scholarly article | Q13442814 |
P50 | author | Shunsuke Ishii | Q55297655 |
P2093 | author name string | M Xu | |
Y Tanaka | |||
T Maekawa | |||
T Nakahata | |||
T Hongo | |||
I Naruse | |||
P2860 | cites work | Sonic Hedgehog-induced activation of the Gli1 promoter is mediated by GLI3 | Q22009022 |
Isolation of angiopoietin-1, a ligand for the TIE2 receptor, by secretion-trap expression cloning | Q24310148 | ||
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome | Q24311679 | ||
Mutations of the TWIST gene in the Saethre-Chotzen syndrome | Q24311736 | ||
Activation of cAMP and mitogen responsive genes relies on a common nuclear factor | Q24313652 | ||
Histone-like TAFs within the PCAF histone acetylase complex | Q24317520 | ||
The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein | Q24318775 | ||
Nuclear protein CBP is a coactivator for the transcription factor CREB | Q24319801 | ||
Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300 | Q24324556 | ||
A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A | Q24336667 | ||
Activation of p53 sequence-specific DNA binding by acetylation of the p53 C-terminal domain | Q27860534 | ||
A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors | Q27860552 | ||
The transcriptional coactivators p300 and CBP are histone acetyltransferases | Q27860843 | ||
A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
The CBP co-activator is a histone acetyltransferase | Q28131758 | ||
Dorso-ventral and rostro-caudal sequential expression of M-twist in the postimplantation murine embryo. | Q52208238 | ||
Drosophila CBP represses the transcription factor TCF to antagonize Wingless signalling. | Q52566206 | ||
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families | Q55670532 | ||
A family of transcriptional adaptor proteins targeted by the E1A oncoprotein | Q59070933 | ||
Adenoviral ElA-associated protein p300 as a functional homologue of the transcriptional co-activator CBP | Q59095054 | ||
CBP as a transcriptional coactivator of c-Myb | Q64382929 | ||
Cephalic neurulation and optic vesicle formation in the early mouse embryo | Q66936792 | ||
Clonal origin of murine hemopoietic colonies with apparent restriction to granuclocyte-macrophage-megakaryocyte (GMM) differentiation | Q70403278 | ||
RNA helicase A mediates association of CBP with RNA polymerase II | Q28250576 | ||
Cellular and developmental control of O2 homeostasis by hypoxia-inducible factor 1 alpha | Q28259513 | ||
Phosphorylated CREB binds specifically to the nuclear protein CBP | Q28265019 | ||
Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300 | Q28270979 | ||
AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis | Q28273478 | ||
The M-twist gene of Mus is expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and the Drosophila twist genes | Q28276195 | ||
Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor | Q28286827 | ||
The signal-dependent coactivator CBP is a nuclear target for pp90RSK | Q28286828 | ||
Cooperation of Stat2 and p300/CBP in signalling induced by interferon-alpha | Q28292603 | ||
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP | Q28295041 | ||
Requisite role of angiopoietin-1, a ligand for the TIE2 receptor, during embryonic angiogenesis | Q28300359 | ||
twist is required in head mesenchyme for cranial neural tube morphogenesis | Q28590860 | ||
The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo | Q28591300 | ||
Hematopoiesis in the fetal liver is impaired by targeted mutagenesis of a gene encoding a non-DNA binding subunit of the transcription factor, polyomavirus enhancer binding protein 2/core binding factor | Q28594445 | ||
An essential role for p300/CBP in the cellular response to hypoxia | Q28678439 | ||
Regulation of transcription by hypoxia requires a multiprotein complex that includes hypoxia-inducible factor 1, an adjacent transcription factor, and p300/CREB binding protein | Q28678484 | ||
Role of CBP/P300 in nuclear receptor signalling | Q29616443 | ||
Interaction and functional cooperation of the leukemia-associated factors AML1 and p300 in myeloid cell differentiation | Q33888879 | ||
Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome | Q33971011 | ||
CREB-binding protein cooperates with transcription factor GATA-1 and is required for erythroid differentiation | Q35901820 | ||
MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3). | Q36556977 | ||
Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein-Taybi syndrome. | Q36584466 | ||
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism | Q38328546 | ||
The dorsal morphogen gradient regulates the mesoderm determinant twist in early Drosophila embryos | Q38333258 | ||
Interaction of the co-activator CBP with Myb proteins: effects on Myb-specific transactivation and on the cooperativity with NF-M | Q41065257 | ||
Regulation of NF-kappaB by cyclin-dependent kinases associated with the p300 coactivator | Q41133317 | ||
Neurulation in the mouse: manner and timing of neural tube closure | Q41243746 | ||
A novel ES cell line, TT2, with high germline-differentiating potency | Q41524060 | ||
Interaction and functional collaboration of p300/CBP and bHLH proteins in muscle and B-cell differentiation | Q42808711 | ||
Regulation of activity of the transcription factor GATA-1 by acetylation | Q42823439 | ||
Acetylation of HMG I(Y) by CBP turns off IFN beta expression by disrupting the enhanceosome | Q44646118 | ||
The CBFbeta subunit is essential for CBFalpha2 (AML1) function in vivo | Q45345510 | ||
Functional analysis of the Drosophila twist promoter reveals a dorsal-binding ventral activator region | Q46065140 | ||
Sequence-specific transactivation of the Drosophila twist gene by the dorsal gene product | Q47070839 | ||
Drosophila CBP is a co-activator of cubitus interruptus in hedgehog signalling | Q47072204 | ||
Conjunction dysfunction: CBP/p300 in human disease. | Q48013074 | ||
Closure of the neural tube in the cephalic region of the mouse embryo | Q48247586 | ||
Drosophila CBP is required for dorsal-dependent twist gene expression. | Q52192359 | ||
Sending and receiving the hedgehog signal: control by the Drosophila Gli protein Cubitus interruptus. | Q52201064 | ||
Expression of M-twist during postimplantation development of the mouse. | Q52205008 | ||
P433 | issue | 1-2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | brain | Q1073 |
bleeding | Q166019 | ||
P304 | page(s) | 133-145 | |
P577 | publication date | 2000-07-01 | |
P1433 | published in | Mechanisms of Development | Q6804657 |
P1476 | title | Extensive brain hemorrhage and embryonic lethality in a mouse null mutant of CREB-binding protein | |
P478 | volume | 95 |
Q38766912 | A Small Molecule Activator of p300/CBP Histone Acetyltransferase Promotes Survival and Neurite Growth in a Cellular Model of Parkinson's Disease. |
Q30357571 | A TDG/CBP/RARα ternary complex mediates the retinoic acid-dependent expression of DNA methylation-sensitive genes |
Q36349016 | A unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice |
Q39598834 | Ablation of CBP in forebrain principal neurons causes modest memory and transcriptional defects and a dramatic reduction of histone acetylation but does not affect cell viability |
Q37249167 | Acetyltransferases (HATs) as targets for neurological therapeutics |
Q44225326 | Age-related changes in CREB binding protein immunoreactivity in the cerebral cortex and hippocampus of rats |
Q41993123 | Amphipathic small molecules mimic the binding mode and function of endogenous transcription factors |
Q37140791 | An overview of nuclear receptor coregulators involved in cerebellar development |
Q37935915 | Bromodomains as therapeutic targets |
Q58721602 | CBP and P300 regulate distinct gene networks required for human primary myoblast differentiation and muscle integrity |
Q92237346 | CBP and SRF co-regulate dendritic growth and synaptic maturation |
Q30436207 | CBP and p300 are essential for renin cell identity and morphological integrity of the kidney |
Q37352828 | CBP/p300 and associated transcriptional co-activators exhibit distinct expression patterns during murine craniofacial and neural tube development |
Q38340711 | CBP/p300 double null cells reveal effect of coactivator level and diversity on CREB transactivation |
Q34080062 | Characterization of an antagonistic switch between histone H3 lysine 27 methylation and acetylation in the transcriptional regulation of Polycomb group target genes |
Q34327866 | Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration. |
Q38151696 | Chromatin-based epigenetics of adult subventricular zone neural stem cells |
Q33593991 | Complex regulation of the transactivation function of hypoxia-inducible factor-1 alpha by direct interaction with two distinct domains of the CREB-binding protein/p300. |
Q38208728 | Crafting the brain - role of histone acetyltransferases in neural development and disease. |
Q37688395 | Crucial roles of histone-modifying enzymes in mediating neural cell-type specification |
Q38037625 | DNA demethylation by TDG. |
Q28591430 | Differential role of p300 and CBP acetyltransferase during myogenesis: p300 acts upstream of MyoD and Myf5 |
Q28589003 | Disruption of Sept6, a fusion partner gene of MLL, does not affect ontogeny, leukemogenesis induced by MLL-SEPT6, or phenotype induced by the loss of Sept4. |
Q34379557 | Distinct roles for CREB-binding protein and p300 in hematopoietic stem cell self-renewal |
Q33522839 | Diversity of mechanisms involved in aromatase regulation and estrogen action in the brain |
Q47423681 | Epigenetic Etiology of Intellectual Disability |
Q26748876 | Epigenetic Mechanisms in Developmental Alcohol-Induced Neurobehavioral Deficits |
Q50421076 | Epigenetic modifiers promote mitochondrial biogenesis and oxidative metabolism leading to enhanced differentiation of neuroprogenitor cells. |
Q34747263 | Epigenetic programming of hypoxic-ischemic encephalopathy in response to fetal hypoxia |
Q34449181 | Epigenetic regulation of cardiac myocyte differentiation. |
Q24672302 | Essential function of p300 acetyltransferase activity in heart, lung and small intestine formation |
Q39067631 | Functions of bromodomain-containing proteins and their roles in homeostasis and cancer. |
Q26996782 | Gene-environment interactions in severe intraventricular hemorrhage of preterm neonates |
Q44296681 | Generation of a conditional allele of the CBP gene in mouse |
Q33713299 | Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study |
Q64246563 | Genetic Association of Phosphodiesterases With Human Cognitive Performance |
Q28593439 | Genetic ablation of the steroid receptor coactivator-ubiquitin ligase, E6-AP, results in tissue-selective steroid hormone resistance and defects in reproduction |
Q24556629 | Genetic deletion of the repressor of estrogen receptor activity (REA) enhances the response to estrogen in target tissues in vivo |
Q28536743 | Genetic interaction between mutations in c-Myb and the KIX domains of CBP and p300 affects multiple blood cell lineages and influences both gene activation and repression |
Q34552276 | Genetics and development of neural tube defects. |
Q34122513 | Genome-wide assessment of differential roles for p300 and CBP in transcription regulation |
Q53290791 | Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate. |
Q24685650 | Global transcriptional coactivators CREB-binding protein and p300 are highly essential collectively but not individually in peripheral B cells |
Q37247908 | Histone acetyltransferase CBP is vital to demarcate conventional and innate CD8+ T-cell development |
Q28585449 | Histone acetyltransferase activities of cAMP-regulated enhancer-binding protein and p300 in tissues of fetal, young, and old mice |
Q26745642 | Histone acetyltransferases: challenges in targeting bi-substrate enzymes |
Q37528712 | Histone posttranslational modifications and cell fate determination: lens induction requires the lysine acetyltransferases CBP and p300. |
Q42524420 | Identification of p300-targeted acetylated residues in GATA4 during hypertrophic responses in cardiac myocytes |
Q87904878 | Identification of transcripts potentially involved in neural tube closure using RNA sequencing |
Q28566098 | Interaction between the HPV E7 oncoprotein and the transcriptional coactivator p300 |
Q38364553 | Intrinsic regulations in neural fate commitment. |
Q36021885 | Is histone acetylation the most important physiological function for CBP and p300? |
Q97565930 | KLF3 Mediates Epidermal Differentiation through the Epigenomic Writer CBP |
Q39747094 | KLF8 recruits the p300 and PCAF co-activators to its amino terminal activation domain to activate transcription |
Q47395308 | Loss of p300 and CBP disrupts histone acetylation at the mouse Sry promoter and causes XY gonadal sex reversal. |
Q38085375 | Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders. |
Q36970331 | MOF maintains transcriptional programs regulating cellular stress response. |
Q28567072 | NF-Y is essential for expression of the proapoptotic bim gene in sympathetic neurons |
Q36012078 | Nuclear receptor coregulators are new players in nervous system development and function |
Q33193939 | Quantitative analysis of CBP- and P300-induced histone acetylations in vivo using native chromatin. |
Q73443708 | Reactive astrocytes express cAMP-response-element-binding protein (CREB) binding protein (CBP) in the central nervous system of transgenic mice expressing a human Cu/Zn superoxide dismutase mutation |
Q39838387 | Retinoid signaling and neurogenin2 function are coupled for the specification of spinal motor neurons through a chromatin modifier CBP |
Q24300183 | Roles of HIPK1 and HIPK2 in AML1- and p300-dependent transcription, hematopoiesis and blood vessel formation |
Q46134600 | Rubinstein-Taybi Syndrome and Epigenetic Alterations. |
Q36973859 | Rubinstein-Taybi syndrome: clinical and molecular overview |
Q32874823 | Setd5 is essential for mammalian development and the co-transcriptional regulation of histone acetylation |
Q38867041 | Small-molecule inhibition of CBP/catenin interactions eliminates drug-resistant clones in acute lymphoblastic leukemia |
Q34692024 | Small-molecule inhibitors of acetyltransferase p300 identified by high-throughput screening are potent anticancer agents. |
Q37122796 | Spatiotemporal expression of histone acetyltransferases, p300 and CBP, in developing embryonic hearts |
Q37242469 | TGF-β signaling in endothelial cells, but not neuroepithelial cells, is essential for cerebral vascular development |
Q37683304 | Target gene context influences the transcriptional requirement for the KAT3 family of CBP and p300 histone acetyltransferases. |
Q36837326 | The Rubinstein-Taybi syndrome: modeling mental impairment in the mouse |
Q58617586 | The many lives of KATs - detectors, integrators and modulators of the cellular environment |
Q38331056 | The transcriptional coactivator Cbp regulates self-renewal and differentiation in adult hematopoietic stem cells. |
Q28572612 | The transcriptional coactivator p300 plays a critical role in the hypertrophic and protective pathways induced by phenylephrine in cardiac cells but is specific to the hypertrophic effect of urocortin |
Q24309357 | Thymine DNA glycosylase is essential for active DNA demethylation by linked deamination-base excision repair |
Q34037768 | Transcription coactivators p300 and CBP are necessary for photoreceptor-specific chromatin organization and gene expression |
Q35280876 | Two histone/protein acetyltransferases, CBP and p300, are indispensable for Foxp3+ T-regulatory cell development and function |
Q39705049 | Two transactivation mechanisms cooperate for the bulk of HIF-1-responsive gene expression. |
Q39960651 | VP16-dependent association of chromatin-modifying coactivators and underrepresentation of histones at immediate-early gene promoters during herpes simplex virus infection |
Q37260433 | beta8 integrins are required for vascular morphogenesis in mouse embryos |
Q92395381 | p300 and cAMP response element-binding protein-binding protein in skeletal muscle homeostasis, contractile function, and survival |
Q35192595 | p300-Dependent ATF5 acetylation is essential for Egr-1 gene activation and cell proliferation and survival |