Search Results - "Rai, Nabham"
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Genetic Delivery and Gene Therapy in Pulmonary Hypertension
Published in International journal of molecular sciences (25-01-2021)“…Pulmonary hypertension (PH) is a progressive complex fatal disease of multiple etiologies. Hyperproliferation and resistance to apoptosis of vascular cells of…”
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Effect of p53 activation on experimental right ventricular hypertrophy
Published in PloS one (19-06-2020)“…The leading cause of death in Pulmonary Arterial Hypertension (PAH) is right ventricular (RV) failure. The tumor suppressor p53 has been associated with left…”
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Effect of Riociguat and Sildenafil on Right Heart Remodeling and Function in Pressure Overload Induced Model of Pulmonary Arterial Banding
Published in BioMed research international (01-01-2018)“…Pulmonary arterial hypertension (PAH) is a progressive disorder characterized by remodeling of the pulmonary vasculature and a rise in right ventricular (RV)…”
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Deficiency of Axl aggravates pulmonary arterial hypertension via BMPR2
Published in Communications biology (24-08-2021)“…Pulmonary arterial hypertension (PAH), is a fatal disease characterized by a pseudo-malignant phenotype. We investigated the expression and the role of the…”
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Author Correction: Deficiency of Axl aggravates pulmonary arterial hypertension via BMPR2
Published in Communications biology (20-01-2022)Get full text
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Evidence for the Fucoidan/P-Selectin Axis as a Therapeutic Target in Hypoxia-induced Pulmonary Hypertension
Published in American journal of respiratory and critical care medicine (01-06-2019)“…Pulmonary arterial hypertension (PAH) is characterized by vascular remodeling and excessive proliferation of pulmonary artery smooth muscle cells (PASMCs)…”
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Targeting peptidyl-prolyl isomerase 1 in experimental pulmonary arterial hypertension
Published in The European respiratory journal (01-08-2022)“…Pulmonary arterial hypertension (PAH) is a progressive disease characterised by pro-proliferative and anti-apoptotic phenotype in vascular cells, leading to…”
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Is PKM2 Phosphorylation a Prerequisite for Oligomer Disassembly in Pulmonary Arterial Hypertension?
Published in American journal of respiratory and critical care medicine (15-12-2019)“…Pulmonary arterial hypertension (PAH) is an incurable vascular disease characterized by pulmonary vascular remodeling and increased pulmonary vascular…”
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Response to: Comment on “Effect of Riociguat and Sildenafil on Right Heart Remodeling and Function in Pressure Overload Induced Model of Pulmonary Arterial Banding”
Published in BioMed research international (01-01-2018)“…We would like to thank Dr. Andersen for careful reading and the comment [1] on the manuscript “Effect of Riociguat and Sildenafil on Right Heart Remodeling and…”
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