Literature DB >> 9379703

Identification of multiple sclerosis-associated genes.

W E Hogancamp1, M Rodriguez, B G Weinshenker.   

Abstract

Multiple sclerosis (MS) is a complex genetic trait. Analyses to identify genetic variants that increase susceptibility to MS have primarily focused on candidate genes, either in family linkage investigations or in association (linkage disequilibrium) studies in sporadic cases and control subjects. Most of the candidate genes considered to date either influence immune function or encode structural myelin proteins. Recently, three preliminary whole genomic surveys were completed, and they reveal multiple loci of possible genetic linkage that are worthy of further study. No convincing evidence for a single strong locus has emerged from analysis of the three studies. Linkage promises to focus the future choice of candidate genes for further investigation.

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Year:  1997        PMID: 9379703     DOI: 10.4065/72.10.965

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  3 in total

Review 1.  Detecting low penetrance genes in cancer: the way ahead.

Authors:  R S Houlston; I P Tomlinson
Journal:  J Med Genet       Date:  2000-03       Impact factor: 6.318

Review 2.  Herpesviruses--a rationale for antiviral treatment in multiple sclerosis.

Authors:  T Bergström
Journal:  Antiviral Res       Date:  1999-02       Impact factor: 5.970

3.  Resilient emotionality and molecular compensation in mice lacking the oligodendrocyte-specific gene Cnp1.

Authors:  N M Edgar; C Touma; R Palme; E Sibille
Journal:  Transl Psychiatry       Date:  2011-09-20       Impact factor: 6.222

  3 in total

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