scholarly article | Q13442814 |
P356 | DOI | 10.1111/GBB.12303 |
P698 | PubMed publication ID | 27251651 |
P2093 | author name string | M Wolter | |
B Christen | |||
O Zaika | |||
B E Kalisch | |||
B D Winters | |||
J M Cloke | |||
K A Mitchnick | |||
M Van Tiggelen | |||
S D Creighton | |||
P2860 | cites work | Translating the Histone Code | Q22065840 |
A mouse model of Rubinstein-Taybi syndrome: defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4 | Q24683143 | ||
The transcriptional coactivators p300 and CBP are histone acetyltransferases | Q27860843 | ||
Analyzing real-time PCR data by the comparative C(T) method | Q28131831 | ||
P/CAF associates with cyclin D1 and potentiates its activation of the estrogen receptor | Q28143534 | ||
CBP histone acetyltransferase activity is a critical component of memory consolidation | Q28267700 | ||
Acetylation of non-histone proteins modulates cellular signalling at multiple levels | Q28294575 | ||
A naturally-occurring histone acetyltransferase inhibitor derived from Garcinia indica impairs newly acquired and reactivated fear memories | Q28485205 | ||
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 | ||
cAMP responsive element-binding protein phosphorylation is necessary for perirhinal long-term potentiation and recognition memory | Q28571881 | ||
Covalent modification of DNA regulates memory formation | Q28576256 | ||
Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning | Q29616330 | ||
New neurons and new memories: how does adult hippocampal neurogenesis affect learning and memory? | Q29619386 | ||
Acetylation and deacetylation of non-histone proteins | Q29619636 | ||
p300/CBP histone acetyltransferase activity is required for newly acquired and reactivated fear memories in the lateral amygdala | Q30443674 | ||
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 | ||
Virtual ligand screening of the p300/CBP histone acetyltransferase: identification of a selective small molecule inhibitor | Q33599508 | ||
Post-training reversible inactivation of the hippocampus enhances novel object recognition memory | Q33706856 | ||
Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity and memory storage. | Q33736104 | ||
Membrane-associated glucocorticoid activity is necessary for modulation of long-term memory via chromatin modification | Q33817894 | ||
Epigenetic alterations are critical for fear memory consolidation and synaptic plasticity in the lateral amygdala | Q33916385 | ||
CBP is required for environmental enrichment-induced neurogenesis and cognitive enhancement | Q34028180 | ||
Metformin activates an atypical PKC-CBP pathway to promote neurogenesis and enhance spatial memory formation | Q34032680 | ||
Histone deacetylase inhibitors enhance memory and synaptic plasticity via CREB:CBP-dependent transcriptional activation | Q34077367 | ||
Genome-wide assessment of differential roles for p300 and CBP in transcription regulation | Q34122513 | ||
Hippocampal histone acetylation regulates object recognition and the estradiol-induced enhancement of object recognition | Q34259302 | ||
Polyisoprenylated benzophenone, garcinol, a natural histone acetyltransferase inhibitor, represses chromatin transcription and alters global gene expression | Q34322167 | ||
Histone acetylation: molecular mnemonics on the chromatin. | Q34322979 | ||
Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration. | Q34327866 | ||
K-Lysine acetyltransferase 2a regulates a hippocampal gene expression network linked to memory formation | Q34332494 | ||
HDAC inhibition modulates hippocampus-dependent long-term memory for object location in a CBP-dependent manner | Q34546622 | ||
Epigenetic targets of HDAC inhibition in neurodegenerative and psychiatric disorders. | Q34587312 | ||
Hippocampal focal knockout of CBP affects specific histone modifications, long-term potentiation, and long-term memory | Q35112173 | ||
The histone acetylase PCAF is a nuclear receptor coactivator. | Q35201383 | ||
A transcription factor-binding domain of the coactivator CBP is essential for long-term memory and the expression of specific target genes | Q35612900 | ||
Selective roles for cAMP response element-binding protein binding protein and p300 protein as coregulators for androgen-regulated gene expression in advanced prostate cancer cells | Q35763204 | ||
Histone acetylation rescues contextual fear conditioning in nNOS KO mice and accelerates extinction of cued fear conditioning in wild type mice | Q35980930 | ||
Transgenic mice expressing an inhibitory truncated form of p300 exhibit long-term memory deficits. | Q36013236 | ||
Low doses of 17β-estradiol rapidly improve learning and increase hippocampal dendritic spines. | Q36174098 | ||
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 | ||
Perirhinal cortical contributions to object perception | Q36392391 | ||
Altered memory capacities and response to stress in p300/CBP-associated factor (PCAF) histone acetylase knockout mice | Q36761722 | ||
Visual perception and memory: a new view of medial temporal lobe function in primates and rodents | Q36785113 | ||
Object recognition memory: neurobiological mechanisms of encoding, consolidation and retrieval. | Q37171360 | ||
Modulation of long-term memory for object recognition via HDAC inhibition | Q37224213 | ||
What pharmacological interventions indicate concerning the role of the perirhinal cortex in recognition memory | Q38030283 | ||
Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders. | Q38085375 | ||
Targeting specific HATs for neurodegenerative disease treatment: translating basic biology to therapeutic possibilities | Q38094663 | ||
Rapid oestrogenic regulation of social and nonsocial learning. | Q38123239 | ||
Participation of Rel/NF-kappaB transcription factors in long-term memory in the crab Chasmagnathus | Q38314992 | ||
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism | Q38328546 | ||
Probing p300/CBP associated factor (PCAF)-dependent pathways with a small molecule inhibitor | Q39168941 | ||
Embelin induces apoptosis in human glioma cells through inactivating NF-κB. | Q39178057 | ||
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 | ||
Inhibition of lysine acetyltransferase KAT3B/p300 activity by a naturally occurring hydroxynaphthoquinone, plumbagin | Q39830457 | ||
Plumbagin (5-hydroxy-2-methyl-1,4-naphthoquinone) suppresses NF-kappaB activation and NF-kappaB-regulated gene products through modulation of p65 and IkappaBalpha kinase activation, leading to potentiation of apoptosis induced by cytokine and chemot | Q40290173 | ||
CBP-Dependent memory consolidation in the prefrontal cortex supports object-location learning. | Q40976579 | ||
The IkappaB kinase regulates chromatin structure during reconsolidation of conditioned fear memories. | Q41652035 | ||
The histone deacetylase inhibitor valproic acid enhances acquisition, extinction, and reconsolidation of conditioned fear | Q42116631 | ||
Differences in specificity and selectivity between CBP and p300 acetylation of histone H3 and H3/H4. | Q42575886 | ||
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 | ||
A novel activator of CBP/p300 acetyltransferases promotes neurogenesis and extends memory duration in adult mice. | Q43833014 | ||
Double dissociation between the effects of peri-postrhinal cortex and hippocampal lesions on tests of object recognition and spatial memory: heterogeneity of function within the temporal lobe. | Q44960342 | ||
Histone deacetylase inhibitors improve learning consolidation in young and in KA-induced-neurodegeneration and SAMP-8-mutant mice | Q46475121 | ||
Insular cortex is involved in consolidation of object recognition memory | Q46698856 | ||
Borders and cytoarchitecture of the perirhinal and postrhinal cortices in the rat. | Q47321124 | ||
Acetylation of nuclear factor-kappaB in rat amygdala improves long-term but not short-term retention of fear memory | Q47717302 | ||
Extending the spontaneous preference test of recognition: evidence of object-location and object-context recognition | Q48096986 | ||
When is the hippocampus involved in recognition memory? | Q48122500 | ||
Differential contributions of de novo and maintenance DNA methyltransferases to object memory processing in the rat hippocampus and perirhinal cortex--a double dissociation | Q48350535 | ||
Dynamic histone marks in the hippocampus and cortex facilitate memory consolidation | Q48416945 | ||
Syndromic features and mild cognitive impairment in mice with genetic reduction on p300 activity: Differential contribution of p300 and CBP to Rubinstein-Taybi syndrome etiology | Q48436070 | ||
Transient inactivation of perirhinal cortex disrupts encoding, retrieval, and consolidation of object recognition memory. | Q48505163 | ||
CB1 receptor antagonism in the granular insular cortex or somatosensory area facilitates consolidation of object recognition memory | Q48669904 | ||
A limited role for the hippocampus in the modulation of novel-object preference by contextual cues | Q48895442 | ||
Nuclear factor κB-dependent histone acetylation is specifically involved in persistent forms of memory. | Q50747275 | ||
Hippocampal lesions that abolish spatial maze performance spare object recognition memory at delays of up to 48 hours. | Q51996194 | ||
Differential role for CBP and p300 CREB-binding domain in motor skill learning. | Q52015251 | ||
Transcriptional coactivator p300/CBP-associated factor and p300/CBP-associated factor type B are required for normal estrogen response of the mouse uterus. | Q52560818 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 542-557 | |
P577 | publication date | 2016-06-02 | |
P1433 | published in | Genes, Brain and Behavior | Q112067 |
P1476 | title | Dissociable roles for histone acetyltransferases p300 and PCAF in hippocampus and perirhinal cortex-mediated object memory | |
P478 | volume | 15 |
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