Toshiya Hirayama mainly investigates Molecular biology, Transfection, Biochemistry, Helicobacter pylori and Microbiology. His Molecular biology research is multidisciplinary, incorporating elements of Secretion, Phospholipase C, Phosphorylation, Internalization and PI3K/AKT/mTOR pathway. Toshiya Hirayama has researched Transfection in several fields, including Protein structure, GSK3B and Complementary DNA.
His work on In vitro, Phosphatase, Protein tyrosine phosphatase and Oligopeptide as part of general Biochemistry study is frequently linked to Peanut agglutinin, bridging the gap between disciplines. His Helicobacter pylori study integrates concerns from other disciplines, such as CagA, Immunology and Tyrosine phosphorylation. His study of Antimicrobial peptides is a part of Microbiology.
His primary areas of study are Microbiology, Molecular biology, Helicobacter pylori, Biochemistry and Immunology. The concepts of his Microbiology study are interwoven with issues in Pseudomonas aeruginosa, Receptor, Vibrio cholerae and Virulence. Toshiya Hirayama combines subjects such as Cell culture, Transfection, HeLa, Mutant and Intracellular with his study of Molecular biology.
His Transfection research integrates issues from DNA, Phosphorylation and Antimicrobial peptides. His Helicobacter pylori research incorporates elements of Inflammation, CagA and Secretion. His work on Peptide, Protein tyrosine phosphatase, Amino acid and Ganglioside as part of general Biochemistry research is frequently linked to Amphiphile, bridging the gap between disciplines.
His scientific interests lie mostly in Helicobacter pylori, Autophagy, CagA, Immunology and Apoptosis. His Helicobacter pylori research incorporates themes from Proinflammatory cytokine, Lung, A549 cell and Microbiology. Within one scientific family, Toshiya Hirayama focuses on topics pertaining to Virulence under Microbiology, and may sometimes address concerns connected to Salmonella enterica and Enterotoxin.
His CagA study also includes
Molecular biology, Apoptosis, Programmed cell death, Autophagy and Immunology are his primary areas of study. The Molecular biology study combines topics in areas such as Virulence factor, Virulence, Periplasmic space, Mutant and Salmonella enterica. His research in Apoptosis intersects with topics in Cell surface receptor, Receptor and Cell biology.
His studies deal with areas such as Unfolded protein response, Endoplasmic reticulum, Signal transduction and Mitochondrion as well as Programmed cell death. His Inflammation study frequently draws parallels with other fields, such as Helicobacter pylori. His Helicobacter pylori research is multidisciplinary, incorporating elements of Tumor necrosis factor alpha, CagA, Cancer, Reactive oxygen species and Microbiology.
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β-Defensin-2 Expression Is Regulated by TLR Signaling in Intestinal Epithelial Cells
Puja Vora;Adrienne Youdim;Lisa S. Thomas;Masayuki Fukata.
Journal of Immunology (2004)
In vitro gene transfection using dendritic poly(L-lysine)
Mio Ohsaki;Tatsuya Okuda;Akihiro Wada;Toshiya Hirayama.
Bioconjugate Chemistry (2002)
Mice deficient in protein tyrosine phosphatase receptor type Z are resistant to gastric ulcer induction by VacA of Helicobacter pylori
Akihiro Fujikawa;Daisuke Shirasaka;Daisuke Shirasaka;Shoichi Yamamoto;Hiroyoshi Ota.
Nature Genetics (2003)
MicroRNA signatures in Helicobacter pylori-infected gastric mucosa.
Kayoko Matsushima;Hajime Isomoto;Naoki Inoue;Toshiyuki Nakayama.
International Journal of Cancer (2011)
Binding of cationic α-helical peptides to plasmid DNA and their gene transfer abilities into cells
Takuro Niidome;Naoya Ohmori;Akitoyo Ichinose;Akihiro Wada.
Journal of Biological Chemistry (1997)
Activation of Helicobacter pylori VacA Toxin by Alkaline or Acid Conditions Increases Its Binding to a 250-kDa Receptor Protein-tyrosine Phosphatase β
Kinnosuke Yahiro;Takuro Niidome;Miyuki Kimura;Tomomitsu Hatakeyama.
Journal of Biological Chemistry (1999)
Reactive Oxygen Species-Induced Autophagic Degradation of Helicobacter pylori CagA Is Specifically Suppressed in Cancer Stem-like Cells
Hitoshi Tsugawa;Hidekazu Suzuki;Hideyuki Saya;Masanori Hatakeyama.
Cell Host & Microbe (2012)
Cutting edge: VacA, a vacuolating cytotoxin of Helicobacter pylori, directly activates mast cells for migration and production of proinflammatory cytokines.
Volaluck Supajatura;Hiroko Ushio;Akihiro Wada;Kinnosuke Yahiro.
Journal of Immunology (2002)
Role of nicotinamide adenine dinucleotide phosphate oxidase 1 in oxidative burst response to toll-like receptor 5 signaling in large intestinal epithelial cells
Tsukasa Kawahara;Yuki Kuwano;Shigetada Teshima-Kondo;Ryu Takeya.
Journal of Immunology (2004)
Helicobacter pylori vacuolating cytotoxin induces activation of the proapoptotic proteins Bax and Bak, leading to cytochrome c release and cell death, independent of vacuolation.
Eiki Yamasaki;Eiki Yamasaki;Akihiro Wada;Akihiro Wada;Atsushi Kumatori;Ichiro Nakagawa.
Journal of Biological Chemistry (2006)
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