What is he best known for?
The fields of study he is best known for:
- Gene
- Enzyme
- Internal medicine
Richard L. Proia mostly deals with Cell biology, Sphingosine, Immunology, Receptor and Sphingosine-1-phosphate.
Richard L. Proia works in the field of Cell biology, namely Signal transduction.
He interconnects Lipid signaling and Kinase in the investigation of issues within Sphingosine.
His work in the fields of Immunology, such as Lymphocyte, intersects with other areas such as Bone mineral.
His Receptor study incorporates themes from Proinflammatory cytokine, Endocrinology and Immune system.
His work carried out in the field of Sphingosine-1-phosphate brings together such families of science as Mast cell, Sphingolipid, Neuroinflammation, Mediator and Degranulation.
His most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1 (1986 citations)
- Edg-1, the G protein-coupled receptor for sphingosine-1-phosphate, is essential for vascular maturation. (990 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Cell biology, Biochemistry, Sphingosine, Immunology and Receptor.
His Cell biology study frequently links to related topics such as Sphingosine-1-phosphate.
As a part of the same scientific study, he usually deals with the Biochemistry, concentrating on Molecular biology and frequently concerns with Complementary DNA and Gene expression.
His research integrates issues of Lipid signaling and Kinase in his study of Sphingosine.
His Immunology research incorporates themes from Tay-Sachs disease, Ganglioside and Sandhoff disease.
His Receptor research integrates issues from Endocrinology, Angiogenesis and Pharmacology.
He most often published in these fields:
- Cell biology (48.02%)
- Biochemistry (22.03%)
- Sphingosine (21.15%)
What were the highlights of his more recent work (between 2016-2021)?
- Cell biology (48.02%)
- S1PR1 (8.81%)
- Receptor (18.06%)
In recent papers he was focusing on the following fields of study:
Richard L. Proia spends much of his time researching Cell biology, S1PR1, Receptor, Sphingosine-1-phosphate and Sphingosine.
His research on Cell biology focuses in particular on Sphingolipid.
His Receptor research is multidisciplinary, relying on both STAT3, Signal transduction and Transplantation.
In general Signal transduction study, his work on Beta-Arrestin-2 often relates to the realm of Bioluminescence imaging, thereby connecting several areas of interest.
His Sphingosine-1-phosphate study integrates concerns from other disciplines, such as Retinal structure, Endocrinology and Function.
His Endocrinology study combines topics from a wide range of disciplines, such as Cell adhesion molecule and Monocyte.
Between 2016 and 2021, his most popular works were:
- Cerebral organoids derived from Sandhoff disease-induced pluripotent stem cells exhibit impaired neurodifferentiation (51 citations)
- De Novo Sphingolipid Biosynthesis Is Required for Adipocyte Survival and Metabolic Homeostasis. (25 citations)
- Bioluminescence imaging of G protein-coupled receptor activation in living mice. (23 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Enzyme
- Internal medicine
Richard L. Proia mainly investigates Cell biology, Receptor, Sphingolipid, G protein-coupled receptor and Cell signaling.
His Cell biology research is multidisciplinary, incorporating elements of HEXB, GM2 gangliosidoses, Tay-Sachs disease, Sandhoff disease and Neurodegeneration.
Many of his research projects under Receptor are closely connected to Collapsin response mediator protein family with Collapsin response mediator protein family, tying the diverse disciplines of science together.
The Sphingolipid study combines topics in areas such as Adipocyte, Cellular differentiation, Ceramide, De novo synthesis and Metabolism.
His G protein-coupled receptor study necessitates a more in-depth grasp of Signal transduction.
His Cell signaling research includes elements of Gene, Metabolic pathway, Disease and Pathogenesis.
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