首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >I/D genetic polymorphism of angiotensin-converting enzyme: pathogenesis evaluation for erectile dysfunction by gene ontology.
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I/D genetic polymorphism of angiotensin-converting enzyme: pathogenesis evaluation for erectile dysfunction by gene ontology.

机译:血管紧张素转换酶的I / D遗传多态性:通过基因本体论评估勃起功能障碍的发病机理。

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OBJECTIVE: Angiotensin-converting enzyme (ACE) is the major regulator of mineralocorticoid synthesis and it is in the renin/angiotensin system. Angiotensin-converting enzyme is responsible for several vascular diseases. It also relates to erectile dysfunction. However, in-depth analysis on the effect of genetic I/D polymorphism of ACE has never been performed. The molecular mechanisms for each genotype expression in erectile dysfunction are poorly understood. DESIGN: Gene ontology technique. SETTING: Chulalongkorn University Hospital, Bangkok, Thailand. PATIENT(S): Men with erectile dysfunction. INTERVENTIONS: In the present study, I have used a new gene ontology technique to predict the molecular function and biological process for the II, ID, and DD genotypes of ACE. MAIN OUTCOME MEASURE(S): Molecular function and biological process. RESULT(S): According to this gene ontology study, it can be shown that the DD genotype lacks molecular function and biological process. CONCLUSION(S): The lack of carboxypeptidase activity in DD genotype might be the clue for erectile dysfunction pathogenesis.
机译:目的:血管紧张素转化酶(ACE)是盐皮质激素合成的主要调节剂,它在肾素/血管紧张素系统中。血管紧张素转换酶负责几种血管疾病。它还与勃起功能障碍有关。但是,从未对ACE的遗传I / D多态性进行深入分析。勃起功能障碍中每种基因型表达的分子机制了解甚少。设计:基因本体技术。地点:泰国曼谷朱拉隆功大学医院。患者:勃起功能障碍的男性。干预措施:在本研究中,我使用了一种新的基因本体技术来预测ACE II,ID和DD基因型的分子功能和生物学过程。主要观察指标:分子功能和生物学过程。结果:根据该基因本体研究,可以证明DD基因型缺乏分子功能和生物学过程。结论:DD基因型缺乏羧肽酶活性可能是勃起功能障碍发病机制的线索。

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