DNA methylation and human disease (Q29615417)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16136652 AND SRC:MED&resulttype=core&format=json

6 January 2020

review article

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title

DNA methylation and human disease (English)

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=16136652

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16136652 AND SRC:MED&resulttype=core&format=json

6 January 2020

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6 January 2020

author name string

Robertson KD

series ordinal

1

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=16136652

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language of work or name

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30 April 2017

publication date

1 August 2005

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6 January 2020

published in

Nature Reviews Genetics

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30 April 2017

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6 January 2020

volume

6

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30 April 2017

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6 January 2020

issue

8

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30 April 2017

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6 January 2020

page(s)

597-610

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30 April 2017

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DNA methylation patterns and epigenetic memory

6 January 2020

cites work

1 reference

CpG-rich islands and the function of DNA methylation

1 May 2017

1 reference

Somatic mutations in the neurofibromatosis 1 gene in human tumors

1 May 2017

1 reference

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

1 May 2017

1 reference

The history of cancer epigenetics

1 May 2017

1 reference

The power and the promise of DNA methylation markers

1 May 2017

1 reference

Genomic imprinting: parental influence on the genome

1 May 2017

1 reference

An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region

1 May 2017

1 reference

CTCF maintains differential methylation at the Igf2/H19 locus

1 May 2017

1 reference

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

1 May 2017

1 reference

NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomas

1 May 2017

1 reference

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 May 2017

1 reference

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 May 2017

1 reference

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 May 2017

1 reference

Disruption of the mouse necdin gene results in early post-natal lethality

1 May 2017

1 reference

RNA and microRNAs in fragile X mental retardation

1 May 2017

1 reference

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

1 May 2017

1 reference

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

1 May 2017

1 reference

Molecular enzymology of the catalytic domains of the Dnmt3a and Dnmt3b DNA methyltransferases

1 May 2017

1 reference

DNMT3B interacts with hSNF2H chromatin remodeling enzyme, HDACs 1 and 2, and components of the histone methylation system

1 May 2017

1 reference

Isolation and characterization of a novel DNA methyltransferase complex linking DNMT3B with components of the mitotic chromosome condensation machinery

1 May 2017

1 reference

DNA methyltransferase 3b regulates nerve growth factor-induced differentiation of PC12 cells by recruiting histone deacetylase 2

1 May 2017

1 reference

Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain

1 May 2017

1 reference

Heterochromatin and ND10 are cell-cycle regulated and phosphorylation-dependent alternate nuclear sites of the transcription repressor Daxx and SWI/SNF protein ATRX

1 May 2017

1 reference

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

1 May 2017

1 reference

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

1 May 2017

1 reference

Worms gang up on bacteria

1 May 2017

1 reference

Boundaries between chromosomal domains of X inactivation and escape bind CTCF and lack CpG methylation during early development

1 May 2017

1 reference

BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma

1 May 2017

1 reference

RNAi-mediated targeting of heterochromatin by the RITS complex

1 May 2017

1 reference

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

1 May 2017

1 reference

Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin

1 May 2017

1 reference

1 May 2017

In search of antisense

1 reference

Transgenic RNAi reveals essential function for CTCF in H19 gene imprinting

1 May 2017

1 reference

In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene

1 May 2017

1 reference

Epigenetic reprogramming in mammalian development

1 May 2017

1 reference

Role for DNA methylation in genomic imprinting

1 May 2017

1 reference

Inappropriate Gene Activation in FSHD

1 May 2017

1 reference

Binary switches and modification cassettes in histone biology and beyond.

1 May 2017

1 reference

DNA methylation and chromatin - unraveling the tangled web.

31 March 2020

1 reference

The methyl-CpG binding domain and the evolving role of DNA methylation in animals

31 March 2020

1 reference

Demethylation of the zygotic paternal genome

31 March 2020

1 reference

Cytosine methylation and the ecology of intragenomic parasites

31 March 2020

1 reference

Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression

31 March 2020

1 reference

DNA hypomethylation can activate Xist expression and silence X-linked genes.

31 March 2020

1 reference

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

31 March 2020

1 reference

Epigenomics and epigenetic therapy of cancer

31 March 2020

1 reference

31 March 2020

1 reference

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

31 March 2020

1 reference

DNA methylation in health and disease

31 March 2020

1 reference

DNA hypomethylation and ovarian cancer biology.

31 March 2020

1 reference

DNA methylation is the primary silencing mechanism for a set of germ line- and tumor-specific genes with a CpG-rich promoter

31 March 2020

1 reference

Hypomethylation of the metastasis-associated S100A4 gene correlates with gene activation in human colon adenocarcinoma cell lines

31 March 2020

1 reference

Cell-Type-Specific Repression of the Maspin Gene Is Disrupted Frequently by Demethylation at the Promoter Region in Gastric Intestinal Metaplasia and Cancer Cells

31 March 2020

1 reference

A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes

31 March 2020

1 reference

CpG island methylator phenotype in cancer

31 March 2020

1 reference

CpG island methylation in aberrant crypt foci of the colorectum

31 March 2020

1 reference

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

31 March 2020

1 reference

DNA methylation and genomic imprinting: insights from cancer into epigenetic mechanisms

31 March 2020

1 reference

Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive

31 March 2020

1 reference

Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes

31 March 2020

1 reference

Effects of culture conditions on IVF outcome

31 March 2020

1 reference

Conservation of methylation reprogramming in mammalian development: aberrant reprogramming in cloned embryos

31 March 2020

1 reference

Tumour-suppressor activity of H19 RNA

31 March 2020

1 reference

Epigenetic lesions at the H19 locus in Wilms' tumour patients

31 March 2020

1 reference

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

31 March 2020

1 reference

Loss of imprinting of Igf2 alters intestinal maturation and tumorigenesis in mice

31 March 2020

1 reference

31 March 2020

Imprinting and disease

1 reference

A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator

31 March 2020

1 reference

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

31 March 2020

1 reference

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome

31 March 2020

1 reference

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

31 March 2020

1 reference

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

31 March 2020

1 reference

Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

31 March 2020

1 reference

Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome.

31 March 2020

1 reference

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

31 March 2020

1 reference

Imprints of disease at GNAS1.

31 March 2020

1 reference

Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB

31 March 2020

1 reference

Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly

31 March 2020

1 reference

Transient neonatal diabetes, a disorder of imprinting.

31 March 2020

1 reference

A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus

31 March 2020

1 reference

A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

31 March 2020

1 reference

Genomic imprinting: CTCF protects the boundaries

31 March 2020

1 reference

Trinucleotide repeats and neurodegenerative disease.

31 March 2020

1 reference

The contribution of <i>cis</i>-elements to disease-associated repeat instability: clinical and experimental evidence

31 March 2020

1 reference

FMR1 and the fragile X syndrome: human genome epidemiology review

31 March 2020

1 reference

31 March 2020

1 reference

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

31 March 2020

1 reference

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

31 March 2020

1 reference

Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome

31 March 2020

1 reference

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

31 March 2020

1 reference

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

31 March 2020

1 reference

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

31 March 2020

1 reference

Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q

31 March 2020

1 reference

The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeat

31 March 2020

1 reference

CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus

31 March 2020

1 reference

DNA triplet repeats mediate heterochromatin-protein-1-sensitive variegated gene silencing

31 March 2020

1 reference

Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells

31 March 2020

1 reference

Genome-wide demethylation destabilizes CTG.CAG trinucleotide repeats in mammalian cells

31 March 2020

1 reference

Age at onset in Huntington's disease and methylation at D4S95

31 March 2020

1 reference

Hypermethylation of telomere-like foldbacks at codon 12 of the human c-Ha-ras gene and the trinucleotide repeat of the FMR-1 gene of fragile X.

31 March 2020

1 reference

The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer

31 March 2020

1 reference

DNA methylation and autoimmune disease

31 March 2020

1 reference

Evidence for impaired T cell DNA methylation in systemic lupus erythematosus and rheumatoid arthritis

31 March 2020

1 reference

Treating activated CD4 T cells with either of two distinct DNA methyltransferase inhibitors, 5-azacytidine or procainamide, is sufficient to cause a lupus-like disease in syngeneic mice

31 March 2020

1 reference

Demethylation of ITGAL (CD11a) regulatory sequences in systemic lupus erythematosus

31 March 2020

1 reference

Overexpression of CD70 and overstimulation of IgG synthesis by lupus T cells and T cells treated with DNA methylation inhibitors

31 March 2020

1 reference

DNA methylation in systemic lupus erythematosus

31 March 2020

1 reference

Hydralazine may induce autoimmunity by inhibiting extracellular signal-regulated kinase pathway signaling

31 March 2020

1 reference

ICF syndrome: a new case and review of the literature

31 March 2020

1 reference

The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease

31 March 2020

1 reference

Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literature

31 March 2020

1 reference

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients

31 March 2020

1 reference

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

31 March 2020

1 reference

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

31 March 2020

1 reference

Defective de novo methylation of viral and cellular DNA sequences in ICF syndrome cells

31 March 2020

1 reference

Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant.

31 March 2020

1 reference

DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements

31 March 2020

1 reference

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes

31 March 2020

1 reference

ATP-dependent chromatin remodeling activities.

31 March 2020

1 reference

ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein

31 March 2020

1 reference

A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein

31 March 2020

1 reference

The fundamental role of epigenetic events in cancer

31 March 2020

1 reference

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

31 March 2020

1 reference

Two RNAi complexes, RITS and RDRC, physically interact and localize to noncoding centromeric RNAs.

31 March 2020

1 reference

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

31 March 2020

1 reference

Transcripts from opposite strands of gamma satellite DNA are differentially expressed during mouse development

31 March 2020

1 reference

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

31 March 2020

1 reference

The binding sites for the chromatin insulator protein CTCF map to DNA methylation-free domains genome-wide

31 March 2020

1 reference

CTCF elements direct allele-specific undermethylation at the imprinted H19 locus

31 March 2020

1 reference

Intracytoplasmic sperm injection may increase the risk of imprinting defects

31 March 2020

1 reference

Parental imprinting of the mouse insulin-like growth factor II gene.

31 March 2020

1 reference

Fetal nutrition and cardiovascular disease in adult life

31 March 2020

1 reference

Selective loss of imprinting in the placenta following preimplantation development in culture

31 March 2020

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=16136652

31 March 2020

Identifiers

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

2068090

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16136652 AND SRC:MED&resulttype=core&format=json

Dimensions Publication ID

6 January 2020

1044723213

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2068090

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Consolidated OpenCitations Corpus – April 2017

2068090

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=16136652

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

9327