Comment onBmpr2 Mutant Rats Develop Pulmonary and Cardiac Characteristics of Pulmonary Arterial Hypertension. [Circulation. 2019]Letter by Nadeau et al Regarding Article, "Bmpr2 Mutant Rats Develop Pulmonary and Cardiac Characteristics of Pulmonary Arterial Hypertension". [Circulation. 2019]International audienceno abstrac
Abstract: Calorie restriction (CR) is one of the most effective nonpharmacological interventions pro...
© 2017 Dr Ling QianPulmonary arterial hypertension is a debilitating disease that results in obstruc...
Translational research is essential to develop strategies for the treatment of pulmonary ...
Comment onBmpr2 Mutant Rats Develop Pulmonary and Cardiac Characteristics of Pulmonary Arterial Hype...
International audienceBACKGROUND: Monoallelic mutations in the gene encoding bone morphogenetic prot...
Comment inThe Janus Faces of Bone Morphogenetic Protein 9 in Pulmonary Arterial Hypertension. [Circ ...
We read with interest the article by Tu et al1 demonstrating that genetic loss of Bmp9 (bone morphog...
To the editor: Kojonazarov et al. recently reported severe emphysema in the SU5416/Hypoxia (SuHx) r...
Echocardiography of pulmonary vascular function in asymptomatic carriers of BMPR2 mutations To the E...
Reduced bone morphogenetic protein receptor 2 (BMPR2) signaling is central to the pathobiology of pu...
I read the article by Pawlinski et al1 with great interest. The authors showed that protease-activat...
In this issue ofBlood, Farha and colleagues have identified amyeloproliferative process that is intr...
Comments on "Hemodynamic, Functional, and Clinical Responses to Pulmonary Artery Denervation in Pati...
We recently reported that a genetic absence of protease activated receptor-1 (PAR-1) improved cardia...
Background: Bmpr2 (bone morphogenetic protein receptor 2) mutations are critical risk factors for he...
Abstract: Calorie restriction (CR) is one of the most effective nonpharmacological interventions pro...
© 2017 Dr Ling QianPulmonary arterial hypertension is a debilitating disease that results in obstruc...
Translational research is essential to develop strategies for the treatment of pulmonary ...
Comment onBmpr2 Mutant Rats Develop Pulmonary and Cardiac Characteristics of Pulmonary Arterial Hype...
International audienceBACKGROUND: Monoallelic mutations in the gene encoding bone morphogenetic prot...
Comment inThe Janus Faces of Bone Morphogenetic Protein 9 in Pulmonary Arterial Hypertension. [Circ ...
We read with interest the article by Tu et al1 demonstrating that genetic loss of Bmp9 (bone morphog...
To the editor: Kojonazarov et al. recently reported severe emphysema in the SU5416/Hypoxia (SuHx) r...
Echocardiography of pulmonary vascular function in asymptomatic carriers of BMPR2 mutations To the E...
Reduced bone morphogenetic protein receptor 2 (BMPR2) signaling is central to the pathobiology of pu...
I read the article by Pawlinski et al1 with great interest. The authors showed that protease-activat...
In this issue ofBlood, Farha and colleagues have identified amyeloproliferative process that is intr...
Comments on "Hemodynamic, Functional, and Clinical Responses to Pulmonary Artery Denervation in Pati...
We recently reported that a genetic absence of protease activated receptor-1 (PAR-1) improved cardia...
Background: Bmpr2 (bone morphogenetic protein receptor 2) mutations are critical risk factors for he...
Abstract: Calorie restriction (CR) is one of the most effective nonpharmacological interventions pro...
© 2017 Dr Ling QianPulmonary arterial hypertension is a debilitating disease that results in obstruc...
Translational research is essential to develop strategies for the treatment of pulmonary ...