Bone morphogenetic protein receptor type II deficiency and increased inflammatory cytokine production. A gateway to pulmonary arterial hypertension
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DNA Damage and Pulmonary HypertensionKidney dysfunction in patients with pulmonary arterial hypertensionHepatic Shunting of Eggs and Pulmonary Vascular Remodeling in Bmpr2(+/-) Mice with Schistosomiasis.Bone Marrow-derived Cells Contribute to the Pathogenesis of Pulmonary Arterial Hypertension.Estrogens in Men: Another Layer of Complexity of Estradiol Metabolism in Pulmonary HypertensionUpdate in Pulmonary Vascular Disease 2015.Constitutive Reprogramming of Fibroblast Mitochondrial Metabolism in Pulmonary Hypertension.Transcription factors, transcriptional coregulators, and epigenetic modulation in the control of pulmonary vascular cell phenotype: therapeutic implications for pulmonary hypertension (2015 Grover Conference series).Oestrogen inhibition reverses pulmonary arterial hypertension and associated metabolic defects.Bone morphogenetic protein signalling in pulmonary hypertension: advances and therapeutic implications.BMPRII influences the response of pulmonary microvascular endothelial cells to inflammatory mediators.Pulmonary arterial hypertension in congenital heart disease: translational opportunities to study the reversibility of pulmonary vascular disease.BMP type II receptor as a therapeutic target in pulmonary arterial hypertension.Reactive Oxygen and Nitrogen Species in the Development of Pulmonary Hypertension.Bone Morphogenetic Protein 9 Protects against Neonatal Hyperoxia-Induced Impairment of Alveolarization and Pulmonary Inflammation.The Roles of Immunity in the Prevention and Evolution of Pulmonary Arterial Hypertension.Pulmonary vascular effect of insulin in a rodent model of pulmonary arterial hypertension.Differential IL-1 signaling induced by BMPR2 deficiency drives pulmonary vascular remodeling.Mitochondrial dysfunction and pulmonary hypertension: Cause, Effect or Both.Bone morphogenetic protein receptor type II and inflammation are bringing old concepts into the new pulmonary arterial hypertension world.Contributions of BMPR2 Mutations and Extrinsic Factors to Cellular Phenotypes of Pulmonary Arterial Hypertension Revealed by iPSC Modeling.Gut-Lung Connection in Pulmonary Arterial Hypertension.Bone morphogenetic protein signaling is required for RAD51-mediated maintenance of genome integrity in vascular endothelial cellsConsequences of BMPR2 Deficiency in the Pulmonary Vasculature and Beyond: Contributions to Pulmonary Arterial Hypertension
P2860
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P2860
Bone morphogenetic protein receptor type II deficiency and increased inflammatory cytokine production. A gateway to pulmonary arterial hypertension
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@ast
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@en
type
label
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@ast
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@en
prefLabel
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@ast
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@en
P2093
P2860
P50
P1476
Bone morphogenetic protein rec ...... ulmonary arterial hypertension
@en
P2093
Alexi Crosby
Kenneth D Bloch
Mark Southwood
Mark Toshner
Paul Upton
Sarah Appleby
Tamara Tajsic
P2860
P304
P356
10.1164/RCCM.201408-1509OC
P407
P577
2015-06-13T00:00:00Z