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云南汉族人群LMP基因多态性与丙型肝炎病毒慢性感染的相关性 被引量:3
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作者 李彤 刘城秀 +3 位作者 姚宇峰 俞建昆 史荔 沈云松 《中华医学遗传学杂志》 CAS CSCD 北大核心 2016年第6期806-810,共5页
目的探讨低分子量蛋白酶体(low molecular weight polypeptide, LMP)基因多态性与丙型肝炎病毒(hepatitis C virus , HCV)慢性感染的相关性。方法选择云南地区汉族人群HCV慢性感染患者427例,健康对照者412名,采用TaqMan探针基因... 目的探讨低分子量蛋白酶体(low molecular weight polypeptide, LMP)基因多态性与丙型肝炎病毒(hepatitis C virus , HCV)慢性感染的相关性。方法选择云南地区汉族人群HCV慢性感染患者427例,健康对照者412名,采用TaqMan探针基因分型方法对LMP2基因单核苷酸多态性( single nucleotide polymorphism, SNP)rs1351383、rs17587、rs2127675和LMP7基因SNPrs2071543进行基因分型,并构建单倍型,统计LMP2和LMP7多态性位点的等位基因频率与基因型频率、单倍型频率,分析SNPs及单倍型与HCV慢性感染的相关性。结果病例组和对照组LMP2基因rs1351383和rs2127675的等位基因频率差异有统计学意义(P〈0.05),rs1351383/rs17587/rs2127675单倍型A-pA和C-G-G差异有统计学意义(P〈0.05);其他位点基因型、等位基因型、单倍型频率在病例组和对照组中差异无统计学意义(P〉0.05)。结论在云南汉族群体中,LMP2基因SNPrs1351383C等位基因和rs2127675G等位基因可能是HCV慢性感染的易感因素,rs1351383/rs17587/rs2127675单倍型A-GA可能是HCV慢性感染的保护因素,单倍型C-G-G可能是HCV慢性感染的危险因素。 展开更多
关键词 丙型肝炎病毒 慢性感染 单核苷酸多态性 LPM2基因 lmp7基因
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Relationship of large multifunctional proteasome 7 gene polymorphism with susceptibility to type 1 diabetes mellitus and DR3 gene
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作者 丁鹤林 程桦 +2 位作者 傅祖植 严励 杨桂芳 《Chinese Medical Journal》 SCIE CAS CSCD 2001年第12期31-34,103,共5页
Objective To study the relationship of the large multifunctional proteasome 7 (LMP7) gene polymorphism with susceptibility to type 1 diabetes mellitus (DM-1) and the DR3 gene in south Chinese Han population.Methods LM... Objective To study the relationship of the large multifunctional proteasome 7 (LMP7) gene polymorphism with susceptibility to type 1 diabetes mellitus (DM-1) and the DR3 gene in south Chinese Han population.Methods LMP7 genotypes and the DR3 gene were identified in 71 DM-1 patients and 86 healthy persons (as controls) by polymerase chain reaction-restriction fragment length polymorphism. DM-1 patients and controls were divided into DR3-positive and DR3-negative subjects. The frequencies of LMP7 genotypes and alleles were compared between DM-1 patients and controls respectively in the random subjects and in the DR3-matched subjects. Furthermore, DM-1 patients were divided into 3 groups according to the age of diabetic onset: group A≤14 years, group B 15-30 years, group C≥31 years.Results In the random subjects, the frequency of LMP7-B/B was lower (39% vs 58%, P<0.05) and that of LMP7-B/A was higher (54% vs 31%, P<0.01) in DM-1 patients than that in controls. In DR3-positive subjects, the frequencies of LMP7 genotypes and alleles showed no differences between DM-1 patients and controls. In DR3-negative subjects, the frequency of LMP7-B/B was decreased (40% vs 61%) and that of LMP7-B/A was increased (55% vs 28%, P<0.01) in DM-1 patients. The frequencies of LMP7 genotypes and alleles showed no significant differences among different ages of diabetic onset.Conclusions LMP7-B/B may be the protective genotype, and LMP7-B/A may be the susceptible genotype of DM-1, and this may not be affected by the DR3 gene. Persons with LMP7-B/B may have a decreased risk, and those with LMP7-B/A have an increased risk suffering from DM-1. The LMP7 gene may not be associated with the age of diabetic onset. 展开更多
关键词 diabetes mellitus · type-1 · gene · large multifunctional proteasome 7 · polymerase chain reaction · restriction fragment length polymorphism
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