Early embryonic chromosome instability results in stable mosaic pattern in human tissues
about
Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genomeSomatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary data.The human genome puzzle - the role of copy number variation in somatic mosaicismCytogenetic contribution to uniparental disomy (UPD).Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia.Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.Somatic genome variations in health and diseaseSomatic genomic variations in extra-embryonic tissuesControlled somatic and germline copy number variation in the mouse modelNew cytogenetically visible copy number variant in region 8q21.2.Hydroxyurea induces de novo copy number variants in human cells.Influence of aflatoxin B1 on copy number variants in human leukocytes in vitroGenomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism.Copy number variation in the region harboring SOX9 gene in dogs with testicular/ovotesticular disorder of sex development (78,XX; SRY-negative)Single cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases.Extensive genetic variation in somatic human tissues.Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells.Chromosomes in a genome-wise order: evidence for metaphase architecture.The human cleavage stage embryo is a cradle of chromosomal rearrangements.Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.Replication stress and mechanisms of CNV formation.Dominant expansion of a cryptic subclone with an abnormal karyotype in B lymphoblastoid cell lines during culture.Microarray analysis of copy number variation in single cells.A time stamp comparative analysis of frequent chromosomal abnormalities in Romanian patients.Somatic mosaicism in cases with small supernumerary marker chromosomes.De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia.Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos.Somatic mosaicism in esophageal atresia.
P2860
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P2860
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@ast
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@en
Early embryonic chromosome instability results in stable mosaic pattern in human tissues.
@nl
type
label
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@ast
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@en
Early embryonic chromosome instability results in stable mosaic pattern in human tissues.
@nl
prefLabel
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@ast
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@en
Early embryonic chromosome instability results in stable mosaic pattern in human tissues.
@nl
P2093
P2860
P1433
P1476
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
@en
P2093
Anja Weise
Anna Polytiko
Elisabeth Ewers
Hasmik Mkrtchyan
Heike Nelle
Kristin Mrasek
Madeleine Gross
Marianne Volleth
Marina Manvelyan
Nadezda Kosyakova
P2860
P356
10.1371/JOURNAL.PONE.0009591
P407
P577
2010-03-09T00:00:00Z