His primary areas of study are Molecular biology, Cell biology, Biochemistry, Microvesicles and Peptide sequence. His studies in Molecular biology integrate themes in fields like Serine protease, Allergen, Complementary DNA, Molecular cloning and Chymotrypsin. His research investigates the link between Complementary DNA and topics such as Nucleic acid sequence that cross with problems in Sequence analysis.
His Cell biology research incorporates themes from Tumor microenvironment, Cell and Immunology. Microvesicles and RNA are commonly linked in his work. His Exosome course of study focuses on Proteomics and Bioinformatics, Blood proteins and Computational biology.
Biochemistry, Molecular biology, Immunology, Cell biology and Peptide sequence are his primary areas of study. His research on Molecular biology often connects related areas such as Complementary DNA. His Immunology research incorporates elements of Cytotoxic T cell, Internal medicine and Endocrinology.
His studies deal with areas such as Microvesicles and Proteomics as well as Cell biology. His Peptide sequence study combines topics in areas such as Chromatography and Peptide. His Chromatography research is multidisciplinary, incorporating perspectives in Polyacrylamide gel electrophoresis and Edman degradation.
Richard J. Simpson focuses on Immunology, Cell biology, Internal medicine, Agronomy and Pasture. His Immunology research integrates issues from Cytotoxic T cell and Hematopoietic stem cell transplantation. His research integrates issues of Microvesicles, Cell, Proteomics and RNA in his study of Cell biology.
His research in Internal medicine intersects with topics in Endocrinology and Oncology. He interconnects Rhizosphere, Nutrient and Root hair in the investigation of issues within Agronomy. His work carried out in the field of Pasture brings together such families of science as Grazing, Soil water, Phosphorus and Shoot.
Richard J. Simpson mostly deals with Cell biology, Microvesicles, Immunology, Extracellular vesicle and Internal medicine. His Cell biology research is multidisciplinary, relying on both Epithelial–mesenchymal transition, Cell, Angiogenesis, Tumor microenvironment and Proteomics. Richard J. Simpson has included themes like Proteome and Cell signaling in his Proteomics study.
Particularly relevant to Exosome is his body of work in Microvesicles. Richard J. Simpson has researched Immunology in several fields, including Cytotoxic T cell, Hematopoietic stem cell transplantation and Cell culture. His Internal medicine research integrates issues from Endocrinology and Oncology.
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.
Identification of DIABLO, a Mammalian Protein that Promotes Apoptosis by Binding to and Antagonizing IAP Proteins
Anne M Verhagen;Paul G Ekert;Paul G Ekert;Miha Pakusch;John Silke.
Anti-phospholipid antibodies are directed against a complex antigen that includes a lipid-binding inhibitor of coagulation: beta 2-glycoprotein I (apolipoprotein H).
H P McNeil;R J Simpson;C N Chesterman;S A Krilis.
Proceedings of the National Academy of Sciences of the United States of America (1990)
Exosomes: extracellular organelles important in intercellular communication.
Suresh Mathivanan;Hong Ji;Richard J. Simpson.
Journal of Proteomics (2010)
Complete amino acid analysis of proteins from a single hydrolysate.
R J Simpson;M R Neuberger;T Y Liu.
Journal of Biological Chemistry (1976)
Exosomes: proteomic insights and diagnostic potential
Richard J Simpson;Justin We Lim;Robert L Moritz;Suresh Mathivanan.
Expert Review of Proteomics (2009)
Soil Microorganisms Mediating Phosphorus Availability Update on Microbial Phosphorus
Alan E. Richardson;Richard J. Simpson.
Plant Physiology (2011)
Vesiclepedia: a compendium for extracellular vesicles with continuous community annotation
Hina Kalra;Richard J. Simpson;Hong Ji;Elena Aikawa.
PLOS Biology (2012)
A common open representation of mass spectrometry data and its application to proteomics research
Patrick G A Pedrioli;Jimmy K Eng;Robert Hubley;Mathijs Vogelzang.
Nature Biotechnology (2004)
Comparison of ultracentrifugation, density gradient separation, and immunoaffinity capture methods for isolating human colon cancer cell line LIM1863-derived exosomes.
Bow J. Tauro;David W. Greening;Rommel A. Mathias;Hong Ji.
Style self-incompatibility gene products of Nicotlana alata are ribonucleases
Bruce A. McClure;Volker Haring;Paul R. Ebert;Marilyn A. Anderson.
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