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The Fas Signaling Pathway: More Than a Paradigm
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1038/35037728openalex-snapshot
CD95's deadly mission in the immune system
inferredcites →https://doi.org/10.1038/82712openalex-snapshot
The multifaceted role of Fas signaling in immune cell homeostasis and autoimmunity
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/10.1126/stke.2002.158.tw417openalex-snapshot
Picking a Signaling Pathway
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/10.1172/jci13779openalex-snapshot
Fas receptor signaling inhibits glycogen synthase kinase 3β and induces cardiac hypertrophy following pressure overload
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/bf02980081openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00011-017-1116-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-018-2795-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00210-003-0801-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00210-011-0637-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00296-013-2793-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00343-022-2129-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00401-024-02722-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-005-0817-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-005-1298-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-006-0575-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-007-0720-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-008-0280-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-009-0339-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-010-0544-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-015-1209-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10495-017-1433-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11010-010-0709-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11033-022-07756-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11255-018-1911-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11356-016-6253-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11596-012-0039-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11686-025-00988-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12011-017-0992-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12011-018-1623-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12011-022-03305-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12011-022-03376-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12032-025-02612-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12094-026-04526-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12257-018-0033-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12672-025-02666-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12975-013-0313-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13273-017-0003-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13273-022-00327-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13277-016-5035-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-08-088504-9.00025-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-384999-1.10009-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.30046-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-416721-6.00020-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-800212-4.00006-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-815762-6.00008-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-816435-8.00010-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-820595-2.00013-8openalex-snapshot
Cell signaling and apoptosis in animals
inferred← citeshttps://doi.org/10.1016/b978-0-12-821666-8.00054-2openalex-snapshot
Genomic and proteomic profiling of osteosarcoma
inferred← citeshttps://doi.org/10.1016/b978-0-323-47674-4.00005-0openalex-snapshot
Pathophysiology of Cancer Cell Death
inferred← citeshttps://doi.org/10.1016/b978-0-443-06694-8.50008-7openalex-snapshot
Cell Life and Death
inferred← citeshttps://doi.org/10.1016/b978-0-443-10513-5.00016-4openalex-snapshot
Pathophysiology: General Principles
inferred← citeshttps://doi.org/10.1016/b978-0-443-10513-5.00023-1openalex-snapshot
Hypoxic-Ischemic Injury in the Term Infant: Pathophysiology
inferred← citeshttps://doi.org/10.1016/b978-0-443-33877-9.00007-0openalex-snapshot
Advancement in the animal model-based therapeutics in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/b978-0-444-64046-8.00014-8openalex-snapshot
Cell Preservation Technology
inferred← citeshttps://doi.org/10.1016/b978-0-7216-9491-7.50108-3openalex-snapshot
Neuropathies with Systemic Vasculitis
inferred← citeshttps://doi.org/10.1016/b978-012160281-9/50009-8openalex-snapshot
The ErbB receptors and their role in cancer progression
inferred← citeshttps://doi.org/10.1016/b978-012639011-7/50021-8openalex-snapshot
The Heat Shock Proteins and Hemeoxygenase Response in Central Nervous System Injuries
inferred← citeshttps://doi.org/10.1016/b978-044452809-4/50162-9openalex-snapshot
An Assessment of the Chances of Antiapoptotic Drug Therapy in Patients with Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1016/b978-1-4557-2865-7.00005-9openalex-snapshot
Pathophysiology of Cancer Cell Death
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2017.08.001openalex-snapshot
Multifaceted Nucleolin Protein and Its Molecular Partners in Oncogenesis
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2021.01.008openalex-snapshot
Apoptosis in health and diseases of the eye and brain
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2025.06.024openalex-snapshot
Role and relation of cell death in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.abb.2016.01.002openalex-snapshot
ERβ up-regulation was involved in silibinin-induced growth inhibition of human breast cancer MCF-7 cells
inferred← citeshttps://doi.org/10.1016/j.acthis.2021.151810openalex-snapshot
Trehalose inhibits proliferation while activates apoptosis and autophagy in rat airway smooth muscle cells
inferred← citeshttps://doi.org/10.1016/j.ajoc.2022.101305openalex-snapshot
Ocular findings associated with FADD deficiency resemble familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.1016/j.apsb.2024.04.034openalex-snapshot
Advancements in precision nanomedicine design targeting the anoikis-platelet interface of circulating tumor cells
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.09.006openalex-snapshot
Targeting post-mitochondrial effectors of apoptosis for neuroprotection
inferred← citeshttps://doi.org/10.1016/j.bbadis.2021.166297openalex-snapshot
The molecular mosaic of regulated cell death in the cardiovascular system
inferred← citeshttps://doi.org/10.1016/j.bbagen.2019.05.018openalex-snapshot
Antitumor activity of methyl (Z)-2-(isothioureidomethyl)-2-pentenoate hydrobromide against leukemia cell lines via mitotic arrest and apoptotic pathways
inferred← citeshttps://doi.org/10.1016/j.bbalip.2009.12.001openalex-snapshot
Electronegative LDL induction of apoptosis in macrophages: Involvement of Nrf2
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2003.10.011openalex-snapshot
Role of Bcl-2 family members in immunity and disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.05.031openalex-snapshot
Apoptosis-inducing factor (AIF) is targeted in IFN-α2a-induced Bid‐mediated apoptosis through Bak activation in ovarian cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.06.026openalex-snapshot
Anoikis molecular pathways and its role in cancer progression
inferred← citeshttps://doi.org/10.1016/j.bbamem.2014.10.030openalex-snapshot
Ion channels in the regulation of apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbapap.2010.04.006openalex-snapshot
Identification and analysis of dominant negative mutants of RAIDD and PIDD
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.188929openalex-snapshot
The innate effects of plant secondary metabolites in preclusion of gynecologic cancers: Inflammatory response and therapeutic action
inferred← citeshttps://doi.org/10.1016/j.bcp.2008.07.023openalex-snapshot
Anoikis: A necessary death program for anchorage-dependent cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2015.11.016openalex-snapshot
Estrogens down-regulate the stem cell factor (SCF)/c-KIT system in prostate cells: Evidence of antiproliferative and proapoptotic effects
inferred← citeshttps://doi.org/10.1016/j.beha.2013.09.007openalex-snapshot
Erythropoiesis stimulating agents and other growth factors in low-risk MDS
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.10.082openalex-snapshot
Molecular mechanisms of anticancer action and cell selectivity of short α-helical peptides
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2022.121522openalex-snapshot
Bottom-up assembly of target-specific cytotoxic synthetic cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103756openalex-snapshot
Incorporation of amino moiety to alepterolic acid improve activity against cancer cell lines: Synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108619openalex-snapshot
Cytotoxic lycorine alkaloids of the plant family Amaryllidaceae
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110735openalex-snapshot
Antitumor potential of Hedyotis diffusa Willd: A systematic review of bioactive constituents and underlying molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111362openalex-snapshot
Apoptotic effects of dehydrocrenatidine via JNK and ERK pathway regulation in oral squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.blre.2007.10.003openalex-snapshot
Supportive care, growth factors, and new therapies in myelodysplastic syndromes
inferred← citeshttps://doi.org/10.1016/j.blre.2010.01.001openalex-snapshot
Novel agents for B-cell non-Hodgkin lymphoma: Science and the promise
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.115044openalex-snapshot
The tetrahydroxanthone-dimer phomoxanthone A is a strong inducer of apoptosis in cisplatin-resistant solid cancer cells
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