Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis.
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 atrophyTechnical considerations for reduced representation bisulfite sequencing with multiplexed librariesN-Acetylglucosamine Inhibits T-helper 1 (Th1)/T-helper 17 (Th17) Cell Responses and Treats Experimental Autoimmune EncephalomyelitisRevealing the genetic basis of multiple sclerosis: are we there yet?Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson's, Huntington's, Alzheimer's, prions, bactericides, chemical toxicology and others as examplesBeyond genotype to phenotype: why the phenotype of an individual cannot always be predicted from their genome sequence and the environment that they experienceThe genetics of multiple sclerosis: review of current and emerging candidatesPromise of personalized omics to precision medicineThe genetics of complex cholestatic disordersHas the microbiota played a critical role in the evolution of the adaptive immune system?Biomarkers in Multiple Sclerosis: An Up-to-Date OverviewEpigenetic Drugs for Multiple SclerosisDNA methylation, its mediators and genome integrityVitamin D Actions on CD4(+) T Cells in Autoimmune DiseaseThe role of epigenetic mechanisms and processes in autoimmune disordersGenetic mosaics and the germ line lineageGenome-wide analysis of copy number variation in type 1 diabetesComparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome.A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.DMAP: differential methylation analysis package for RRBS and WGBS data.Differences of DNA methylation profiles between monozygotic twins' blood samples.The background puzzle: how identical mutations in the same gene lead to different disease symptoms.The genetic basis of multiple sclerosis: a model for MS susceptibility.Whole genome and exome sequencing of monozygotic twins with trisomy 21, discordant for a congenital heart defect and epilepsySystems biology: personalized medicine for the future?Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia.Deficient Vitamin E Uptake During Development Impairs Neural Tube Closure in Mice Lacking Lipoprotein Receptor SR-BI.Differential methylation at MHC in CD4+ T cells is associated with multiple sclerosis independently of HLA-DRB1Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.The role of replicates for error mitigation in next-generation sequencing.Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation.The use of the twin model to investigate the genetics and epigenetics of skin diseases with genomic, transcriptomic and methylation data.Contribution of genetic, epigenetic and transcriptomic differences to twin discordance in multiple sclerosis.Increased expression and altered methylation of HERVWE1 in the human placentas of smaller fetuses from monozygotic, dichorionic, discordant twinsTransgenerational epigenetic inheritance: more questions than answers.Comprehensive carrier screening and molecular diagnostic testing for recessive childhood diseases.Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs.Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences.In depth comparison of an individual's DNA and its lymphoblastoid cell line using whole genome sequencing.Genome-wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels.
P2860
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P2860
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis.
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին 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
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@ast
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@en
type
label
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@ast
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@en
prefLabel
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@ast
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@en
P2093
P2860
P50
P356
P1433
P1476
Genome, epigenome and RNA sequ ...... ordant for multiple sclerosis.
@en
P2093
Andrew D Farmer
Callum J Bell
Elena E Ganusova
Faye D Schilkey
Gary P Schroth
Gregory D May
Irina Khrebtukova
Jim J Huntley
Jimmy E Woodward
Joann Mudge
P2860
P2888
P304
P356
10.1038/NATURE08990
P407
P50
P577
2010-04-01T00:00:00Z