Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q33774256

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Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution Alterations in specific gene expression and focal neoplastic growth during spontaneous hepatocarcinogenesis in albumin-SV40 T antigen transgenic rats The imprinting mechanism of the Prader-Willi/Angelman regional control center.Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome 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 Blockade of EphA receptor tyrosine kinase activation inhibits vascular endothelial cell growth factor-induced angiogenesis.Chromatin regulators of genomic imprinting Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center.Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome MyoD regulates p57kip2 expression by interacting with a distant cis-element and modifying a higher order chromatin structure A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome.DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts.Insulin gene expression is regulated by DNA methylation Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region.Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome.Beckwith-Wiedemann syndrome: imprinting in clusters revisited.Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.Investigation of elements sufficient to imprint the mouse Air promoter.DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.Domain-specific response of imprinted genes to reduced DNMT1.The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality.Imprinting in the germ line.Differentiation-driven nucleolar association of the mouse imprinted Kcnq1 locus.Genetic mapping and developmental timing of transmission ratio distortion in a mouse interspecific backcross.Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.DNA methylation in genomic imprinting, development, and disease.Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.Autonomous silencing of the imprinted Cdkn1c gene in stem cells.Effects of DNMT1 and HDAC inhibitors on gene-specific methylation reprogramming during porcine somatic cell nuclear transfer.Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.Epigenetic risks related to assisted reproductive technologies: short- and long-term consequences for the health of children conceived through assisted reproduction technology: more reason for caution?Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation.

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P2860

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

http://www.wikidata.org/entity/Q33774256

description

1998 nî lūn-bûn

@nan

1998 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի հունիսին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

@zh-tw

1998年论文

@wuu

name

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

@ast

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

@en

type

label

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

@ast

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

@en

prefLabel

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

@ast

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

@en

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Molecular and Cellular Biology

P1476

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

@en

P2093

C C Baker

http://www.w3.org/2001/XMLSchema#string

M A Cleary

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S M Tilghman

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T Caspary

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X J Guan

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P2860

Parental imprinting of the mouse H19 gene

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

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

UBE3A/E6-AP mutations cause Angelman syndrome

Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development

A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

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

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

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3466-3474

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scholarly article

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10.1128/MCB.18.6.3466

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6

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18

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13700278

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9584186

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108927

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