Therapeutic efficacy of the novel selective RNA polymerase I inhibitor CX‐5461 on pulmonary arterial hypertension and associated vascular remodelling-Reference-Cited by-同舟云学术

Therapeutic efficacy of the novel selective RNA polymerase I inhibitor CX‐5461 on pulmonary arterial hypertension and associated vascular remodelling

Published:2021-03 Issue:7 Volume:178 Page:1605-1619
ISSN:0007-1188
Container-title:British Journal of Pharmacology
language:en
Short-container-title:Br J Pharmacol

Author:

Xu Xia¹,Feng Hua²,Dai Chaochao¹,Lu Weida¹,Zhang Jun³,Guo Xiaosun⁴,Yin Qihui⁴,Wang Jianli⁵,Cui Xiaopei¹,Jiang Fan¹⁴^ORCID

Affiliation:

1. Department of Geriatrics & Key Laboratory of Cardiovascular Proteomics of Shandong Province Qilu Hospital, Cheeloo College of Medicine, Shandong University Jinan Shandong China

2. Department of gastroenterology Shandong Provincial Hospital Affiliated to Shandong First Medical University Jinan Shandong Province China

3. Department of Cardiovascular Surgery Qilu Hospital, Cheeloo College of Medicine, Shandong University Jinan Shandong Province China

4. Department of Physiology and Pathophysiology, School of Basic Medicine Shandong University Jinan Shandong China

5. Department of Obstetrics and Gynecology Qilu Hospital of Shandong University Jinan Shandong China

Funder

Key Technology Research and Development Program of Shandong

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

Wiley

Subject

Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bph.15385

Reference68 articles.

1. p21-Dependent Protective Effects of a Carbon Monoxide–Releasing Molecule-3 in Pulmonary Hypertension

2. THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Enzymes

3. Goals and practicalities of immunoblotting and immunohistochemistry: A guide for submission to the British Journal of Pharmacology

4. Roles for the CX3CL1/CX3CR1 and CCL2/CCR2 Chemokine Systems in Hypoxic Pulmonary Hypertension

5. T lymphocyte subset abnormalities in the blood and lung in pulmonary arterial hypertension

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