What is he best known for?
The fields of study he is best known for:
- Gene
- Enzyme
- Organic chemistry
Hiroyuki Kagechika spends much of his time researching Stereochemistry, Retinoic acid, Retinoid X receptor, Retinoic acid receptor and Retinoid.
His Stereochemistry research is multidisciplinary, incorporating perspectives in Biological activity, Benzoic acid, Molecule and Amide.
Hiroyuki Kagechika has researched Retinoic acid in several fields, including Receptor, Ligand, Mechanism of action and Cell biology.
Retinoid X receptor is a subfield of Biochemistry that Hiroyuki Kagechika tackles.
His Retinoic acid receptor research is multidisciplinary, relying on both Interleukin 12 and Cancer research.
His Retinoid research is multidisciplinary, incorporating elements of Substituent and Pharmacology.
His most cited work include:
- The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity (4196 citations)
- Retinoic Acid Imprints Gut-Homing Specificity on T Cells (1185 citations)
- Retinoid X receptor gamma signaling accelerates CNS remyelination (360 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Stereochemistry, Retinoic acid, Retinoid, Biochemistry and Retinoid X receptor.
His Stereochemistry research includes elements of Benzoic acid, Molecule and Amide.
His research integrates issues of Receptor, Cellular differentiation and Cell biology in his study of Retinoic acid.
The study incorporates disciplines such as Cancer research, In vitro and Pharmacology in addition to Retinoid.
The concepts of his Biochemistry study are interwoven with issues in Cell culture and Leukemia.
His biological study spans a wide range of topics, including Agonist, Endocrinology, Retinoid X receptor alpha and Internal medicine.
He most often published in these fields:
- Stereochemistry (30.47%)
- Retinoic acid (21.35%)
- Retinoid (19.79%)
What were the highlights of his more recent work (between 2017-2021)?
- RYR1 (2.60%)
- Cell biology (11.98%)
- Cancer research (10.42%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include RYR1, Cell biology, Cancer research, Pharmacology and Ryanodine receptor.
His work carried out in the field of Cell biology brings together such families of science as Secretion, High-throughput screening and Retinoic acid.
His research in High-throughput screening tackles topics such as Characterization which are related to areas like Biochemistry.
His study in Retinoic acid is interdisciplinary in nature, drawing from both Babylonia japonica, Retinoid X receptor and Raf kinase.
His work is dedicated to discovering how Cell growth, Scaffold protein are connected with Retinoid and other disciplines.
His research in Stereochemistry intersects with topics in Binding affinities and Transactivation.
Between 2017 and 2021, his most popular works were:
- Prevention of hepatocellular carcinoma by targeting MYCN-positive liver cancer stem cells with acyclic retinoid. (36 citations)
- Efficient High-Throughput Screening by Endoplasmic Reticulum Ca2+ Measurement to Identify Inhibitors of Ryanodine Receptor Ca2+-Release Channels (21 citations)
- AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus (18 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Enzyme
- Organic chemistry
His main research concerns Cancer research, Antagonist, Cell biology, Progesterone receptor and Endoplasmic reticulum.
His Cancer research research is multidisciplinary, incorporating elements of Cancer, Epithelial cell adhesion molecule, Cell culture, Stem cell and Androgen receptor.
The concepts of his Antagonist study are interwoven with issues in Triazine, 1,3,5-Triazine, IC50, Stereochemistry and Pharmacology.
His Cell biology study integrates concerns from other disciplines, such as Prostaglandin E2, Receptor, Cell growth and Secretion.
His MAPK/ERK pathway study combines topics in areas such as Binding domain and Retinoic acid.
His work on Retinoid as part of general Retinoic acid study is frequently linked to Hormone response element, bridging the gap between disciplines.
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