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新生儿呼吸窘迫综合征的遗传学研究进展 被引量:5

The heredity of research in neonatal respiratory distress syndrome
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摘要 新生儿呼吸窘迫综合征(neonatalrespiratorydistresssyndrome,NRDS)是新生儿期最常见的危重症,目前认为遗传因素在NRDS发病中起着重要作用。目前与NRDS相关的遗传性的蛋白、基因被越来越多的学者研究,本文主要综述肺表面活性物质蛋白、ATP结合盒转运蛋白A3基因(ABCA3)、甘露糖结合凝集素、甲状腺转录因子与NRDS的相关性。 Neonatal respiratory distress syndrome (NRDS)is the most critical disease in neonatal pe- riod. Studies have proved that genetic factors play an important role in the pathogenesis of NRDS. More and more proteins and genes which are associated with NRDS are researched. This article mainly reviewed the re- search of surfactant protein, ATP-binding cassette transporters A3, mannose-binding lectin, thyroid transcrip- tion factor-1 and NRDS.
出处 《中国小儿急救医学》 CAS 2016年第4期259-262,共4页 Chinese Pediatric Emergency Medicine
基金 基金项目:国家自然科学基金(gjzr12107) 内蒙古自治区自然科学基金项目[2011MS1111,2015MS(LH)0810]
关键词 呼吸窘迫综合征 肺表面活性蛋白 ATP结合盒转运蛋白A3基因 甘露糖结合凝集素 甲状腺转录因子 Respiratory distress syndrome Surfactant protein ATP-binding cassette transporters A3 Mannose-binding lectin Thyroid transcription factor-1
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