What is he best known for?
The fields of study he is best known for:
Takashi Hashimoto mainly focuses on Biochemistry, Peroxisome, Enzyme, Molecular biology and Dehydrogenase.
Takashi Hashimoto performs multidisciplinary study on Biochemistry and Phthalate in his works.
The concepts of his Peroxisome study are interwoven with issues in Endocrinology, Internal medicine and Biosynthesis.
As part of one scientific family, he deals mainly with the area of Enzyme, narrowing it down to issues related to the Gel electrophoresis, and often Substrate, Column chromatography, Cofactor, Chromatography and Sedimentation equilibrium.
His studies deal with areas such as Catalase, Oxidase test, Acyl-CoA oxidase and Complementary DNA, Gene as well as Molecular biology.
Takashi Hashimoto combines subjects such as Beta oxidation and Mitochondrion with his study of Dehydrogenase.
His most cited work include:
- Altered Constitutive Expression of Fatty Acid-metabolizing Enzymes in Mice Lacking the Peroxisome Proliferator-activated Receptor α (PPARα) (756 citations)
- The 70-kDa peroxisomal membrane protein is a member of the Mdr (P-glycoprotein)-related ATP-binding protein superfamily. (337 citations)
- Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting (248 citations)
What are the main themes of his work throughout his whole career to date?
Takashi Hashimoto mostly deals with Biochemistry, Peroxisome, Molecular biology, Enzyme and Thiolase.
His study in Biochemistry concentrates on Peptide sequence, Dehydrogenase, Beta oxidation, Enoyl-CoA hydratase and Amino acid.
His study looks at the intersection of Peroxisome and topics like Oxidase test with Matrix.
His Molecular biology research incorporates elements of Genetics, Nucleic acid sequence, Complementary DNA, Gene and Exon.
His Enzyme research incorporates themes from Endocrinology and Mitochondrion.
His Thiolase research focuses on Mitochondrial trifunctional protein and how it connects with HADHB.
He most often published in these fields:
- Biochemistry (73.06%)
- Peroxisome (41.63%)
- Molecular biology (36.33%)
What were the highlights of his more recent work (between 1995-2008)?
- Biochemistry (73.06%)
- Molecular biology (36.33%)
- Peroxisome (41.63%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Biochemistry, Molecular biology, Peroxisome, Enzyme and Thiolase.
His Biochemistry study is mostly concerned with Dehydrogenase, Enoyl-CoA hydratase, 3-Hydroxyacyl-CoA Dehydrogenase, Peptide sequence and Mitochondrion.
His work carried out in the field of Molecular biology brings together such families of science as Mutation, Protein subunit, Gene, Complementary DNA and Acyl CoA dehydrogenase.
His Peroxisome research is multidisciplinary, relying on both Cell fractionation, Dehydratase and Fatty acid metabolism.
His work on Polyacrylamide gel electrophoresis, Oxidase test and Catalase as part of general Enzyme study is frequently linked to Ultraviolet light, bridging the gap between disciplines.
His Thiolase research integrates issues from Mitochondrial trifunctional protein, Internal medicine, Endocrinology and Cytosol.
Between 1995 and 2008, his most popular works were:
- Altered Constitutive Expression of Fatty Acid-metabolizing Enzymes in Mice Lacking the Peroxisome Proliferator-activated Receptor α (PPARα) (756 citations)
- Role of peroxisome proliferator-activated receptor alpha in altered cell cycle regulation in mouse liver. (138 citations)
- MOLECULAR CLONING OF CDNA ENCODING RAT VERY LONG-CHAIN ACYL-COA SYNTHETASE (138 citations)
In his most recent research, the most cited papers focused on:
Takashi Hashimoto spends much of his time researching Biochemistry, Peroxisome, Thiolase, Enzyme and D-bifunctional protein deficiency.
His Biochemistry study which covers Molecular biology that intersects with Complementary DNA.
His research in Peroxisome intersects with topics in Oxidase test, Beta oxidation, Mitochondrion and Fatty acid metabolism.
His Thiolase study incorporates themes from HADHB, Enzyme complex, Point mutation, Mitochondrial trifunctional protein and Pristanic acid.
His studies in Enzyme integrate themes in fields like Reactive oxygen species and Antioxidant.
His D-bifunctional protein deficiency research focuses on Dehydratase and how it relates to Coenzyme A and Messenger RNA.
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