(Q34378421)

1 August 2017

DNA methylation in genomic imprinting, development, and disease (English)

1 reference

1 August 2017

0 references

Paulsen M

1

1 reference

PubMed ID

11568896

1 August 2017

Ferguson-Smith AC

series ordinal

2

1 reference

1 August 2017

1 September 2001

1 reference

1 August 2017

1 reference

1 August 2017

195

1 reference

1 August 2017

97-110

1 reference

1 August 2017

1

1 reference

DNA Methylation and Gene Function

1 August 2017

1 reference

Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases

21 January 2018

1 reference

Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells

21 January 2018

1 reference

The DNA methyltransferases of mammals

21 January 2018

1 reference

DNA methylation and imprinting: why bother?

21 January 2018

1 reference

Decreased methylation of the major mouse long interspersed repeated DNA during aging and in myeloma cells

21 January 2018

1 reference

DNA methylation differences associated with tumor tissues identified by genome scanning analysis

21 January 2018

1 reference

DNA hypomethylation leads to elevated mutation rates

21 January 2018

1 reference

Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

21 January 2018

1 reference

DNA methylation and cancer

21 January 2018

1 reference

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

21 January 2018

1 reference

MECP2 mutations account for most cases of typical forms of Rett syndrome.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

21 January 2018

1 reference

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Imprinting in Prader-Willi and Angelman syndromes.

21 January 2018

1 reference

Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

21 January 2018

1 reference

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

21 January 2018

1 reference

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain.

21 January 2018

1 reference

Genomic imprinting: implications for human disease

21 January 2018

1 reference

Genomic imprinting and Wilms' tumor

21 January 2018

1 reference

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

21 January 2018

1 reference

Role of paternal and maternal genomes in mouse development

21 January 2018

1 reference

Cytosine methylation and the ecology of intragenomic parasites

21 January 2018

1 reference

Active demethylation of the paternal genome in the mouse zygote

21 January 2018

1 reference

Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.

21 January 2018

1 reference

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

21 January 2018

1 reference

Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes.

21 January 2018

1 reference

Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting

21 January 2018

1 reference

Number of CpG islands and genes in human and mouse

21 January 2018

1 reference

The expected equilibrium of the CpG dinucleotide in vertebrate genomes under a mutation model

21 January 2018

1 reference

CpG islands as gene markers in the human genome.

21 January 2018

1 reference

DNA methylation inhibits elongation but not initiation of transcription in Neurospora crassa.

21 January 2018

1 reference

The DNA methylation paradox

21 January 2018

1 reference

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

21 January 2018

1 reference

PAX6 methylation and ectopic expression in human tumor cells

21 January 2018

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

21 January 2018

1 reference

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

21 January 2018

1 reference

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

21 January 2018

1 reference

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

21 January 2018

1 reference

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1).

21 January 2018

1 reference

Effects of DNA methylation on DNA-binding proteins and gene expression.

21 January 2018

1 reference

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

21 January 2018

1 reference

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

21 January 2018

1 reference

Binding of histone H1 to DNA is indifferent to methylation at CpG sequences.

21 January 2018

1 reference

Histone H1 is dispensable for methylation-associated gene silencing in Ascobolus immersus and essential for long life span

21 January 2018

1 reference

DNA methyltransferase Dnmt1 associates with histone deacetylase activity

21 January 2018

1 reference

DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci

21 January 2018

1 reference

Human DNA-(Cytosine-5) Methyltransferase-PCNA Complex as a Target for p21WAF1

21 January 2018

1 reference

Identification and characterization of a family of mammalian methyl-CpG binding proteins

21 January 2018

1 reference

DNA methylation specifies chromosomal localization of MeCP2.

21 January 2018

1 reference

Active repression of methylated genes by the chromosomal protein MBD1

21 January 2018

1 reference

Identification of a mammalian protein that binds specifically to DNA containing methylated CpGs.

21 January 2018

1 reference

The role of histone acetylation in the allelic expression of the imprinted human insulin-like growth factor II gene

21 January 2018

1 reference

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

21 January 2018

1 reference

Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region

21 January 2018

1 reference

Allele-specific replication timing of imprinted gene regions

21 January 2018

1 reference

Asynchronous replication of imprinted genes is established in the gametes and maintained during development

21 January 2018

1 reference

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation

21 January 2018

1 reference

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

21 January 2018

1 reference

Imprinting in Angelman and Prader-Willi syndromes.

21 January 2018

1 reference

Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila

21 January 2018

1 reference

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

21 January 2018

1 reference

In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit

21 January 2018

1 reference

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting

21 January 2018

1 reference

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

21 January 2018

1 reference

Parental imprinting of the mouse H19 gene

21 January 2018

1 reference

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

21 January 2018

1 reference

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

21 January 2018

1 reference

An enhancer deletion affects both H19 and Igf2 expression

21 January 2018

1 reference

Disruption of imprinting caused by deletion of the H19 gene region in mice

21 January 2018

1 reference

A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprinting

21 January 2018

1 reference

Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element

21 January 2018

1 reference

Role of a 461-bp G-rich repetitive element in H19 transgene imprinting.

21 January 2018

1 reference

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

21 January 2018

1 reference

Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.

21 January 2018

1 reference

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

21 January 2018

1 reference

An imprinting element from the mouse H19 locus functions as a silencer in Drosophila.

21 January 2018

1 reference

A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice.

21 January 2018

1 reference

Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

21 January 2018

1 reference

Inhibition of tumorigenesis by a cytosine-DNA, methyltransferase, antisense oligodeoxynucleotide

21 January 2018

1 reference

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

21 January 2018

1 reference

Aberrant methylation of p16(INK4a) is an early event in lung cancer and a potential biomarker for early diagnosis

21 January 2018

1 reference

Alterations of H19 Imprinting and IGF2 Replication Timing Are Infrequent in Beckwith–Wiedemann Syndrome

21 January 2018

1 reference

Growing Y-junction carbon nanotubes

21 January 2018

1 reference

Demethylation of the zygotic paternal genome

21 January 2018

1 reference

The imprinting box of the mouse Igf2r gene

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PATH.890

1 reference

1 August 2017

1 reference

PubMed ID

11568896