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 by Sierra-Filardi, Elena, Puig-Kröger, Amaya, Blanco, Francisco J., Nieto, Concha, Bragado, Rafael, Palomero, M. Isabel, Bernabéu, Carmelo, Vega, Miguel A., Corbí, Angel L.

    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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    Journal Article
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    Pregnancy-Induced High Plasma Levels of Soluble Endoglin in Mice Lead to Preeclampsia Symptoms and Placental Abnormalities by Pérez-Roque, Lucía, Núñez-Gómez, Elena, Rodríguez-Barbero, Alicia, Bernabéu, Carmelo, López-Novoa, José M, Pericacho, Miguel

    “…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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    Journal Article
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    The Splicing Factor SRSF1 as a Marker for Endothelial Senescence by Blanco, Francisco Javier, Bernabéu, Carmelo

    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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    Journal Article
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    The role of endoglin in post-ischemic revascularization by Núñez-Gómez, Elena, Pericacho, Miguel, Ollauri-Ibáñez, Claudia, Bernabéu, Carmelo, López-Novoa, José M.

    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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    Journal Article Book Review
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    Propranolol as antiangiogenic candidate for the therapy of hereditary haemorrhagic telangiectasia by Albiñana, Virginia, Recio-Poveda, Lucía, Zarrabeitia, Roberto, Bernabéu, Carmelo, Botella, Luisa María

    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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    Journal Article
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    Bazedoxifene, a new orphan drug for the treatment of bleeding in hereditary haemorrhagic telangiectasia by Zarrabeitia, Roberto, Ojeda-Fernandez, Luisa, Recio, Lucia, Bernabéu, Carmelo, Parra, Jose A, Albiñana, Virginia, Botella, Luisa M

    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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    Journal Article
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    L- and S-endoglin differentially modulate TGFβ1 signaling mediated by ALK1 and ALK5 in L₆E₉ myoblasts by Velasco, Soraya, Alvarez-Muñoz, Patricia, Pericacho, Miguel, Dijke, Peter ten, Bernabéu, Carmelo, López-Novoa, José M, Rodríguez-Barbero, Alicia

    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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    The role of the TGF-β coreceptor endoglin in cancer by Pérez-Gómez, Eduardo, Del Castillo, Gaelle, Juan Francisco, Santibáñez, López-Novoa, Jose Miguel, Bernabéu, Carmelo, Quintanilla, Miguel

    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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    Journal Article
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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 by Albiñana, Virginia, Sanz-Rodríguez, Francisco, Recio-Poveda, Lucía, Bernabéu, Carmelo, Botella, Luisa M

    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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    Journal Article
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    Extracellular signal–regulated protein kinase signaling pathway negatively regulates the phenotypic and functional maturation of monocyte-derived human dendritic cells by Puig-Kröger, Amaya, Relloso, Miguel, Fernández-Capetillo, Oskar, Zubiaga, Ana, Silva, Augusto, Bernabéu, Carmelo, Corbı́, Angel L.

    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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    Journal Article
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    Review of Pharmacological Strategies with Repurposed Drugs for Hereditary Hemorrhagic Telangiectasia Related Bleeding by Albiñana, Virginia, Cuesta, Angel M, Rojas-P, Isabel de, Gallardo-Vara, Eunate, Recio-Poveda, Lucía, Bernabéu, Carmelo, Botella, Luisa María

    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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    Journal Article
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    Estrogen therapy for hereditary haemorrhagic telangiectasia (HHT): Effects of raloxifene, on Endoglin and ALK1 expression in endothelial cells by Albiñana, Virginia, Bernabeu-Herrero, Maria E, Zarrabeitia, Roberto, Bernabéu, Carmelo, Botella, Luisa M

    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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    Journal Article
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    Research on potential biomarkers in hereditary hemorrhagic telangiectasia by Botella, Luisa-María, Albiñana, Virginia, Ojeda-Fernandez, Luisa, Recio-Poveda, Lucia, Bernabéu, Carmelo

    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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    Journal Article
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    Soluble endoglin antagonizes Met signaling in spindle carcinoma cells by del Castillo, Gaelle, Sánchez-Blanco, Esther, Martín-Villar, Ester, Valbuena-Diez, Ana C, Langa, Carmen, Pérez-Gómez, Eduardo, Renart, Jaime, Bernabéu, Carmelo, Quintanilla, Miguel

    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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    Journal Article
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    Hereditary Hemorrhagic Telangiectasia, a Vascular Dysplasia Affecting the TGF-β Signaling Pathway by Africa Fernández-L, Francisco Sanz-Rodriguez, Francisco J. Blanco, Carmelo Bernabéu, Luisa M. Botella

    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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    Journal Article
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    Characterization of murine S-endoglin isoform and its effects on tumor development by PEREZ-GOMEZ, Eduardo, ELENO, Nélida, LOPEZ-NOVOA, Jose Miguel, RAMIREZ, Jose Ramon, VELASCO, Beatriz, LETARTE, Michelle, BERNABEU, Carmelo, QUINTANILLA, Miguel

    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 by PEREZ-GOMEZ, Eduardo, VILLA-MORALES, Maria, SANTOS, Javier, FERNANDEZ-PIQUERAS, José, GAMALLO, Carlos, DOTOR, Javier, BERNABEU, Carmelo, QUINTANILLA, Miguel

    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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    Journal Article