Somatic genomic variations in early human prenatal development. - Wikidata - wikimedia - TriplyDB

Somatic genomic variations in early human prenatal development.

Somatic genomic variations in early human prenatal development.

http://www.wikidata.org/entity/Q34479598

about

Array comparative genomic hybridization analyses of all blastomeres of a cohort of embryos from young IVF patients revealed significant contribution of mitotic errors to embryo mosaicism at the cleavage stage ATRX contributes to epigenetic asymmetry and silencing of major satellite transcripts in the maternal genome of the mouse embryo Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism.Hypomethylation and Genetic Instability in Monosomy Blastocysts May Contribute to Decreased Implantation Potential.Single cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases.Implications of aneuploidy for stem cell biology and brain therapeutics Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos.

P2860

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P2860

Somatic genomic variations in early human prenatal development.

http://www.wikidata.org/entity/Q34479598

description

2010 nî lūn-bûn

@nan

2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Somatic genomic variations in early human prenatal development.

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Somatic genomic variations in early human prenatal development.

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Somatic genomic variations in early human prenatal development.

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type

label

Somatic genomic variations in early human prenatal development.

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Somatic genomic variations in early human prenatal development.

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Somatic genomic variations in early human prenatal development.

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prefLabel

Somatic genomic variations in early human prenatal development.

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Somatic genomic variations in early human prenatal development.

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Somatic genomic variations in early human prenatal development.

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Current Genomics

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Somatic genomic variations in early human prenatal development.

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Anne Pexsters

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Caroline Robberecht

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Evelyne Vanneste

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Joris R Vermeesch

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Thierry Voet

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

P2860

Confined placental mosaicism

Global variation in copy number in the human genome

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction

Prospective prenatal investigations on potential uniparental disomy in cases of confined placental trisomy

Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling

Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism.

Aneuploidy and confined chromosomal mosaicism in the developing human brain.

Natural selection of human embryos: decidualizing endometrial stromal cells serve as sensors of embryo quality upon implantation

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397-401

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6

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11

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