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1
Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster.载脂蛋白AI-CIII-AIV基因簇中哈迪-温伯格平衡及成对不平衡的估计。
Am J Hum Genet. 1991 Aug;49(2):350-65.
2
Variation at the apolipoprotein (apo) AI-CIII-AIV gene cluster and apo B gene loci is associated with lipoprotein and apolipoprotein levels in Italian children.载脂蛋白(apo)AI-CIII-AIV基因簇和apo B基因位点的变异与意大利儿童的脂蛋白及载脂蛋白水平相关。
Am J Hum Genet. 1990 Sep;47(3):429-39.
3
Linkage disequilibrium of the Apo AI-CIII-AIV gene cluster and their relationship to plasma triglyceride, apolipoprotein AI and CIII levels in Koreans.韩国人载脂蛋白AI-CIII-AIV基因簇的连锁不平衡及其与血浆甘油三酯、载脂蛋白AI和CIII水平的关系。
Mol Cells. 1998 Feb 28;8(1):12-8.
4
DNA polymorphisms of the apolipoprotein AII and AI-CIII-AIV genes: a study in men selected for differences in high-density-lipoprotein cholesterol concentration.载脂蛋白AII和AI-CIII-AIV基因的DNA多态性:一项针对高密度脂蛋白胆固醇浓度存在差异的男性的研究。
Am J Hum Genet. 1988 Mar;42(3):458-67.
5
DNA restriction polymorphisms of the apolipoprotein AI-CIII-AIV gene cluster: a genetic determinant of atherosclerosis in type 2 (non-insulin-dependent) diabetes mellitus.载脂蛋白AI - CIII - AIV基因簇的DNA限制性多态性:2型(非胰岛素依赖型)糖尿病动脉粥样硬化的遗传决定因素。
Diabet Med. 1991 May;8(4):354-60. doi: 10.1111/j.1464-5491.1991.tb01609.x.
6
Associations of genotypes at the apolipoprotein AI-CIII-AIV, apolipoprotein B and lipoprotein lipase gene loci with coronary atherosclerosis and high density lipoprotein subclasses.载脂蛋白AI-CIII-AIV、载脂蛋白B和脂蛋白脂肪酶基因位点的基因型与冠状动脉粥样硬化及高密度脂蛋白亚类的关联。
Clin Genet. 1994 Oct;46(4):273-82. doi: 10.1111/j.1399-0004.1994.tb04159.x.
7
Polymorphisms in the apolipoprotein (apo) AI-CIII-AIV gene cluster: detection of genetic variation determining plasma apo AI, apo CIII and apo AIV concentrations.载脂蛋白(apo)AI-CIII-AIV基因簇中的多态性:决定血浆apo AI、apo CIII和apo AIV浓度的遗传变异检测。
Hum Genet. 1992 Feb;88(4):439-46. doi: 10.1007/BF00215679.
8
A PvuII polymorphism in the 5' flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration.载脂蛋白AIV基因5'侧翼区的PvuII多态性:用于研究决定血清脂质和载脂蛋白浓度的遗传变异
Hum Genet. 1988 Mar;78(3):237-9. doi: 10.1007/BF00291668.
9
Within-individual variation in serum cholesterol levels: association with DNA polymorphisms at the apolipoprotein B and AI-CIII-AIV loci in patients with peripheral arterial disease.外周动脉疾病患者血清胆固醇水平的个体内变异:与载脂蛋白B及AI-CIII-AIV基因座处DNA多态性的关联
Clin Genet. 1991 Apr;39(4):260-73. doi: 10.1111/j.1399-0004.1991.tb03024.x.
10
Association between genetic variations of apo AI-CIII-AIV cluster gene and hypertriglyceridemic subjects.载脂蛋白AI-CIII-AIV基因簇的遗传变异与高甘油三酯血症患者之间的关联。
Clin Chem. 1997 Jan;43(1):13-7.

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Association of lipoprotein lipase and apolipoprotein C-III genes polymorphism with acute myocardial infarction in diabetic patients.载脂蛋白 C-III 基因多态性与脂蛋白脂肪酶基因多态性与糖尿病患者急性心肌梗死的关系。
Mol Cell Biochem. 2011 Aug;354(1-2):141-50. doi: 10.1007/s11010-011-0813-6. Epub 2011 Apr 17.
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Apolipoprotein C3 polymorphisms, cognitive function and diabetes in Caribbean origin Hispanics.加勒比裔西班牙人中载脂蛋白C3基因多态性、认知功能与糖尿病
PLoS One. 2009;4(5):e5465. doi: 10.1371/journal.pone.0005465. Epub 2009 May 8.
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Association of the TNF-alpha-308 (G-->A) polymorphism with self-reported history of childhood asthma.肿瘤坏死因子-α -308(G→A)基因多态性与儿童哮喘自我报告病史的关联。
Hum Genet. 2000 Dec;107(6):591-6. doi: 10.1007/s004390000410.
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Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase.基于人类脂蛋白脂肪酶核苷酸序列变异的单倍型结构与群体遗传学推断
Am J Hum Genet. 1998 Aug;63(2):595-612. doi: 10.1086/301977.
5
Apolipoprotein AI-CIII-AIV genetic polymorphisms and coronary heart disease in type 2 diabetes mellitus.载脂蛋白AI-CIII-AIV基因多态性与2型糖尿病患者的冠心病
Acta Diabetol. 1995 Dec;32(4):251-6. doi: 10.1007/BF00576258.
6
Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.连锁不平衡可预测结肠腺瘤性息肉病区域的物理距离。
Am J Hum Genet. 1994 May;54(5):884-98.
7
Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping.神经纤维瘤病1型(NF1)区域的连锁不平衡:对基因定位的影响。
Am J Hum Genet. 1993 Nov;53(5):1038-50.
8
Linkage disequilibrium of three polymorphic RFLP markers in the apolipoprotein AI-CIII gene cluster on chromosome 11.位于11号染色体上的载脂蛋白AI - CIII基因簇中三个多态性限制性片段长度多态性(RFLP)标记的连锁不平衡
Hum Genet. 1993 Mar;91(2):169-74. doi: 10.1007/BF00222719.
9
Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.来自不同人群的有和没有家族性高胆固醇血症的受试者中低密度脂蛋白受体基因位点的多态性单倍型和重组率。
Am J Hum Genet. 1993 Apr;52(4):808-26.
10
Polymorphisms and linkage disequilibrium in the COL6A1 and COL6A2 gene cluster: novel DNA polymorphisms in the region of a candidate gene for congenital heart defects in Down's syndrome.COL6A1和COL6A2基因簇中的多态性与连锁不平衡:唐氏综合征先天性心脏缺陷候选基因区域的新型DNA多态性。
Hum Genet. 1993 Jan;90(5):521-5. doi: 10.1007/BF00217452.

本文引用的文献

1
The two apolipoprotein loci apo A-I and apo A-IV are closely linked in man.载脂蛋白A-I和载脂蛋白A-IV这两个基因座在人类中紧密连锁。
Hum Genet. 1984;68(2):181-4. doi: 10.1007/BF00279311.
2
Human apolipoprotein A-I and C-III genes reside in the p11----q13 region of chromosome 11.人类载脂蛋白A-I和C-III基因位于11号染色体的p11----q13区域。
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Apolipoprotein A-I as a marker of angiographically assessed coronary-artery disease.载脂蛋白A-I作为血管造影评估冠状动脉疾病的标志物。
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Genetics of coronary heart disease.冠心病的遗传学
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The effects of subfractions of high density lipoprotein on cholesterol efflux from cultured fibroblasts. Regulation of low density lipoprotein receptor activity.高密度脂蛋白亚组分对培养成纤维细胞胆固醇流出的影响。低密度脂蛋白受体活性的调节。
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DNA polymorphism adjacent to human apoprotein A-1 gene: relation to hypertriglyceridaemia.人类载脂蛋白A-1基因附近的DNA多态性:与高甘油三酯血症的关系。
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Analysis of multilocus genetic systems in Tecumseh, Michigan. II. Consideration of the correlation between nonalleles in gametes.密歇根州蒂卡姆西多位点遗传系统分析。II. 配子中非等位基因间相关性的考量。
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Estimation of linkage disequilibrium in randomly mating populations.随机交配群体中连锁不平衡的估计。
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载脂蛋白AI-CIII-AIV基因簇中哈迪-温伯格平衡及成对不平衡的估计。

Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster.

作者信息

Haviland M B, Kessling A M, Davignon J, Sing C F

机构信息

Department of Human Genetics, University of Michigan, Ann Arbor.

出版信息

Am J Hum Genet. 1991 Aug;49(2):350-65.

PMID:1678249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1683298/
Abstract

Departures from Hardy-Weinberg (HW) equilibria and pairwise disequilibria were estimated in a sample of unrelated healthy individuals typed for six RFLPs in the apo AI-CIII-AIV gene region. The sample was composed of males and females, selected for health, from two populations, those of exclusively French-Canadian (FC) and those of some non-French-Canadian (NFC) ancestry. An approach suggested by Weir and Cockerham, which includes estimates of nonrandom association (disequilibria) between three and four alleles at two loci as well as the traditional associations between two alleles, at two loci was used. The pattern of departures from HW equilibria suggested that the genetic structures of the FC and NFC are different. Departure from HW equilibrium at an RFLP locus could not be predicted from information about other loci in the same gene region. Nonrandom associations were also evident from the pairwise analyses. Two pairs of loci had significant diallelic disequilibria, while two other pairs had significant triallelic disequilibria. All of the RFLP pairs had at least one measure of disequilibrium at its maximum value determined by allele frequencies. Inferences about pairwise disequilibria depended on the statistical approach used. Sizes of the pairwise disequilibria were not correlated with the physical distance between loci. The impact of these disequilibria on RFLP-phenotype association studies is discussed.

摘要

在一个对载脂蛋白AI-CIII-AIV基因区域的6个限制性片段长度多态性(RFLP)进行分型的无亲缘关系健康个体样本中,估计了哈迪-温伯格(HW)平衡的偏离情况和成对不平衡情况。该样本由来自两个群体的男性和女性组成,这些个体因健康状况而被挑选出来,这两个群体分别是纯法裔加拿大人(FC)群体和一些非法裔加拿大人(NFC)血统的群体。采用了Weir和Cockerham提出的一种方法,该方法包括估计两个位点上三个和四个等位基因之间的非随机关联(不平衡)以及传统的两个位点上两个等位基因之间的关联。偏离HW平衡的模式表明FC和NFC的遗传结构不同。无法根据同一基因区域中其他位点的信息预测RFLP位点偏离HW平衡的情况。成对分析中也明显存在非随机关联。两对位点具有显著的双等位基因不平衡,而另外两对位点具有显著的三等位基因不平衡。所有RFLP对至少有一项不平衡测量值达到由等位基因频率决定的最大值。关于成对不平衡的推断取决于所使用的统计方法。成对不平衡的大小与位点之间的物理距离无关。讨论了这些不平衡对RFLP-表型关联研究的影响。