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首页> 外文期刊>Neuromuscular disorders: NMD >Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women.
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Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women.

机译:白人女性中的雌激素受体α基因内含子多态性和自身免疫性重症肌无力。

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摘要

Autoimmune myasthenia gravis is a disorder with a complex pathomechanism in which sex hormones, in particular oestrogen, have long been considered to play a role. Here we report the result of a case-control study which evaluated the association of two oestrogen receptor alpha gene polymorphisms with myasthenia gravis in Caucasian patients. PvuII (rs2234693) and XbaI (rs9340799) restriction fragment polymorphisms of the oestrogen receptor alpha gene were analyzed in 113 female myasthenia patients and 184 female controls. Distribution of these polymorphisms was compared with PCR-RFLP. Patients were divided into groups according to their oestrogen receptoralpha genotypes, and acetylcholine receptor antibody status and age of onset were compared between the groups. We found no significant difference between any of the groups implying that these two polymorphisms probably do not play a role in the pathomechanism of myasthenia gravis in Caucasian women.
机译:自身免疫性重症肌无力是一种具有复杂病理机制的疾病,长期以来一直认为性激素(尤其是雌激素)起着作用。在这里,我们报告了一项病例对照研究的结果,该研究评估了两种雌激素受体α基因多态性与白种人患者重症肌无力的关系。在113位女性肌无力患者和184位女性对照中分析了雌激素受体α基因的PvuII(rs2234693)和XbaI(rs9340799)限制性片段多态性。将这些多态性的分布与PCR-RFLP进行比较。根据患者的雌激素受体α基因型将其分为两组,并比较两组之间的乙酰胆碱受体抗体状态和发病年龄。我们发现两组之间均无显着差异,这暗示着这两个多态性可能在白人女性重症肌无力的发病机制中不起作用。

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