What is he best known for?
The fields of study he is best known for:
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.
His most cited work include:
- Cellular uptake of arginine-rich peptides: roles for macropinocytosis and actin rearrangement. (567 citations)
- Systematic subcellular localization of novel proteins identified by large‐scale cDNA sequencing (329 citations)
- Evidence for a COP-I-independent transport route from the Golgi complex to the endoplasmic reticulum (321 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Cell biology (61.59%)
- Golgi apparatus (23.91%)
- Endoplasmic reticulum (21.01%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (61.59%)
- Biofilm (3.62%)
- Computational biology (10.14%)
In recent papers he was focusing on the following fields of study:
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.
Between 2018 and 2021, his most popular works were:
- NeurodegenERation: The Central Role for ER Contacts in Neuronal Function and Axonopathy, Lessons From Hereditary Spastic Paraplegias and Related Diseases (20 citations)
- The Challenges and Possibilities of Extracellular Vesicles as Therapeutic Vehicles (17 citations)
- Precise Targeting of miRNA Sites Restores CFTR Activity in CF Bronchial Epithelial Cells. (10 citations)
In his most recent research, the most cited papers focused on:
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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