医学
焦点粘着
促炎细胞因子
成纤维细胞
纤维化
特发性肺纤维化
博莱霉素
肺纤维化
背景(考古学)
炎症
信号转导
肌成纤维细胞
肺
机械转化
癌症研究
病理
生物
细胞生物学
免疫学
内科学
细胞培养
古生物学
化疗
遗传学
作者
Artem A. Trotsyuk,Kellen Chen,Sun Hyung,Kun Ma,Dominic Henn,Alana M. Mermin-Bunnell,Smiti Mittal,Jagannath Padmanabhan,Madelyn R. Larson,Sydney R. Steele,Dharshan Sivaraj,Clark A. Bonham,Chikage Noishiki,Mélanie Rodrigues,Yuanwen Jiang,Serena L. Jing,Simiao Niu,Arhana Chattopadhyay,David Perrault,Melissa C. Leeolou
标识
DOI:10.1089/wound.2021.0077
摘要
Objective: Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease that affects 63 in every 100,000 Americans. Its etiology remains unknown, although inflammatory pathways appear to be important. Given the dynamic environment of the lung, we examined the significance of mechanotransduction on both inflammatory and fibrotic signaling during IPF.
科研通智能强力驱动
Strongly Powered by AbleSci AI