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Autor:
Niu, Rui1, Liu, Ying2, Zhang, Ying1, Zhang, Yuan3, Wang, Hui1, Wang, Yongbin1, Wang, Wei1 ww8160@163.com, Li, Xiaohui4
Publikováno v:
PLoS ONE. 1/25/2017, Vol. 12 Issue 1, p1-18. 18p.
Autor:
Zhang, Fenming1, Xu, Chengfu1, Ning, Longgui1, Hu, Fengling1, Shan, Guodong1, Chen, Hongtan1, Yang, Ming1, Chen, Wenguo1, Yu, Jiekai2, Xu, Guoqiang1 xuguoqi@mail.hz.zj.cn
Publikováno v:
PLoS ONE. 12/20/2016, Vol. 11 Issue 12, p1-18. 18p.
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170741 (2017)
PLoS ONE
PLoS ONE
Idiopathic pulmonary fibrosis (IPF) is a gradual lung disease with a survival of less than 5 years post-diagnosis for most patients. Poor molecular description of IPF has led to unsatisfactory interpretation of the pathogenesis of this disease, resul