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组蛋白去乙酰化酶及其抑制剂与特发性肺纤维化的研究进展 预览 被引量:1

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摘要 特发性肺纤维化(idiopathic pulmonary fibrosis,IPF)是一种伴有弥漫性肺泡损伤的进展性间质性肺疾病,具有寻常型间质性肺炎的组织病理学特征,表现为上皮细胞损伤,成纤维母细胞和肌成纤维细胞的聚集,细胞外基质的大量沉积。IPF是一种毁灭性的疾病,发病率大概为50/10万,平均生存时间只有3~5年。
出处 《实用医学杂志》 CAS 北大核心 2015年第3期505-506,共2页 The Journal of Practical Medicine
基金 贵州省卫生厅基金资助项目(编号:gzwjkj2014-1-064)
作者简介 通信作者:刘代顺E-mail:ldsdoc@126.com
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参考文献16

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