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E2F-7: a distinctive E2F family member with an unusual organization of DNA-binding domains

https://doi.org/10.1038/sj.onc.1207649
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb06116.xopenalex-snapshot
Functional synergy between DP‐1 and E2F‐1 in the cell cycle‐regulating transcription factor DRTF1/E2F.
inferredcites →https://doi.org/10.1016/0092-8674(87)90453-3openalex-snapshot
An adenovirus E1A-like transcription factor is regulated during the differentiation of murine embryonal carcinoma stem cells
inferredcites →https://doi.org/10.1016/0092-8674(94)90582-7openalex-snapshot
Negative regulation of the growth-promoting transcription factor E2F-1 by a stably bound cyclin A-dependent protein kinase
inferredcites →https://doi.org/10.1016/s0003-9861(03)00054-7openalex-snapshot
E2F and cell cycle control: a double-edged sword
inferredcites →https://doi.org/10.1016/s0092-8674(00)81254-4openalex-snapshot
Tumor Induction and Tissue Atrophy in Mice Lacking E2F-1
inferredcites →https://doi.org/10.1016/s0092-8674(00)81255-6openalex-snapshot
E2F-1 Functions in Mice to Promote Apoptosis and Suppress Proliferation
inferredcites →https://doi.org/10.1016/s0092-8674(00)81683-9openalex-snapshot
The Hallmarks of Cancer
inferredcites →https://doi.org/10.1016/s0955-0674(00)00201-5openalex-snapshot
DNA-PK, ATM and ATR as sensors of DNA damage: variations on a theme?
inferredcites →https://doi.org/10.1016/s1097-2765(00)00029-0openalex-snapshot
E2F4 Is Essential for Normal Erythrocyte Maturation and Neonatal Viability
inferredcites →https://doi.org/10.1016/s1097-2765(00)00030-7openalex-snapshot
Loss of E2F4 Activity Leads to Abnormal Development of Multiple Cellular Lineages
inferredcites →https://doi.org/10.1016/s1097-2765(00)00071-xopenalex-snapshot
E2F4 and E2F5 Play an Essential Role in Pocket Protein–Mediated G1 Control
inferredcites →https://doi.org/10.1038/35008660openalex-snapshot
Regulation of E2F transcription by cyclin E–Cdk2 kinase mediated through p300/CBP co-activators
inferredcites →https://doi.org/10.1038/35078527openalex-snapshot
Apaf-1 is a transcriptional target for E2F and p53
inferredcites →https://doi.org/10.1038/35106593openalex-snapshot
The E2F1–3 transcription factors are essential for cellular proliferation
inferredcites →https://doi.org/10.1038/ncb974openalex-snapshot
Chk2 activates E2F-1 in response to DNA damage
inferredcites →https://doi.org/10.1038/nrm714openalex-snapshot
Sibling rivalry in the E2F family
inferredcites →https://doi.org/10.1038/sj.onc.1204793openalex-snapshot
Role of LXCXE motif-dependent interactions in the activity of the retinoblastoma protein
inferredcites →https://doi.org/10.1073/pnas.91.23.10918openalex-snapshot
Deregulated transcription factor E2F-1 expression leads to S-phase entry and p53-mediated apoptosis.
inferredcites →https://doi.org/10.1073/pnas.94.16.8427openalex-snapshot
Purification and characterization of a CENP-B homologue protein that binds to the centromeric K-type repeat DNA of Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1074/jbc.m200913200openalex-snapshot
E2Ls, E2F-like Repressors of Arabidopsis That Bind to E2F Sites in a Monomeric Form
inferredcites →https://doi.org/10.1074/jbc.m308105200openalex-snapshot
Identification and Characterization of E2F7, a Novel Mammalian E2F Family Member Capable of Blocking Cellular Proliferation
inferredcites →https://doi.org/10.1093/emboj/18.17.4597openalex-snapshot
Crystal structure of a prokaryotic replication initiator protein bound to DNA at 2.6 Å resolution
inferredcites →https://doi.org/10.1093/emboj/cdg613openalex-snapshot
E2F7, a novel E2F featuring DP‐independent repression of a subset of E2F‐regulated genes
inferredcites →https://doi.org/10.1093/nar/gkg520openalex-snapshot
SWISS-MODEL: an automated protein homology-modeling server
inferredcites →https://doi.org/10.1101/gad.10.1.27openalex-snapshot
Oct-1 POU domain-DNA interactions: cooperative binding of isolated subdomains and effects of covalent linkage.
inferredcites →https://doi.org/10.1101/gad.12.15.2245openalex-snapshot
The regulation of E2F by pRB-family proteins
inferredcites →https://doi.org/10.1101/gad.12.8.1092openalex-snapshot
A specific, nonproliferative role for E2F-5 in choroid plexus function revealed by gene targeting
inferredcites →https://doi.org/10.1101/gad.13.6.666openalex-snapshot
Structural basis of DNA recognition by the heterodimeric cell cycle transcription factor E2F-DP
inferredcites →https://doi.org/10.1126/science.1069861openalex-snapshot
A Complex with Chromatin Modifiers That Occupies E2F- and Myc-Responsive Genes in G 0 Cells
inferredcites →https://doi.org/10.1128/mcb.14.12.8166openalex-snapshot
Deregulated Expression of E2F-1 Induces S-Phase Entry and Leads to Apoptosis
inferredcites →https://doi.org/10.1128/mcb.19.5.3704openalex-snapshot
Transcription Factor E2F-1 Is Upregulated in Response to DNA Damage in a Manner Analogous to That of p53
inferredcites →https://doi.org/10.1242/jcs.109.10.2443openalex-snapshot
Nuclear accumulation of the E2F heterodimer regulated by subunit composition and alternative splicing of a nuclear localization signal

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4048928openalex-extracted
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200500022openalex-snapshot
Replication and the Cell Cycle
inferred← citeshttps://doi.org/10.1002/dvdy.21516openalex-snapshot
E2f6 and Bmi1 cooperate in axial skeletal development
inferred← citeshttps://doi.org/10.1002/hep.31259openalex-snapshot
E2F7 Is a Potent Inhibitor of Liver Tumor Growth in Adult Mice
inferred← citeshttps://doi.org/10.1002/jcp.21243openalex-snapshot
Cyclin D1/cdk4 can interact with E2F4/DP1 and disrupts its DNA‐binding capacity
inferred← citeshttps://doi.org/10.1002/jcp.24329openalex-snapshot
RB1 in cancer: Different mechanisms of RB1 inactivation and alterations of pRb pathway in tumorigenesis
inferred← citeshttps://doi.org/10.1007/0-387-33915-9_6openalex-snapshot
Diverse Regulatory Functions of the E2F Family of Transcription Factors
inferred← citeshttps://doi.org/10.1007/400_002openalex-snapshot
The Retinoblastoma Gene Family in Cell Cycle Regulation and Suppression of Tumorigenesis
inferred← citeshttps://doi.org/10.1007/978-1-4939-2957-3_4openalex-snapshot
E2F Transcription Factors Control the Roller Coaster Ride of Cell Cycle Gene Expression
inferred← citeshttps://doi.org/10.1007/978-90-481-9069-0_3openalex-snapshot
A Catalogue of Eukaryotic Transcription Factor Types, Their Evolutionary Origin, and Species Distribution
inferred← citeshttps://doi.org/10.1007/978-981-32-9005-1_5openalex-snapshot
p53 and Aging
inferred← citeshttps://doi.org/10.1007/s12156-009-0028-1openalex-snapshot
E2F-1 as an anticancer drug target
inferred← citeshttps://doi.org/10.1007/s12185-015-1895-9openalex-snapshot
Molecular genetic and cytogenetic analysis of a primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma
inferred← citeshttps://doi.org/10.1007/s13258-014-0218-5openalex-snapshot
Identification and expression analysis of the E2F/DP genes under salt stress in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/b978-0-12-820472-6.00102-xopenalex-snapshot
E2F Transcription Factors in Cancer, More than the Cell Cycle
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117147openalex-snapshot
Posttranslational modifications of E2F family members in the physiological state and in cancer: Roles, mechanisms and therapeutic targets
inferred← citeshttps://doi.org/10.1016/j.cardiores.2004.09.003openalex-snapshot
Therapeutic opportunities for cell cycle re-entry and cardiac regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.10.017openalex-snapshot
Synergistic Function of E2F7 and E2F8 Is Essential for Cell Survival and Embryonic Development
inferred← citeshttps://doi.org/10.1016/j.dnarep.2004.03.034openalex-snapshot
The emerging role of E2F-1 in the DNA damage response and checkpoint control
inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.05.004openalex-snapshot
Crosstalk between P53 and DNA damage response in ageing
inferred← citeshttps://doi.org/10.1016/j.ejca.2005.08.005openalex-snapshot
Involvement of E2F transcription factor family in cancer
inferred← citeshttps://doi.org/10.1016/j.gde.2004.07.003openalex-snapshot
Hitting their targets: an emerging picture of E2F and cell cycle control
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e34362openalex-snapshot
The roles of E2F7 in cancer: Current knowledge and future prospects
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.108027openalex-snapshot
E2F1 and E2F7 regulate gastric cancer cell proliferation, respectively, through transcriptional activation and transcriptional repression of MYBL2
inferred← citeshttps://doi.org/10.1016/j.micpath.2022.105679openalex-snapshot
Fibrillarin RNA methylase is an interacting protein of Cryptosporidium parvum calmodulin-like protein (CpCML)
inferred← citeshttps://doi.org/10.1016/j.molmed.2006.02.002openalex-snapshot
E2F1-induced apoptosis: turning killers into therapeutics
inferred← citeshttps://doi.org/10.1016/j.semcancer.2023.03.004openalex-snapshot
Role of E2F transcription factor in oral cancer: Recent insight and advancements
inferred← citeshttps://doi.org/10.1016/j.tcb.2009.01.002openalex-snapshot
Atypical E2Fs: new players in the E2F transcription factor family
inferred← citeshttps://doi.org/10.1021/acs.biochem.4c00640openalex-snapshot
Fine-Tuning of ATF4 DNA Binding Activity by a Secondary Basic Motif Unique to the ATF-X Subfamily of bZip Transcription Factors
inferred← citeshttps://doi.org/10.1038/cdd.2010.70openalex-snapshot
E2F-1 regulation by an unusual DNA damage-responsive DP partner subunit
inferred← citeshttps://doi.org/10.1038/gene.2008.70openalex-snapshot
Defining a transcriptional fingerprint of murine splenic B-cell development
inferred← citeshttps://doi.org/10.1038/ncb2585openalex-snapshot
E2F8 is essential for polyploidization in mammalian cells
inferred← citeshttps://doi.org/10.1038/onc.2012.640openalex-snapshot
Senescence and aging: the critical roles of p53
inferred← citeshttps://doi.org/10.1038/onc.2016.251openalex-snapshot
Synergistic functions of E2F7 and E2F8 are critical to suppress stress-induced skin cancer
inferred← citeshttps://doi.org/10.1038/s41388-018-0494-7openalex-snapshot
E2F1 and E2F7 differentially regulate KPNA2 to promote the development of gallbladder cancer
inferred← citeshttps://doi.org/10.1038/s41416-020-01032-yopenalex-snapshot
E2F7−EZH2 axis regulates PTEN/AKT/mTOR signalling and glioblastoma progression
inferred← citeshttps://doi.org/10.1038/s41419-018-0529-6openalex-snapshot
Functional interplay between E2F7 and ribosomal rRNA gene transcription regulates protein synthesis
inferred← citeshttps://doi.org/10.1038/s41419-023-05603-8openalex-snapshot
Adding pieces to the puzzle of differentiated-to-anaplastic thyroid cancer evolution: the oncogene E2F7
inferred← citeshttps://doi.org/10.1038/s41598-018-26613-zopenalex-snapshot
E2F signature is predictive for the pancreatic adenocarcinoma clinical outcome and sensitivity to E2F inhibitors, but not for the response to cytotoxic-based treatments
inferred← citeshttps://doi.org/10.1038/sj.embor.7401158openalex-snapshot
DNA‐damage response control of E2F7 and E2F8
inferred← citeshttps://doi.org/10.1038/sj.onc.1208608openalex-snapshot
Cell cycle in mouse development
inferred← citeshttps://doi.org/10.1038/sj.onc.1208612openalex-snapshot
The E2F transcriptional network: old acquaintances with new faces
inferred← citeshttps://doi.org/10.1038/sj.onc.1208703openalex-snapshot
E2F-8: an E2F family member with a similar organization of DNA-binding domains to E2F-7
inferred← citeshttps://doi.org/10.1038/sj.onc.1208814openalex-snapshot
Stabilization of E2F1 protein by MDM2 through the E2F1 ubiquitination pathway
inferred← citeshttps://doi.org/10.1038/sj.onc.1209343openalex-snapshot
A functionally distinct member of the DP family of E2F subunits
inferred← citeshttps://doi.org/10.1074/jbc.m109.012047openalex-snapshot
A Novel WRKY-like Protein Involved in Transcriptional Activation of Cyst Wall Protein Genes in Giardia lamblia
inferred← citeshttps://doi.org/10.1074/jbc.m110.217158openalex-snapshot
Genome-wide Analysis of Transcription Factor E2F1 Mutant Proteins Reveals That N- and C-terminal Protein Interaction Domains Do Not Participate in Targeting E2F1 to the Human Genome
inferred← citeshttps://doi.org/10.1074/jbc.m111.280206openalex-snapshot
A Novel E2F-like Protein Involved in Transcriptional Activation of Cyst Wall Protein Genes in Giardia lamblia
inferred← citeshttps://doi.org/10.1074/jbc.m113.467506openalex-snapshot
Interaction of E2F7 Transcription Factor with E2F1 and C-terminal-binding Protein (CtBP) Provides a Mechanism for E2F7-dependent Transcription Repression
inferred← citeshttps://doi.org/10.1074/jbc.m501410200openalex-snapshot
Cloning and Characterization of Mouse E2F8, a Novel Mammalian E2F Family Member Capable of Blocking Cellular Proliferation
inferred← citeshttps://doi.org/10.1074/jbc.m503587200openalex-snapshot
Characterization of the Condensin Component Cnap1 and Protein Kinase Melk as Novel E2F Target Genes Down-regulated by 1,25-Dihydroxyvitamin D3
inferred← citeshttps://doi.org/10.1074/jbc.m506797200openalex-snapshot
Silencing of the Meiotic Genes SMC1β and STAG3 in Somatic Cells by E2F6
inferred← citeshttps://doi.org/10.1074/jbc.m603800200openalex-snapshot
CDCA4 Is an E2F Transcription Factor Family-induced Nuclear Factor That Regulates E2F-dependent Transcriptional Activation and Cell Proliferation
inferred← citeshttps://doi.org/10.1074/jbc.m604705200openalex-snapshot
Bok, Bcl-2-related Ovarian Killer, Is Cell Cycle-regulated and Sensitizes to Stress-induced Apoptosis
inferred← citeshttps://doi.org/10.1074/jbc.m606169200openalex-snapshot
Human TFDP3, a Novel DP Protein, Inhibits DNA Binding and Transactivation by E2F
inferred← citeshttps://doi.org/10.1074/jbc.m705986200openalex-snapshot
RhoBTB2 (DBC2) Is a Mitotic E2F1 Target Gene with a Novel Role in Apoptosis
inferred← citeshttps://doi.org/10.1093/molehr/gam091openalex-snapshot
Gene expression analysis of human endometrial endothelial cells exposed to op′-DDT
inferred← citeshttps://doi.org/10.1093/nar/gki855openalex-snapshot
Characterization of E2F8, a novel E2F-like cell-cycle regulated repressor of E2F-activated transcription
inferred← citeshttps://doi.org/10.1093/nar/gkr1203openalex-snapshot
E2F7 represses a network of oscillating cell cycle genes to control S-phase progression
inferred← citeshttps://doi.org/10.1096/fj.202402520ropenalex-snapshot
Ascending E2F7a/b ratio facilitates KLF13 transcription in hepatocellular carcinoma and correlates with the abundance of binuclear hepatocytes ( ABH ) modulation for short‐term recurrence
inferred← citeshttps://doi.org/10.1097/cm9.0000000000004312openalex-snapshot
E2F7 promotes lung adenocarcinoma progression by affecting phosphorylation and stabilization of β-catenin
inferred← citeshttps://doi.org/10.1097/md.0000000000029253openalex-snapshot
High expression of E2F transcription factors 7: An independent predictor of poor prognosis in patients with lung adenocarcinoma
inferred← citeshttps://doi.org/10.1097/md.0000000000038574openalex-snapshot
The predictive value of E2F7 in immunotherapy efficacy for lung adenocarcinoma: An observational study
inferred← citeshttps://doi.org/10.1101/gad.1255204openalex-snapshot
Identification of a Drosophila Myb-E2F2/RBF transcriptional repressor complex
inferred← citeshttps://doi.org/10.1101/gad.184911.111openalex-snapshot
E2F7, a novel target, is up-regulated by p53 and mediates DNA damage-dependent transcriptional repression
inferred← citeshttps://doi.org/10.1101/gad.196238.112openalex-snapshot
The atypical E2F family member E2F7 couples the p53 and RB pathways during cellular senescence
inferred← citeshttps://doi.org/10.1101/gr.080622.108openalex-snapshot
E2F in vivo binding specificity: Comparison of consensus versus nonconsensus binding sites
inferred← citeshttps://doi.org/10.1104/pp.104.054155openalex-snapshot
Genome-Wide Annotation and Expression Profiling of Cell Cycle Regulatory Genes in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1111/1759-7714.14941openalex-snapshot
Circ_0010235 confers cisplatin resistance in lung cancer by upregulating E2F7 through absorbing miR ‐379‐5p
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2007.00030.xopenalex-snapshot
E2F1 death pathways as targets for cancer therapy
inferred← citeshttps://doi.org/10.1128/mcb.02100-06openalex-snapshot
Unique Requirement for Rb/E2F3 in Neuronal Migration: Evidence for Cell Cycle-Independent Functions
inferred← citeshttps://doi.org/10.1128/mcb.02147-05openalex-snapshot
E2f1, E2f2, and E2f3 Control E2F Target Expression and Cellular Proliferation via a p53-Dependent Negative Feedback Loop
inferred← citeshttps://doi.org/10.1128/mcb.02147-06openalex-snapshot
E2f1, E2f2, and E2f3 Control E2F Target Expression and Cellular Proliferation via a p53-Dependent Negative Feedback Loop
inferred← citeshttps://doi.org/10.1128/mcb.25.8.3027-3039.2005openalex-snapshot
dDP Is Needed for Normal Cell Proliferation
inferred← citeshttps://doi.org/10.1146/annurev.genet.40.110405.090431openalex-snapshot
Cell Cycle Regulation in Plant Development
inferred← citeshttps://doi.org/10.1155/2021/5790416openalex-snapshot
Comprehensive Analysis of the Expression and Prognosis for E2Fs in Human Clear Cell Renal Cell Carcinoma
inferred← citeshttps://doi.org/10.1182/blood-2005-09-008656openalex-snapshot
E2f4 regulates fetal erythropoiesis through the promotion of cellular proliferation
inferred← citeshttps://doi.org/10.1186/1750-2187-2-3openalex-snapshot
E2F8 is a nonreceptor activator of heterotrimeric G proteins
inferred← citeshttps://doi.org/10.13028/h6jf-nf65openalex-snapshot
Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002831openalex-snapshot
S Phase–Coupled E2f1 Destruction Ensures Homeostasis in Proliferating Tissues
inferred← citeshttps://doi.org/10.14670/hh-21.403openalex-snapshot
The transcription factor E2F: a crucial switch in the control of homeostasis and tumorigenesis.
inferred← citeshttps://doi.org/10.17169/refubium-15113openalex-snapshot
Expression und Funktion Endothelin-Konvertierungsenzym-1 regulierender Transkriptionsfaktoren in humanen neuroepithelialen und meningealen Tumoren
inferred← citeshttps://doi.org/10.17615/ek0g-9846openalex-snapshot
Changes in Protein Abundance are Essential for Proper Cell Cycle Regulation
inferred← citeshttps://doi.org/10.18632/oncotarget.7003openalex-snapshot
MiR-129 triggers autophagic flux by regulating a novel Notch-1/ E2F7/Beclin-1 axis to impair the viability of human malignant glioma cells
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2767947/v1openalex-snapshot
A novel defined apoptosis-related gene signature as a prognostic tool in lung adenocarcinoma
inferred← citeshttps://doi.org/10.2165/00129785-200505050-00005openalex-snapshot
Oncogenes as Novel Targets for Cancer Therapy (Part III)
inferred← citeshttps://doi.org/10.2165/00129785-200505060-00006openalex-snapshot
Oncogenes as Novel Targets for Cancer Therapy (Part IV)
inferred← citeshttps://doi.org/10.22034/apjcp.2017.18.1.271openalex-snapshot
Identification of a Low-Frequency Missense Variant in E2F Transcription Factor 7 Associated with Colorectal Cancer Risk In A Chinese Population
inferred← citeshttps://doi.org/10.2337/db08-0931openalex-snapshot
Genome-Wide Linkage and Admixture Mapping of Type 2 Diabetes in African American Families From the American Diabetes Association GENNID (Genetics of NIDDM) Study Cohort
inferred← citeshttps://doi.org/10.24875/ric.23000180openalex-snapshot
Transcription Factor E2F7 Activates PKMYT1 to Partially Suppress Adriamycin Sensitivity in Gastric Cancer Through the MAPK Signaling Pathway
inferred← citeshttps://doi.org/10.3389/fonc.2021.723137openalex-snapshot
Emerging Role of E2F Family in Cancer Stem Cells
inferred← citeshttps://doi.org/10.3389/fpls.2018.00638openalex-snapshot
The Canonical E2Fs Are Required for Germline Development in Arabidopsis
inferred← citeshttps://doi.org/10.3390/cancers13092033openalex-snapshot
Atypical E2Fs either Counteract or Cooperate with RB during Tumorigenesis Depending on Tissue Context
inferred← citeshttps://doi.org/10.3390/ijms12128947openalex-snapshot
The Role of the E2F Transcription Factor Family in UV-Induced Apoptosis
inferred← citeshttps://doi.org/10.3390/ijms23158154openalex-snapshot
A Journey to the Core of the Plant Cell Cycle
inferred← citeshttps://doi.org/10.3748/wjg.v19.i21.3189openalex-snapshot
E2F transcription factors and digestive system malignancies: How much do we know?
inferred← citeshttps://doi.org/10.3892/ijo.2018.4492openalex-snapshot
A miR-26a/E2F7 feedback loop contributes to tamoxifen resistance in ER-positive breast cancer
inferred← citeshttps://doi.org/10.4018/978-1-60566-685-3.ch002openalex-snapshot
Introduction to GRNs
inferred← citeshttps://doi.org/10.4161/cc.26078openalex-snapshot
E2F-7 couples DNA damage-dependent transcription with the DNA repair process
inferred← citeshttps://doi.org/10.4161/cc.6.23.4997openalex-snapshot
Specific In Vivo Roles for E2Fs in Differentiation and Development
inferred← citeshttps://doi.org/10.5282/edoc.6324openalex-snapshot
Purification and Characterization of Retinoblastoma like Factor-containing Protein Complexes from Drosophila melanogaster
inferred← citeshttps://doi.org/10.5772/intechopen.82448openalex-snapshot
Distinct E2F-Mediated Transcriptional Mechanisms in Cell Proliferation, Endoreplication and Apoptosis
inferred← citeshttps://doi.org/10.70675/cf9df440zf3faz43bezb940z28698183447dopenalex-snapshot
Rôle de E2F1 dans la sécrétion d'insuline, le métabolisme oxydatif, la néoglucogenèse et la lipogenèse. Implication dans le diabète, la dystrophie musculaire et le cancer
inferred← citeshttps://doi.org/10.7150/ijbs.1.87openalex-snapshot
Signalling In The Epidermis: The E2f Cell Cycle Regulatory Pathway In Epidermal Morphogenesis, Regeneration And Transformation
inferred← citeshttps://doi.org/10.7150/jca.18255openalex-snapshot
E2F8 is a Potential Therapeutic Target for Hepatocellular Carcinoma
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