FISIOPATOLOGÍA CARDIOVASCULAR Y RENAL
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Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Centro de Investigación Biomédica en Red sobre Enfermedades Raras (11)
2020
2018
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Human endoglin as a potential new partner involved in platelet–endothelium interactions
Cellular and Molecular Life Sciences, Vol. 75, Núm. 7, pp. 1269-1284
2017
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The role of endoglin in post-ischemic revascularization
Angiogenesis, Vol. 20, Núm. 1
2016
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Endoglin regulates mural cell adhesion in the circulatory system
Cellular and Molecular Life Sciences, Vol. 73, Núm. 8, pp. 1715-1739
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Overexpression of the short endoglin isoform reduces renal fibrosis and inflammation after unilateral ureteral obstruction
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1862, Núm. 9, pp. 1801-1814
2012
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C3G transgenic mouse models with specific expression in platelets reveal a new role for C3G in platelet clotting through its GEF activity
Biochimica et Biophysica Acta - Molecular Cell Research, Vol. 1823, Núm. 8, pp. 1366-1377
2011
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Diminished thrombogenic responses by deletion of the Podocalyxin gene in mouse megakaryocytes
PLoS ONE, Vol. 6, Núm. 10
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Release of podocalyxin into the extracellular space. Role of metalloproteinases
Biochimica et Biophysica Acta - Molecular Cell Research, Vol. 1813, Núm. 8, pp. 1504-1510
2010
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Reduced plasma levels of Ang-2 and sEng as novel biomarkers in hereditary hemorrhagic telangiectasia (HHT)
Clinica Chimica Acta, Vol. 411, Núm. 7-8, pp. 494-499
2008
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L- and S-endoglin differentially modulate TGFβ1 signaling mediated by ALK1 and ALK5 in L6E9 myoblasts
Journal of Cell Science, Vol. 121, Núm. 6, pp. 913-919
2007
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Gene expression fingerprinting for human hereditary hemorrhagic telangiectasia
Human Molecular Genetics, Vol. 16, Núm. 13, pp. 1515-1533