human | Q5 |
P496 | ORCID iD | 0000-0001-6392-6802 |
P3829 | Publons author ID | 2491853 |
P1053 | ResearcherID | K-7306-2014 |
P735 | given name | Ramón | Q18218536 |
Ramón | Q18218536 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q33200129 | A modified chorioallantoic membrane assay allows for specific detection of endothelial apoptosis induced by antiangiogenic substances. |
Q50471938 | A simple technique of image analysis for specific nuclear immunolocalization of proteins. |
Q68745244 | Anatomical studies of the coronary system in elasmobranchs: I. Coronary arteries in lamnoid sharks |
Q68163763 | Anatomical studies of the coronary system in elasmobranchs: II. Coronary arteries in hexanchoid, squaloid, and carcharhinoid sharks |
Q71857761 | Anatomy and histology of the cardiac conal valves of the adult dogfish (Scyliorhinus canicula) |
Q37402641 | Building the vertebrate heart - an evolutionary approach to cardiac development. |
Q37766199 | Cardiogenesis: an embryological perspective. |
Q34589642 | Cells derived from the coelomic epithelium contribute to multiple gastrointestinal tissues in mouse embryos. |
Q36884230 | Challenges of antiangiogenic cancer therapy: trials and errors, and renewed hope |
Q38659781 | Coelomic epithelium-derived cells in visceral morphogenesis. |
Q49923297 | Comparative developmental biology of the cardiac inflow tract. |
Q37265937 | Conditional deletion of WT1 in the septum transversum mesenchyme causes congenital diaphragmatic hernia in mice |
Q52092901 | Contribution of mesothelium-derived cells to liver sinusoids in avian embryos. |
Q73804188 | Contribution of the primitive epicardium to the subepicardial mesenchyme in hamster and chick embryos |
Q43836682 | Coronary myointimal lesions in the dogfish shark Scyliorhinus canicula |
Q39941554 | DTD, an anti-inflammatory ditriazine, inhibits angiogenesis in vitro and in vivo |
Q41087765 | Development of the coronary arteries and cardiac veins in the dogfish (Scyliorhinus canicula). |
Q73556346 | Development of the coronary arteries in a murine model of transposition of great arteries |
Q37259213 | Developmental and tumoral vascularization is regulated by G protein-coupled receptor kinase 2 |
Q77422727 | Differentiation of hemangioblasts from embryonic mesothelial cells? A model on the origin of the vertebrate cardiovascular system |
Q96956411 | Embryonic circulating endothelial progenitor cells |
Q34969022 | Epithelial-mesenchymal transitions: a mesodermal cell strategy for evolutive innovation in Metazoans. |
Q44042836 | Experimental studies on the spatiotemporal expression of WT1 and RALDH2 in the embryonic avian heart: a model for the regulation of myocardial and valvuloseptal development by epicardially derived cells (EPDCs). |
Q36498224 | Extracardiac septum transversum/proepicardial endothelial cells pattern embryonic coronary arterio-venous connections |
Q57103262 | Fusion of valve cushions as a key factor in the formation of congenital bicuspid aortic valves in Syrian hamsters |
Q39035179 | GATA4 loss in the septum transversum mesenchyme promotes liver fibrosis in mice |
Q42524186 | Hyperplastic conotruncal endocardial cushions and transposition of great arteries in perlecan-null mice. |
Q81444715 | IB05204, a dichloropyridodithienotriazine, inhibits angiogenesis in vitro and in vivo |
Q52170989 | Immunolocalization of the transcription factor Slug in the developing avian heart. |
Q52183533 | Immunoreactivity of the ets-1 transcription factor correlates with areas of epithelial-mesenchymal transition in the developing avian heart. |
Q51184853 | In vitro self-assembly of proepicardial cell aggregates: an embryonic vasculogenic model for vascular tissue engineering. |
Q82462288 | In vivo and in vitro analysis of the vasculogenic potential of avian proepicardial and epicardial cells |
Q73724818 | Localization of the Wilm's tumour protein WT1 in avian embryos |
Q28297755 | Met signaling in cardiomyocytes is required for normal cardiac function in adult mice |
Q42872685 | Molecular evolution of nitric oxide synthases in metazoans. |
Q37294086 | Peritoneal repairing cells: a type of bone marrow derived progenitor cells involved in mesothelial regeneration |
Q92350016 | Retinoids in Stellate Cells: Development, Repair, and Regeneration |
Q37673265 | Role of Vitamin A/Retinoic Acid in Regulation of Embryonic and Adult Hematopoiesis |
Q79846648 | Study of puupehenone and related compounds as inhibitors of angiogenesis |
Q64230573 | The Wilms' tumor suppressor gene regulates pancreas homeostasis and repair |
Q72148390 | The effects of calcitonin on serum calcium levels in immature brown trout, Salmo trutta |
Q37755436 | The embryonic epicardium: an essential element of cardiac development |
Q36176445 | The origin of the endothelial cells: an evo-devo approach for the invertebrate/vertebrate transition of the circulatory system. |
Q47709534 | The origin of the subepicardial mesenchyme in the avian embryo: an immunohistochemical and quail-chick chimera study |
Q34278378 | The origin, formation and developmental significance of the epicardium: a review. |
Q47395804 | The proepicardium keeps a potential for glomerular marker expression which supports its evolutionary origin from the pronephros |
Q47842713 | Two genes encoding distinct cytosolic glutamine synthetases are closely linked in the pine genome |
Q46889320 | Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis |
Q42052856 | Wt1 controls retinoic acid signalling in embryonic epicardium through transcriptional activation of Raldh2. |
Q42945812 | Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherin. |
Q45765307 | Wt1-expressing progenitors contribute to multiple tissues in the developing lung |
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