A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.
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The Association Between Genetic Polymorphism rs703842 in CYP27B1 and Multiple Sclerosis: A Meta-AnalysisWhole-Genome DNA Methylation Analysis of Peripheral Blood Mononuclear Cells in Multiple Sclerosis Patients with Different Disease Courses.Viruses and Multiple Sclerosis: From Mechanisms and Pathways to Translational Research Opportunities.Heterozygote galactocerebrosidase (GALC) mutants have reduced remyelination and impaired myelin debris clearance following demyelinating injury.Neuroinflammation as modifier of genetically caused neurological disorders of the central nervous system: Understanding pathogenesis and chances for treatment.Environmental control of autoimmune inflammation in the central nervous system.The remedy within: will the microbiome fulfill its therapeutic promise?Meta-analysis of the correlation between the rs17401966 polymorphism in kinesin family member 1B and susceptibility to hepatitis B virus related hepatocellular carcinoma.Cytokine Signaling in Multiple Sclerosis and Its Therapeutic Applications.PLXNA3 Variant rs5945430 is Associated with Severe Clinical Course in Male Multiple Sclerosis Patients.Altered intestinal permeability in patients with relapsing-remitting multiple sclerosis: A pilot study.Pathogenic inflammation in the CNS of mice carrying human PLP1 mutations.Common genetic variation within miR-146a predicts disease onset and relapse in multiple sclerosis.Common genetic etiology between "multiple sclerosis-like" single-gene disorders and familial multiple sclerosis.Another Round of "Clue" to Uncover the Mystery of Complex Traits.Heterozygous carriers of galactocerebrosidase mutations that cause Krabbe disease have impaired microglial function and defective repair of myelin damage.Gut Microbiota in Multiple Sclerosis and Experimental Autoimmune Encephalomyelitis: Current Applications and Future Perspectives.Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis: the impact of genome-wide association studies identified disease risk loci
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P2860
A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
A review of genome-wide associ ...... hypothesis-driven approaches.
@en
type
label
A review of genome-wide associ ...... hypothesis-driven approaches.
@en
prefLabel
A review of genome-wide associ ...... hypothesis-driven approaches.
@en
P2093
P2860
P1433
P1476
A review of genome-wide associ ...... d hypothesis-driven approaches
@en
P2093
A V Favorov
O G Kulakova
V V Bashinskaya
P2860
P2888
P304
P356
10.1007/S00439-015-1601-2
P577
2015-09-25T00:00:00Z
P5875
P6179
1012627285