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Neuroimmunotherapies Targeting T Cells: From Pathophysiology to Therapeutic Applications.Defining a new biomarker for the autoimmune component of Multiple Sclerosis: Th40 cells.Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study.Small non-coding RNA signature in multiple sclerosis patients after treatment with interferon-β.TRAIL/TRAIL receptor system and susceptibility to multiple sclerosisIL7Rα contributes to experimental autoimmune encephalomyelitis through altered T cell responses and nonhematopoietic cell lineagesCharacterisation of genome-wide association epistasis signals for serum uric acid in human population isolatesGenetic association of rs1520333 G/A polymorphism in the IL7 gene with multiple sclerosis susceptibility in Isfahan population.Association of CD58 Polymorphism with Multiple Sclerosis and Response to Interferon ß Therapy in A Subset of Iranian PopulationThe POLG Polyglutamine Tract Variants in Iranian Patients with Multiple SclerosisAnti-CCP antibody levels are not associated with MS: results from a case-control study.Statistical Optimization of Pharmacogenomics Association Studies: Key Considerations from Study Design to AnalysisGenome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genes.The genetic basis of graves' disease.Gene network analysis of small molecules with autoimmune disease associated genes predicts a novel strategy for drug efficacy.Genome-wide association analysis identifies genetic variations in subjects with myalgic encephalomyelitis/chronic fatigue syndrome.Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases.MicroRNAs and Multiple Sclerosis.New insight into the functions of the interleukin-17 receptor adaptor protein Act1 in psoriatic arthritis.Polymorphism in Leptin and Leptin Receptor Genes May Modify Leptin Levels and Represent Risk Factors for Multiple Sclerosis.Association of missense mutations of Mediterranean fever (MEFV) gene with multiple sclerosis in Turkish population.Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis.The promoter SNP, but not the alternative splicing SNP, is linked to multiple sclerosis among Jordanian patients.Multiple sclerosis and cognitive decline: is ApoE-4 a surrogate marker?The Association of Interleukin-16 Gene Polymorphisms with IL-16 Serum Levels and Risk of Multiple Sclerosis.Association of AIRE Polymorphism and the Susceptibility to Multiple Sclerosis in Iranian Population.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 05 May 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The genetics of multiple sclerosis: an update 2010.
@en
The genetics of multiple sclerosis: an update 2010.
@nl
type
label
The genetics of multiple sclerosis: an update 2010.
@en
The genetics of multiple sclerosis: an update 2010.
@nl
prefLabel
The genetics of multiple sclerosis: an update 2010.
@en
The genetics of multiple sclerosis: an update 2010.
@nl
P1476
The genetics of multiple sclerosis: an update 2010.
@en
P2093
Denis A Akkad
Sabine Hoffjan
P304
P356
10.1016/J.MCP.2010.04.006
P577
2010-05-05T00:00:00Z