Donald G. Payan mainly investigates Cell biology, Molecular biology, Immunology, Receptor and Inflammation. His Cell biology research is multidisciplinary, incorporating elements of Free nerve ending, Biochemistry, Peptide and Histamine. His Molecular biology study combines topics in areas such as Gene expression, Substance P, Endocytosis, Protein kinase domain and Endosome.
His Immunology research includes elements of Fostamatinib, Syk and AXL receptor tyrosine kinase. His study in Receptor is interdisciplinary in nature, drawing from both Endocrinology, Antibody, Transfection and Trypsin. His Inflammation study deals with Arthritis intersecting with Asthma, Inflammatory bowel disease and Pathogenesis.
Donald G. Payan mainly focuses on Biochemistry, Cell biology, Molecular biology, Receptor and Internal medicine. He interconnects Epitope and Immunoglobulin E in the investigation of issues within Biochemistry. His Cell biology research is multidisciplinary, incorporating perspectives in Neuropeptide, Cell, Internalization and Mast cell.
Donald G. Payan has included themes like Cell culture, Transfection, Gene expression, Peptide sequence and Intracellular in his Molecular biology study. Donald G. Payan combines subjects such as Antibody and Lymphoblast with his study of Receptor. In his study, Immunology is inextricably linked to Endocrinology, which falls within the broad field of Internal medicine.
His primary areas of study are Stereochemistry, Internal medicine, Cancer research, Immunology and Kinase. His Internal medicine course of study focuses on Endocrinology and T cell. His research integrates issues of Degranulation and Syk in his study of Immunology.
His study looks at the relationship between Degranulation and topics such as Salt, which overlap with Biochemistry. His Kinase research includes themes of Cell, Cell culture, In vivo and Transcription factor. His Cell research incorporates themes from Muscle tissue, Molecular biology and Signal transduction, Receptor signaling.
His primary scientific interests are in Internal medicine, Cancer research, Endocrinology, Immunology and Pharmacology. His work deals with themes such as AMP-activated protein kinase and AMPK, which intersect with Internal medicine. His studies in Cancer research integrate themes in fields like Hematology, Cancer and Kinase.
Donald G. Payan works in the field of Endocrinology, focusing on Nitric oxide in particular. His Immunology study combines topics in areas such as Metastasis and Syk. His T cell research is multidisciplinary, incorporating perspectives in Inflammation, Receptor, Lesion and Psoriasis.
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Molecular cloning, expression and potential functions of the human proteinase-activated receptor-2
Stephan K. Böhm;Wuyi Kong;Dieter Brömme;Steven P. Smeekens.
Biochemical Journal (1996)
R428, a Selective Small Molecule Inhibitor of Axl Kinase, Blocks Tumor Spread and Prolongs Survival in Models of Metastatic Breast Cancer
Sacha J Holland;Alison Pan;Christian Franci;Yuanming Hu.
Cancer Research (2010)
R406, an Orally Available Spleen Tyrosine Kinase Inhibitor Blocks Fc Receptor Signaling and Reduces Immune Complex-Mediated Inflammation
Sylvia Braselmann;Vanessa Taylor;Haoran Zhao;Su Wang.
Journal of Pharmacology and Experimental Therapeutics (2006)
Substance P selectively activates TNF-alpha gene expression in murine mast cells.
John C. Ansel;Jeffrey R. Brown;Donald G. Payan;Melissa A. Brown.
Journal of Immunology (1993)
Structure and expression of a rat agrin.
Fabio Rupp;Donald G. Payan;Catherine Magill-Solc;David M. Cowan.
Neuron (1991)
Mast cell tryptase regulates rat colonic myocytes through proteinase-activated receptor 2.
Carlos U. Corvera;Olivier Déry;K. McConalogue;Stephan K. Böhm.
Journal of Clinical Investigation (1997)
NEUROPEPTIDES AND INFLAMMATION: The Role of Substance P
Donald G. Payan.
Annual Review of Medicine (1989)
Substance P recognition by a subset of human T lymphocytes.
D G Payan;D R Brewster;A Missirian-Bastian;E J Goetzl.
Journal of Clinical Investigation (1984)
Neutrophil rolling altered by inhibition of L-selectin shedding in vitro.
B. Walcheck;J. Kahn;J. M. Fisher;B. B. Wang.
Nature (1996)
Luminal trypsin may regulate enterocytes through proteinase-activated receptor 2
Wuyi Kong;Karen McConalogue;Lev M. Khitin;Morley D. Hollenberg.
Proceedings of the National Academy of Sciences of the United States of America (1997)
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