Search Results - "Van der Feen, Diederik E"
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Converging Paths of Pulmonary Arterial Hypertension and Cellular Senescence
Published in American journal of respiratory cell and molecular biology (01-07-2019)“…Cellular senescence is recognized as a crucial contributor to the pathobiology of various degenerative and cardiovascular diseases, such as idiopathic…”
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Pulmonary arterial hypertension in congenital heart disease: translational opportunities to study the reversibility of pulmonary vascular disease
Published in European heart journal (07-07-2017)“…Pulmonary arterial hypertension (PAH) is a progressive and lethal pulmonary vascular disease (PVD). Although in recent years outcome has improved by new…”
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Assessment of reversibility in pulmonary arterial hypertension and congenital heart disease
Published in Heart (British Cardiac Society) (01-02-2019)“…Pulmonary arterial hypertension (PAH) in congenital heart disease (CHD) can be reversed by early shunt closure, but this potential is lost beyond a certain…”
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Inhibition of the prolyl isomerase Pin1 improves endothelial function and attenuates vascular remodelling in pulmonary hypertension by inhibiting TGF-β signalling
Published in Angiogenesis (London) (01-02-2022)“…Pulmonary arterial hypertension (PAH) is a devastating disease, characterized by obstructive pulmonary vascular remodelling ultimately leading to right…”
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Egr-1 identifies neointimal remodeling and relates to progression in human pulmonary arterial hypertension
Published in The Journal of heart and lung transplantation (01-04-2016)“…Background Pulmonary arterial hypertension (PAH) is hallmarked by the development of neointimal lesions. The transcription factor Egr-1 seems to play a…”
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Volume Load-Induced Right Ventricular Failure in Rats Is Not Associated With Myocardial Fibrosis
Published in Frontiers in physiology (26-02-2021)“…Right ventricular (RV) function and failure are key determinants of morbidity and mortality in various cardiovascular diseases. Myocardial fibrosis is regarded…”
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Pirfenidone ameliorates pulmonary arterial pressure and neointimal remodeling in experimental pulmonary arterial hypertension by suppressing NLRP3 inflammasome activation
Published in Pulmonary circulation (01-07-2022)“…Pulmonary arterial hypertension (PAH) is a fatal disease characterized by increased pulmonary arterial pressure, inflammation, and neointimal remodeling of…”
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Multicenter Preclinical Validation of BET Inhibition for the Treatment of Pulmonary Arterial Hypertension
Published in American journal of respiratory and critical care medicine (01-10-2019)“…Pulmonary arterial hypertension (PAH) is a degenerative arteriopathy that leads to right ventricular (RV) failure. BRD4 (bromodomain-containing protein 4), a…”
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A novel method optimizing the normalization of cardiac parameters in small animal models: the importance of dimensional indexing
Published in American journal of physiology. Heart and circulatory physiology (01-06-2019)“…For indexing cardiac measures in small animal models, tibia length (TL) is a recommended surrogate for body weight (BW) that aims to avoid biases because of…”
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Neuregulin-1 enhances cell-cycle activity, delays cardiac fibrosis, and improves cardiac performance in rat pups with right ventricular pressure load
Published in The Journal of thoracic and cardiovascular surgery (01-12-2022)“…Right ventricular (RV) failure is a leading cause of death in patients with congenital heart disease. RV failure is kept at bay during childhood. Limited…”
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Animal models of right heart failure
Published in Cardiovascular diagnosis and therapy (01-10-2020)“…Right heart failure may be the ultimate cause of death in patients with acute or chronic pulmonary hypertension (PH). As PH is often secondary to other…”
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Reply to Piquereau and Perros and to Pullamsetti and de Jesus Perez
Published in American journal of respiratory and critical care medicine (01-11-2019)Get full text
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Shunt Surgery, Right Heart Catheterization, and Vascular Morphometry in a Rat Model for Flow-induced Pulmonary Arterial Hypertension
Published in Journal of visualized experiments (11-02-2017)“…In this protocol, PAH is induced by combining a 60 mg/kg monocrotalin (MCT) injection with increased pulmonary blood flow through an aorto-caval shunt…”
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Abstract 16556: BRD4 Antagonist RVX208 Reverses Vascular Remodeling and Supports the Right Ventricle in Pulmonary Arterial Hypertension via PLK1 and FoxM1
Published in Circulation (New York, N.Y.) (06-11-2018)“…IntroductionPulmonary arterial hypertension (PAH) is a degenerative arteriopathy that leads to right ventricular (RV) failure. BMPR2 loss and DNA damage are…”
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A neonate with anaemia of prematurity: zinc protoporphyrin identifies iron deficiency anaemia without iron deficiency
Published in Nederlands tijdschrift voor geneeskunde (2015)“…Anaemia is a common problem in premature infants and is generally easy to treat with iron supplementation. If the anaemia persists despite appropriate…”
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