Source:http://linkedlifedata.com/resource/pubmed/id/15584484
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2004-12-8
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pubmed:abstractText |
Solute carrier 11a1 (SLC11A1; formerly NRAMP1, where NRAMP stands for natural resistance-associated macrophage protein) is a proton/bivalent cation antiporter that localizes to late endosomes/lysosomes. SLC11A1 regulates macrophage functions that are of potential importance in the induction and/or maintenance of autoimmune diseases such as rheumatoid arthritis, type I diabetes and Crohn's disease. We investigated SLC11A1 gene as a candidate gene for genetic susceptibility to multiple sclerosis (MS) in our population. Four SLC11A1 gene polymorphisms (5'GT repeat, D543N, 1729 + 55del4 and 1729 + 271del4) were analysed in a case-control study of 195 patients with MS and 125 control subjects. We found no evidence of association between SLC11A1 polymorphisms and MS susceptibility in the Spanish population.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1352-4585
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
618-20
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pubmed:meshHeading |
pubmed-meshheading:15584484-Adult,
pubmed-meshheading:15584484-Case-Control Studies,
pubmed-meshheading:15584484-Cation Transport Proteins,
pubmed-meshheading:15584484-Female,
pubmed-meshheading:15584484-Genetic Predisposition to Disease,
pubmed-meshheading:15584484-Humans,
pubmed-meshheading:15584484-Male,
pubmed-meshheading:15584484-Middle Aged,
pubmed-meshheading:15584484-Multiple Sclerosis, Chronic Progressive,
pubmed-meshheading:15584484-Multiple Sclerosis, Relapsing-Remitting,
pubmed-meshheading:15584484-Polymorphism, Genetic,
pubmed-meshheading:15584484-Risk Factors,
pubmed-meshheading:15584484-Spain
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pubmed:year |
2004
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pubmed:articleTitle |
Genetic analysis of SLC11A1 polymorphisms in multiple sclerosis patients.
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pubmed:affiliation |
Department of Neurology, Unitat de Neuroimmunologia Clínica, Hospital Universitari Vall d'Hebron, Barcelona, Spain. mcomabel@vhebron.net
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pubmed:publicationType |
Journal Article
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