Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. - Test2 - elhamkhani - TriplyDB

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

http://www.wikidata.org/entity/Q33680910

about

Genomic imprinting in mammals: emerging themes and established theories High-resolution analysis of parent-of-origin allelic expression in the mouse brain DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency A family of neofunctionalized Ty3/gypsy retrotransposon genes in mammalian genomes Role of Tet1 in erasure of genomic imprinting Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome Identification of tammar wallaby SIRH12, derived from a marsupial-specific retrotransposition event Genetic and molecular analyses of PEG10 reveal new aspects of genomic organization, transcription and translation Retrotransposon silencing by DNA methylation can drive mammalian genomic imprinting Novel gene expression patterns along the proximo-distal axis of the mouse embryo before gastrulation.Exclusive paternal expression and novel alternatively spliced variants of epsilon-sarcoglycan mRNA in mouse brain.A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation Sex dependent imprinting effects on complex traits in mice.Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.An in vitro ES cell imprinting model shows that imprinted expression of the Igf2r gene arises from an allele-specific expression bias LTRs of Endogenous Retroviruses as a Source of Tbx6 Binding Sites.Asymmetric DNA methylation of CpG dyads is a feature of secondary DMRs associated with the Dlk1/Gtl2 imprinting cluster in mouse Positive selection and multiple losses of the LINE-1-derived L1TD1 gene in mammals suggest a dual role in genome defense and pluripotency.Mouse oocyte methylomes at base resolution reveal genome-wide accumulation of non-CpG methylation and role of DNA methyltransferases.Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.Selective expression of sense and antisense transcripts of the sushi-ichi-related retrotransposon--derived family during mouse placentogenesis A survey for novel imprinted genes in the mouse placenta by mRNA-seq Allelic Imbalance Is a Prevalent and Tissue-Specific Feature of the Mouse Transcriptome.Silencing of Paternally Expressed Gene 10 Inhibits Trophoblast Proliferation and Invasion Quantitative and functional interrogation of parent-of-origin allelic expression biases in the brain.Ultra-Deep Bisulfite Sequencing to Detect Specific DNA Methylation Patterns of Minor Cell Types in Heterogeneous Cell Populations: An Example of the Pituitary Tissue.Allele-specific demethylation at an imprinted mammalian promoter Genomic imprinting in the placenta.Imprinted genes in placental growth and obstetric disorders.Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing.Linkage disequilibrium analysis of allelic heterogeneity in DNA methylation.Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues.Transcription is required for establishment of germline methylation marks at imprinted genes The MBD protein family-reading an epigenetic mark?A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.An imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages.Epigenetic modifications at DMRs of placental genes are subjected to variations in normal gestation, pathological conditions and folate supplementation.Genomic imprinting mechanisms in embryonic and extraembryonic mouse tissues A survey of tissue-specific genomic imprinting in mammals.

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P2860

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

http://www.wikidata.org/entity/Q33680910

description

2003 nî lūn-bûn

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2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2003 թվականի հուլիսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@ast

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@en

type

label

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@ast

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@en

prefLabel

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@ast

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@en

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Genome Research

P1476

Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

@en

P2093

Fumitoshi Ishino

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

Hirosuke Shiura

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

Hiroyuki Aburatani

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

Ryuichi Ono

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

Takashi Kohda

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

Tomoko Kaneko-Ishino

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P2860

The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarin

Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family

Isoform-specific imprinting of the human PEG1/MEST gene

Neurabin: a novel neural tissue-specific actin filament-binding protein involved in neurite formation

The Tnfrh1 (Tnfrsf23) gene is weakly imprinted in several organs and expressed at the trophoblast-decidua interface

A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21

Paraoxonase-2 is a ubiquitously expressed protein with antioxidant properties and is capable of preventing cell-mediated oxidative modification of low density lipoprotein

No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

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1696-1705

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scholarly article

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10.1101/GR.906803

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7

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13

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2003-07-01T00:00:00Z

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6691414

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12840045

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403743

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