A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group.
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N-Acetylglucosamine Inhibits T-helper 1 (Th1)/T-helper 17 (Th17) Cell Responses and Treats Experimental Autoimmune EncephalomyelitisMapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.Thomas John (Jock) Murray, OC, MD, FRCP(C), MACP, LLD(HON), DSc(Hon), FRCP(Lon): a conversation with the editor. Interview by William Clifford Roberts.Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosisThe genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genesEpidemiology and genetic aspects of multiple sclerosis in IndiaEnvironmental risk factors for multiple sclerosis: a review with a focus on molecular mechanismsAssociation of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosisA genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22A dinucleotide deletion in CD24 confers protection against autoimmune diseasesA survey of endogenous retrovirus (ERV) sequences in the vicinity of multiple sclerosis (MS)-associated single nucleotide polymorphisms (SNPs).Migration of engrafted neural stem cells is mediated by CXCL12 signaling through CXCR4 in a viral model of multiple sclerosis.Two-photon imaging of remyelination of spinal cord axons by engrafted neural precursor cells in a viral model of multiple sclerosis.Identification of susceptibility genes for experimental autoimmune encephalomyelitis that overcome the effect of protective alleles at the eae2 locus.PRKCA and multiple sclerosis: association in two independent populations.Variation of the myelin oligodendrocyte glycoprotein gene is not primarily associated with multiple sclerosis in the Sardinian population.The inheritance of resistance alleles in multiple sclerosis.Endogenous retroviruses and multiple sclerosis-new pieces to the puzzle.The causal cascade to multiple sclerosis: a model for MS pathogenesis.Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.The genetic aspects of multiple sclerosis.Progress in determining the causes and treatment of multiple sclerosis.Fine-mapping resolves Eae23 into two QTLs and implicates ZEB1 as a candidate gene regulating experimental neuroinflammation in rat.The genetic basis of multiple sclerosis: a model for MS susceptibility.Risks of multiple sclerosis in relatives of patients in Flanders, BelgiumGenetic epidemiology of multiple sclerosisGenetic counselling in multiple sclerosis: risks to sibs and children of affected individuals.Elevated Epstein-Barr virus-encoded nuclear antigen-1 immune responses predict conversion to multiple sclerosisGenetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.The genetic epidemiology of multiple sclerosis.Initiation and exacerbation of autoimmune demyelination of the central nervous system via virus-induced molecular mimicry: implications for the pathogenesis of multiple sclerosis.Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.The genetics of multiple sclerosis.Refining the association of MHC with multiple sclerosis in African Americans.A high-density screen for linkage in multiple sclerosis.Cell replacement therapies to promote remyelination in a viral model of demyelinationGenetic and functional studies in multiple sclerosis patients from Martinique attest for a specific and direct role of the HLA-DR locus in the syndrome.HLA-DRB1-DQB1 haplotypes confer susceptibility and resistance to multiple sclerosis in Sardinia.Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.Systemic inflammation and the brain: novel roles of genetic, molecular, and environmental cues as drivers of neurodegeneration.
P2860
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P2860
A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group.
description
1995 nî lūn-bûn
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1995年の論文
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1995年論文
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1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
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1995年論文
@zh-tw
1995年论文
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1995年论文
@zh
1995年论文
@zh-cn
name
A genetic basis for familial a ...... ian Collaborative Study Group.
@en
A genetic basis for familial a ...... ian Collaborative Study Group.
@nl
type
label
A genetic basis for familial a ...... ian Collaborative Study Group.
@en
A genetic basis for familial a ...... ian Collaborative Study Group.
@nl
prefLabel
A genetic basis for familial a ...... ian Collaborative Study Group.
@en
A genetic basis for familial a ...... ian Collaborative Study Group.
@nl
P2093
P356
P1433
P1476
A genetic basis for familial a ...... ian Collaborative Study Group.
@en
P2093
P2888
P304
P356
10.1038/377150A0
P407
P577
1995-09-01T00:00:00Z
P6179
1009126775