His primary areas of investigation include Cell biology, Angiogenesis, Endothelium, Vascular endothelial growth factor A and Cancer research. The concepts of his Cell biology study are interwoven with issues in Autocrine signalling, Cellular differentiation and Anatomy. His Angiogenesis research incorporates themes from Inflammation, Proteolytic enzymes and In vivo.
His work carried out in the field of Endothelium brings together such families of science as Endothelial stem cell and Regulation of gene expression. His Vascular endothelial growth factor A study is associated with Vascular endothelial growth factor. The various areas that M. Luisa Iruela-Arispe examines in his Cancer research study include Carcinogenesis, Cancer, Prostate and Immunology.
His scientific interests lie mostly in Cell biology, Angiogenesis, Cancer research, Endothelial stem cell and Immunology. He has included themes like Vascular endothelial growth factor A and Endothelium in his Cell biology study. M. Luisa Iruela-Arispe combines subjects such as Growth factor, Vascular endothelial growth factor and Thrombospondin with his study of Angiogenesis.
His studies in Cancer research integrate themes in fields like Cancer cell, Cancer, Metastasis and Pathology. His Endothelial stem cell research is multidisciplinary, incorporating elements of Integrin and Cell growth. In his study, Monocyte is inextricably linked to Progenitor cell, which falls within the broad field of Immunology.
M. Luisa Iruela-Arispe mainly investigates Cell biology, Cancer research, Endothelium, Transcriptome and Phenotype. His Cell biology research integrates issues from Cancer cell and Monocyte. His work deals with themes such as Metastasis, Circulating tumor cell, Germ layer and Extravasation, which intersect with Cancer research.
The Endothelium study combines topics in areas such as Endothelial stem cell, Actin cytoskeleton, Cytoskeleton, Vascular permeability and Ectopic expression. M. Luisa Iruela-Arispe interconnects In vitro, Mutation, Phosphatase, Prostate cancer and Kinase in the investigation of issues within Phenotype. Within one scientific family, M. Luisa Iruela-Arispe focuses on topics pertaining to Cell cycle under Cellular differentiation, and may sometimes address concerns connected to Angiogenesis.
His main research concerns Cell biology, Cancer cell, Cancer research, Angiogenesis and Signal transduction. His work on Myocyte as part of general Cell biology study is frequently linked to Population, therefore connecting diverse disciplines of science. His Cancer cell research is multidisciplinary, incorporating perspectives in Chemotherapy, Microvesicles, Annexin, Monocyte and Cytotoxic T cell.
The study incorporates disciplines such as Epithelium, Hypoxia, Enteritis, Breast cancer and Experimental pathology in addition to Cancer research. His Angiogenesis research includes themes of Ex vivo, In vivo, ATF3, Parabiosis and Regeneration. His biological study spans a wide range of topics, including Endothelial stem cell, Phenotype, Cell physiology, Receptor and Mechanotransduction.
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Dll4 signalling through Notch1 regulates formation of tip cells during angiogenesis
Mats Hellström;Li Kun Phng;Jennifer J. Hofmann;Elisabet Wallgard.
Autocrine VEGF Signaling Is Required for Vascular Homeostasis
Sunyoung Lee;Tom T. Chen;Chad L. Barber;Maria C. Jordan.
Myc-driven murine prostate cancer shares molecular features with human prostate tumors.
Katharine Ellwood-Yen;Thomas G. Graeber;John Wongvipat;M. Luisa Iruela-Arispe.
Cancer Cell (2003)
Processing of VEGF-A by matrix metalloproteinases regulates bioavailability and vascular patterning in tumors
Sunyoung Lee;Shahla M. Jilani;Ganka V. Nikolova;Darren R. Carpizo.
Journal of Cell Biology (2005)
Fate tracing reveals the endothelial origin of hematopoietic stem cells.
Ann C. Zovein;Jennifer J. Hofmann;Maureen Lynch;Wendy J. French.
Cell Stem Cell (2008)
Dicer-dependent endothelial microRNAs are necessary for postnatal angiogenesis.
Yajaira Suárez;Carlos Fernández-Hernando;Jun Yu;Scott A. Gerber.
Proceedings of the National Academy of Sciences of the United States of America (2008)
Thrombospondin-1 suppresses spontaneous tumor growth and inhibits activation of matrix metalloproteinase-9 and mobilization of vascular endothelial growth factor
Juan Carlos Rodríguez-Manzaneque;Timothy F. Lane;María Asunción Ortega;Richard O. Hynes.
Proceedings of the National Academy of Sciences of the United States of America (2001)
METH-1, a Human Ortholog of ADAMTS-1, and METH-2 Are Members of a New Family of Proteins with Angio-inhibitory Activity
Francisca Vázquez;Gregg Hastings;Maria Asunción Ortega;Timothy F Lane.
Journal of Biological Chemistry (1999)
Versican V1 proteolysis in human aorta in vivo occurs at the Glu441-Ala442 bond, a site that is cleaved by recombinant ADAMTS-1 and ADAMTS-4.
John D. Sandy;Jennifer Westling;Richard D. Kenagy;M. Luisa Iruela-Arispe.
Journal of Biological Chemistry (2001)
Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels.
Natividad Villa;Liberty Walker;Claire E. Lindsell;Judith Gasson.
Mechanisms of Development (2001)
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