Xiao-jian Wang

Key Laboratory Of Pulmonary Vascular Medicine, State Key Laboratory Of Cardiovascular Disease, Chinese Academy Medical Sciences And Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 14 publications

Editorial: Progresses in the Drug Treatment of Chronic Cardiopulmonary Diseases.

Editorial: Progresses in the Drug Treatment of Chronic Cardiopulmonary Diseases.

Journal: Frontiers in pharmacology
Published: April 01, 2022

Text Mining-Based Drug Discovery for Connective Tissue Disease-Associated Pulmonary Arterial Hypertension.

Text Mining-Based Drug Discovery for Connective Tissue Disease-Associated Pulmonary Arterial Hypertension.

Journal: Frontiers in pharmacology
Published: July 17, 2021

Association of Rare PTGIS Variants With Susceptibility and Pulmonary Vascular Response in Patients With Idiopathic Pulmonary Arterial Hypertension.

Association of Rare PTGIS Variants With Susceptibility and Pulmonary Vascular Response in Patients With Idiopathic Pulmonary Arterial Hypertension.

Journal: JAMA cardiology
Published: April 03, 2020

Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension.

Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension.

Journal: The European respiratory journal
Published: August 24, 2018

Metabolic reprogramming of the urea cycle pathway in experimental pulmonary arterial hypertension rats induced by monocrotaline.

Metabolic reprogramming of the urea cycle pathway in experimental pulmonary arterial hypertension rats induced by monocrotaline.

Journal: Respiratory research
Published: March 05, 2018

Inhibition of CRTH2-mediated Th2 activation attenuates pulmonary hypertension in mice.

Inhibition of CRTH2-mediated Th2 activation attenuates pulmonary hypertension in mice.

Journal: The Journal of experimental medicine
Published: September 25, 2017

Hypermethylation of BMPR2 Promoter Occurs in Patients with Heritable Pulmonary Arterial Hypertension and Inhibits BMPR2 Expression.

Hypermethylation of BMPR2 Promoter Occurs in Patients with Heritable Pulmonary Arterial Hypertension and Inhibits BMPR2 Expression.

Journal: American journal of respiratory and critical care medicine
Published: February 08, 2017

Elevated levels of plasma transforming growth factor-β1 in idiopathic and heritable pulmonary arterial hypertension.

Elevated levels of plasma transforming growth factor-β1 in idiopathic and heritable pulmonary arterial hypertension.

Journal: International journal of cardiology
Published: May 31, 2016

Profiling nitric oxide metabolites in patients with idiopathic pulmonary arterial hypertension.

Profiling nitric oxide metabolites in patients with idiopathic pulmonary arterial hypertension.

Journal: The European respiratory journal
Published: February 01, 2016

Differential expression of microRNAs in aortic tissue and plasma in patients with acute aortic dissection.

Differential expression of microRNAs in aortic tissue and plasma in patients with acute aortic dissection.

Journal: Journal of geriatric cardiology : JGC
Published: January 21, 2016

BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis.

BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis.

Journal: The Lancet. Respiratory medicine
Published: October 16, 2015

Research update for articles published in EJCI in 2013.

Research update for articles published in EJCI in 2013.

Journal: European journal of clinical investigation
Published: August 04, 2015
Showing 1-12 of 14

Last Updated: 09/26/2026