Genomewide scan of multiple sclerosis in Finnish multiplex families.
about
Genomewide scans of complex human diseases: true linkage is hard to findA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosisPECAM-1, a key player in neuroinflammationExtracellular nucleotides induce migration of renal mesangial cells by upregulating sphingosine kinase-1 expression and activityCognitive impairments in multiple sclerosis: a review.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.An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians.Genetic analysis of the exon 1 position 49 CD152 dimorphism in multiple sclerosisGenome-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.Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.The genetic epidemiology of multiple sclerosis.A second-generation genomic screen for multiple sclerosisThe genetics of multiple sclerosis.A high-density screen for linkage in multiple sclerosis.Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q.Meta-analysis of genome-wide linkage studies across autoimmune diseases.Replication of linkage studies of complex traits: an examination of variation in location estimates.Eae19, a new locus on rat chromosome 15 regulating experimental autoimmune encephalomyelitis.Recent advances in the genetics of schizophrenia.Multiple sclerosis complexity in selected populations: the challenge of Sardinia, insular Italy.Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.Genetics and pathogenesis of multiple sclerosis.Genetics and genomics of asthma and allergic diseases.Candidate gene regions and genetic heterogeneity in gluten sensitivity.Multiple sclerosis in sibling pairs: an analysis of 250 familiesIdentification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis.Current gene-mapping strategies in experimental models of multiple sclerosis.Comparison of GenFlex Tag array and Pyrosequencing in SNP genotyping.Sphingosine kinase signalling in immune cells.Finding disease candidate genes by liquid associationHLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility.Genetic Factors and Orofacial Clefting.The complex genetics of multiple sclerosis: pitfalls and prospectsUse of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.A follow-up study of chromosome 19q13 in multiple sclerosis susceptibilityNo evidence for shared etiology in two demyelinative disorders, MS and PLOSL
P2860
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P2860
Genomewide scan of multiple sclerosis in Finnish multiplex families.
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@ast
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@en
type
label
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@ast
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@en
prefLabel
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@ast
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@en
P2093
P2860
P356
P1476
Genomewide scan of multiple sclerosis in Finnish multiplex families.
@en
P2093
E S Lander
J D Terwilliger
J Wikström
L Peltonen
M Gschwend
P J Tienari
S Kuokkanen
P2860
P304
P356
10.1086/301637
P407
P577
1997-12-01T00:00:00Z