The scientist’s investigation covers issues in Cell biology, Endoplasmic reticulum, Golgi apparatus, Biochemistry and Transport protein. Jeremy C. Simpson interconnects Endocytic cycle and Programmed cell death in the investigation of issues within Cell biology. His Golgi apparatus research is multidisciplinary, incorporating elements of Molecular biology and Image acquisition.
In general Biochemistry study, his work on Glycosylation, Protein degradation, SEC Translocation Channels and Translocon often relates to the realm of Ricin, thereby connecting several areas of interest. The various areas that Jeremy C. Simpson examines in his Transport protein study include Luminescent Proteins, Pinocytosis, Actin, Computational biology and Organelle. Jeremy C. Simpson has researched Secretory pathway in several fields, including Secretion and Secretory protein.
Jeremy C. Simpson mainly focuses on Cell biology, Golgi apparatus, Endoplasmic reticulum, Secretory pathway and Biochemistry. His research related to Rab, GTPase, Endosome, Transport protein and Function might be considered part of Cell biology. His Golgi apparatus research focuses on subjects like Organelle, which are linked to Proteome.
His Endoplasmic reticulum study incorporates themes from Receptor and Microtubule. His biological study spans a wide range of topics, including Secretion and Secretory protein. His work on Glycosylation and Mutant as part of general Biochemistry research is often related to Ricin, thus linking different fields of science.
Cell biology, Biofilm, Computational biology, Nanoparticle and Microbiology are his primary areas of study. He regularly ties together related areas like PLGA in his Cell biology studies. His Computational biology research is multidisciplinary, relying on both Proteome, Deep learning, Artificial intelligence and Secretory pathway.
In his research, Nanomedicine and 3D cell culture is intimately related to Confocal microscopy, which falls under the overarching field of Nanoparticle. His Golgi apparatus study combines topics from a wide range of disciplines, such as CDC42 and Organelle. As a member of one scientific family, Jeremy C. Simpson mostly works in the field of Endocytosis, focusing on GTPase and, on occasion, Endoplasmic reticulum.
Jeremy C. Simpson mainly investigates Cell biology, Rab, Organelle, Computational biology and Autophagy. His Cell biology research includes themes of microRNA, Untranslated region and PLGA. His studies deal with areas such as Sonic hedgehog, Cilium, Zebrafish, Confocal microscopy and Nanomedicine as well as Rab.
His research in Organelle intersects with topics in Axon, Endoplasmic reticulum, Neurodegeneration and Mitochondrion. His study in Computational biology is interdisciplinary in nature, drawing from both Spheroid, Cell, 3D cell culture and Nanoparticle. His research brings together the fields of Golgi apparatus and Autophagy.
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Cellular uptake of arginine-rich peptides: roles for macropinocytosis and actin rearrangement.
Ikuhiko Nakase;Miki Niwa;Toshihide Takeuchi;Kazuhiro Sonomura.
Molecular Therapy (2004)
Systematic subcellular localization of novel proteins identified by large‐scale cDNA sequencing
Jeremy C. Simpson;Ruth Wellenreuther;Annemarie Poustka;Rainer Pepperkok.
EMBO Reports (2000)
Evidence for a COP-I-independent transport route from the Golgi complex to the endoplasmic reticulum
A Girod;B Storrie;J C Simpson;L Johannes.
Nature Cell Biology (1999)
Cytoglobin is a respiratory protein in connective tissue and neurons, which is up-regulated by hypoxia.
Marc Schmidt;Frank Gerlach;Aaron Avivi;Tilmann Laufs.
Journal of Biological Chemistry (2004)
Malectin – A Novel Carbohydrate-binding Protein of the Endoplasmic Reticulum and a Candidate Player in the Early Steps of Protein N-glycosylation
T Schallus;C Jaeckh;K Feher;A.S Palma.
Molecular Biology of the Cell (2008)
Analysis of Intraviral Protein-Protein Interactions of the SARS Coronavirus ORFeome
Albrecht von Brunn;Carola Teepe;Jeremy C. Simpson;Rainer Pepperkok.
PLOS ONE (2007)
Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells
Charlotte Stadler;Elton Rexhepaj;Vasanth R Singan;Robert F Murphy.
Nature Methods (2013)
The KDEL retrieval system is exploited by Pseudomonas exotoxin A, but not by Shiga-like toxin-1, during retrograde transport from the Golgi complex to the endoplasmic reticulum
M.E. Jackson;J.C. Simpson;A. Girod;R. Pepperkok.
Journal of Cell Science (1999)
Genome-wide RNAi screening identifies human proteins with a regulatory function in the early secretory pathway
Jeremy C. Simpson;Brigitte Joggerst;Vibor Laketa;Fatima Verissimo.
Nature Cell Biology (2012)
Ricin A chain utilises the endoplasmic reticulum‐associated protein degradation pathway to enter the cytosol of yeast
Jeremy C. Simpson;Lynne M. Roberts;Karin Römisch;John Davey.
FEBS Letters (1999)
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