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Somatic mosaicism: implications for disease and transmission geneticsSensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) methodRepublished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetimeParental somatic mosaicism is underrecognized and influences recurrence risk of genomic disordersNon-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetimeMulti-Color Spectral Transcript Analysis (SPECTRA) for Phenotypic Characterization of Tumor Cells.A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approachRapid mechanisms for generating genome diversity: whole ploidy shifts, aneuploidy, and loss of heterozygosityIn silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome research.Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism.The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin FibroblastsSingle cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases.Implications of aneuploidy for stem cell biology and brain therapeuticsSomatic deletions implicated in functional diversity of brain cells of individuals with schizophrenia and unaffected controls.New insights into the troubles of aneuploidyX chromosome aneuploidy in the Alzheimer's disease brain.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.A prescription for 'stress'--the role of Hsp90 in genome stability and cellular adaptationLow-grade chromosomal mosaicism in human somatic and embryonic stem cell populations.An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseGenomic instability in chronic renal failure patients.Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes.Aneuploidy-driven non-heritable genomic variations demonstrate area-specific distribution in the Alzheimer’s disease brain.Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort.Aneuploidy: an important model system to understand salient aspects of functional genomics.Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.The DNA replication stress hypothesis of Alzheimer's disease.Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis.Risk Factors for Gastric Cancer: A Systematic ReviewHow to talk about genome editing.Yuri B. Yurov (1951-2017).An advanced enrichment method for rare somatic retroelement insertions sequencing
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին 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
Somatic genome variations in health and disease
@ast
Somatic genome variations in health and disease
@en
Somatic genome variations in health and disease
@nl
type
label
Somatic genome variations in health and disease
@ast
Somatic genome variations in health and disease
@en
Somatic genome variations in health and disease
@nl
prefLabel
Somatic genome variations in health and disease
@ast
Somatic genome variations in health and disease
@en
Somatic genome variations in health and disease
@nl
P2093
P2860
P1433
P1476
Somatic genome variations in health and disease
@en
P2093
I Y Iourov
S G Vorsanova
P2860
P304
P356
10.2174/138920210793176065
P577
2010-09-01T00:00:00Z