Search Results - "Bernabéu, Carmelo"
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Activin A skews macrophage polarization by promoting a proinflammatory phenotype and inhibiting the acquisition of anti-inflammatory macrophage markers
Published in Blood (12-05-2011)“…M-CSF favors the generation of folate receptor β–positive (FRβ+), IL-10–producing, immunosuppressive, M2-polarized macrophages [M2 (M-CSF)], whereas GM-CSF…”
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Pregnancy-Induced High Plasma Levels of Soluble Endoglin in Mice Lead to Preeclampsia Symptoms and Placental Abnormalities
Published in International journal of molecular sciences (26-12-2020)“…Preeclampsia is a pregnancy-specific disease of high prevalence characterized by the onset of hypertension, among other maternal or fetal signs. Its…”
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Co-injection of mesenchymal stem cells with endothelial progenitor cells accelerates muscle recovery in hind limb ischemia through an endoglin-dependent mechanism
Published in Thrombosis and haemostasis (05-10-2017)“…Endothelial colony-forming cells (ECFCs) are progenitor cells committed to endothelial lineages and have robust vasculogenic properties. Mesenchymal stem cells…”
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4
The Splicing Factor SRSF1 as a Marker for Endothelial Senescence
Published in Frontiers in physiology (01-01-2012)“…Aging is the major risk factor per se for the development of cardiovascular diseases. The senescence of the endothelial cells (ECs) that line the lumen of…”
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The role of endoglin in post-ischemic revascularization
Published in Angiogenesis (01-02-2017)“…Following arterial occlusion, blood vessels respond by forming a new network of functional capillaries (angiogenesis), by reorganizing preexisting capillaries…”
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Propranolol as antiangiogenic candidate for the therapy of hereditary haemorrhagic telangiectasia
Published in Thrombosis and haemostasis (01-07-2012)“…The β-blocker propranolol, originally designed for cardiological indications (angina, cardiac arrhythmias and high blood pressure), is nowadays, considered the…”
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Bazedoxifene, a new orphan drug for the treatment of bleeding in hereditary haemorrhagic telangiectasia
Published in Thrombosis and haemostasis (02-06-2016)“…Hereditary haemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is a dominant genetic vascular disorder. In HHT, blood vessels are weak and prone…”
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L- and S-endoglin differentially modulate TGFβ1 signaling mediated by ALK1 and ALK5 in L₆E₉ myoblasts
Published in Journal of cell science (15-03-2008)“…TGFβ regulates cellular processes by binding to type I and type II TGFβ receptors (TβRI and TβRII, respectively). In addition to these signaling receptors,…”
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Vascular Injury Triggers Krüppel-Like Factor 6 Mobilization and Cooperation With Specificity Protein 1 to Promote Endothelial Activation Through Upregulation of the Activin Receptor-Like Kinase 1 Gene
Published in Circulation research (04-01-2013)“…RATIONALE:Activin receptor-like kinase-1 (ALK1) is an endothelial transforming growth factor β receptor involved in angiogenesis. ALK1 expression is high in…”
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The role of the TGF-β coreceptor endoglin in cancer
Published in TheScientificWorld (01-01-2010)“…Endoglin (CD105) is an auxiliary membrane receptor of transforming growth factor beta (TGF-β) that interacts with type I and type II TGF-β receptors and…”
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Immunosuppressor FK506 increases endoglin and activin receptor-like kinase 1 expression and modulates transforming growth factor-β1 signaling in endothelial cells
Published in Molecular pharmacology (01-05-2011)“…Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is an autosomal-dominant vascular disease. The clinical manifestations are…”
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12
Extracellular signal–regulated protein kinase signaling pathway negatively regulates the phenotypic and functional maturation of monocyte-derived human dendritic cells
Published in Blood (01-10-2001)“…Dendritic cells (DC) are highly specialized antigen-presenting cells that on activation by inflammatory stimuli (eg, tumor necrosis factor α [TNF-α] and…”
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Review of Pharmacological Strategies with Repurposed Drugs for Hereditary Hemorrhagic Telangiectasia Related Bleeding
Published in Journal of clinical medicine (06-06-2020)“…The diagnosis of hereditary hemorrhagic telangiectasia (HHT) is based on the Curaçao criteria: epistaxis, telangiectases, arteriovenous malformations in…”
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Estrogen therapy for hereditary haemorrhagic telangiectasia (HHT): Effects of raloxifene, on Endoglin and ALK1 expression in endothelial cells
Published in Thrombosis and haemostasis (01-03-2010)“…Hereditary haemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is an autosomal dominant vascular disease. The clinical manifestations are…”
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Research on potential biomarkers in hereditary hemorrhagic telangiectasia
Published in Frontiers in genetics (31-03-2015)“…Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous disorder, involving mutations in two predominant genes known as Endoglin (ENG; HHT1)…”
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Soluble endoglin antagonizes Met signaling in spindle carcinoma cells
Published in Carcinogenesis (New York) (01-02-2015)“…Increased levels of soluble endoglin (Sol-Eng) correlate with poor outcome in human cancer. We have previously shown that shedding of membrane endoglin, and…”
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Transcriptional activation of endoglin and transforming growth factor-β signaling components by cooperative interaction between Sp1 and KLF6: their potential role in the response to vascular injury
Published in Blood (01-12-2002)“…Endoglin is an endothelial membrane glycoprotein involved in cardiovascular morphogenesis and vascular remodeling. It associates with transforming growth…”
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Hereditary Hemorrhagic Telangiectasia, a Vascular Dysplasia Affecting the TGF-β Signaling Pathway
Published in Clinical medicine & research (01-03-2006)“…Hereditary hemorrhagic telangiectasia (HHT) is caused by mutations in endoglin (ENG; HHT1) or ACVRL1/ALK1 (HHT2) genes and is an autosomal dominant vascular…”
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Characterization of murine S-endoglin isoform and its effects on tumor development
Published in Oncogene (23-06-2005)“…Endoglin is a transmembrane glycoprotein that acts as an auxiliary receptor for transforming growth factor-beta (TGF-beta) and modulates cellular responses to…”
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A Role for Endoglin as a Suppressor of Malignancy during Mouse Skin Carcinogenesis
Published in Cancer research (Chicago, Ill.) (01-11-2007)“…Endoglin is a membrane glycoprotein that acts as a coreceptor for transforming growth factor-beta. We and others have previously suggested a function of…”
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