Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies (Q37615626)

21 August 2017

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title

Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies (English)

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21 August 2017

3

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21 August 2017

Jose V Sanchez-Mut

2

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Rocío G Urdinguio

object named as

Rocio G Urdinguio

series ordinal

1

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language of work or name

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1 November 2009

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21 August 2017

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21 August 2017

volume

8

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21 August 2017

issue

11

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21 August 2017

page(s)

1056-1072

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DNA methylation and epigenetic defects in carcinogenesis

21 August 2017

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Epigenetic reprogramming in mammalian development

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MBD family proteins: reading the epigenetic code

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The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues

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Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition

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The role of citrullinated proteins suggests a novel mechanism in the pathogenesis of multiple sclerosis

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Cancer epigenomics: DNA methylomes and histone-modification maps

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Inactivation of the DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents

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7 January 2021

MGMT gene silencing and benefit from temozolomide in glioblastoma

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7 January 2021

CpG island hypermethylation of the DNA repair enzyme methyltransferase predicts response to temozolomide in primary gliomas

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Chromatin modifications and their function

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The mammalian epigenome

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The emerging functions of histone demethylases

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Transcriptional therapy with the histone deacetylase inhibitor trichostatin A ameliorates experimental autoimmune encephalomyelitis.

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7 January 2021

Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator

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7 January 2021

HDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse model

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7 January 2021

Long intronic GAA*TTC repeats induce epigenetic changes and reporter gene silencing in a molecular model of Friedreich ataxia

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7 January 2021

Posttranscriptional control of neuronal development by microRNA networks

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7 January 2021

Epigenetic principles and mechanisms underlying nervous system functions in health and disease

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7 January 2021

The epigenomics of cancer

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7 January 2021

Epigenetics in cancer

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7 January 2021

Relevance of DNA methylation in the management of cancer

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7 January 2021

Hypomethylation distinguishes genes of some human cancers from their normal counterparts

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7 January 2021

Aberrant CpG-island methylation has non-random and tumour-type-specific patterns.

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7 January 2021

A microarray-based DNA methylation study of glioblastoma multiforme

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7 January 2021

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

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7 January 2021

Clustering of gene hypermethylation associated with clinical risk groups in neuroblastoma

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https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Towards the human cancer epigenome: a first draft of histone modifications

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https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Global histone modification patterns predict risk of prostate cancer recurrence

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7 January 2021

The story of Rett syndrome: from clinic to neurobiology

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7 January 2021

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.

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7 January 2021

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

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7 January 2021

The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.

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7 January 2021

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

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7 January 2021

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

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7 January 2021

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

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7 January 2021

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

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7 January 2021

Mecp2-null mice provide new neuronal targets for Rett syndrome.

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7 January 2021

Histone H3 and H4 modification profiles in a Rett syndrome mouse model.

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7 January 2021

Reversal of neurological defects in a mouse model of Rett syndrome

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7 January 2021

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

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7 January 2021

Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation

1 reference

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7 January 2021

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

1 reference

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7 January 2021

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

MeCP2, a key contributor to neurological disease, activates and represses transcription

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

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7 January 2021

Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome

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https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Rubinstein-Taybi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Rubinstein-Taybi syndrome: molecular findings and therapeutic approaches to improve cognitive dysfunction

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7 January 2021

DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease

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7 January 2021

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

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7 January 2021

Genotype-phenotype correlations in Rubinstein-Taybi syndrome.

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7 January 2021

Phosphorylated CREB binds specifically to the nuclear protein CBP

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7 January 2021

The CBP co-activator is a histone acetyltransferase

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7 January 2021

CBP and p300: HATs for different occasions

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7 January 2021

Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity and memory storage.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Monoallele deletion of CBP leads to pericentromeric heterochromatin condensation through ESET expression and histone H3 (K9) methylation

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7 January 2021

The Coffin-Lowry syndrome

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7 January 2021

Coffin-Lowry syndrome: clinical and molecular features

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7 January 2021

A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome

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7 January 2021

Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome

1 reference

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7 January 2021

Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation

1 reference

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7 January 2021

Mitogen-activated protein kinases: specific messages from ubiquitous messengers

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7 January 2021

Rsk-2 activity is necessary for epidermal growth factor-induced phosphorylation of CREB protein and transcription of c-fos gene

1 reference

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7 January 2021

Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylase activities

1 reference

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7 January 2021

The p53 protein is a novel substrate of ribosomal S6 kinase 2 and a critical intermediary for ribosomal S6 kinase 2 and histone H3 interaction.

1 reference

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7 January 2021

Phosphoacetylation of histone H3 on c-fos- and c-jun-associated nucleosomes upon gene activation

1 reference

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7 January 2021

Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).

1 reference

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7 January 2021

Alpha thalassaemia-mental retardation, X linked

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7 January 2021

Mutations in the chromatin-associated protein ATRX.

1 reference

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7 January 2021

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

1 reference

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7 January 2021

Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions

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7 January 2021

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

PHD fingers in human diseases: disorders arising from misinterpreting epigenetic marks

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Loss of ATRX leads to chromosome cohesion and congression defects

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 protein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Structural basis for the recognition and cross-linking of amyloid fibrils by human apolipoprotein E

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

The epigenetic effects of amyloid-beta(1-40) on global DNA and neprilysin genes in murine cerebral endothelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Neprilysin gene expression requires binding of the amyloid precursor protein intracellular domain to its promoter: implications for Alzheimer disease

1 reference

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7 January 2021

Reduced neprilysin in high plaque areas of Alzheimer brain: a possible relationship to deficient degradation of beta-amyloid peptide

1 reference

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7 January 2021

Age-dependent decline of neprilysin in Alzheimer's disease and normal brain: inverse correlation with A beta levels.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Exchange of N-CoR corepressor and Tip60 coactivator complexes links gene expression by NF-kappaB and beta-amyloid precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Inhibition of histone deacetylation enhances the neurotoxicity induced by the C-terminal fragments of amyloid precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Fe65 is required for Tip60-directed histone H4 acetylation at DNA strand breaks

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Evidence of DNA damage in Alzheimer disease: phosphorylation of histone H2AX in astrocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

HDAC2 negatively regulates memory formation and synaptic plasticity.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

DNA methylation in the human cerebral cortex is dynamically regulated throughout the life span and involves differentiated neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

S100A2 induces metastasis in non-small cell lung cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

S100B-mediated protection against the pro-apoptotic effects of ethanol on fetal rhombencephalic neurons

1 reference

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7 January 2021

Phosphorylation by extracellular signal-regulated kinase of a multidomain adaptor protein, vinexin, at synapses

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Age-specific epigenetic drift in late-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

DNA methylation signatures within the human brain

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Alpha-synuclein acts in the nucleus to inhibit histone acetylation and promote neurotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Sirtuin 2 inhibitors rescue alpha-synuclein-mediated toxicity in models of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Striatal histone modifications in models of levodopa-induced dyskinesia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Different methylation of the TNF-alpha promoter in cortex and substantia nigra: Implications for selective neuronal vulnerability

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Interleukin (IL)-1 beta, IL-2, IL-4, IL-6 and transforming growth factor-alpha levels are elevated in ventricular cerebrospinal fluid in juvenile parkinsonism and Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription

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https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Modulation of nucleosome dynamics in Huntington's disease

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https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histones associated with downregulated genes are hypo-acetylated in Huntington's disease models

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Valproic acid induces up- or down-regulation of gene expression responsible for the neuronal excitation and inhibition in rat cortical neurons through its epigenetic actions.

1 reference

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7 January 2021

Phase 2 study of sodium phenylbutyrate in ALS.

1 reference

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7 January 2021

Combined lithium and valproate treatment delays disease onset, reduces neurological deficits and prolongs survival in an amyotrophic lateral sclerosis mouse model

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

The genetics of multiple sclerosis: SNPs to pathways to pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

HLA-DRB1*1501, -DQB1*0301, -DQB1*0302, -DQB1*0602, and -DQB1*0603 alleles are associated with more severe disease outcome on MRI in patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Concordance for multiple sclerosis in Danish twins: an update of a nationwide study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Risk for multiple sclerosis in dizygotic and monozygotic twins

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

The multiple sclerosis trait and the development of multiple sclerosis: genetic vulnerability and environmental effect

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Twin concordance and sibling recurrence rates in multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Men transmit MS more often to their children vs women: the Carter effect

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Peptidyl argininedeiminase 2 CpG island in multiple sclerosis white matter is hypomethylated

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

The role of charge microheterogeneity of basic protein in the formation and maintenance of the multilayered structure of myelin: a possible role in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Myelin in multiple sclerosis is developmentally immature

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Autocatalytic cleavage of myelin basic protein: an alternative to molecular mimicry

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Deimination of membrane-bound myelin basic protein in multiple sclerosis exposes an immunodominant epitope

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Current approaches to the identification and management of breakthrough disease in patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Mechanisms of human inherited epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone modifications in kainate-induced status epilepticus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Altered histone acetylation at glutamate receptor 2 and brain-derived neurotrophic factor genes is an early event triggered by status epilepticus.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone modifications at gene promoter regions in rat hippocampus after acute and chronic electroconvulsive seizures.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Gcn5- and Elp3-induced histone H3 acetylation regulates hsp70 gene transcription in yeast

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: Its modulation by the proteasome and Hsp70

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Hsp27 and Hsp70 administered in combination have a potent protective effect against FALS-associated SOD1-mutant-induced cell death in mammalian neuronal cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Treatment of spinal muscular atrophy by sodium butyrate

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Benefit of valproic acid in suppressing disease progression of ALS model mice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

In vitro reactivation of the FMR1 gene involved in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

CBP histone acetyltransferase activity is a critical component of memory consolidation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone deacetylase inhibitors enhance memory and synaptic plasticity via CREB:CBP-dependent transcriptional activation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Regulation of histone acetylation during memory formation in the hippocampus.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Acetylation of nuclear factor-kappaB in rat amygdala improves long-term but not short-term retention of fear memory

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Sodium phenylbutyrate in Huntington's disease: a dose-finding study.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Neprilysin: an enzyme candidate to slow the progression of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Recovery of learning and memory is associated with chromatin remodelling

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

Transgenerational epigenetic effects.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970262-5

7 January 2021

10.1016/S1474-4422(09)70262-5

Identifiers

DOI

1 reference

21 August 2017

1 reference