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国家自然科学基金(30771029)

作品数:4 被引量:18H指数:2
相关作者:王莹王伟于意王德芬倪继红更多>>
相关机构:上海交通大学医学院附属瑞金医院更多>>
发文基金:国家自然科学基金国家高技术研究发展计划国家杰出青年科学基金更多>>
相关领域:医药卫生生物学更多>>

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ASSOCIATION ANALYSIS OF POLYMORPHISMS IN SIX GENES WITHIN THE GH/IGF-1 AXIS IN PATIENTS WITH IDIOPATHIC SHORT STATURE IN THE CHINESE HAN POPULATION被引量:1
2012年
Objective To investigate relationships of polymorphisms in six genes(GHR,IGF-1, IGF-1R,IGFBP-3,JAK2,and STAT5b)in the growth hormone(GH)/insulin-like growth factor-1 (IGF-1)axis with idiopathic short stature(ISS)in the Chinese Han population.Methods A casecontrol study was carried out on a cohort of 198 ISS patients and 306 healthy controls.A total of 106 tagging single nucleotide polymorphisms(tagSNPs)from the six genes were selected from the HapMap(haplotype map of the human genome)Han Chinese in the Beijing subset.Results of genotyping conducted by highthroughput Illumina GoldenGate?Assay were analyzed by statistical software.Results Both individual tagSNPs and haplotypes showed an association with ISS in the Han Chinese population(P <0.05).For each single test,both allele and genotype were tested.By allele frequency analysis,six positive SNP sites (rsNo.l,rsNo.2,rsNo.3,rsNo.4,rsNo.5,and rsNo.6)of 3 genes(JAK2,IGF-1 R,and GHR)were found having associations with ISS.By genotype frequency analysis,there were significant differences between the patient and control groups in the following SNP sites;4 sites in JAK2 gene(rsNo.1,rsNo.2, rsNo.3,and rsNo.4)and 1 site in GHR gene(rsNo.6).The risk which affected ISS was found related to the JAK2 gene in 4 sites(increase in rsNo.1 and decrease in rsNo.2,rsNo.3,and rsNo.4)and to the GHR gene in 1 site(decrease in rsNo.6).They were four haplotypes in gene of IGF-1 R as "TGC","CGCT", "TA",and " CA",one haplotype in IGFBP-3 as "TA",and one haplotype in JAK2 as " CTG",which revealed high significance for risks of affecting ISS.At last,multivariate logistic regression analysis of specific site rsNo.6 of the GHR gene revealed that the serum IGF-1 was related to genotypes AA and AC, with genotype CC as the reference(P=0.015).Conclusion Genetic variances in six genes within the GH/IGF-1 axis may be important etiological factors for ISS in the Chinese Han population.
滕月春王伟黄薇王莹杨玉卫海燕陈少科陈临琪王德芬
关键词:中国汉族人群多态性分析人类基因组单体型图等位基因频率
全基因组关联分析在人类复杂疾病研究中的应用被引量:4
2010年
早在1996年,Risch和Merikangas[1]首先提出了常见疾病可能是由于常见基因变异引起的,关联分析通常比连锁分析具有更高的检测效率,而全基因组关联分析(genome-wide association study,GWAS)是发现人类复杂疾病相关遗传变异最有力和最有效的研究方法。
王莹王艺黄薇
关键词:全基因组关联分析复杂疾病单核苷酸多态性
生长激素受体基因多态性与特发性矮小遗传易感性的关系被引量:13
2011年
目的探讨人生长激素受体(GHR)基因的单核苷酸多态性(SNP)与中国汉族人群特发性矮小(ISS)遗传易感性的关系。方法采用病例对照法,在199例ISS患儿(ISS组)和469名身高正常成人(对照组)中,对GHR基因16个SNP位点进行基因分型和比较,筛查阳性SNP位点(特异基因型频率差异有统计学意义),分析阳性SNP位点基因型与ISS发病风险及血清胰岛素样生长因子1(IGF-1)等相关临床变量的关系。结果在ISS组和对照组中,发现3个阳性SNP位点rs6182(P=0.027)、rs4410646(P=0.01)和rs10044169(P=0.024)。①rs6182(G/T):在T显性模式下,TT和GT基因型的ISS发病风险降低(OR=0.624,95%CI:0.402~0.969,P=0.021)。②rs4410646(A/C):在C显性模式下AA基因型的ISS发病风险降低(OR=0.674,95%CI:0.475~0.958,P=0.016);该位点的多因素Logistics回归分析显示,以CC基因型为参照,血清IGF-1与基因型AA(OR=1.011,95%CI:1.002~1.020,P=0.018...
于意王伟王莹黄嶶董治亚滕月春倪继红肖园王德芬
关键词:特发性矮小生长激素受体单核苷酸多态性胰岛素样生长因子1遗传易感性
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