What is he best known for?
The fields of study he is best known for:
Toshiaki Katada mainly investigates Cell biology, Biochemistry, Molecular biology, G protein and Signal transduction.
His work deals with themes such as Integral membrane protein, Endocytic cycle, Poly-Binding Protein I and Messenger RNA, which intersect with Cell biology.
His study in GTP-binding protein regulators, GTP', Protein subunit, Peptide sequence and Poly-binding protein is carried out as part of his studies in Biochemistry.
His Molecular biology study combines topics from a wide range of disciplines, such as Amino acid, DNA damage, Homologous recombination and Complementary DNA, Molecular cloning.
His G protein research is multidisciplinary, incorporating elements of Guanosine, Biophysics and Cell surface receptor.
His study in Signal transduction is interdisciplinary in nature, drawing from both Calcium, Cell and Kinase, Protein kinase A.
His most cited work include:
- Direct modification of the membrane adenylate cyclase system by islet-activating protein due to ADP-ribosylation of a membrane protein. (672 citations)
- Subunit structure of islet-activating protein, pertussis toxin, in conformity with the A-B model. (397 citations)
- Molecular cloning and sequence determination of cDNAs for alpha subunits of the guanine nucleotide-binding proteins Gs, Gi, and Go from rat brain. (288 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Cell biology, Biochemistry, Molecular biology, G protein and GTP-binding protein regulators.
GTPase, Small GTPase, Signal transduction, Protein kinase A and Kinase are the primary areas of interest in his Cell biology study.
His studies in GTP', Pertussis toxin, NAD+ kinase, ADP-ribosylation and Peptide sequence are all subfields of Biochemistry research.
His NAD+ kinase research focuses on Cyclase and how it relates to Cyclic ADP-ribose.
His work carried out in the field of Molecular biology brings together such families of science as Cellular differentiation, Antigen, Complementary DNA, Messenger RNA and Retinoic acid.
Toshiaki Katada focuses mostly in the field of G protein, narrowing it down to matters related to Biophysics and, in some cases, Muscarinic acetylcholine receptor.
He most often published in these fields:
- Cell biology (47.33%)
- Biochemistry (46.62%)
- Molecular biology (24.91%)
What were the highlights of his more recent work (between 2009-2021)?
- Cell biology (47.33%)
- Biochemistry (46.62%)
- GTPase (11.03%)
In recent papers he was focusing on the following fields of study:
His main research concerns Cell biology, Biochemistry, GTPase, Endoplasmic reticulum and Secretion.
His Cell biology research is multidisciplinary, incorporating perspectives in Caenorhabditis elegans and Mutant.
His GTPase research includes elements of Cytoplasm, Conformational change, RHOA and Endosome.
His research in RHOA intersects with topics in Mutation, GTP-binding protein regulators and Molecular biology.
To a larger extent, Toshiaki Katada studies G protein with the aim of understanding GTP-binding protein regulators.
His biological study spans a wide range of topics, including Secretory protein and Gene isoform.
Between 2009 and 2021, his most popular works were:
- Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans (142 citations)
- cTAGE5 mediates collagen secretion through interaction with TANGO1 at endoplasmic reticulum exit sites (113 citations)
- Genetically encoded calcium indicator illuminates calcium dynamics in primary cilia (90 citations)
In his most recent research, the most cited papers focused on:
Toshiaki Katada mostly deals with Cell biology, Transport protein, Molecular biology, Caenorhabditis elegans and Signal transduction.
His studies in Cell biology integrate themes in fields like Secretion and Genetics.
In his work, Coatomer is strongly intertwined with Integral membrane protein, which is a subfield of Transport protein.
His research integrates issues of Embryonic stem cell, Kinase, Cellular differentiation and p38 mitogen-activated protein kinases in his study of Molecular biology.
His NAD+ kinase research is classified as research in Biochemistry.
His Biochemistry research integrates issues from Nestin and Nervous system.
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