scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Jose P Lopez-Atalaya | Q58883299 |
Angel Barco | Q37387292 | ||
Luis M. Valor | Q43154749 | ||
P2093 | author name string | Jose Viosca | |
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Rubinstein‐Taybi syndrome medical guidelines | Q52105470 | ||
Inhibition of histone deacetylation protects wild-type but not gelsolin-deficient neurons from oxygen/glucose deprivation. | Q52931322 | ||
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Adenoviral ElA-associated protein p300 as a functional homologue of the transcriptional co-activator CBP | Q59095054 | ||
Acetylation control of the retinoblastoma tumour-suppressor protein | Q64379714 | ||
Acetylation of MyoD by p300 requires more than its histone acetyltransferase domain | Q74568433 | ||
p300/CREB-binding protein interacts with ATR and is required for the DNA replication checkpoint | Q79710648 | ||
Further case of Rubinstein-Taybi syndrome due to a deletion in EP300 | Q83624716 | ||
Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity | Q95721056 | ||
Epigenetic mechanisms in memory formation. | Q36011654 | ||
Pleiotropic protective effects of phytochemicals in Alzheimer's disease | Q36012073 | ||
Transgenic mice expressing an inhibitory truncated form of p300 exhibit long-term memory deficits. | Q36013236 | ||
Is histone acetylation the most important physiological function for CBP and p300? | Q36021885 | ||
Joining the dots: from chromatin remodeling to neuronal plasticity | Q36032226 | ||
Paraquat induces epigenetic changes by promoting histone acetylation in cell culture models of dopaminergic degeneration | Q36123405 | ||
Paradoxical enhancement of fear extinction memory and synaptic plasticity by inhibition of the histone acetyltransferase p300 | Q36281272 | ||
p300/CBP-associated factor selectively regulates the extinction of conditioned fear | Q36303815 | ||
Regulation of CRE-dependent transcription by presenilins: prospects for therapy of Alzheimer's disease | Q36335999 | ||
An essential role for histone deacetylase 4 in synaptic plasticity and memory formation | Q36344938 | ||
Selective histone deacetylase (HDAC) inhibition imparts beneficial effects in Huntington's disease mice: implications for the ubiquitin-proteasomal and autophagy systems. | Q36435854 | ||
Epigenetic mechanisms: a common theme in vertebrate and invertebrate memory formation. | Q36441080 | ||
Histone deacetylase (HDAC) inhibitors targeting HDAC3 and HDAC1 ameliorate polyglutamine-elicited phenotypes in model systems of Huntington's disease. | Q36482299 | ||
Altered memory capacities and response to stress in p300/CBP-associated factor (PCAF) histone acetylase knockout mice | Q36761722 | ||
The Rubinstein-Taybi syndrome: modeling mental impairment in the mouse | Q36837326 | ||
Mapping of cellular protein-binding sites on the products of early-region 1A of human adenovirus type 5. | Q36845795 | ||
Rubinstein-Taybi syndrome: clinical and molecular overview | Q36973859 | ||
Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner | Q36981055 | ||
Beyond transcription factors: the role of chromatin modifying enzymes in regulating transcription required for memory | Q37201297 | ||
Modulation of long-term memory for object recognition via HDAC inhibition | Q37224213 | ||
Structure and chemistry of the p300/CBP and Rtt109 histone acetyltransferases: implications for histone acetyltransferase evolution and function | Q37290564 | ||
Regulation of chromatin structure in memory formation | Q37347946 | ||
CBP/p300 and associated transcriptional co-activators exhibit distinct expression patterns during murine craniofacial and neural tube development | Q37352828 | ||
Decoding the epigenetic language of neuronal plasticity | Q37358580 | ||
Dynamic bookmarking of primary response genes by p300 and RNA polymerase II complexes. | Q37429059 | ||
Histone acetyl transferases as emerging drug targets. | Q37540911 | ||
Histone deacetylase inhibition-mediated neuronal differentiation of multipotent adult neural progenitor cells | Q37610451 | ||
Persistent improvement in synaptic and cognitive functions in an Alzheimer mouse model after rolipram treatment | Q37625928 | ||
Target gene context influences the transcriptional requirement for the KAT3 family of CBP and p300 histone acetyltransferases. | Q37683304 | ||
Protein acetylation in synaptic plasticity and memory | Q37706786 | ||
CREB's control of intrinsic and synaptic plasticity: implications for CREB-dependent memory models. | Q37707617 | ||
Aberrant histone acetylation, altered transcription, and retinal degeneration in a Drosophila model of polyglutamine disease are rescued by CREB-binding protein | Q35965543 | ||
HATs and HDACs in neurodegeneration: a tale of disconcerted acetylation homeostasis. | Q35968237 | ||
Huntington's gene finally found | Q45291214 | ||
CRE-mediated transcription is increased in Huntington's disease transgenic mice. | Q45292425 | ||
Phosphodiesterase type IV inhibition prevents sequestration of CREB binding protein, protects striatal parvalbumin interneurons and rescues motor deficits in the R6/2 mouse model of Huntington's disease | Q45293113 | ||
p53 mediates cellular dysfunction and behavioral abnormalities in Huntington's disease | Q45297400 | ||
Striatal modulation of cAMP-response-element-binding protein (CREB) after excitotoxic lesions: implications with neuronal vulnerability in Huntington's disease. | Q45299845 | ||
Metabolic and glutamatergic disturbances in the Huntington's disease transgenic mouse. | Q45299857 | ||
Differential contributions of Caenorhabditis elegans histone deacetylases to huntingtin polyglutamine toxicity. | Q45300254 | ||
Neuronal intranuclear inclusions and neuropil aggregates in HdhCAG(150) knockin mice | Q45303809 | ||
CREB-binding protein modulates repeat instability in a Drosophila model for polyQ disease | Q45304348 | ||
Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity. | Q45305295 | ||
Huntingtin inclusions do not deplete polyglutamine-containing transcription factors in HD mice | Q45305847 | ||
Dysregulation of histone acetylation in the APP/PS1 mouse model of Alzheimer's disease. | Q45922651 | ||
Phenylbutyrate ameliorates cognitive deficit and reduces tau pathology in an Alzheimer's disease mouse model | Q46162286 | ||
Identification of long chain alkylidenemalonates as novel small molecule modulators of histone acetyltransferases. | Q46628836 | ||
Behavioral characteristics of three children with the broad thumb-hallux (Rubinstein-Taybi) syndrome | Q46704858 | ||
Inhibition of histone deacetylation protects wildtype but not gelsolin-deficient mice from ischemic brain injury | Q46782849 | ||
Systemic or intrahippocampal delivery of histone deacetylase inhibitors facilitates fear extinction | Q46972944 | ||
Intrinsically fluorescent carbon nanospheres as a nuclear targeting vector: delivery of membrane-impermeable molecule to modulate gene expression in vivo. | Q47341033 | ||
Polyglutamine-expanded spinocerebellar ataxia-7 protein disrupts normal SAGA and SLIK histone acetyltransferase activity | Q27931763 | ||
Extensive brain hemorrhage and embryonic lethality in a mouse null mutant of CREB-binding protein | Q28141517 | ||
Stimulation of NF-E2 DNA binding by CREB-binding protein (CBP)-mediated acetylation | Q28142527 | ||
A CBP binding transcriptional repressor produced by the PS1/epsilon-cleavage of N-cadherin is inhibited by PS1 FAD mutations | Q28185270 | ||
HATs and HDACs: from structure, function and regulation to novel strategies for therapy and prevention | Q28240437 | ||
Genome-wide mapping of HATs and HDACs reveals distinct functions in active and inactive genes | Q28255974 | ||
Phosphorylated CREB binds specifically to the nuclear protein CBP | Q28265019 | ||
CBP histone acetyltransferase activity is a critical component of memory consolidation | Q28267700 | ||
Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300 | Q28270979 | ||
Loss of HDAC5 impairs memory function: implications for Alzheimer's disease | Q28273493 | ||
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP | Q28295041 | ||
Selective modulation of some forms of schaffer collateral-CA1 synaptic plasticity in mice with a disruption of the CPEB-1 gene | Q28513435 | ||
Spatial memory consolidation is associated with induction of several lysine-acetyltransferase (histone acetyltransferase) expression levels and H2B/H4 acetylation-dependent transcriptional events in the rat hippocampus. | Q28564318 | ||
α-Synuclein negatively regulates protein kinase Cδ expression to suppress apoptosis in dopaminergic neurons by reducing p300 histone acetyltransferase activity | Q28572683 | ||
Mutant huntingtin represses CBP, but not p300, by binding and protein degradation | Q28574845 | ||
Loss of presenilin function causes impairments of memory and synaptic plasticity followed by age-dependent neurodegeneration | Q28590719 | ||
New nomenclature for chromatin-modifying enzymes | Q29616425 | ||
Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila | Q29616737 | ||
Alzheimer's disease | Q29616743 | ||
p300/CBP proteins: HATs for transcriptional bridges and scaffolds | Q29617981 | ||
Function and regulation of CREB family transcription factors in the nervous system | Q29619559 | ||
Recovery of learning and memory is associated with chromatin remodelling | Q29619784 | ||
Proteome-wide prediction of acetylation substrates | Q30437029 | ||
Subregion-specific p300 conditional knock-out mice exhibit long-term memory impairments | Q30470054 | ||
CREB binding protein is required for both short-term and long-term memory formation | Q30476167 | ||
Inhibitors of class 1 histone deacetylases reverse contextual memory deficits in a mouse model of Alzheimer's disease | Q30498541 | ||
Quantitative analysis of CBP- and P300-induced histone acetylations in vivo using native chromatin. | Q33193939 | ||
Virtual ligand screening of the p300/CBP histone acetyltransferase: identification of a selective small molecule inhibitor | Q33599508 | ||
Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity and memory storage. | Q33736104 | ||
Environmental neurotoxic pesticide increases histone acetylation to promote apoptosis in dopaminergic neuronal cells: relevance to epigenetic mechanisms of neurodegeneration | Q33762517 | ||
Membrane-associated glucocorticoid activity is necessary for modulation of long-term memory via chromatin modification | Q33817894 | ||
Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration | Q33854083 | ||
HATs off: selective synthetic inhibitors of the histone acetyltransferases p300 and PCAF. | Q33908350 | ||
CREB is a key regulator of striatal vulnerability in chemical and genetic models of Huntington's disease | Q33908482 | ||
Epigenetic alterations are critical for fear memory consolidation and synaptic plasticity in the lateral amygdala | Q33916385 | ||
Dynamic epigenetic regulation in neurons: enzymes, stimuli and signaling pathways | Q37803122 | ||
Targeting the correct HDAC(s) to treat cognitive disorders | Q37803453 | ||
CREB: a multifaceted regulator of neuronal plasticity and protection | Q37806285 | ||
Chemical biology of histone acetyltransferase natural compounds modulators | Q37825449 | ||
Epigenetic regulation of gene expression in physiological and pathological brain processes | Q37870034 | ||
Genetic approaches to investigate the role of CREB in neuronal plasticity and memory. | Q37938886 | ||
Challenges associated with curcumin therapy in Alzheimer disease | Q37952439 | ||
The potential of HDAC inhibitors as cognitive enhancers. | Q38072102 | ||
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism | Q38328546 | ||
CBP/p300 double null cells reveal effect of coactivator level and diversity on CREB transactivation | Q38340711 | ||
Suppression of aggregate formation of mutant huntingtin potentiates CREB-binding protein sequestration and apoptotic cell death | Q39436375 | ||
Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein-Taybi syndrome. | Q39460830 | ||
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 | Q39598834 | ||
Partial depletion of CREB-binding protein reduces life expectancy in a mouse model of Huntington disease. | Q39706773 | ||
The identification of a novel natural activator of p300 histone acetyltranferase provides new insights into the modulation mechanism of this enzyme. | Q39717695 | ||
HDAC inhibitor trichostatin A-inhibited survival of dopaminergic neuronal cells | Q39786674 | ||
p300 activation by Presenilin 1 but not by its M146L mutant. | Q40188420 | ||
Distribution of histone deacetylases 1-11 in the rat brain | Q40225359 | ||
Depletion of CBP is directly linked with cellular toxicity caused by mutant huntingtin | Q40269204 | ||
CREB-binding protein activation by presenilin 1 but not by its M146L mutant | Q40273213 | ||
Critical loss of CBP/p300 histone acetylase activity by caspase-6 during neurodegeneration. | Q40323686 | ||
Using proteomics and network analysis to elucidate the consequences of synaptic protein oxidation in a PS1 + AbetaPP mouse model of Alzheimer's disease | Q40366410 | ||
Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington's disease | Q40782711 | ||
CREB binding protein recruitment to the transcription complex requires growth factor-dependent phosphorylation of its GF box. | Q40791260 | ||
CREB-binding protein sequestration by expanded polyglutamine | Q40859094 | ||
Regulation of NF-kappaB by cyclin-dependent kinases associated with the p300 coactivator | Q41133317 | ||
Acetylation of general transcription factors by histone acetyltransferases | Q41586010 | ||
The IkappaB kinase regulates chromatin structure during reconsolidation of conditioned fear memories. | Q41652035 | ||
Acetylation targets mutant huntingtin to autophagosomes for degradation | Q41773329 | ||
Post-training intrahippocampal inhibition of class I histone deacetylases enhances long-term object-location memory | Q41873212 | ||
Histone modifications around individual BDNF gene promoters in prefrontal cortex are associated with extinction of conditioned fear | Q42628513 | ||
Regulation of activity of the transcription factor GATA-1 by acetylation | Q42823439 | ||
Alteration of working memory but not in anxiety or stress response in p300/CBP associated factor (PCAF) histone acetylase knockout mice bred on a C57BL/6 background. | Q43108180 | ||
Genetic heterogeneity in Rubinstein-Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300. | Q43163937 | ||
Histone acetylation is recruited in consolidation as a molecular feature of stronger memories | Q43268931 | ||
Beta -amyloid-(1-42) impairs activity-dependent cAMP-response element-binding protein signaling in neurons at concentrations in which cell survival Is not compromised | Q43559766 | ||
Phenylbutyrate rescues dendritic spine loss associated with memory deficits in a mouse model of Alzheimer disease | Q43648215 | ||
Phosphorylation of CBP mediates transcriptional activation by neural activity and CaM kinase IV. | Q43968740 | ||
Integration of long-term-memory-related synaptic plasticity involves bidirectional regulation of gene expression and chromatin structure | Q44220427 | ||
Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome | Q44302108 | ||
Small molecule modulators of histone acetyltransferase p300. | Q44353899 | ||
Histone Deacetylase Inhibition by Sodium Butyrate Chemotherapy Ameliorates the Neurodegenerative Phenotype in Huntington's Disease Mice | Q44619618 | ||
Chromatin remodeling and neuronal response: multiple signaling pathways induce specific histone H3 modifications and early gene expression in hippocampal neurons | Q44660996 | ||
Decreased cAMP response element-mediated transcription: an early event in exon 1 and full-length cell models of Huntington's disease that contributes to polyglutamine pathogenesis | Q44662096 | ||
Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy | Q44854729 | ||
Valproic acid reduces brain damage induced by transient focal cerebral ischemia in rats: potential roles of histone deacetylase inhibition and heat shock protein induction | Q44930696 | ||
Regulation of histone acetylation during memory formation in the hippocampus. | Q44992481 | ||
Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease | Q45115023 | ||
Inducible PC12 cell model of Huntington's disease shows toxicity and decreased histone acetylation | Q45288904 | ||
Alcohol exposure decreases CREB binding protein expression and histone acetylation in the developing cerebellum | Q33927405 | ||
Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease | Q33942130 | ||
CBP and p300: HATs for different occasions | Q33980693 | ||
CBP is required for environmental enrichment-induced neurogenesis and cognitive enhancement | Q34028180 | ||
Histone deacetylase inhibitors enhance memory and synaptic plasticity via CREB:CBP-dependent transcriptional activation | Q34077367 | ||
A transcriptional switch mediated by cofactor methylation | Q34101080 | ||
Viral replication and the coactivators p300 and CBP. | Q34104253 | ||
Altered histone acetylation is associated with age-dependent memory impairment in mice. | Q34114011 | ||
Tuning acetylation levels with HAT activators: Therapeutic strategy in neurodegenerative diseases | Q34137377 | ||
HDAC3 is a critical negative regulator of long-term memory formation | Q34158695 | ||
Histone deacetylase complexes promote trinucleotide repeat expansions | Q34169694 | ||
Epigenetic changes induced by curcumin and other natural compounds. | Q34180255 | ||
Amyloid beta -peptide inhibition of the PKA/CREB pathway and long-term potentiation: reversibility by drugs that enhance cAMP signaling | Q34192226 | ||
CREB-binding protein controls response to cocaine by acetylating histones at the fosB promoter in the mouse striatum | Q34245266 | ||
Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration. | Q34327866 | ||
Crebinostat: a novel cognitive enhancer that inhibits histone deacetylase activity and modulates chromatin-mediated neuroplasticity | Q34329880 | ||
Cellular targets for transformation by the adenovirus E1A proteins | Q34438094 | ||
Histone deactylase inhibition combined with behavioral therapy enhances learning and memory following traumatic brain injury | Q34441350 | ||
CBP gene transfer increases BDNF levels and ameliorates learning and memory deficits in a mouse model of Alzheimer's disease | Q34450215 | ||
The versatile functions of the transcriptional coactivators p300 and CBP and their roles in disease | Q34606655 | ||
Curcumin: a potential neuroprotective agent in Parkinson's disease | Q34634749 | ||
Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease | Q34763178 | ||
CREBBP mutations in relapsed acute lymphoblastic leukaemia | Q34792792 | ||
Experience-dependent epigenetic modifications in the central nervous system. | Q34954649 | ||
Dynamic acetylation of all lysine-4 trimethylated histone H3 is evolutionarily conserved and mediated by p300/CBP | Q34977966 | ||
CBP-mediated acetylation of histone H3 lysine 27 antagonizes Drosophila Polycomb silencing. | Q34998982 | ||
Hippocampal focal knockout of CBP affects specific histone modifications, long-term potentiation, and long-term memory | Q35112173 | ||
Protective effects of valproic acid on the nigrostriatal dopamine system in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model of Parkinson's disease | Q35385117 | ||
A transcription factor-binding domain of the coactivator CBP is essential for long-term memory and the expression of specific target genes | Q35612900 | ||
Drosophila dCBP is involved in establishing the DNA replication checkpoint | Q35641689 | ||
Increased EID1 nuclear translocation impairs synaptic plasticity and memory function associated with pathogenesis of Alzheimer's disease | Q35748624 | ||
Alpha-synuclein: normal function and role in neurodegenerative diseases. | Q35749928 | ||
The effects of ethanol on the developing cerebellum and eyeblink classical conditioning. | Q35949348 | ||
P275 | copyright license | Creative Commons Attribution 2.5 Generic | Q18810333 |
P433 | issue | 28 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | transcription factor | Q407384 |
targeted therapy | Q492646 | ||
neurodegeneration | Q1755122 | ||
cell | Q7868 | ||
cognitive disorder | Q3065932 | ||
nerve tissue protein | Q6996861 | ||
enzyme | Q8047 | ||
nervous system | Q9404 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | 5051-5064 | |
P577 | publication date | 2013-01-01 | |
P1433 | published in | Current Pharmaceutical Design | Q5195068 |
P1476 | title | Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders | |
P478 | volume | 19 |
Q38766912 | A Small Molecule Activator of p300/CBP Histone Acetyltransferase Promotes Survival and Neurite Growth in a Cellular Model of Parkinson's Disease. |
Q43833014 | A novel activator of CBP/p300 acetyltransferases promotes neurogenesis and extends memory duration in adult mice. |
Q47575767 | A role for histone acetylation mechanisms in adolescent alcohol exposure-induced deficits in hippocampal brain-derived neurotrophic factor expression and neurogenesis markers in adulthood |
Q37249167 | Acetyltransferases (HATs) as targets for neurological therapeutics |
Q28070096 | Adolescent Alcohol Exposure Persistently Impacts Adult Neurobiology and Behavior |
Q92237346 | CBP and SRF co-regulate dendritic growth and synaptic maturation |
Q38815116 | CREB-binding protein regulates lung cancer growth by targeting MAPK and CPSF4 signaling pathway |
Q39423291 | Chemical modulators for epigenome reader domains as emerging epigenetic therapies for cancer and inflammation |
Q47128083 | Chemical probes and inhibitors of bromodomains outside the BET family |
Q35112822 | Curcumin alleviates neuropathic pain by inhibiting p300/CBP histone acetyltransferase activity-regulated expression of BDNF and cox-2 in a rat model. |
Q49949196 | Discovery of Spiro Oxazolidinediones as Selective, Orally Bioavailable Inhibitors of p300/CBP Histone Acetyltransferases |
Q48701393 | Dissociable roles for histone acetyltransferases p300 and PCAF in hippocampus and perirhinal cortex-mediated object memory |
Q35772931 | Drosophila Eye Model to Study Neuroprotective Role of CREB Binding Protein (CBP) in Alzheimer's Disease |
Q28088777 | Drosophila as an In Vivo Model for Human Neurodegenerative Disease |
Q28077090 | Dysregulation of Acetylation Enzymes Inanimal Models of Psychostimulant use Disorders: Evolving Stories |
Q90388893 | Early Drug-Discovery Efforts towards the Identification of EP300/CBP Histone Acetyltransferase (HAT) Inhibitors |
Q47423681 | Epigenetic Etiology of Intellectual Disability |
Q30358152 | Epigenetic assays for chemical biology and drug discovery. |
Q34323841 | Epigenetic memory: the Lamarckian brain |
Q54765415 | Epigenetics, fragile X syndrome and transcriptional therapy. |
Q97533922 | Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann-Steiner and Rubinstein-Taybi syndromes |
Q38246625 | Genetic findings in obsessive-compulsive disorder connect to brain-derived neutrophic factor and mammalian target of rapamycin pathways: implications for drug development |
Q43690913 | Genomic landscape of transcriptional and epigenetic dysregulation in early onset polyglutamine disease. |
Q91655544 | Histone Acetyltransferase p300 Induces De Novo Super-Enhancers to Drive Cellular Senescence |
Q35853603 | Histone acetylation inhibitors promote axon growth in adult dorsal root ganglia neurons |
Q34683308 | Histone hyperacetylation up-regulates protein kinase Cδ in dopaminergic neurons to induce cell death: relevance to epigenetic mechanisms of neurodegeneration in Parkinson disease |
Q27003952 | Histone-modifying enzymes, histone modifications and histone chaperones in nucleosome assembly: Lessons learned from Rtt109 histone acetyltransferases |
Q96134406 | Identification of lysine acetylome in cervical cancer by label-free quantitative proteomics |
Q38363468 | Inhibition of different histone acetyltransferases (HATs) uncovers transcription-dependent and -independent acetylation-mediated mechanisms in memory formation |
Q47869988 | Insights into intermolecular interactions, electrostatic properties and the stability of C646 in the binding pocket of p300 histone acetyltransferase enzyme: a combined molecular dynamics and charge density study |
Q39376004 | Integration of Bioorthogonal Probes and Q-FRET for the Detection of Histone Acetyltransferase Activity |
Q36812681 | Involvement of phosphorylated Apis mellifera CREB in gating a honeybee's behavioral response to an external stimulus |
Q95660209 | KAT3-dependent acetylation of cell type-specific genes maintains neuronal identity in the adult mouse brain |
Q90643583 | Lifespan-increasing drug nordihydroguaiaretic acid inhibits p300 and activates autophagy |
Q89459080 | MicroRNA-132 provides neuroprotection for tauopathies via multiple signaling pathways |
Q60458527 | Modulating the masters: chemical tools to dissect CBP and p300 function |
Q29247921 | Modulation of proteostasis by transcription factor NRF2 and impact in neurodegenerative diseases |
Q33972484 | Molecular targets of chromatin repressive mark H3K9me3 in primate progenitor cells within adult neurogenic niches. |
Q60924003 | Nutrient-Dependent Changes of Protein Palmitoylation: Impact on Nuclear Enzymes and Regulation of Gene Expression |
Q30405868 | Prefrontal consolidation supports the attainment of fear memory accuracy |
Q92450973 | Promoting tau secretion and propagation by hyperactive p300/CBP via autophagy-lysosomal pathway in tauopathy |
Q55248558 | Proteasomal degradation of the histone acetyl transferase p300 contributes to beta-cell injury in a diabetes environment. |
Q57054631 | Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator |
Q91755231 | Role of SIRT1 in Modulating Acetylation of the Sarco-Endoplasmic Reticulum Ca2+-ATPase in Heart Failure |
Q27026861 | Sirtuins in epigenetic regulation |
Q38973220 | Spatial genome organization and cognition |
Q40271872 | Structure-Activity Relationships on Cinnamoyl Derivatives as Inhibitors of p300 Histone Acetyltransferase. |
Q58546879 | The Epigenetic Factor CBP Is Required for the Differentiation and Function of Medial Ganglionic Eminence-Derived Interneurons |
Q64898882 | The Regulatory Effects of Acetyl-CoA Distribution in the Healthy and Diseased Brain. |
Q35111862 | The epigenetic landscape of alcoholism |
Q35024695 | Transcription, epigenetics and ameliorative strategies in Huntington's Disease: a genome-wide perspective |
Q58700177 | Ubiquitin Regulation: The Histone Modifying Enzyme's Story |
Q50660192 | Vitamin A deficiency impairs spatial learning and memory: the mechanism of abnormal CBP-dependent histone acetylation regulated by retinoic acid receptor alpha. |
Q26740071 | Where Environment Meets Cognition: A Focus on Two Developmental Intellectual Disability Disorders |
Q50542122 | [Epigenetic regulations and cerebral plasticity: towards new therapeutic options in neurodegenerative diseases?] |
Q36705321 | p300 is not required for metabolic adaptation to endurance exercise training. |
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