His primary scientific interests are in Molecular biology, Biochemistry, Superoxide dismutase, Endocrinology and Internal medicine. The study incorporates disciplines such as Neurotoxicity, Mutation, Mutant, Knockout mouse and Cerebral amyloid angiopathy in addition to Molecular biology. SOD2 is closely connected to Genetically modified mouse in his research, which is encompassed under the umbrella topic of Knockout mouse.
His Superoxide dismutase study is related to the wider topic of Oxidative stress. His Oxidative stress research includes themes of Lipofuscin, Senescence, Paraquat and Caenorhabditis elegans. Takuji Shirasawa has researched Endocrinology in several fields, including Superoxide and Mitochondrion.
Molecular biology, Internal medicine, Endocrinology, Biochemistry and Cell biology are his primary areas of study. The concepts of his Molecular biology study are interwoven with issues in Genetics, Mutant, Complementary DNA, Peptide sequence and Exon. His Endocrinology research integrates issues from Gene expression and Neuron.
His study in Biochemistry is interdisciplinary in nature, drawing from both Neurotoxicity and In vivo. His Cell biology research includes elements of Immunology, Embryonic stem cell, Downregulation and upregulation and Transgene. The Oxidative stress study combines topics in areas such as Antioxidant and Pathogenesis, Pathology.
His main research concerns Endocrinology, Internal medicine, Coenzyme Q – cytochrome c reductase, Cell biology and Mitochondrion. His biological study spans a wide range of topics, including Superoxide and CYP17A1. His Coenzyme Q – cytochrome c reductase research is under the purview of Biochemistry.
His Biochemistry study often links to related topics such as Respiratory system. He has included themes like Molecular biology and Caenorhabditis elegans, Gene in his Cell biology study. Specifically, his work in Oxidative stress is concerned with the study of Superoxide dismutase.
Takuji Shirasawa focuses on Endocrinology, Internal medicine, SOD2, Superoxide and Superoxide dismutase. His Hypothalamus and Cerebral cortex study in the realm of Endocrinology interacts with subjects such as Androgen receptor and Estrogen receptor alpha. His Internal medicine research is multidisciplinary, incorporating elements of Coenzyme Q – cytochrome c reductase, Biochemistry and CYP17A1.
His work deals with themes such as Paraquat and Bone cell, which intersect with Superoxide. His research integrates issues of Molecular biology and Mitochondrion, Cell biology in his study of Superoxide dismutase. As part of one scientific family, Takuji Shirasawa deals mainly with the area of Molecular biology, narrowing it down to issues related to the Periodic acid–Schiff stain, and often Goblet cell and Conjunctiva.
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Inhibition of autophagy in the heart induces age-related cardiomyopathy.
Manabu Taneike;Osamu Yamaguchi;Atsuko Nakai;Shungo Hikoso.
Autophagy (2010)
Carnosic acid, a catechol-type electrophilic compound, protects neurons both in vitro and in vivo through activation of the Keap1/Nrf2 pathway via S-alkylation of targeted cysteines on Keap1.
Takumi Satoh;Kunio Kosaka;Ken Itoh;Akira Kobayashi.
Journal of Neurochemistry (2008)
Neurotoxicity and Physicochemical Properties of Aβ Mutant Peptides from Cerebral Amyloid Angiopathy: IMPLICATION FOR THE PATHOGENESIS OF CEREBRAL AMYLOID ANGIOPATHY AND ALZHEIMER'S DISEASE
Kazuma Murakami;Kazuhiro Irie;Akira Morimoto;Hajime Ohigashi.
Journal of Biological Chemistry (2003)
μ1B, a novel adaptor medium chain expressed in polarized epithelial cells1
Hiroshi Ohno;Takuya Tomemori;Fubito Nakatsu;Yasushi Okazaki.
FEBS Letters (1999)
Effects of a potent antioxidant, platinum nanoparticle, on the lifespan of Caenorhabditis elegans.
Juewon Kim;Mayumi Takahashi;Takahiko Shimizu;Takuji Shirasawa.
Mechanisms of Ageing and Development (2008)
SOD1 (copper/zinc superoxide dismutase) deficiency drives amyloid β protein oligomerization and memory loss in mouse model of Alzheimer disease.
Kazuma Murakami;Nakaba Murata;Yoshihiro Noda;Shoichi Tahara.
Journal of Biological Chemistry (2011)
Racemization of Asp23 residue affects the aggregation properties of Alzheimer amyloid beta protein analogues.
T Tomiyama;S Asano;Y Furiya;T Shirasawa.
Journal of Biological Chemistry (1994)
Senescence Marker Protein-30 Knockout Mouse Liver Is Highly Susceptible to Tumor Necrosis Factor-α- and Fas-Mediated Apoptosis
Akihito Ishigami;Toshiko Fujita;Setsuko Handa;Takuji Shirasawa.
American Journal of Pathology (2002)
Synthesis, aggregation, neurotoxicity, and secondary structure of various Aβ1–42 mutants of familial Alzheimer's disease at positions 21–23
Kazuma Murakami;Kazuhiro Irie;Akira Morimoto;Hajime Ohigashi.
Biochemical and Biophysical Research Communications (2002)
Cytoplasmic superoxide causes bone fragility owing to low‐turnover osteoporosis and impaired collagen cross‐linking
Hidetoshi Nojiri;Yoshitomo Saita;Daichi Morikawa;Keiji Kobayashi.
Journal of Bone and Mineral Research (2011)
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