
The TNF-receptor-associated factor family
inferredcites →https://doi.org/10.1016/s0952-7915(98)80167-2openalex-snapshot
Cytokine regulation of secondary lymphoid organ development
inferredcites →https://doi.org/10.1016/s0960-9822(07)00420-4openalex-snapshot
Essential requirement for caspase-8/FLICE in the initiation of the Fas-induced apoptotic cascade
inferredcites →https://doi.org/10.1016/s0960-9822(98)00019-0openalex-snapshot
Synergistic activation of SAPK1/JNK1 by two MAP kinase kinases in vitro
inferredcites →https://doi.org/10.1016/s0960-9822(98)70083-1openalex-snapshot
A model of the microtubule–kinesin complex based on electron cryomicroscopy and X-ray crystallography
inferredcites →https://doi.org/10.1016/s0960-9822(98)70121-6openalex-snapshot
MADD is highly homologous to a Rab3 guanine-nucleotide exchange protein (Rab3-GEP)
inferredcites →https://doi.org/10.1016/s0962-8924(01)02064-5openalex-snapshot
Signal transduction by tumor necrosis factor and its relatives
inferredcites →https://doi.org/10.1016/s0968-0004(00)01617-0openalex-snapshot
The Rel/NF-κB family: friend and foe
inferredcites →https://doi.org/10.1016/s0968-0004(97)01164-xopenalex-snapshot
Modularity in the TNF-receptor family
inferredcites →https://doi.org/10.1016/s1074-7613(00)80038-2openalex-snapshot
Impaired On/Off Regulation of TNF Biosynthesis in Mice Lacking TNF AU-Rich Elements
inferredcites →https://doi.org/10.1016/s1074-7613(00)80042-4openalex-snapshot
Embryonic Lethality, Liver Degeneration, and Impaired NF-κB Activation in IKK-β-Deficient Mice
inferredcites →https://doi.org/10.1016/s1074-7613(00)80183-1openalex-snapshot
Recruitment of the IKK Signalosome to the p55 TNF Receptor
inferredcites →https://doi.org/10.1016/s1074-7613(00)80194-6openalex-snapshot
The Distinct Roles of TRAF2 and RIP in IKK Activation by TNF-R1
inferredcites →https://doi.org/10.1016/s1074-7613(00)80211-3openalex-snapshot
FADD/MORT1 and Caspase-8 Are Recruited to TRAIL Receptors 1 and 2 and Are Essential for Apoptosis Mediated by TRAIL Receptor 2
inferredcites →https://doi.org/10.1016/s1074-7613(00)80212-5openalex-snapshot
Apo2L/TRAIL-Dependent Recruitment of Endogenous FADD and Caspase-8 to Death Receptors 4 and 5
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)80252-6openalex-snapshot
TNF-Dependent Recruitment of the Protein Kinase RIP to the TNF Receptor-1 Signaling Complex
inferredcites →https://doi.org/10.1016/s1074-7613(00)80390-8openalex-snapshot
TRAF2 Is Essential for JNK but Not NF-κB Activation and Regulates Lymphocyte Proliferation and Survival
inferredcites →https://doi.org/10.1016/s1074-7613(00)80391-xopenalex-snapshot
Early Lethality, Functional NF-κB Activation, and Increased Sensitivity to TNF-Induced Cell Death in TRAF2-Deficient Mice
inferredcites →https://doi.org/10.1016/s1074-7613(00)80535-xopenalex-snapshot
The Death Domain Kinase RIP Mediates the TNF-Induced NF-κB Signal
inferredcites →https://doi.org/10.1016/s1074-7613(00)80609-3openalex-snapshot
Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally
inferredcites →https://doi.org/10.1016/s1074-7613(01)00104-2openalex-snapshot
IKKβ Is Essential for Protecting T Cells from TNFα-Induced Apoptosis
inferredcites →https://doi.org/10.1016/s1074-7613(01)00207-2openalex-snapshot
TRAF1 Is a Negative Regulator of TNF Signaling
inferredcites →https://doi.org/10.1016/s1097-2765(00)00109-xopenalex-snapshot
JunD Protects Cells from p53-Dependent Senescence and Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80262-2openalex-snapshot
Female Mice Heterozygous for IKKγ/NEMO Deficiencies Develop a Dermatopathy Similar to the Human X-Linked Disorder Incontinentia Pigmenti
inferredcites →https://doi.org/10.1016/s1097-2765(00)80263-4openalex-snapshot
NEMO/IKKγ-Deficient Mice Model Incontinentia Pigmenti
inferredcites →https://doi.org/10.1016/s1097-2765(00)80283-xopenalex-snapshot
ASK1 Is Essential for JNK/SAPK Activation by TRAF2
inferredcites →https://doi.org/10.1016/s1097-2765(00)80445-1openalex-snapshot
IKKε Is Part of a Novel PMA-Inducible IκB Kinase Complex
inferredcites →https://doi.org/10.1016/s1097-2765(01)00361-6openalex-snapshot
Targeted Disruption of the ζPKC Gene Results in the Impairment of the NF-κB Pathway
inferredcites →https://doi.org/10.1016/s1097-2765(01)00380-xopenalex-snapshot
Blocking Caspase-3-Mediated Proteolysis of IKKβ Suppresses TNF-α-Induced Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(02)00450-1openalex-snapshot
TNF-Induced Recruitment and Activation of the IKK Complex Require Cdc37 and Hsp90
inferredcites →https://doi.org/10.1021/bi952182topenalex-snapshot
Human pro-Tumor Necrosis Factor Is a Homotrimer
inferredcites →https://doi.org/10.1038/12050openalex-snapshot
Apoptosis overrides survival signals through a caspase-mediated dominant-negative NF-κB loop
inferredcites →https://doi.org/10.1038/26261openalex-snapshot
IKK-γ is an essential regulatory subunit of the IκB kinase complex
inferredcites →https://doi.org/10.1038/316552a0openalex-snapshot
Identity of tumour necrosis factor and the macrophage-secreted factor cachectin
inferredcites →https://doi.org/10.1038/32681openalex-snapshot
Fas-mediated apoptosis and activation-induced T-cell proliferation are defective in mice lacking FADD/Mort1
inferredcites →https://doi.org/10.1038/337661a0openalex-snapshot
Prolonged activation of jun and collagenase genes by tumour necrosis factor-α
inferredcites →https://doi.org/10.1038/35008109openalex-snapshot
NAK is an IκB kinase-activating kinase
inferredcites →https://doi.org/10.1038/35008667openalex-snapshot
TRAIL receptor-2 signals apoptosis through FADD and caspase-8
inferredcites →https://doi.org/10.1038/35017574openalex-snapshot
Requirement for glycogen synthase kinase-3β in cell survival and NF-κB activation
inferredcites →https://doi.org/10.1038/35022514openalex-snapshot
Structural and biochemical basis of apoptotic activation by Smac/DIABLO
inferredcites →https://doi.org/10.1038/35065000openalex-snapshot
Mammalian MAP kinase signalling cascades
inferredcites →https://doi.org/10.1038/35071111openalex-snapshot
HIV-1 Nef inhibits ASK1-dependent death signalling providing a potential mechanism for protecting the infected host cell
inferredcites →https://doi.org/10.1038/35085008openalex-snapshot
Four deaths and a funeral: from caspases to alternative mechanisms
inferredcites →https://doi.org/10.1038/35104560openalex-snapshot
Induction of gadd45β by NF-κB downregulates pro-apoptotic JNK signalling
inferredcites →https://doi.org/10.1038/35104568openalex-snapshot
Inhibition of JNK activation through NF-κB target genes
inferredcites →https://doi.org/10.1038/376167a0openalex-snapshot
Embryonic lethality and liver degeneration in mice lacking the RelA component of NF-κB
inferredcites →https://doi.org/10.1038/377750a0openalex-snapshot
Activation of the SAPK pathway by the human STE20 homologue germinal centre kinase
inferredcites →https://doi.org/10.1038/378307a0openalex-snapshot
Phosphorylation of Raf by ceramide-activated protein kinase
inferredcites →https://doi.org/10.1038/385350a0openalex-snapshot
Stress-signalling kinase Sek1 protects thymocytes from apoptosis mediated by CD95 and CD3
inferredcites →https://doi.org/10.1038/385729a0openalex-snapshot
A metalloproteinase disintegrin that releases tumour-necrosis factor-α from cells
inferredcites →https://doi.org/10.1038/39899openalex-snapshot
Absence of excitotoxicity-induced apoptosis in the hippocampus of mice lacking the Jnk3 gene
inferredcites →https://doi.org/10.1038/41493openalex-snapshot
A cytokine-responsive IκB kinase that activates the transcription factor NF-κB
inferredcites →https://doi.org/10.1038/416345aopenalex-snapshot
TNF-RII and c-IAP1 mediate ubiquitination and degradation of TRAF2
inferredcites →https://doi.org/10.1038/43466openalex-snapshot
NF-κB activation by tumour necrosis factor requires the Akt serine–threonine kinase
inferredcites →https://doi.org/10.1038/43474openalex-snapshot
NF-κB is a target of AKT in anti-apoptotic PDGF signalling
inferredcites →https://doi.org/10.1038/6854openalex-snapshot
Amino-terminal phosphorylation of c-Jun regulates stress-induced apoptosis and cellular proliferation
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/10.1038/89769openalex-snapshot
The essential role of MEKK3 in TNF-induced NF-κB activation
inferredcites →https://doi.org/10.1038/ncb0502-e131openalex-snapshot
AP-1 as a regulator of cell life and death
inferredcites →https://doi.org/10.1038/ncb1201-1035openalex-snapshot
Regulation of microglial expression of integrins by poly(ADP-ribose) polymerase-1
inferredcites →https://doi.org/10.1038/nm0498-408openalex-snapshot
Evidence for the involvement of endotheliai cell integrin αVβ3 in the disruption of the tumor vascuiature induced by TNF and IFN-γ
inferredcites →https://doi.org/10.1038/scientificamerican0588-59openalex-snapshot
Tumor Necrosis Factor
inferredcites →https://doi.org/10.1038/sj.cdd.4400467openalex-snapshot
JNK/SAPK activity contributes to TRAIL-induced apoptosis
inferredcites →https://doi.org/10.1038/sj.cdd.4400821openalex-snapshot
Baculoviruses and apoptosis: the good, the bad, and the ugly
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.onc.1202094openalex-snapshot
TNF-α activates at least two apoptotic signaling cascades
inferredcites →https://doi.org/10.1038/sj.onc.1202975openalex-snapshot
Mediation of TNF receptor-associated factor effector functions by apoptosis signal-regulating kinase-1 (ASK1)
inferredcites →https://doi.org/10.1038/sj.onc.1203445openalex-snapshot
Somatic mutagenesis studies of NF-κB signaling in human T cells: evidence for an essential role of IKKγ in NF-κB activation by T-cell costimulatory signals and HTLV-I Tax protein
inferredcites →https://doi.org/10.1038/sj.onc.1203824openalex-snapshot
Caspase-8/FLICE functions as an executioner caspase in anticancer drug-induced apoptosis
inferredcites →https://doi.org/10.1038/sj.onc.1204570openalex-snapshot
NF-κB activation results in rapid inactivation of JNK in TNFα-treated Ewing sarcoma cells: a mechanism for the anti-apoptotic effect of NF-κB
inferredcites →https://doi.org/10.1038/sj.onc.1205348openalex-snapshot
Differential effects of JNK1 and JNK2 on signal specific induction of apoptosis
inferredcites →https://doi.org/10.1042/0264-6021:3510459openalex-snapshot
Phosphatidylcholine-specific phospholipase C and phospholipase D are respectively implicated in mitogen-activated protein kinase and nuclear factor κB activation in tumour-necrosis-factor-α-treated immature acute-myeloid-leukaemia cells
inferredcites →https://doi.org/10.1042/0264-6021:3590525openalex-snapshot
Type II tumour necrosis factor-α receptor (TNFR2) activates c-Jun N-terminal kinase (JNK) but not mitogen-activated protein kinase (MAPK) or p38 MAPK pathways
inferredcites →https://doi.org/10.1042/bj2890587openalex-snapshot
Tumour necrosis factor-α induces superoxide anion generation in mitochondria of L929 cells
inferredcites →https://doi.org/10.1042/bj3460641openalex-snapshot
Evidence for regulation of NF-κB by poly(ADP-ribose) polymerase
inferredcites →https://doi.org/10.1046/j.1432-1327.1998.2540439.xopenalex-snapshot
Apoptosis signaling by death receptors
inferredcites →https://doi.org/10.1053/jhep.2002.32534openalex-snapshot
NF-κB inhibition sensitizes hepatocytes to TNF-induced apoptosis through a sustained activation of JNK and c-Jun
inferredcites →https://doi.org/10.1056/nejmra002709openalex-snapshot
The Pathogenesis of Vasodilatory Shock
inferredcites →https://doi.org/10.1073/pnas.052712399openalex-snapshot
Poly(ADP-ribose) polymerase-1 dependence of stress-induced transcription factors and associated gene expression in glia
inferredcites →https://doi.org/10.1073/pnas.130176697openalex-snapshot
MEK kinase 1 gene disruption alters cell migration and c-Jun NH 2 -terminal kinase regulation but does not cause a measurable defect in NF-κB activation
inferredcites →https://doi.org/10.1073/pnas.90.7.2774openalex-snapshot
Mechanisms of rejection induced by tumor cell-targeted gene transfer of interleukin 2, interleukin 4, interleukin 7, tumor necrosis factor, or interferon gamma.
inferredcites →https://doi.org/10.1073/pnas.92.24.11294openalex-snapshot
Spontaneous inflammatory demyelinating disease in transgenic mice showing central nervous system-specific expression of tumor necrosis factor alpha.
inferredcites →https://doi.org/10.1073/pnas.93.13.6721openalex-snapshot
The tumor necrosis factor-inducible zinc finger protein A20 interacts with TRAF1/TRAF2 and inhibits NF-kappaB activation.
inferredcites →https://doi.org/10.1073/pnas.93.24.13973openalex-snapshot
The tumor necrosis factor receptor 2 signal transducers TRAF2 and c-IAP1 are components of the tumor necrosis factor receptor 1 signaling complex
inferredcites →https://doi.org/10.1073/pnas.94.15.8093openalex-snapshot
Characterization of tumor necrosis factor-deficient mice
inferredcites →https://doi.org/10.1073/pnas.94.18.9687openalex-snapshot
Activation of the c-Jun N-terminal kinase pathway by a novel protein kinase related to human germinal center kinase
inferredcites →https://doi.org/10.1073/pnas.94.18.9792openalex-snapshot
Tumor necrosis factor (TNF)-mediated kinase cascades: Bifurcation of Nuclear Factor-κB and c-jun N-terminal kinase (JNK/SAPK) pathways at TNF receptor-associated factor 2
inferredcites →https://doi.org/10.1073/pnas.94.19.10057openalex-snapshot
Suppression of tumor necrosis factor-induced cell death by inhibitor of apoptosis c-IAP2 is under NF-κB control
inferredcites →https://doi.org/10.1073/pnas.94.4.1441openalex-snapshot
Initiation of liver growth by tumor necrosis factor: Deficient liver regeneration in mice lacking type I tumor necrosis factor receptor
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.96.16.9136openalex-snapshot
NF-κB-mediated up-regulation of Bcl-x and Bfl-1/A1 is required for CD40 survival signaling in B lymphocytes
inferredcites →https://doi.org/10.1073/pnas.96.17.9803openalex-snapshot
Targeted disruption of Traf5 gene causes defects in CD40- and CD27-mediated lymphocyte activation
inferredcites →https://doi.org/10.1073/pnas.96.24.13978openalex-snapshot
Poly(ADP-ribose) polymerase is a mediator of necrotic cell death by ATP depletion
inferredcites →https://doi.org/10.1073/pnas.96.3.1042openalex-snapshot
Identification of a cell protein (FIP-3) as a modulator of NF-κB activity and as a target of an adenovirus inhibitor of tumor necrosis factor α-induced apoptosis
inferredcites →https://doi.org/10.1073/pnas.96.7.3763openalex-snapshot
Requirement of mitogen-activated protein kinase kinase 3 (MKK3) for tumor necrosis factor-induced cytokine expression
inferredcites →https://doi.org/10.1073/pnas.96.7.3775openalex-snapshot
Deletion of the loop region of Bcl-2 completely blocks paclitaxel-induced apoptosis
inferredcites →https://doi.org/10.1073/pnas.97.10.5243openalex-snapshot
MEK kinase 1 is critically required for c-Jun N-terminal kinase activation by proinflammatory stimuli and growth factor-induced cell migration
inferredcites →https://doi.org/10.1074/jbc.270.21.12343openalex-snapshot
Activation of the B-cell Surface Receptor CD40 Induces A20, a Novel Zinc Finger Protein That Inhibits Apoptosis
inferredcites →https://doi.org/10.1074/jbc.270.8.3574openalex-snapshot
Identification of a Protein with Homology to hsp90 That Binds the Type 1 Tumor Necrosis Factor Receptor
inferredcites →https://doi.org/10.1074/jbc.272.18.12069openalex-snapshot
MADD, a Novel Death Domain Protein That Interacts with the Type 1 Tumor Necrosis Factor Receptor and Activates Mitogen-activated Protein Kinase
inferredcites →https://doi.org/10.1074/jbc.272.40.25238openalex-snapshot
Bcl-2 Undergoes Phosphorylation by c-Jun N-terminal Kinase/Stress-activated Protein Kinases in the Presence of the Constitutively Active GTP-binding Protein Rac1
inferredcites →https://doi.org/10.1074/jbc.272.47.29419openalex-snapshot
Phosphorylation of IκB-α Inhibits Its Cleavage by Caspase CPP32 in Vitro
inferredcites →https://doi.org/10.1074/jbc.272.51.32102openalex-snapshot
Activation of Stress-activated Protein Kinase/c-Jun N-terminal Kinase, but Not NF-κB, by the Tumor Necrosis Factor (TNF) Receptor 1 through a TNF Receptor-associated Factor 2- and Germinal Center Kinase Related-dependent Pathway
inferredcites →https://doi.org/10.1074/jbc.273.10.5916openalex-snapshot
TNF Receptor Death Domain-associated Proteins TRADD and FADD Signal Activation of Acid Sphingomyelinase
inferredcites →https://doi.org/10.1074/jbc.273.17.10232openalex-snapshot
Early Activation of c-Jun N-terminal Kinase and p38 Kinase Regulate Cell Survival in Response to Tumor Necrosis Factor α
inferredcites →https://doi.org/10.1074/jbc.273.17.10362openalex-snapshot
Inhibition of the Expression of Mitogen-activated Protein Phosphatase-1 Potentiates Apoptosis Induced by Tumor Necrosis Factor-α in Rat Mesangial Cells
inferredcites →https://doi.org/10.1074/jbc.273.28.17477openalex-snapshot
Reactive Oxygen Species- and Dimerization-induced Activation of Apoptosis Signal-regulating Kinase 1 in Tumor Necrosis Factor-α Signal Transduction
inferredcites →https://doi.org/10.1074/jbc.273.35.22681openalex-snapshot
Tumor Necrosis Factor Signaling to Stress-activated Protein Kinase (SAPK)/Jun NH2-terminal Kinase (JNK) and p38
inferredcites →https://doi.org/10.1074/jbc.273.38.24832openalex-snapshot
Regulation of Interleukin-1β-induced Interleukin-6 Gene Expression in Human Fibroblast-like Synoviocytes by p38 Mitogen-activated Protein Kinase
inferredcites →https://doi.org/10.1074/jbc.273.47.31245openalex-snapshot
Tumor Necrosis Factor Induces Ceramide Oscillations and Negatively Controls Sphingolipid Synthases by Caspases in Apoptotic Kym-1 Cells
inferredcites →https://doi.org/10.1074/jbc.273.49.33091openalex-snapshot
TRAIL/Apo2L Activates c-Jun NH2-terminal Kinase (JNK) via Caspase-dependent and Caspase-independent Pathways
inferredcites →https://doi.org/10.1074/jbc.273.6.3285openalex-snapshot
p38 and Extracellular Signal-regulated Kinase Mitogen-activated Protein Kinase Pathways Are Required for Nuclear Factor-κB p65 Transactivation Mediated by Tumor Necrosis Factor
inferredcites →https://doi.org/10.1074/jbc.273.7.4027openalex-snapshot
Correlation between Sustained c-Jun N-terminal Protein Kinase Activation and Apoptosis Induced by Tumor Necrosis Factor-α in Rat Mesangial Cells
inferredcites →https://doi.org/10.1074/jbc.274.13.8531openalex-snapshot
Tumor Necrosis Factor Induces Bcl-2 and Bcl-x Expression through NFκB Activation in Primary Hippocampal Neurons
inferredcites →https://doi.org/10.1074/jbc.274.15.10203openalex-snapshot
Inhibition of Receptor Internalization by Monodansylcadaverine Selectively Blocks p55 Tumor Necrosis Factor Receptor Death Domain Signaling
inferredcites →https://doi.org/10.1074/jbc.274.18.12722openalex-snapshot
A Novel Pathway for Tumor Necrosis Factor-α and Ceramide Signaling Involving Sequential Activation of Tyrosine Kinase, p21 , and Phosphatidylinositol 3-Kinase
inferredcites →https://doi.org/10.1074/jbc.274.19.13594openalex-snapshot
Regulation of NF-κB RelA Phosphorylation and Transcriptional Activity by p21 and Protein Kinase Cζ in Primary Endothelial Cells
inferredcites →https://doi.org/10.1074/jbc.274.27.19368openalex-snapshot
The Human Tumor Necrosis Factor (TNF) Receptor-associated Factor 1 Gene (TRAF1) Is Up-regulated by Cytokines of the TNF Ligand Family and Modulates TNF-induced Activation of NF-κB and c-Jun N-terminal Kinase
inferredcites →https://doi.org/10.1074/jbc.274.27.19411openalex-snapshot
Tumor Necrosis Factor Induces Phosphorylation and Translocation of BAD through a Phosphatidylinositide-3-OH Kinase-dependent Pathway
inferredcites →https://doi.org/10.1074/jbc.274.34.24372openalex-snapshot
Roles of Phosphatidylinositol 3-Kinase and Rac in the Nuclear Signaling by Tumor Necrosis Factor-α in Rat-2 Fibroblasts
inferredcites →https://doi.org/10.1074/jbc.274.4.2118openalex-snapshot
A Novel Human STE20-related Protein Kinase, HGK, That Specifically Activates the c-Jun N-terminal Kinase Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.274.43.30729openalex-snapshot
TNIK, a Novel Member of the Germinal Center Kinase Family That Activates the c-Jun N-terminal Kinase Pathway and Regulates the Cytoskeleton
inferredcites →https://doi.org/10.1074/jbc.274.51.36817openalex-snapshot
Resistance to the Cytotoxic Effects of Tumor Necrosis Factor α Can Be Overcome by Inhibition of a FADD/Caspase-dependent Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.274.9.5259openalex-snapshot
Signaling by the Germinal Center Kinase Family of Protein Kinases
inferredcites →https://doi.org/10.1074/jbc.274.9.5267openalex-snapshot
Requirement of FADD for Tumor Necrosis Factor-induced Activation of Acid Sphingomyelinase
inferredcites →https://doi.org/10.1074/jbc.275.13.9303openalex-snapshot
Caspase-8 Activation and Bid Cleavage Contribute to MCF7 Cellular Execution in a Caspase-3-dependent Manner during Staurosporine-mediated Apoptosis
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.275.17.12684openalex-snapshot
Selective Involvement of Superoxide Anion, but Not Downstream Compounds Hydrogen Peroxide and Peroxynitrite, in Tumor Necrosis Factor-α-induced Apoptosis of Rat Mesangial Cells
inferredcites →https://doi.org/10.1074/jbc.275.5.3305openalex-snapshot
The hsp90-related Protein TRAP1 Is a Mitochondrial Protein with Distinct Functional Properties
inferredcites →https://doi.org/10.1074/jbc.c100340200openalex-snapshot
A Kinase-independent Function of Ask1 in Caspase-independent Cell Death
inferredcites →https://doi.org/10.1074/jbc.m000811200openalex-snapshot
Inhibition of Death Receptor-mediated Gene Induction by a Cycloheximide-sensitive Factor Occurs at the Level of or Upstream of Fas-associated Death Domain Protein (FADD)
inferredcites →https://doi.org/10.1074/jbc.m001009200openalex-snapshot
NESK, a Member of the Germinal Center Kinase Family That Activates the c-Jun N-terminal Kinase Pathway and Is Expressed during the Late Stages of Embryogenesis
inferredcites →https://doi.org/10.1074/jbc.m001358200openalex-snapshot
Tumor Necrosis Factor α-induced Phosphorylation of RelA/p65 on Ser529 Is Controlled by Casein Kinase II
inferredcites →https://doi.org/10.1074/jbc.m003280200openalex-snapshot
Sensitization to Death Receptor Cytotoxicity by Inhibition of Fas-associated Death Domain Protein (FADD)/Caspase Signaling
inferredcites →https://doi.org/10.1074/jbc.m003412200openalex-snapshot
Execution of Apoptosis Signal-regulating Kinase 1 (ASK1)-induced Apoptosis by the Mitochondria-dependent Caspase Activation
inferredcites →https://doi.org/10.1074/jbc.m006353200openalex-snapshot
Cell Autonomous Apoptosis Defects in Acid Sphingomyelinase Knockout Fibroblasts
inferredcites →https://doi.org/10.1074/jbc.m008343200openalex-snapshot
Caspase-mediated Cleavage of Hematopoietic Progenitor Kinase 1 (HPK1) Converts an Activator of NFκB into an Inhibitor of NFκB
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Reverse Signalling
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Signalling by Cytokines
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An Adaptive Role for TNFα in Synaptic Plasticity and Neuronal Function
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Mechanisms of Tumor Necrosis Factor‐induced Cell Death
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Redox Regulation of Apoptosis in Immune Cells
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Silicate Nanoplatelets Promotes Neuronal Differentiation of Neural Stem Cells and Restoration of Spinal Cord Injury
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Triazine‐Trione Thermosets with High Processability for Scaffold Applications in Bone Tissue Engineering
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Development of a New Positron Emission Tomography Imaging Radioligand Targeting RIPK1 in the Brain and Characterization in Alzheimer's Disease
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Tumor necrosis factor‐α regulates interleukin‐33 expression through extracellular signal‐regulated kinase, p38, and nuclear factor–κB pathways in airway epithelial cells
inferred← citeshttps://doi.org/10.1002/alr.21855openalex-snapshot
Role of the type I tumor necrosis factor receptor in inflammation‐associated olfactory dysfunction
inferred← citeshttps://doi.org/10.1002/ange.200907360openalex-snapshot
Structure‐Based Discovery of Natural‐Product‐like TNF‐α Inhibitors
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A Metal‐Based Inhibitor of Tumor Necrosis Factor‐α
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Structure‐Based Discovery of Natural‐Product‐like TNF‐α Inhibitors
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A Metal‐Based Inhibitor of Tumor Necrosis Factor‐α
inferred← citeshttps://doi.org/10.1002/ar.a.20229openalex-snapshot
Tumor necrosis factor‐α‐induced changes in insulin‐producing β‐cells
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Neutrophils from patients with TNFRSF1A mutations display resistance to tumor necrosis factor–induced apoptosis: Pathogenetic and clinical implications
inferred← citeshttps://doi.org/10.1002/art.23123openalex-snapshot
Abnormal tumor necrosis factor receptor I cell surface expression and NF‐κB activation in tumor necrosis factor receptor–associated periodic syndrome
inferred← citeshttps://doi.org/10.1002/art.24145openalex-snapshot
Tumor necrosis factor receptor–associated periodic syndrome: Toward a molecular understanding of the systemic autoinflammatory diseases
inferred← citeshttps://doi.org/10.1002/art.24905openalex-snapshot
The 423Q polymorphism of the X‐linked inhibitor of apoptosis gene influences monocyte function and is associated with periodic fever
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Selective Blockade of Tumor Necrosis Factor Receptor I Inhibits Proinflammatory Cytokine and Chemokine Production in Human Rheumatoid Arthritis Synovial Membrane Cell Cultures
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Selective Activation of Tumor Necrosis Factor Receptor II Induces Antiinflammatory Responses and Alleviates Experimental Arthritis
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The isoform‐specific functions of the c‐Jun N‐terminal Kinases (JNKs): differences revealed by gene targeting
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Skin regenerative potentials of curcumin
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Morin exerts neuroprotection via attenuation of ROS induced oxidative damage and neuroinflammation in experimental diabetic neuropathy
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Survival and apoptotic pathways initiated by TNF‐α: Modeling and predictions
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Tumor necrosis factor‐α regulates matrix metalloproteinase‐2 expression and cell migration via ERK pathway in rat glomerular mesangial cells
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Gold‐Catalyzed Cycloisomerization and Diels–Alder Reaction of 1,4,9‐Dienyne Esters to 3 a,6‐Methanoisoindole Esters with Pro‐Inflammatory Cytokine Antagonist Activity
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Structure‐Based Repurposing of FDA‐Approved Drugs as TNF‐α Inhibitors
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Death receptor expression is associated with poor response to chemotherapy and shorter survival in metastatic ovarian carcinoma
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Fever, Immunity, and Molecular Adaptations
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Trans‐System Mechanisms Against Ischemic Myocardial Injury
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IgG promotes TNF‐α induced osteoclastogenesis by upregulating the expression of TNFR1 and the NF‐κB signalling pathway
inferred← citeshttps://doi.org/10.1002/dc.21095openalex-snapshot
Cell survival and apoptosis‐related molecules in cancer cells in effusions: A comprehensive review
inferred← citeshttps://doi.org/10.1002/ece3.5724openalex-snapshot
Differential gene expression in chronic wasting disease‐positive white‐tailed deer (Odocoileus virginianus)
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Calcium and 1α,25‐dihydroxyvitamin D3 target the TNF‐α pathway to suppress experimental inflammatory bowel disease
inferred← citeshttps://doi.org/10.1002/eji.200425818openalex-snapshot
GITR: a multifaceted regulator of immunity belonging to the tumor necrosis factor receptor superfamily
inferred← citeshttps://doi.org/10.1002/eji.202048988openalex-snapshot
TNFR2 expression is a hallmark of human memory B cells with suppressive function
inferred← citeshttps://doi.org/10.1002/glia.20089openalex-snapshot
Astroglial‐derived lymphotoxin‐α exacerbates inflammation and demyelination, but not remyelination
inferred← citeshttps://doi.org/10.1002/glia.22401openalex-snapshot
Proinflammatory cytokine regulation of cyclic AMP‐phosphodiesterase 4 signaling in microglia in vitro and following CNS injury
inferred← citeshttps://doi.org/10.1002/hep.20174openalex-snapshot
Topoisomerase inhibitor camptothecin sensitizes mouse hepatocytes in vitro and in vivo to TNF-mediated apoptosis
inferred← citeshttps://doi.org/10.1002/hep.22541openalex-snapshot
Switch from type II to I Fas/CD95 death signaling on in vitro culturing of primary hepatocytes
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.23945openalex-snapshot
Mmp23b Promotes Liver Development and Hepatocyte Proliferation Through the Tumor Necrosis Factor Pathway in Zebrafish
inferred← citeshttps://doi.org/10.1002/hep.24239openalex-snapshot
Ron receptor regulates Kupffer cell-dependent cytokine production and hepatocyte survival following endotoxin exposure in mice
inferred← citeshttps://doi.org/10.1002/hup.2301openalex-snapshot
Levels of TNF‐α, soluble TNF receptors (sTNFR1, sTNFR2), and cognition in bipolar disorder
inferred← citeshttps://doi.org/10.1002/iid3.197openalex-snapshot
T cells responding to Trypanosoma cruzi detected by membrane TNF‐α and CD154 in chagasic patients
inferred← citeshttps://doi.org/10.1002/ijc.21734openalex-snapshot
TAK1‐mediated stress signaling pathways are essential for TNF‐α‐promoted pulmonary metastasis of murine colon cancer cells
inferred← citeshttps://doi.org/10.1002/ijc.24789openalex-snapshot
Inflammatory disease and cancer with a decrease in Kupffer cell numbers in Nucling‐knockout mice
inferred← citeshttps://doi.org/10.1002/ijc.25232openalex-snapshot
Elevated expression of tumor necrosis factor‐α signaling molecules in colonic tumors of Zucker obese (fa/fa) rats
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2014.tb00544.xopenalex-snapshot
Fever, Immunity, and Molecular Adaptations
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2015.tb00606.xopenalex-snapshot
Trans‐System Mechanisms Against Ischemic Myocardial Injury
inferred← citeshttps://doi.org/10.1002/jat.3543openalex-snapshot
Protective effect of metoclopramide against organophosphate‐induced apoptosis in the murine skin fibroblast L929
inferred← citeshttps://doi.org/10.1002/jbt.22424openalex-snapshot
Anti‐inflammatory effects of doxepin hydrochloride against LPS‐induced C6‐glioma cell inflammatory reaction by PI3K‐mediated Akt signaling
inferred← citeshttps://doi.org/10.1002/jbt.70585openalex-snapshot
Protective Role of Coenzyme Q10 Against Isoniazid and Rifampicin‐Induced Hepatotoxicity in Rats via Modulation of PPAR‐γ, iNOS, and NF‐κB
inferred← citeshttps://doi.org/10.1002/jcb.20569openalex-snapshot
Sp1 and Sp3 regulate the basal transcription of receptor activator of nuclear factor kappa B ligand gene in osteoblasts and bone marrow stromal cells
inferred← citeshttps://doi.org/10.1002/jcb.22068openalex-snapshot
Secretory products from human adipocytes stimulate proinflammatory cytokine secretion from human endothelial cells
inferred← citeshttps://doi.org/10.1002/jcb.24227openalex-snapshot
Apoptosis signal‐regulating kinase 1 is mediated in TNF‐α‐induced CCL2 expression in human synovial fibroblasts
inferred← citeshttps://doi.org/10.1002/jcb.24441openalex-snapshot
Kallikrein‐binding protein inhibits LPS‐induced TNF‐α by upregulating SOCS3 expression
inferred← citeshttps://doi.org/10.1002/jcb.26152openalex-snapshot
Tumor Necrosis Factor‐α Induced Apoptosis in U937 Cells Promotes Cathepsin D‐Independent Stefin B Degradation
inferred← citeshttps://doi.org/10.1002/jcb.27807openalex-snapshot
Effects of alpha lipoic acid and its derivative “andrographolid‐lipoic acid‐1” on ulcerative colitis: A systematic review with meta‐analysis of animal studies
inferred← citeshttps://doi.org/10.1002/jcb.30173openalex-snapshot
Review of cancer cell resistance mechanisms to apoptosis and actual targeted therapies
inferred← citeshttps://doi.org/10.1002/jcp.21070openalex-snapshot
Psychosine‐induced apoptosis and cytokine activation in immune peripheral cells of Krabbe patients
inferred← citeshttps://doi.org/10.1002/jcp.21142openalex-snapshot
Enamel matrix derivative protects human gingival fibroblasts from TNF‐induced apoptosis by inhibiting caspase activation
inferred← citeshttps://doi.org/10.1002/jcp.22221openalex-snapshot
TRUSS, TNF‐R1, and TRPC ion channels synergistically reverse endoplasmic reticulum Ca2+ storage reduction in response to m1 muscarinic acetylcholine receptor signaling
inferred← citeshttps://doi.org/10.1002/jcp.22805openalex-snapshot
Distinct cellular responses induced by saporin and a transferrin–saporin conjugate in two different human glioblastoma cell lines
inferred← citeshttps://doi.org/10.1002/jcp.24256openalex-snapshot
Tumor necrosis factor‐α enhances the transcription of smad ubiquitination regulatory factor 1 in an activating protein‐1‐ and runx2‐dependent manner
inferred← citeshttps://doi.org/10.1002/jcp.25186openalex-snapshot
Stress‐Induced Activation of Apoptosis Signal‐Regulating Kinase 1 Promotes Osteoarthritis
inferred← citeshttps://doi.org/10.1002/jcp.25438openalex-snapshot
Ascorbic Acid Induces Necrosis in Human Laryngeal Squamous Cell Carcinoma via ROS, PKC, and Calcium Signaling
inferred← citeshttps://doi.org/10.1002/jcp.27265openalex-snapshot
HDAC1/2‐mediated regulation of JNK and ERK phosphorylation in bovine mammary epithelial cells in response to TNF‐α
inferred← citeshttps://doi.org/10.1002/jcp.29743openalex-snapshot
KIF15 promotes the evolution of gastric cancer cells through inhibition of reactive oxygen species‐mediated apoptosis
inferred← citeshttps://doi.org/10.1002/jcp.31176openalex-snapshot
Epitranscriptomics m 6 A analyses reveal distinct m 6 A marks under tumor necrosis factor α (TNF‐α)‐induced apoptotic conditions in HeLa cells
inferred← citeshttps://doi.org/10.1002/jgm.3010openalex-snapshot
Low penetrance genetic polymorphisms as potential biomarkers for colorectal cancer predisposition
inferred← citeshttps://doi.org/10.1002/jlb.2ma0121-082ropenalex-snapshot
Differential role of TNFR1 and TNFR2 in the development of imiquimod-induced mouse psoriasis
inferred← citeshttps://doi.org/10.1002/jlb.2mr0120-510ropenalex-snapshot
Distinct modes of TNF signaling through its two receptors in health and disease
inferred← citeshttps://doi.org/10.1002/jmv.25588openalex-snapshot
Chikungunya virus modulates the miRNA expression patterns in human synovial fibroblasts
inferred← citeshttps://doi.org/10.1002/jnr.10878openalex-snapshot
TNFα increases activity of γ‐glutamyl transpeptidase in cultured rat astroglial cells
inferred← citeshttps://doi.org/10.1002/jnr.20531openalex-snapshot
Microglia-derived tumor necrosis factor-α exaggerates death of newborn hippocampal progenitor cells in vitro
inferred← citeshttps://doi.org/10.1002/jnr.21253openalex-snapshot
A decoy oligonucleotide inhibiting nuclear factor‐κB binding to the IgGκB consensus site reduces cerebral injury and apoptosis in neonatal hypoxic‐ischemic encephalopathy
inferred← citeshttps://doi.org/10.1002/jnr.21697openalex-snapshot
Preconditioning with cobalt chloride or desferrioxamine protects oligodendrocyte cell line (MO3.13) from tumor necrosis factor‐α‐mediated cell death
inferred← citeshttps://doi.org/10.1002/jnr.23409openalex-snapshot
Propofol anesthesia induces proapoptotic tumor necrosis factor‐α and pro‐nerve growth factor signaling and prosurvival Akt and XIAP expression in neonatal rat brain
inferred← citeshttps://doi.org/10.1002/jsp2.70011openalex-snapshot
Targeting nucleus pulposus cell death in the treatment of intervertebral disc degeneration
inferred← citeshttps://doi.org/10.1002/kjm2.70201openalex-snapshot
Protective Effects of Riociguat Against Contrast‐Induced Nephropathy: An Experimental and Machine Learning‐Based Study in Rats
inferred← citeshttps://doi.org/10.1002/lary.23190openalex-snapshot
Tumor necrosis factor‐α receptor expression correlates with mucosal changes and biofilm presence in chronic rhinosinusitis with nasal polyposis
inferred← citeshttps://doi.org/10.1002/mc.21990openalex-snapshot
IL‐32γ enhances TNF‐α‐induced cell death in colon cancer
inferred← citeshttps://doi.org/10.1002/med.21273openalex-snapshot
The Generation, Detection, and Effects of Reactive Drug Metabolites
inferred← citeshttps://doi.org/10.1002/med.21893openalex-snapshot
Inflammatory bowel disease biomarkers
inferred← citeshttps://doi.org/10.1002/minf.201800011openalex-snapshot
3D Modeling of Tumor Necrosis Factor Receptor and Tumor Necrosis Factor‐bound Receptor Systems
inferred← citeshttps://doi.org/10.1002/prca.201200087openalex-snapshot
Apolipoprotein A ‐ I : Insights from redox proteomics for its role in neurodegeneration
inferred← citeshttps://doi.org/10.1002/pro.70817openalex-snapshot
Structural dynamics and pH ‐regulated membrane binding of the TRAF2 ‐ NC trimer
inferred← citeshttps://doi.org/10.1002/rmb2.12489openalex-snapshot
The impact of oocyte death on mouse primordial follicle formation and ovarian reserve
inferred← citeshttps://doi.org/10.1002/rnc.1786openalex-snapshot
Steady‐state robustness of qualitative gene regulation networks
inferred← citeshttps://doi.org/10.1002/stem.2819openalex-snapshot
In Vitro Fusion of Normal and Neoplastic Breast Epithelial Cells with Human Mesenchymal Stroma/Stem Cells Partially Involves Tumor Necrosis Factor Receptor Signaling
inferred← citeshttps://doi.org/10.1007/0-387-30395-2_9openalex-snapshot
TNF-α in CNS: Physiologic and Pathologic Roles
inferred← citeshttps://doi.org/10.1007/0-387-34573-6_6openalex-snapshot
Fas—More Than an Apoptosis Inducer
inferred← citeshttps://doi.org/10.1007/1-4020-8107-3_14openalex-snapshot
Molecular Signaling in Thyroid Cancer
inferred← citeshttps://doi.org/10.1007/3-540-27194-5_10openalex-snapshot
Nature and Function of Hepatic Tumor Necrosis Factor-α Signaling
inferred← citeshttps://doi.org/10.1007/400_2008_22openalex-snapshot
Death Ligands Designed to Kill: Development and Application of Targeted Cancer Therapeutics Based on Proapoptotic TNF Family Ligands
inferred← citeshttps://doi.org/10.1007/400_2008_23openalex-snapshot
Impact of TNF-R1 and CD95 Internalization on Apoptotic and Antiapoptotic Signaling
inferred← citeshttps://doi.org/10.1007/400_2008_26openalex-snapshot
The Role of TNF in Cancer
inferred← citeshttps://doi.org/10.1007/4243_2012_60openalex-snapshot
TNF Receptor Membrane Dynamics Studied with Fluorescence Microscopy and Spectroscopy
inferred← citeshttps://doi.org/10.1007/978-0-387-34133-0_5openalex-snapshot
Chondrocyte Signaling and Artificial Matrices for Articular Cartilage Engineering
inferred← citeshttps://doi.org/10.1007/978-0-387-69147-3_5openalex-snapshot
Interrelationship of the Fanconi Anemia/BRCA Pathway
inferred← citeshttps://doi.org/10.1007/978-0-387-70630-6_2openalex-snapshot
TRAF1 and Its Biological Functions
inferred← citeshttps://doi.org/10.1007/978-0-387-70830-0_1openalex-snapshot
Inflammation and Neuronal Susceptibility to Excitotoxic Cell Death
inferred← citeshttps://doi.org/10.1007/978-0-387-73894-9_5openalex-snapshot
Cytokines in CNS Inflammation and Disease
inferred← citeshttps://doi.org/10.1007/978-0-387-77976-8_3openalex-snapshot
Cytokine Receptors and Signaling
inferred← citeshttps://doi.org/10.1007/978-0-387-84851-8_4openalex-snapshot
Molecular Basis of Cytokine Function
inferred← citeshttps://doi.org/10.1007/978-0-85729-697-9_3openalex-snapshot
Ovarian/Primary Peritoneal Carcinoma
inferred← citeshttps://doi.org/10.1007/978-0-85729-697-9_9openalex-snapshot
Ovarian/Primary Peritoneal Carcinoma
inferred← citeshttps://doi.org/10.1007/978-1-0716-1450-1_2openalex-snapshot
Treatment of Autoimmune Diseases with Therapeutic Antibodies: Lessons Learned from PID Patients Allow for Stratification of the Infection Risk
inferred← citeshttps://doi.org/10.1007/978-1-4419-0131-6_5openalex-snapshot
Targeting of Apoptosis Signaling Pathways and Their Mediators for Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-1-4419-6612-4_59openalex-snapshot
TNFR2 – Target for Therapeutics Against Neurodegenerative Diseases?
inferred← citeshttps://doi.org/10.1007/978-1-4419-6612-4_65openalex-snapshot
TNF/TNF Receptor 1-Mediated Apoptosis in Hepatocytes
inferred← citeshttps://doi.org/10.1007/978-1-4419-6612-4_66openalex-snapshot
Regulation of Cell Death by c-FLIP Phosphorylation
inferred← citeshttps://doi.org/10.1007/978-1-4419-7104-3_2openalex-snapshot
Molecular Mechanisms of Neuronal Death
inferred← citeshttps://doi.org/10.1007/978-1-4419-8999-4_23openalex-snapshot
Overview of Cytokine Structure and Function
inferred← citeshttps://doi.org/10.1007/978-1-4419-9072-3_22openalex-snapshot
A Paradigm for Gene Regulation: Inflammation, NF-κB and PPAR
inferred← citeshttps://doi.org/10.1007/978-1-4614-4009-3_5openalex-snapshot
Systems Biology of Cell Death in Hepatocytes
inferred← citeshttps://doi.org/10.1007/978-1-4614-8256-7_15openalex-snapshot
Cytokines in Inflammatory Bowel Disease
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/10.1007/978-1-59745-221-2_2openalex-snapshot
The Extrinsic Pathway of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-59745-518-3_27openalex-snapshot
Role of Immune Response in Nonalcoholic Fatty Liver Disease
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_24openalex-snapshot
Apoptosis in Liver Injury and Liver Diseases
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_29openalex-snapshot
Lysosomal Proteases in Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_5openalex-snapshot
The Death Receptor Pathway
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_8openalex-snapshot
Reactive Oxygen Species in Cell Fate Decisions
inferred← citeshttps://doi.org/10.1007/978-1-60327-530-9_10openalex-snapshot
The NF-κB Transcription Factor Pathway as a Therapeutic Target in Cancer: Methods for Detection of NF-κB Activity
inferred← citeshttps://doi.org/10.1007/978-1-60327-538-5_12openalex-snapshot
Signalling in Immune Reactions
inferred← citeshttps://doi.org/10.1007/978-1-61779-391-2_4openalex-snapshot
C-Peptide Signaling in the Kidney and Protection from Diabetic Nephropathy
inferred← citeshttps://doi.org/10.1007/978-3-030-11815-0_14openalex-snapshot
Pathogenesis of Gestational Diabetes Mellitus
inferred← citeshttps://doi.org/10.1007/978-3-030-19055-2_13openalex-snapshot
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS)
inferred← citeshttps://doi.org/10.1007/978-3-030-19922-7_2openalex-snapshot
Modulation of the Innate Immune System
inferred← citeshttps://doi.org/10.1007/978-3-030-19922-7_7openalex-snapshot
Mechanisms of Autoimmunity and Pharmacologic Treatments
inferred← citeshttps://doi.org/10.1007/978-3-030-22827-9_7openalex-snapshot
Biologics Targeting Tumor Necrosis Factor
inferred← citeshttps://doi.org/10.1007/978-3-030-43093-1_9openalex-snapshot
Extracellular Vesicles in the Tumor Microenvironment: Various Implications in Tumor Progression
inferred← citeshttps://doi.org/10.1007/978-3-030-98256-0_14openalex-snapshot
Regenerative Medicine Procedures Under Ultrasound Guidance
inferred← citeshttps://doi.org/10.1007/978-3-031-25519-9_15openalex-snapshot
Pathogenesis of Gestational Diabetes Mellitus
inferred← citeshttps://doi.org/10.1007/978-3-031-39721-9_2openalex-snapshot
Obesity and Inflammation
inferred← citeshttps://doi.org/10.1007/978-3-031-92785-0_1openalex-snapshot
Molecular Cell Biology of Apoptosis in Health and Disease
inferred← citeshttps://doi.org/10.1007/978-3-032-10997-2_1openalex-snapshot
Mechanisms of Liver Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-0346-0168-9_2openalex-snapshot
Heterogeneity in responses of microvascular endothelial cells during inflammation
inferred← citeshttps://doi.org/10.1007/978-3-0348-0837-8_9openalex-snapshot
The Role of Inflammation in Kidney Cancer
inferred← citeshttps://doi.org/10.1007/978-3-211-85578-2_80openalex-snapshot
Effect of traumatic brain injury on cognitive function in mice lacking p55 and p75 tumor necrosis factor receptors
inferred← citeshttps://doi.org/10.1007/978-3-319-04111-7_4openalex-snapshot
Contribution of Receptors, Transcription Factors, and Genes in the Induction of Neuroinflammation
inferred← citeshttps://doi.org/10.1007/978-3-319-17807-3_11openalex-snapshot
Pancreatic Cancer Resistance to TRAIL Therapy: Regulators of the Death Inducing Signaling Complex
inferred← citeshttps://doi.org/10.1007/978-3-319-28558-0_8openalex-snapshot
Cancer-Induced Fatigue and Cachexia
inferred← citeshttps://doi.org/10.1007/978-3-319-28576-4_2openalex-snapshot
The Putative Role of Measles Virus in the Pathogenesis of Otosclerosis
inferred← citeshttps://doi.org/10.1007/978-3-319-30273-7_3openalex-snapshot
Cytokine Receptors and Signaling
inferred← citeshttps://doi.org/10.1007/978-3-319-53659-0_6openalex-snapshot
NF-κB and Its Implication in Liver Health and Cancer Development
inferred← citeshttps://doi.org/10.1007/978-3-319-58106-4_6openalex-snapshot
Beta-Catenin and the Survival of Hepatocytes
inferred← citeshttps://doi.org/10.1007/978-3-319-59963-2_1openalex-snapshot
Comorbidity in Rheumatic Diseases
inferred← citeshttps://doi.org/10.1007/978-3-319-66884-0_13openalex-snapshot
Tumor Necrosis Factor Inhibition
inferred← citeshttps://doi.org/10.1007/978-3-319-76478-8_9openalex-snapshot
Ovarian Cancer
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_14openalex-snapshot
Absolute Threshold
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_3868openalex-snapshot
Neuroinflammation: Brain and Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/978-3-540-72569-5_5openalex-snapshot
Effektorreaktionen von angeborener und erworbener Immunität
inferred← citeshttps://doi.org/10.1007/978-3-642-00150-5_10openalex-snapshot
TNF/TNF Receptors
inferred← citeshttps://doi.org/10.1007/978-3-642-16135-3_29openalex-snapshot
Global Uncertainty Analysis for a Model of TNF-Induced NF-κB Signalling
inferred← citeshttps://doi.org/10.1007/978-3-662-60410-6_56openalex-snapshot
TRAPS bei Kindern und Jugendlichen
inferred← citeshttps://doi.org/10.1007/978-3-662-60411-3_56-1openalex-snapshot
TRAPS bei Kindern und Jugendlichen
inferred← citeshttps://doi.org/10.1007/978-4-431-87704-2_11openalex-snapshot
The Apoptotic Signaling Network Dynamically Interprets the Outputs of Individual Signaling Pathways in an Early Analog and Late Digital Manner
inferred← citeshttps://doi.org/10.1007/978-90-481-2976-8_1openalex-snapshot
Role of HSF1 in Infectious Disease
inferred← citeshttps://doi.org/10.1007/978-90-481-9713-2_9openalex-snapshot
Nuclear Apoptosis and Sarcopenia
inferred← citeshttps://doi.org/10.1007/978-94-007-6331-9_1openalex-snapshot
Sphingomyelin and Its Role in Cellular Signaling
inferred← citeshttps://doi.org/10.1007/978-981-10-2041-4_4openalex-snapshot
Inflammation and Fibrosis in ADPKD
inferred← citeshttps://doi.org/10.1007/978-981-13-9077-7_1openalex-snapshot
Lipid Homeostasis on Cell Membrane
inferred← citeshttps://doi.org/10.1007/978-981-15-1568-2_14openalex-snapshot
Oxidative Stress and Inflammation Can Fuel Cancer
inferred← citeshttps://doi.org/10.1007/978-981-32-9393-9_8openalex-snapshot
Role of Inflammatory Cytokines in the Initiation and Progression of Pancreatic Cancer
inferred← citeshttps://doi.org/10.1007/s00005-011-0133-2openalex-snapshot
Soluble TNF-α Receptor I Encoded on Plasmid Vector and Its Application in Experimental Gene Therapy of Radiation-Induced Lung Fibrosis
inferred← citeshttps://doi.org/10.1007/s00011-013-0633-0openalex-snapshot
TNF-α signalling and inflammation: interactions between old acquaintances
inferred← citeshttps://doi.org/10.1007/s00011-017-1029-3openalex-snapshot
HCV-induced regulatory alterations of IL-1β, IL-6, TNF-α, and IFN-ϒ operative, leading liver en-route to non-alcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1007/s00018-007-7063-5openalex-snapshot
Adult hippocampal neurogenesis: regulation by HIV and drugs of abuse
inferred← citeshttps://doi.org/10.1007/s00018-013-1431-0openalex-snapshot
Domain structure and function of matrix metalloprotease 23 (MMP23): role in potassium channel trafficking
inferred← citeshttps://doi.org/10.1007/s00018-014-1757-2openalex-snapshot
Cell death controlling complexes and their potential therapeutic role
inferred← citeshttps://doi.org/10.1007/s00018-018-2757-4openalex-snapshot
SLC52A3 expression is activated by NF-κB p65/Rel-B and serves as a prognostic biomarker in esophageal cancer
inferred← citeshttps://doi.org/10.1007/s00018-021-03900-zopenalex-snapshot
TRIMs: selective recruitment at different steps of the NF-κB pathway—determinant of activation or resolution of inflammation
inferred← citeshttps://doi.org/10.1007/s00018-022-04616-4openalex-snapshot
What is the ability of inflamed endothelium to uptake exogenous saturated fatty acids? A proof-of-concept study using spontaneous Raman, SRS and CARS microscopy
inferred← citeshttps://doi.org/10.1007/s00018-024-05560-1openalex-snapshot
Glial-derived TNF/Eiger signaling promotes somatosensory neurite sculpting
inferred← citeshttps://doi.org/10.1007/s00044-017-1856-3openalex-snapshot
Ganoderic acid modulating TNF and its receptors: in silico and in vitro study
inferred← citeshttps://doi.org/10.1007/s00109-006-0073-1openalex-snapshot
A CD40–CD95L fusion protein interferes with CD40L-induced prosurvival signaling and allows membrane CD40L-restricted activation of CD95
inferred← citeshttps://doi.org/10.1007/s00109-015-1334-7openalex-snapshot
CD147 promotes IKK/IκB/NF-κB pathway to resist TNF-induced apoptosis in rheumatoid arthritis synovial fibroblasts
inferred← citeshttps://doi.org/10.1007/s00109-025-02549-6openalex-snapshot
Single intracerebroventricular TNFR2 agonist injection impacts remyelination in the cuprizone model
inferred← citeshttps://doi.org/10.1007/s00125-011-2183-8openalex-snapshot
mRNA of the pro-apoptotic gene BBC3 serves as a molecular marker for TNF-α-induced islet damage in humans
inferred← citeshttps://doi.org/10.1007/s00125-016-4141-yopenalex-snapshot
Salt-inducible kinase 2 and -3 are downregulated in adipose tissue from obese or insulin-resistant individuals: implications for insulin signalling and glucose uptake in human adipocytes
inferred← citeshttps://doi.org/10.1007/s00204-011-0722-1openalex-snapshot
Evaluation of the cytotoxic and inflammatory potential of differentially shaped zinc oxide nanoparticles
inferred← citeshttps://doi.org/10.1007/s00204-012-0814-6openalex-snapshot
Cytokines in alcoholic liver disease
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/s00204-020-02903-2openalex-snapshot
Organophosphorus flame retardants are developmental neurotoxicants in a rat primary brainsphere in vitro model
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