Immunology, Cell biology, Endothelium, Cell adhesion molecule and Endothelial stem cell are his primary areas of study. His research investigates the connection between Immunology and topics such as Stromal cell that intersect with problems in T cell. His work deals with themes such as CD18, Integrin, In vitro, Cell migration and Inflammation, which intersect with Cell biology.
His studies in Endothelium integrate themes in fields like Molecular biology, Innate immune system, CXC chemokine receptors and Systemic inflammation. Gerard B. Nash has included themes like Receptor and Cell adhesion, Soluble cell adhesion molecules in his Cell adhesion molecule study. His Endothelial stem cell research incorporates themes from Neutrophile, Cytokine, P-selectin, Umbilical vein and Cell–cell interaction.
His scientific interests lie mostly in Immunology, Cell biology, Biophysics, Endothelial stem cell and Inflammation. His Immunology study integrates concerns from other disciplines, such as Endothelium, Umbilical vein and Stromal cell. His Cell biology study combines topics in areas such as Tumor necrosis factor alpha, Platelet, Integrin and Cell adhesion.
His Integrin research is multidisciplinary, relying on both Integrin alpha M and Chemotaxis. His Biophysics study also includes fields such as
His primary areas of study are Cell biology, Immunology, Inflammation, Platelet and Endothelial stem cell. His Cell biology research includes elements of Tumor necrosis factor alpha, Endothelium, Cell adhesion and Podoplanin. His biological study spans a wide range of topics, including Selectin and Cell adhesion molecule.
His Immunology research includes themes of Phenotype and Rheology. His Inflammation research integrates issues from Stromal cell, Pathogenesis, Downregulation and upregulation, Stimulation and Monocyte. His Platelet research is multidisciplinary, incorporating elements of Vesicle, Src family, Receptor and Whole blood.
Cell biology, Immunology, Inflammation, Platelet and Endothelial stem cell are his primary areas of study. The concepts of his Cell biology study are interwoven with issues in Tumor necrosis factor alpha, Lymphatic Endothelium, Receptor, Cell adhesion and Platelet activation. His research in Immunology intersects with topics in Endothelium and Biomedical engineering.
His study in Inflammation is interdisciplinary in nature, drawing from both Stromal cell, Mesenchymal stem cell and Stroma. The Platelet study combines topics in areas such as Hemostasis, Vesicle, Rheology and Biophysics. The study incorporates disciplines such as Angiogenesis and Cellular differentiation in addition to Endothelial stem cell.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Rapid switching to multiple antigenic and adhesive phenotypes in malaria
David J. Roberts;Alister G. Craig;Anthony R. Berendt;Robert Pinches.
Nature (1992)
New guidelines for hemorheological laboratory techniques
Oguz K Baskurt;Michel Boynard;Giles C Cokelet;Philippe Connes.
Clinical Hemorheology and Microcirculation (2009)
The junctional adhesion molecule JAM-C regulates polarized transendothelial migration of neutrophils in vivo
Abigail Woodfin;Mathieu-Benoit Voisin;Martina Beyrau;Bartomeu Colom.
Nature Immunology (2011)
White cell accumulation in dependent legs of patients with venous hypertension: a possible mechanism for trophic changes in the skin
P R S Thomas;G B Nash;J A Dormandy.
BMJ (1988)
A stromal address code defined by fibroblasts.
Greg Parsonage;Andrew D. Filer;Oliver Haworth;Gerard B. Nash.
Trends in Immunology (2005)
Selectin-mediated rolling of neutrophils on immobilized platelets.
Stephen M. Buttrum;Raymond Hatton;Gerard B. Nash.
Blood (1993)
Abnormalities in the mechanical properties of red blood cells caused by Plasmodium falciparum
GB Nash;E O'Brien;EC Gordon-Smith;JA Dormandy.
Blood (1989)
Identification of a phenotypically and functionally distinct population of long-lived neutrophils in a model of reverse endothelial migration.
Christopher D. Buckley;Ewan A. Ross;Helen M. McGettrick;Chloe. E. Osborne.
Journal of Leukocyte Biology (2006)
Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake
Lisa C. Willcocks;Paul A. Lyons;Menna R. Clatworthy;James I. Robinson.
Journal of Experimental Medicine (2008)
Rolling and stationary cytoadhesion of red blood cells parasitized by Plasmodium falciparum: separate roles for ICAM‐1, CD36 and thrombospondin
Brian M. Cooke;Anthony R. Berendt;Alister G. Craig;John MacGregor.
British Journal of Haematology (1994)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Oxford
University Hospitals Birmingham NHS Foundation Trust
University of Birmingham
University of Southampton
GlaxoSmithKline (United Kingdom)
University of Oxford
Liverpool School of Tropical Medicine
University of Birmingham
University of Cambridge
Wellcome Sanger Institute
McMaster University
Fondazione Bruno Kessler
University of California, Berkeley
Colorado State University
University of Manchester
Harvard University
Pacific Northwest National Laboratory
Technical University of Kaiserslautern
British Geological Survey
University of New South Wales
California Institute of Technology
Vanderbilt University
Brown University
University of Washington
University of Barcelona
Rice University