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[肾脏病学中的分子遗传学。遗传性肾脏疾病为理解蛋白尿的发病机制提供线索]

[Molecular genetics in nephrology. Genetic kidney diseases provide clues for understanding the pathogenesis of proteinuria].

作者信息

Huber T B, Benzing Th

机构信息

Medizinische Klinik IV, Nephrologie, Universitätsklinik Freiburg, Freiburg, Deutschland.

出版信息

Ther Umsch. 2003 Aug;60(8):435-7. doi: 10.1024/0040-5930.60.8.435.

Abstract

Recent progress in defining the genetic basis of inherited glomerular diseases has provided a completely new understanding of the glomerular filter of the kidney and has helped illuminate the pathogenesis of acquired and inherited renal proteinuric diseases. Based on the findings of molecular genetics in nephrology we will discuss the current understanding of the glomerular filter and provide an idea how genetic testing in the future may help to guide therapy in patients suffering from nephrotic syndrome and progressive renal failure.

摘要

在确定遗传性肾小球疾病的遗传基础方面取得的最新进展,为肾脏的肾小球滤过器提供了全新的认识,并有助于阐明获得性和遗传性肾蛋白尿性疾病的发病机制。基于肾脏病分子遗传学的研究结果,我们将讨论目前对肾小球滤过器的认识,并提出未来基因检测如何有助于指导肾病综合征和进行性肾衰竭患者治疗的思路。

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