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1.
Neuromolecular Med ; 18(2): 155-6, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-26972434

RESUMO

Liu et al. have carried out a meta-analysis of case-control studies to investigate the association between PICALM gene rs3851179 polymorphism and Alzheimer's disease in an Asian population. However, several important issues should be noted.


Assuntos
Doença de Alzheimer , Proteínas Monoméricas de Montagem de Clatrina/genética , Povo Asiático , Predisposição Genética para Doença , Humanos , Polimorfismo de Nucleotídeo Único
2.
Oncotarget ; 7(37): 58862-58875, 2016 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-27556856

RESUMO

Myosin IXB (MYO9B) gene polymorphisms have been extensively investigated in terms of their associations with inflammatory bowel disease (IBD), with contradictory results. The aim of this meta-analysis was to evaluate associations between MY09B gene polymorphisms and the risk of IBD, Crohn's disease (CD) and ulcerative colitis (UC). Eligible studies from PubMed, Embase, and CNKI databases were identified. Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated. Ten studies published in eight papers reporting 8,975 cases and 9,482 controls were included in this meta-analysis. Five MY09B gene polymorphisms were evaluated: rs1545620, rs962917, rs1457092, rs2305764, and rs2305767. Our data suggested that the rs1545620 polymorphism was associated with a decreased risk of IBD. A similar result was found for rs2305767 and UC. The rs962917 single nucleotide polymorphism (SNP) increased the risk of IBD, CD and UC. Moreover, rs1457092 increased the risk of IBD and UC. Rs2305764 was also associated with an increased risk of IBD. Furthermore, stratification analyses indicated that rs1545620 decreased the risk of IBD, while rs962917 increased the risk of IBD, CD and UC in Caucasian populations. To sum up, our data indicate that these five SNPs in MY09B are significantly associated with the risk of IBD.


Assuntos
Genótipo , Doenças Inflamatórias Intestinais/genética , Miosinas/genética , Estudos de Associação Genética , Predisposição Genética para Doença , Humanos , Doenças Inflamatórias Intestinais/epidemiologia , Razão de Chances , Polimorfismo de Nucleotídeo Único , Risco , População Branca
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