(Q36626596)

15 August 2017

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title

Implication of abnormal epigenetic patterns for human diseases (English)

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15 August 2017

Santos-Rebouças CB

1

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15 August 2017

Pimentel MM

series ordinal

2

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15 August 2017

publication date

18 October 2006

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European Journal of Human Genetics

15 August 2017

published in

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15 August 2017

volume

15

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15 August 2017

issue

1

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15 August 2017

page(s)

10-17

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201727

15 August 2017

exact match

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cites work

Syndromes of disordered chromatin remodeling

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MAP kinase-mediated signalling to nucleosomes and immediate-early gene induction

21 January 2018

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A role for Saccharomyces cerevisiae histone H2A in DNA repair.

21 January 2018

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X-linked Coffin-Lowry syndrome (CLS, MIM 303600, RPS6KA3 gene, protein product known under various names: pp90(rsk2), RSK2, ISPK, MAPKAP1)

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Role of histone H3 lysine 27 methylation in X inactivation

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Identification and characterization of a novel human histone H3 lysine 36-specific methyltransferase

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

The SWI/SNF complex--chromatin and cancer.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Genomic imprinting in mammals.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

High-resolution methylation analysis of the human hypoxanthine phosphoribosyltransferase gene 5' region on the active and inactive X chromosomes: correlation with binding sites for transcription factors

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Centromeres and kinetochores: from epigenetics to mitotic checkpoint signaling

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

DNA methylation and autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Evidence that DNA (cytosine-5) methyltransferase regulates synaptic plasticity in the hippocampus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Gene/environment causes of cleft lip and/or palate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Maternal folate polymorphisms and the etiology of human nondisjunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

21 January 2018

Homocysteine and stroke

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Genetic polymorphism of methylenetetrahydrofolate reductase as a risk factor for diabetic nephropathy in Chinese type 2 diabetic patients

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Methylation and acetylation in nervous system development and neurodegenerative disorders

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Folic acid - vitamin and panacea or genetic time bomb?

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

DNA methyltransferase Dnmt1 associates with histone deacetylase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Two substrates are better than one: dual specificities for Dnmt2 methyltransferases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Reconstitution and mechanism of the stimulation of de novo methylation by human DNMT3L

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Genetic disruption of cytosine DNA methyltransferase enzymes induces chromosomal instability in human cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Methyl-CpG-binding domain 2: a protective role in bladder carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

MBD1, MBD2 and CGBP genes at chromosome 18q21 are infrequently mutated in human colon and lung cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

A decade of molecular studies of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Transgenerational epigenetic inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Genomic imprinting in mammalian development: a parental tug-of-war

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

X-chromosome inactivation: counting, choice and initiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Hairpin RNAs and retrotransposon LTRs effect RNAi and chromatin-based gene silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

The non-coding Air RNA is required for silencing autosomal imprinted genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

RNAi-mediated targeting of heterochromatin by the RITS complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

RITS acts in cis to promote RNA interference-mediated transcriptional and post-transcriptional silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Induction of DNA methylation and gene silencing by short interfering RNAs in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

DNA methylation and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

H19 and Igf2--enhancing the confusion?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Birth of parthenogenetic mice that can develop to adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Polycomb, epigenomes, and control of cell identity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Histone methyltransferase activity associated with a human multiprotein complex containing the Enhancer of Zeste protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

ALL-1 is a histone methyltransferase that assembles a supercomplex of proteins involved in transcriptional regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Xist RNA and the mechanism of X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Xite, X-inactivation intergenic transcription elements that regulate the probability of choice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

A developmental switch in H4 acetylation upstream of Xist plays a role in X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

CTCF, a candidate trans-acting factor for X-inactivation choice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Establishment of histone h3 methylation on the inactive X chromosome requires transient recruitment of Eed-Enx1 polycomb group complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

The polycomb group protein EZH2 is involved in progression of prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Poorly differentiated breast carcinoma is associated with increased expression of the human polycomb group EZH2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Inappropriate Gene Activation in FSHD

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Effects of 5-aza-2'-deoxycytidine on fetal hemoglobin levels, red cell adhesion, and hematopoietic differentiation in patients with sickle cell disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Phase 1 study of low-dose prolonged exposure schedules of the hypomethylating agent 5-aza-2'-deoxycytidine (decitabine) in hematopoietic malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Specific inhibition of DNMT1 by antisense oligonucleotides induces re-expression of estrogen receptor-alpha (ER) in ER-negative human breast cancer cell lines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Histone deacetylase inhibitors: discovery and development as anticancer agents

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Inhibition of histone deacetylation blocks cardiac hypertrophy induced by angiotensin II infusion and aortic banding

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Histone deacetylase inhibitors reduce polyglutamine toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Modulation of radiation response by histone deacetylase inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Reactivating the expression of methylation silenced genes in human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

7 January 2021

Altered folate and vitamin B12 metabolism in families with spina bifida offspring

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

7 January 2021

Folate levels in psychiatric outpatients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

7 January 2021

Why have ten or so nontoxic, retrovirus integrase inhibitors not been made available for AIDS treatment? A ten-year experience [correction of experiment] must liberate them

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

7 January 2021

Enox, a novel gene that maps 10 kb upstream of Xist and partially escapes X inactivation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

7 January 2021

Alteration of DNA methylation levels in MRL lupus mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201727

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201727

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Dimensions Publication ID

15 August 2017

1043024096

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1 reference