CCL5 deficiency rescues pulmonary vascular dysfunction, and reverses pulmonary hypertension via caveolin-1-dependent BMPR2 activation-Reference-Cited by-同舟云学术

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CCL5 deficiency rescues pulmonary vascular dysfunction, and reverses pulmonary hypertension via caveolin-1-dependent BMPR2 activation

Published:2018-03 Issue: Volume:116 Page:41-56
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Nie Xiaowei^ORCID,Tan Jianxin,Dai Youai,Liu Yun,Zou Jian,Sun Jie,Ye Shugao,Shen Chenyou,Fan Li,Chen Jingyu,Bian Jin-Song

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Jiangsu Provincial Commission of Health and Family Planning

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference61 articles.

1. Pathology of pulmonary hypertension;Tuder;Clin. Chest Med.,2007

2. Modern age pathology of pulmonary arterial hypertension;Stacher;Am. J. Respir. Crit. Care Med.,2012

3. Novel therapeutic approaches for pulmonary arterial hypertension: unique molecular targets to site-specific drug delivery;Vaidya;J. Control. Rel.,2015

4. The genetics of pulmonary arterial hypertension;Austin;Circ. Res.,2014

5. Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor;Atkinson;Circulation,2002

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