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ΔN-P63α and TA-P63α exhibit intrinsic differences in transactivation specificities that depend on distinct features of DNA target sites
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1 of the 81 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1371/journal.pgen.1000680 (notice 2023-03-27).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1097-0061(20000630)16:9<857::aid-yea561>3.0.co;2-bopenalex-snapshot
Rapid and reliable protein extraction from yeast
inferredcites →https://doi.org/10.1002/humu.22304openalex-snapshot
EEC- and ADULT-AssociatedTP63Mutations Exhibit Functional Heterogeneity Toward P63 Responsive Sequences
inferredcites →https://doi.org/10.1002/ijc.24280openalex-snapshot
ΔNp63α‐dependent expression of Id‐3 distinctively suppresses the invasiveness of human squamous cell carcinoma
inferredcites →https://doi.org/10.1007/s00018-008-8119-xopenalex-snapshot
p63 in epithelial development
inferredcites →https://doi.org/10.1016/j.cell.2009.01.039openalex-snapshot
A Mutant-p53/Smad Complex Opposes p63 to Empower TGFβ-Induced Metastasis
inferredcites →https://doi.org/10.1016/j.cell.2011.01.013openalex-snapshot
DNA Damage in Oocytes Induces a Switch of the Quality Control Factor TAp63α from Dimer to Tetramer
inferredcites →https://doi.org/10.1016/j.celrep.2013.04.008openalex-snapshot
p53 DNA Binding Cooperativity Is Essential for Apoptosis and Tumor Suppression In Vivo
inferredcites →https://doi.org/10.1016/j.celrep.2013.05.028openalex-snapshot
Mutant Mice Lacking the p53 C-Terminal Domain Model Telomere Syndromes
inferredcites →https://doi.org/10.1016/j.jmb.2005.03.014openalex-snapshot
Comparative Binding of p53 to its Promoter and DNA Recognition Elements
inferredcites →https://doi.org/10.1016/j.molcel.2010.02.037openalex-snapshot
DNA Binding Cooperativity of p53 Modulates the Decision between Cell-Cycle Arrest and Apoptosis
inferredcites →https://doi.org/10.1016/s0076-6879(05)09019-1openalex-snapshot
The Delitto Perfetto Approach to In Vivo Site‐Directed Mutagenesis and Chromosome Rearrangements with Synthetic Oligonucleotides in Yeast
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/10.1038/21697openalex-snapshot
Interaction of c-Abl and p73α and their collaboration to induce apoptosis
inferredcites →https://doi.org/10.1038/416560aopenalex-snapshot
p63 and p73 are required for p53-dependent apoptosis in response to DNA damage
inferredcites →https://doi.org/10.1038/90837openalex-snapshot
In vivo site-directed mutagenesis using oligonucleotides
inferredcites →https://doi.org/10.1038/cdd.2010.35openalex-snapshot
p53-family proteins and their regulators: hubs and spokes in tumor suppression
inferredcites →https://doi.org/10.1038/cdd.2013.23openalex-snapshot
Analysis of the oligomeric state and transactivation potential of TAp73α
inferredcites →https://doi.org/10.1038/cddis.2010.49openalex-snapshot
Novel p63 target genes involved in paracrine signaling and keratinocyte differentiation
inferredcites →https://doi.org/10.1038/nature05337openalex-snapshot
p63 protects the female germ line during meiotic arrest
inferredcites →https://doi.org/10.1038/nature09459openalex-snapshot
TAp63 suppresses metastasis through coordinate regulation of Dicer and miRNAs
inferredcites →https://doi.org/10.1038/ncb1988openalex-snapshot
TAp63 induces senescence and suppresses tumorigenesis in vivo
inferredcites →https://doi.org/10.1038/ng0492-45openalex-snapshot
Definition of a consensus binding site for p53
inferredcites →https://doi.org/10.1038/nm.2033openalex-snapshot
Inhibition of the c-Abl–TAp63 pathway protects mouse oocytes from chemotherapy-induced death
inferredcites →https://doi.org/10.1038/nrc2730openalex-snapshot
The expanding universe of p53 targets
inferredcites →https://doi.org/10.1038/nrm3086openalex-snapshot
The p53 family: guardians of maternal reproduction
inferredcites →https://doi.org/10.1038/onc.2008.37openalex-snapshot
Mechanisms of regulatory diversity within the p53 transcriptional network
inferredcites →https://doi.org/10.1038/sj.cdd.4401914openalex-snapshot
p53/p63/p73 isoforms: an orchestra of isoforms to harmonise cell differentiation and response to stress
inferredcites →https://doi.org/10.1038/sj.emboj.7600708openalex-snapshot
TAp63α induces apoptosis by activating signaling via death receptors and mitochondria
inferredcites →https://doi.org/10.1038/sj.onc.1204149openalex-snapshot
p73 is transcriptionally regulated by DNA damage, p53, and p73
inferredcites →https://doi.org/10.1038/sj.onc.1204427openalex-snapshot
p63α and ΔNp63α can induce cell cycle arrest and apoptosis and differentially regulate p53 target genes
inferredcites →https://doi.org/10.1038/sj.onc.1205465openalex-snapshot
DN-p73 is activated after DNA damage in a p53-dependent manner to regulate p53-induced cell cycle arrest
inferredcites →https://doi.org/10.1038/sj.onc.1206859openalex-snapshot
Differential regulation of p63 and p73 expression
inferredcites →https://doi.org/10.1038/sj.onc.1207129openalex-snapshot
Positive and negative regulation of ΔN-p63 promoter activity by p53 and ΔN-p63-α contributes to differential regulation of p53 target genes
inferredcites →https://doi.org/10.1038/sj.onc.1208215openalex-snapshot
The expression of TA and ΔNp63 are regulated by different mechanisms in liver cells
inferredcites →https://doi.org/10.1038/sj.onc.1210561openalex-snapshot
p63 consensus DNA-binding site: identification, analysis and application into a p63MH algorithm
inferredcites →https://doi.org/10.1073/pnas.0704694105openalex-snapshot
Functional evolution of the p53 regulatory network through its target response elements
inferredcites →https://doi.org/10.1073/pnas.0909129107openalex-snapshot
Estrogen receptor acting in cis enhances WT and mutant p53 transactivation at canonical and noncanonical p53 target sequences
inferredcites →https://doi.org/10.1073/pnas.1013657108openalex-snapshot
Structures of p63 DNA binding domain in complexes with half-site and with spacer-containing full response elements
inferredcites →https://doi.org/10.1073/pnas.1016201108openalex-snapshot
Endogenous retrovirus drives hitherto unknown proapoptotic p63 isoforms in the male germ line of humans and great apes
inferredcites →https://doi.org/10.1073/pnas.1115463109openalex-snapshot
Structure of p73 DNA-binding domain tetramer modulates p73 transactivation
inferredcites →https://doi.org/10.1073/pnas.1205971109openalex-snapshot
Low-level p53 expression changes transactivation rules and reveals superactivating sequences
inferredcites →https://doi.org/10.1073/pnas.1633803100openalex-snapshot
Functional mutants of the sequence-specific transcription factor p53 and implications for master genes of diversity
inferredcites →https://doi.org/10.1074/jbc.m111.315820openalex-snapshot
Pliable DNA Conformation of Response Elements Bound to Transcription Factor p63
inferredcites →https://doi.org/10.1074/jbc.m112.408039openalex-snapshot
Crystal Structures of the DNA-binding Domain Tetramer of the p53 Tumor Suppressor Family Member p73 Bound to Different Full-site Response Elements
inferredcites →https://doi.org/10.1093/nar/29.9.e45openalex-snapshot
A new mathematical model for relative quantification in real-time RT-PCR
inferredcites →https://doi.org/10.1093/nar/gkm1040openalex-snapshot
Algorithm for prediction of tumour suppressor p53 affinity for binding sites in DNA
inferredcites →https://doi.org/10.1093/nar/gkp674openalex-snapshot
Identification and functional characterization of two new transcriptional variants of the human p63 gene
inferredcites →https://doi.org/10.1093/nar/gkq1044openalex-snapshot
Sequence-dependent cooperative binding of p53 to DNA targets and its relationship to the structural properties of the DNA targets
inferredcites →https://doi.org/10.1093/nar/gks389openalex-snapshot
Genome-wide analysis of p63 binding sites identifies AP-2 factors as co-regulators of epidermal differentiation
inferredcites →https://doi.org/10.1093/nar/gkt504openalex-snapshot
Diverse stresses dramatically alter genome-wide p53 binding and transactivation landscape in human cancer cells
inferredcites →https://doi.org/10.1093/nar/gkt657openalex-snapshot
Transactivation specificity is conserved among p53 family proteins and depends on a response element sequence code
inferredcites →https://doi.org/10.1101/cshperspect.a001131openalex-snapshot
Phylogeny and Function of the Invertebrate p53 Superfamily
inferredcites →https://doi.org/10.1101/gad.1165104openalex-snapshot
p63 is the molecular switch for initiation of an epithelial stratification program
inferredcites →https://doi.org/10.1101/gad.224386.113openalex-snapshot
The C terminus of p53 regulates gene expression by multiple mechanisms in a target- and tissue-specific manner in vivo
inferredcites →https://doi.org/10.1128/mcb.22.24.8612-8625.2002openalex-snapshot
Differential Transactivation by the p53 Transcription Factor Is Highly Dependent on p53 Level and Promoter Target Sequence
inferredcites →https://doi.org/10.1128/mcb.22.24.8659-8668.2002openalex-snapshot
Complex Transcriptional Effects of p63 Isoforms: Identification of Novel Activation and Repression Domains†
inferredcites →https://doi.org/10.1128/mcb.25.14.6077-6089.2005openalex-snapshot
Differential Recognition of Response Elements Determines Target Gene Specificity forp53 and p63
inferredcites →https://doi.org/10.1158/0008-5472.758.65.3openalex-snapshot
ΔNp63α Up-Regulates the Hsp70 Gene in Human Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-11-0046openalex-snapshot
Physical Association of HDAC1 and HDAC2 with p63 Mediates Transcriptional Repression and Tumor Maintenance in Squamous Cell Carcinoma
inferredcites →https://doi.org/10.1158/1535-7163.mct-09-0912openalex-snapshot
Interactions of the p53 Protein Family in Cellular Stress Response in Gastrointestinal Tumors
inferredcites →https://doi.org/10.1172/jci30866openalex-snapshot
The p63/p73 network mediates chemosensitivity to cisplatin in a biologically defined subset of primary breast cancers
inferredcites →https://doi.org/10.1177/1947601911408893openalex-snapshot
p53 Isoforms: An Intracellular Microprocessor?
inferredcites →https://doi.org/10.1186/1471-2164-10-628openalex-snapshot
Conservation of DNA-binding specificity and oligomerisation properties within the p53 family
inferredcites →https://doi.org/10.1186/1471-2199-8-43openalex-snapshot
Novel in vivo targets of ΔNp63 in keratinocytes identified by a modified chromatin immunoprecipitation approach
inferredcites →https://doi.org/10.1186/1471-2407-13-552openalex-snapshot
Identification of new p53 target microRNAs by bioinformatics and functional analysis
inferredcites →https://doi.org/10.1242/jcs.049619openalex-snapshot
Regulation of VDR by ΔNp63α is associated with inhibition of cell invasion
inferredcites →https://doi.org/10.1242/jcs.113.10.1661openalex-snapshot
The p53/p63/p73 family of transcription factors: overlapping and distinct functions
inferredcites →https://doi.org/10.1371/journal.pgen.1000104openalex-snapshot
Noncanonical DNA Motifs as Transactivation Targets by Wild Type and Mutant p53
inferredcites →https://doi.org/10.1371/journal.pgen.1000680openalex-snapshot
p63 and p73 Transcriptionally Regulate Genes Involved in DNA Repair
inferredcites →https://doi.org/10.1371/journal.pone.0005623openalex-snapshot
An Active Role of the ΔN Isoform of p63 in Regulating Basal Keratin Genes K5 and K14 and Directing Epidermal Cell Fate
inferredcites →https://doi.org/10.1371/journal.pone.0010236openalex-snapshot
The Coordinated P53 and Estrogen Receptor Cis-Regulation at an FLT1 Promoter SNP Is Specific to Genotoxic Stress and Estrogenic Compound
inferredcites →https://doi.org/10.1371/journal.pone.0020643openalex-snapshot
p53 Transactivation and the Impact of Mutations, Cofactors and Small Molecules Using a Simplified Yeast-Based Screening System
inferredcites →https://doi.org/10.1371/journal.pone.0047889openalex-snapshot
Stability of p53 Homologs
inferredcites →https://doi.org/10.1371/journal.pone.0069152openalex-snapshot
P53 Family Members Modulate the Expression of PRODH, but Not PRODH2, via Intronic p53 Response Elements
inferredcites →https://doi.org/10.4161/cc.10.24.18567openalex-snapshot
Conservation of all three p53 family members and Mdm2 and Mdm4 in the cartilaginous fish
inferredcites →https://doi.org/10.4161/cc.24309openalex-snapshot
Interaction between p53 and estradiol pathways in transcriptional responses to chemotherapeutics
inferredcites →https://doi.org/10.4161/cc.4.8.1904openalex-snapshot
Functional Diversity in the Gene Network Controlled by the Master Regulator p53 in Humans
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.4781335openalex-extracted
The Abl1 Tyrosine Kinase and p53 are Key Players in Doxorubicin-Induced Cardiomyopathy and Their Cell Death Signaling Differs in Atrial and Ventricular Cardiomyocytes
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.11.027openalex-snapshot
Impact of cadmium, cobalt and nickel on sequence-specific DNA binding of p63 and p73 in vitro and in cells
inferred← citeshttps://doi.org/10.1016/j.biochi.2023.09.026openalex-snapshot
Transactivation by partial function P53 family mutants is increased by the presence of G-quadruplexes at a promoter site
inferred← citeshttps://doi.org/10.1016/j.neo.2018.06.008openalex-snapshot
ETV7-Mediated DNAJC15 Repression Leads to Doxorubicin Resistance in Breast Cancer Cells
inferred← citeshttps://doi.org/10.1016/j.omto.2020.06.012openalex-snapshot
Monocarboxylate Transporter 4 Is a Therapeutic Target in Non-small Cell Lung Cancer with Aerobic Glycolysis Preference
inferred← citeshttps://doi.org/10.1016/j.yexcr.2014.09.028openalex-snapshot
Studying p53 family proteins in yeast: Induction of autophagic cell death and modulation by interactors and small molecules
inferred← citeshttps://doi.org/10.1021/acsbiomedchemau.4c00124openalex-snapshot
Chromatin Immunoprecipitation Reveals p53 Binding to G-Quadruplex DNA Sequences in Myeloid Leukemia Cell Lines
inferred← citeshttps://doi.org/10.1038/s41419-021-04005-yopenalex-snapshot
ETV7 regulates breast cancer stem-like cell features by repressing IFN-response genes
inferred← citeshttps://doi.org/10.1038/s41419-023-05718-yopenalex-snapshot
ETV7 reduces inflammatory responses in breast cancer cells by repressing the TNFR1/NF-κB axis
inferred← citeshttps://doi.org/10.1038/s41420-025-02891-1openalex-snapshot
Exploring p53 isoforms: unraveling heterogeneous p53 tumor suppressor functionality in uveal melanoma
inferred← citeshttps://doi.org/10.1038/s41598-019-51349-9openalex-snapshot
Regulatory Crosstalk of Doxorubicin, Estradiol and TNFα Combined Treatment in Breast Cancer-derived Cell Lines
inferred← citeshttps://doi.org/10.1042/bsr20192114openalex-snapshot
P63 modulates the expression of theWDFY2gene which is implicated in cancer regulation and limb development
inferred← citeshttps://doi.org/10.1042/bsr20231348openalex-snapshot
The presence of a G-quadruplex prone sequence upstream of a minimal promoter increases transcriptional activity in the yeast Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1093/femsyr/fow083openalex-snapshot
Human transcription factors in yeast: the fruitful examples of P53 and NF-кB
inferred← citeshttps://doi.org/10.1101/2023.06.23.546269openalex-snapshot
The presence of a G-quadruplex prone sequence upstream of a minimal promoter increases transcriptional activity in the yeast S. cerevisiae
inferred← citeshttps://doi.org/10.1186/s12864-015-1643-9openalex-snapshot
Whole-genome cartography of p53 response elements ranked on transactivation potential
inferred← citeshttps://doi.org/10.1186/s12967-024-05623-8openalex-snapshot
The Abl1 tyrosine kinase is a key player in doxorubicin-induced cardiomyopathy and its p53/p73 cell death mediated signaling differs in atrial and ventricular cardiomyocytes
inferred← citeshttps://doi.org/10.1371/journal.pone.0116177openalex-snapshot
Evolution of p53 Transactivation Specificity through the Lens of a Yeast-Based Functional Assay
inferred← citeshttps://doi.org/10.1371/journal.pone.0130170openalex-snapshot
Quantitative Analysis of NF-κB Transactivation Specificity Using a Yeast-Based Functional Assay
inferred← citeshttps://doi.org/10.18632/oncotarget.11774openalex-snapshot
The dominant-negative interplay between p53, p63 and p73: A family affair
inferred← citeshttps://doi.org/10.18632/oncotarget.18506openalex-snapshot
p53, p63 and p73 in the wonderland ofS. cerevisiae
inferred← citeshttps://doi.org/10.18632/oncotarget.5090openalex-snapshot
p73 regulates basal and starvation-induced liver metabolismin vivo
inferred← citeshttps://doi.org/10.3390/cancers13205231openalex-snapshot
Altered Expression of Shorter p53 Family Isoforms Can Impact Melanoma Aggressiveness
inferred← citeshttps://doi.org/10.3390/genes12020277openalex-snapshot
Evaluating the Influence of a G-Quadruplex Prone Sequence on the Transactivation Potential by Wild-Type and/or Mutant P53 Family Proteins through a Yeast-Based Functional Assay
inferred← citeshttps://doi.org/10.3390/ijms25020714openalex-snapshot
Proline Dehydrogenase (PRODH) Is Expressed in Lung Adenocarcinoma and Modulates Cell Survival and 3D Growth by Inducing Cellular Senescence
inferred← citeshttps://doi.org/10.70675/df567380z9a01z4262z9a43z7666c8df7b0fopenalex-snapshot
Coopération entre les isoformes TAp73 et la signalisation TGF-β dans la régulation de l'expression de la NO Synthase inductible
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