Somatic gene mutation and human disease other than cancer.
about
Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophySomatic mosaicism in the human genomeBAK1 gene variation and abdominal aortic aneurysmsRepublished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetimeNon-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetimeSomatic mutation, genomic variation, and neurological diseaseMutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).Somatic mutations, genome mosaicism, cancer and aging.Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.Gene × environment interaction by a longitudinal epigenome-wide association study (LEWAS) overcomes limitations of genome-wide association study (GWAS)Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences.Aging genomes: a necessary evil in the logic of life.Stem cell transplantation for treating Duchenne muscular dystrophy: A Web of Science-based literature analysisA random mutation capture assay to detect genomic point mutations in mouse tissueDirect mutation analysis by high-throughput sequencing: from germline to low-abundant, somatic variantsTwo novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birthMonozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancerPhenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.Structural and Kinetic Analysis of Miscoding Opposite the DNA Adduct 1,N6-Ethenodeoxyadenosine by Human Translesion DNA Polymerase η.Understanding what determines the frequency and pattern of human germline mutations.Recombination as a mechanism for sporadic mutation in the surfactant protein-C geneDYZ1 arrays show sequence variation between the monozygotic malesWhen Should Genetic Testing Be Performed in Epilepsy Patients?Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease.Congenital heart disease: the crossroads of genetics, epigenetics and environment.A high-fidelity method for genomic sequencing of single somatic cells reveals a very high mutational burden.Genetic toxicology at the crossroads-from qualitative hazard evaluation to quantitative risk assessment.Cerebral vasculopathy in a Chinese family with neurofibromatosis type I mutation.Somatic mutations in cardiac malformations.Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency.
P2860
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P2860
Somatic gene mutation and human disease other than cancer.
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Somatic gene mutation and human disease other than cancer.
@ast
Somatic gene mutation and human disease other than cancer.
@en
type
label
Somatic gene mutation and human disease other than cancer.
@ast
Somatic gene mutation and human disease other than cancer.
@en
prefLabel
Somatic gene mutation and human disease other than cancer.
@ast
Somatic gene mutation and human disease other than cancer.
@en
P1433
P1476
Somatic gene mutation and human disease other than cancer.
@en
P2093
Robert P Erickson
P304
P356
10.1016/S1383-5742(03)00010-3
P407
P577
2003-03-01T00:00:00Z