about
Genome-wide association study of severity in multiple sclerosis.HLA-DRB1*07:01 is associated with a higher risk of asparaginase allergies.Endophenotypes in schizophrenia: a selective review.Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphismsGenomic NGFB variation and multiple sclerosis in a case control study.Differential micro RNA expression in PBMC from multiple sclerosis patients.An application of Random Forests to a genome-wide association dataset: methodological considerations & new findingsGenetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosisThe association of -330 interleukin-2 gene polymorphism with its plasma concentration in Iranian multiple sclerosis patients.SHP-1 deficiency and increased inflammatory gene expression in PBMCs of multiple sclerosis patients.Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.Genetics and pathogenesis of multiple sclerosis.Common viruses associated with lower pediatric multiple sclerosis risk.Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans.Incidence of acquired CNS demyelinating syndromes in a multiethnic cohort of children.High-throughput, high-fidelity HLA genotyping with deep sequencing.Polymorphism of Apo lipoprotein E gene and the risk of multiple sclerosis.Bioinformatics for study of autoimmunity.Fetal risks related to the treatment of multiple sclerosis during pregnancy and breastfeeding.Exchangeable models of complex inherited diseasesVariation within DNA repair pathway genes and risk of multiple sclerosis.The association of -475 and -631 interleukin-2 gene polymorphism with multiple sclerosis in Iranian patients.Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.Systems biology approaches for the study of multiple sclerosis.No evidence for shared etiology in two demyelinative disorders, MS and PLOSLMacrophages of multiple sclerosis patients display deficient SHP-1 expression and enhanced inflammatory phenotypeGene expression profiling in multiple sclerosis brain.The human microbiome in multiple sclerosis: pathogenic or protective constituents?Annotation of functional variation within non-MHC MS susceptibility loci through bioinformatics analysis.A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactomeRole of socioeconomic position in multiple sclerosis etiology.A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis.Adverse socioeconomic position during the life course is associated with multiple sclerosis.Effects of acute and repeated exposure to lipopolysaccharide on cytokine and corticosterone production during remyelinationThe innate immune response to adjuvants dictates the adaptive immune response to autoantigens.The association of -330 interleukin-2 gene polymorphism and HLA-DR15 allele in Iranian patients with multiple sclerosis.Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.The payer's perspective: What is the burden of MS and how should the patient's perspective be integrated in health technology assessment conducted for taking decisions on access to care and treatment?Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients.Frequency of HLA-A alleles in the Syrian population genotyped by sequence-based typing.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Multiple sclerosis genetics: leaving no stone unturned.
@ast
Multiple sclerosis genetics: leaving no stone unturned.
@en
type
label
Multiple sclerosis genetics: leaving no stone unturned.
@ast
Multiple sclerosis genetics: leaving no stone unturned.
@en
prefLabel
Multiple sclerosis genetics: leaving no stone unturned.
@ast
Multiple sclerosis genetics: leaving no stone unturned.
@en
P2860
P356
P1433
P1476
Multiple sclerosis genetics: leaving no stone unturned.
@en
P2093
Barcellos LF
Oksenberg JR
P2860
P2888
P304
P356
10.1038/SJ.GENE.6364237
P577
2005-08-01T00:00:00Z