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利用11号染色体q13区域与特应性及对乙酰甲胆碱的支气管高反应性之间连锁的DNA多态性进行遗传分析。

Genetic analysis using DNA polymorphism of the linkage between chromosome 11q13 and atopy and bronchial hyperresponsiveness to methacholine.

作者信息

Lympany P, Welsh K, MacCochrane G, Kemeny D M, Lee T H

机构信息

Department of Allergy and Allied Respiratory Disorders, United Medical School, Guy's Hospital, London, England.

出版信息

J Allergy Clin Immunol. 1992 Feb;89(2):619-28. doi: 10.1016/0091-6749(92)90330-5.

Abstract

Previous studies have suggested that there is a genetic predisposition for the development of asthma and atopy. A recent study has also demonstrated that there is a striking link between chromosome 11q and the IgE response underlying asthma and rhinitis. To assess the linkage between chromosome 11q (region D11S97) and atopy or bronchial hyperresponsiveness (BH), we have studied nine families of two and, in many instances, three generations with the index case having asthma and/or atopy. With variable number of tandem repeat analysis with the probe, p lambda-MS.51, we have been unable to confirm a significant link between region D11S97 of chromosome 11q and either atopy or BH to methacholine. We have demonstrated that atopy and BH produce similar log of odds scores with linkage analysis at each recombination fraction from 0.001 to 0.5 with both Hinf1 and Taq1 restriction digests and that the use of either a positive skin prick test or positive RAST as a definition of atopy does not significantly alter the log of odds score.

摘要

先前的研究表明,哮喘和特应性疾病的发生存在遗传易感性。最近一项研究还证明,11号染色体q区与哮喘和鼻炎所潜在的IgE反应之间存在显著联系。为了评估11号染色体q区(D11S97区域)与特应性疾病或支气管高反应性(BH)之间的联系,我们研究了9个家庭,这些家庭中有两代人,在许多情况下还有三代人,索引病例患有哮喘和/或特应性疾病。通过使用探针p lambda-MS.51进行可变数目串联重复分析,我们未能证实11号染色体q区的D11S97区域与特应性疾病或对乙酰甲胆碱的支气管高反应性之间存在显著联系。我们已经证明,在从0.001到0.5的每个重组分数下,使用Hinf1和Taq1限制性酶切进行连锁分析时,特应性疾病和支气管高反应性产生相似的优势对数分数,并且使用阳性皮肤点刺试验或阳性放射变应原吸附试验作为特应性疾病的定义不会显著改变优势对数分数。

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