2023 - Research.com Biology and Biochemistry in Japan Leader Award
Cell biology, Green fluorescent protein, Fluorescence, Biophysics and Förster resonance energy transfer are his primary areas of study. His study in Cell biology is interdisciplinary in nature, drawing from both Cameleon and Autophagy. His Green fluorescent protein research is multidisciplinary, relying on both Protein structure, Photochemistry, Calmodulin and Fusion protein.
His studies deal with areas such as Biochemistry, Monomer and Luminescent Proteins as well as Fluorescence. His research in Biophysics intersects with topics in Mutagenesis, Chromophore, Cytosol, Photobleaching and Fluorescence spectrometry. The Förster resonance energy transfer study combines topics in areas such as Cyan, Visualization, Bimolecular fluorescence complementation and Yellow fluorescent protein.
His primary scientific interests are in Cell biology, Fluorescence, Green fluorescent protein, Biophysics and Optics. In his work, Cell growth is strongly intertwined with Cell cycle, which is a subfield of Cell biology. His Fluorescence study combines topics from a wide range of disciplines, such as Photochemistry, Chromophore and Biochemistry.
Atsushi Miyawaki works mostly in the field of Photochemistry, limiting it down to concerns involving Dronpa and, occasionally, Photochromism. His research in Biochemistry is mostly focused on Amino acid. His Green fluorescent protein study integrates concerns from other disciplines, such as Molecular biology and Fusion protein.
Atsushi Miyawaki mainly investigates Cell biology, Fluorescence, Optics, Biophysics and Microscopy. In his study, Cell division is inextricably linked to Cell cycle, which falls within the broad field of Cell biology. The various areas that Atsushi Miyawaki examines in his Fluorescence study include Microscope and Green fluorescent protein.
Atsushi Miyawaki has included themes like Ligand, Bioluminescence, Luciferase, Calmodulin and In vivo in his Biophysics study. Atsushi Miyawaki interconnects Photochemistry and Near-infrared spectroscopy in the investigation of issues within Bioluminescence. His work carried out in the field of Microscopy brings together such families of science as Image resolution and Two-photon excitation microscopy.
His primary areas of investigation include Cell biology, Luciferase, Neuroscience, Luciferin and Bioluminescence. His work often combines Cell biology and State studies. His study in the field of Premovement neuronal activity and Brain mapping also crosses realms of Clinical biomarker and Transgenic lines.
His research on Luciferin also deals with topics like
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Fluorescent indicators for Ca2+based on green fluorescent proteins and calmodulin
Atsushi Miyawaki;Juan Llopis;Roger Heim;J. Michael McCaffery.
Nature (1997)
A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications
Takeharu Nagai;Keiji Ibata;Eun Sun Park;Mie Kubota.
Nature Biotechnology (2002)
Visualizing Spatiotemporal Dynamics of Multicellular Cell-Cycle Progression
Asako Sakaue-Sawano;Hiroshi Kurokawa;Toshifumi Morimura;Aki Hanyu.
Cell (2008)
Scale: a chemical approach for fluorescence imaging and reconstruction of transparent mouse brain.
Hiroshi Hama;Hiroshi Kurokawa;Hiroyuki Kawano;Ryoko Ando.
Nature Neuroscience (2011)
Circularly permuted green fluorescent proteins engineered to sense Ca2
Takeharu Nagai;Asako Sawano;Eun Sun Park;Atsushi Miyawaki.
Proceedings of the National Academy of Sciences of the United States of America (2001)
Measurement of cytosolic, mitochondrial, and Golgi pH in single living cells with green fluorescent proteins.
J Llopis;J M McCaffery;A Miyawaki;M G Farquhar.
Proceedings of the National Academy of Sciences of the United States of America (1998)
An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein
Ryoko Ando;Hiroshi Hama;Miki Yamamoto-Hino;Hideaki Mizuno.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Expanded dynamic range of fluorescent indicators for Ca(2+) by circularly permuted yellow fluorescent proteins.
Takeharu Nagai;Shuichi Yamada;Takashi Tominaga;Michinori Ichikawa.
Proceedings of the National Academy of Sciences of the United States of America (2004)
Dynamic and quantitative Ca2+ measurements using improved cameleons.
Atsushi Miyawaki;Oliver Griesbeck;Roger Heim;Roger Y. Tsien.
Proceedings of the National Academy of Sciences of the United States of America (1999)
Whole-Brain Imaging with Single-Cell Resolution Using Chemical Cocktails and Computational Analysis
Etsuo A. Susaki;Kazuki Tainaka;Kazuki Tainaka;Dimitri Perrin;Fumiaki Kishino.
Cell (2014)
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