What is he best known for?
The fields of study he is best known for:
His primary areas of study are Fluorescence, Biochemistry, Microscopy, Internal medicine and Endocrinology.
His studies in Fluorescence integrate themes in fields like Luminescent Proteins, Fluorescent protein, Green fluorescent protein and Molecular biology, Cleavage.
His research on Biochemistry often connects related areas such as Biophysics.
He has researched Biophysics in several fields, including Calcium, Electrophysiology, Protein–protein interaction, Förster resonance energy transfer and Quantum yield.
His Microscopy research includes themes of Fluorescence microscope, Photobleaching, Two-photon excitation microscopy and Fluorescence-lifetime imaging microscopy.
His Type 2 diabetes research extends to the thematically linked field of Internal medicine.
His most cited work include:
- An improved cyan fluorescent protein variant useful for FRET. (979 citations)
- Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy. (705 citations)
- Bone morphogenetic proteins (BMPs) as regulators of dorsal forebrain development (637 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Internal medicine, Endocrinology, Biophysics, Cell biology and Insulin.
His study ties his expertise on Receptor together with the subject of Endocrinology.
David W. Piston interconnects Autofluorescence, Fluorescence, Förster resonance energy transfer and Protein–protein interaction in the investigation of issues within Biophysics.
David W. Piston combines subjects such as Green fluorescent protein, Luminescent Proteins, Biochemistry and Microscopy with his study of Fluorescence.
His Microscopy study combines topics from a wide range of disciplines, such as Confocal microscopy, Fluorescence-lifetime imaging microscopy, Two-photon excitation microscopy and Fluorescence microscope.
The study incorporates disciplines such as Cell, Calcium and Paracrine signalling in addition to Cell biology.
He most often published in these fields:
- Internal medicine (25.95%)
- Endocrinology (25.95%)
- Biophysics (21.45%)
What were the highlights of his more recent work (between 2015-2021)?
- Cell biology (20.42%)
- Islet (19.38%)
- Fluorescence (18.69%)
In recent papers he was focusing on the following fields of study:
David W. Piston mainly focuses on Cell biology, Islet, Fluorescence, Glucagon secretion and Insulin.
His Cell biology research is multidisciplinary, incorporating perspectives in Cell and Calcium.
His Islet research also covers Endocrinology and Internal medicine studies.
The various areas that David W. Piston examines in his Fluorescence study include Luminescent Proteins, Spectroscopy, Biophysics, Biochemistry and Biological system.
His study in the fields of Oxidative stress under the domain of Biochemistry overlaps with other disciplines such as Ribonucleoprotein.
His Insulin study integrates concerns from other disciplines, such as Unfolded protein response, Endoplasmic reticulum, Wolfram syndrome and Homeostasis.
Between 2015 and 2021, his most popular works were:
- Quantitative assessment of fluorescent proteins (241 citations)
- Quantitative assessment of fluorescent proteins (241 citations)
- Precommitment low-level Neurog3 expression defines a long-lived mitotic endocrine-biased progenitor pool that drives production of endocrine-committed cells (38 citations)
In his most recent research, the most cited papers focused on:
David W. Piston mainly investigates Cell biology, Islet, Pancreatic islets, Fluorescence and Secretion.
His Islet research is under the purview of Insulin.
His Insulin study combines Internal medicine and Endocrinology studies.
The concepts of his Pancreatic islets study are interwoven with issues in Oxidative stress, Biochemistry and Ribosomal protein.
The Fluorescence study combines topics in areas such as Confocal microscopy, Biological system, Microscopy and Luminescent Proteins.
In Intracellular, he works on issues like Biophysics, which are connected to Signal transduction.
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