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Expression and prognostic significance of apoptotic genes in oral squamous cell carcinoma
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Characterization of the expression pattern of p63α and δnp63α in benign and malignant oral epithelial lesions
inferredcites →https://doi.org/10.1006/gyno.2000.5953openalex-snapshot
Expression of the p53 Homologue p63 in Early Cervical Neoplasia
inferredcites →https://doi.org/10.1007/s00432-008-0365-7openalex-snapshot
ATM in oral carcinogenesis: association with clinicopathological features
inferredcites →https://doi.org/10.1016/j.cell.2011.02.013openalex-snapshot
Hallmarks of Cancer: The Next Generation
inferredcites →https://doi.org/10.1016/j.humpath.2004.12.003openalex-snapshot
p63 overexpression associates with poor prognosis in head and neck squamous cell carcinoma
inferredcites →https://doi.org/10.1016/j.it.2010.05.005openalex-snapshot
FADD: a regulator of life and death
inferredcites →https://doi.org/10.1016/j.oraloncology.2003.09.012openalex-snapshot
Induction of apoptosis in oral cancer cells: agents and mechanisms for potential therapy and prevention
inferredcites →https://doi.org/10.1016/j.oraloncology.2010.06.012openalex-snapshot
Overexpression of p63 is associated with radiation resistance and prognosis in oral squamous cell carcinoma
inferredcites →https://doi.org/10.1016/s0002-9440(10)64814-6openalex-snapshot
p63 Is a Prostate Basal Cell Marker and Is Required for Prostate Development
inferredcites →https://doi.org/10.1016/s0092-8674(00)80434-1openalex-snapshot
Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade
inferredcites →https://doi.org/10.1016/s0092-8674(00)80501-2openalex-snapshot
Apaf-1, a Human Protein Homologous to C. elegans CED-4, Participates in Cytochrome c–Dependent Activation of Caspase-3
inferredcites →https://doi.org/10.1016/s0092-8674(00)81874-7openalex-snapshot
Apoptosis by Death Factor
inferredcites →https://doi.org/10.1016/s0304-419x(01)00036-1openalex-snapshot
p53, p63 and p73 – solos, alliances and feuds among family members
inferredcites →https://doi.org/10.1016/s0952-7915(98)80222-7openalex-snapshot
Mechanisms of CD95 (APO-1/Fas)-mediated apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80095-7openalex-snapshot
Autoactivation of Procaspase-9 by Apaf-1-Mediated Oligomerization
inferredcites →https://doi.org/10.1016/s1097-2765(00)80275-0openalex-snapshot
p63, a p53 Homolog at 3q27–29, Encodes Multiple Products with Transactivating, Death-Inducing, and Dominant-Negative Activities
inferredcites →https://doi.org/10.1016/s1535-6108(02)00024-7openalex-snapshot
A matter of life and death
inferredcites →https://doi.org/10.1034/j.1600-0560.2002.290902.xopenalex-snapshot
p63 expression in normal skin and usual cutaneous carcinomas
inferredcites →https://doi.org/10.1034/j.1600-0560.2003.300102.xopenalex-snapshot
p63 expression in normal human epidermis and epidermal appendages and their tumors
inferredcites →https://doi.org/10.1038/19539openalex-snapshot
p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
inferredcites →https://doi.org/10.1038/385086a0openalex-snapshot
RAIDD is a new 'death' adaptor molecule
inferredcites →https://doi.org/10.1038/sj.cdd.4401186openalex-snapshot
The CD95(APO-1/Fas) DISC and beyond
inferredcites →https://doi.org/10.1073/pnas.0507367103openalex-snapshot
ATM promotes apoptosis and suppresses tumorigenesis in response to Myc
inferredcites →https://doi.org/10.1073/pnas.96.20.10964openalex-snapshot
Caspase activation: The induced-proximity model
inferredcites →https://doi.org/10.1083/jcb.147.4.809openalex-snapshot
The Pro-Apoptotic Proteins, Bid and Bax, Cause a Limited Permeabilization of the Mitochondrial Outer Membrane That Is Enhanced by Cytosol
inferredcites →https://doi.org/10.1093/emboj/16.10.2794openalex-snapshot
FLICE is activated by association with the CD95 death‐inducing signaling complex (DISC)
inferredcites →https://doi.org/10.1097/00000478-200108000-00010openalex-snapshot
p63, a p53 Homologue, Is a Selective Nuclear Marker of Myoepithelial Cells of the Human Breast
inferredcites →https://doi.org/10.1097/00001622-199901000-00014openalex-snapshot
Mechanisms of apoptosis avoidance in cancer
inferredcites →https://doi.org/10.1101/gad.914401openalex-snapshot
Cell cycle checkpoint signaling through the ATM and ATR kinases
inferredcites →https://doi.org/10.1177/039463200601900323openalex-snapshot
Genetic Analysis of Oral Squamous Cell Carcinoma by cDNA Microarrays Focused Apoptotic Pathway
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Arecoline‐regulated ataxia telangiectasia mutated expression level in oral cancer progression
inferred← citeshttps://doi.org/10.1007/978-3-030-33832-9_22openalex-snapshot
Biomarkers in Head and Neck Oncology: From Early Diagnosis to Tailored Cancer Therapy
inferred← citeshttps://doi.org/10.1007/s10495-013-0806-xopenalex-snapshot
Effects of aging on apoptosis gene expression in oral mucosal tissues
inferred← citeshttps://doi.org/10.1016/j.crbiot.2024.100253openalex-snapshot
Identification of a prognostic model based on cuproptosis and ferroptosis-related genes in patients with head and neck squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2021.112181openalex-snapshot
Combined photodynamic therapy with chloroaluminum phthalocyanine and doxorubicin nanoemulsions in breast cancer model
inferred← citeshttps://doi.org/10.1016/j.oooo.2012.11.007openalex-snapshot
Clinicopathological and immunohistochemical analysis of 19 cases of oral eosinophilic ulcers
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Expression of DNA repair genes in oral squamous cell carcinoma using reverse transcription-quantitative polymerase chain reaction
inferred← citeshttps://doi.org/10.1016/j.oraloncology.2023.106659openalex-snapshot
A senescence-related lncRNA signature predicts prognosis and reflects immune landscape in HNSCC
inferred← citeshttps://doi.org/10.1038/srep15391openalex-snapshot
Synergistic Effect of Sorafenib and Radiation on Human Oral Carcinoma in vivo
inferred← citeshttps://doi.org/10.1089/dna.2021.0023openalex-snapshot
Mechanisms of Ferroptosis and Application to Head and Neck Squamous Cell Carcinoma Treatments
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Novel Hydroxyapatite Biomaterial Covalently Linked to Raloxifene
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MG63 and MC3T3-E1 Osteoblastic Cell Lines Response to Raloxifene
inferred← citeshttps://doi.org/10.1371/journal.pone.0071272openalex-snapshot
RNA-Mediated Gene Silencing of Nicotinamide N-Methyltransferase Is Associated with Decreased Tumorigenicity in Human Oral Carcinoma Cells
inferred← citeshttps://doi.org/10.18632/oncotarget.15752openalex-snapshot
Interplay between ΔNp63 and miR-138-5p regulates growth, metastasis and stemness of oral squamous cell carcinoma
inferred← citeshttps://doi.org/10.18632/oncotarget.2721openalex-snapshot
Dichloroacetate, a selective mitochondria-targeting drug for oral squamous cell carcinoma: a metabolic perspective of treatment
inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2018.0022openalex-snapshot
ATM in breast and brain tumors: a comprehensive review
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4342492/v1openalex-snapshot
Analysis of cuproptosis-related genes signature in prognosis and immune landscape in Head and neck squamous cell carcinoma
inferred← citeshttps://doi.org/10.21608/ajdsm.2017.107497openalex-snapshot
Evaluation of caspase 9 expression in induced hamster buccal pouch carcinoma
inferred← citeshttps://doi.org/10.21608/ajdsm.2017.107498openalex-snapshot
Electron microscopic evaluation of cisplatin conjugated nanogold and laser irradiation on hamster buccal pouch carcinoma
inferred← citeshttps://doi.org/10.21608/ajdsm.2018.71607openalex-snapshot
Chemopreventive efficacy of carvacrol on experimentally induced hamster buccal pouch carcinogenesis
inferred← citeshttps://doi.org/10.21608/edj.2020.42856.1262openalex-snapshot
Effect of rosmarinic acid as a chemopreventive modality on experimentally induced hamster buccal pouch carcinogenesis
inferred← citeshttps://doi.org/10.3390/ijms23031562openalex-snapshot
Proliferation and Apoptosis Pathways and Factors in Oral Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.36611/upjohns/volume14/issue1/4openalex-snapshot
THE CONTRIBUTORY ROLE OF LONG NON-CODING RNAs TINCR, LUCAT1, AND CASC2 IN HEAD AND NECK SQUAMOUS CELL CARCINOMA
inferred← citeshttps://doi.org/10.3892/ijmm.2018.3721openalex-snapshot
Telomerase reverse transcriptase interference synergistically promotes tumor necrosis factor‑related apoptosis‑inducing ligand‑induced oral squamous cell carcinoma apoptosis and suppresses proliferation in�vitro and in�vivo
inferred← citeshttps://doi.org/10.4081/oncol.2020.472openalex-snapshot
Apoptosis and genes involved in oral cancer - a comprehensive review
inferred← citeshttps://doi.org/10.4317/medoral.19805openalex-snapshot
Analysis of methylation and mRNA expression status of FADD and FAS genes in patients with oral squamous cell carcinoma
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