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Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies

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Europe PubMed Central

PubMed publication ID

21 August 2017

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Europe PubMed Central

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

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Europe PubMed Central

PubMed publication ID

21 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Jose V Sanchez-Mut

object named as

Jose V Sanchez-Mut

2

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Rocío G Urdinguio

object named as

Rocio G Urdinguio

1

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language of work or name

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publication date

1 November 2009

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Europe PubMed Central

PubMed publication ID

21 August 2017

Lancet Neurology

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Europe PubMed Central

PubMed publication ID

21 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

1056-1072

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

DNA methylation and epigenetic defects in carcinogenesis

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic plasticity and the epigenetics of human disease

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenetic differences arise during the lifetime of monozygotic twins

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Rett Syndrome: The First Forty Years 1966-2006

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA methylation patterns and epigenetic memory

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenetic reprogramming in mammalian development

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Environmental exposures and gene regulation in disease etiology

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanisms regulating imprinted genes in clusters.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The DNA methyltransferases of mammals

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

MBD family proteins: reading the epigenetic code

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteins that bind methylated DNA and human cancer: reading the wrong words

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer epigenomics: DNA methylomes and histone-modification maps

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

MGMT gene silencing and benefit from temozolomide in glioblastoma

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromatin modifications and their function

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The mammalian epigenome

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The emerging functions of histone demethylases

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

HDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse model

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Posttranscriptional control of neuronal development by microRNA networks

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The epigenomics of cancer

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenetics in cancer

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Relevance of DNA methylation in the management of cancer

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Hypomethylation distinguishes genes of some human cancers from their normal counterparts

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

A microarray-based DNA methylation study of glioblastoma multiforme

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Clustering of gene hypermethylation associated with clinical risk groups in neuroblastoma

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Global histone modification patterns predict risk of prostate cancer recurrence

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The story of Rett syndrome: from clinic to neurobiology

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Reversal of neurological defects in a mouse model of Rett syndrome

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Rubinstein-Taybi syndrome.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Genotype-phenotype correlations in Rubinstein-Taybi syndrome.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Phosphorylated CREB binds specifically to the nuclear protein CBP

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The CBP co-activator is a histone acetyltransferase

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

CBP and p300: HATs for different occasions

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

The Coffin-Lowry syndrome

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Coffin-Lowry syndrome: clinical and molecular features

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitogen-activated protein kinases: specific messages from ubiquitous messengers

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Alpha thalassaemia-mental retardation, X linked

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the chromatin-associated protein ATRX.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

DNA methylation signatures within the human brain

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Modulation of nucleosome dynamics in Huntington's disease

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Phase 2 study of sodium phenylbutyrate in ALS.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Myelin in multiple sclerosis is developmentally immature

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Mechanisms of human inherited epilepsies

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Histone modifications in kainate-induced status epilepticus

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Transgenerational epigenetic effects.

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1474-4422(09)70262-5

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

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