Koji Hase mostly deals with Immune system, Immunology, Microbiology, Epithelium and Biochemistry. His studies deal with areas such as Gut flora, Antigen and B cell as well as Immune system. His Immunology research is multidisciplinary, relying on both Cell and Cell biology.
Koji Hase has researched Microbiology in several fields, including Probiotic, Bacteria, Innate immune system and Cellular differentiation. His Biochemistry study combines topics from a wide range of disciplines, such as Lipopolysaccharide and Liver injury, Pharmacology. His FOXP3 research includes elements of Clostridia, Human microbiome, Virulence and Bacterial antigen.
Cell biology, Immunology, Immune system, Antigen and Microfold cell are his primary areas of study. His study in Cell biology is interdisciplinary in nature, drawing from both Epithelium, Stromal cell, Transcription factor and Cellular differentiation. His Cellular differentiation research incorporates elements of Adoptive cell transfer and Intestinal mucosa.
His research integrates issues of DNA methylation, Antibody, Microbiology and Cancer research in his study of Immune system. His Microbiology study frequently draws connections to adjacent fields such as T cell. His biological study spans a wide range of topics, including Transcytosis, Molecular biology and Lymphatic system.
His primary areas of study are Cell biology, Immunology, Gut flora, Antigen and Immune system. His work deals with themes such as Inflammation and Macrophage, which intersect with Cell biology. His Immunology study often links to related topics such as Metabolomics.
The study incorporates disciplines such as Microbiome, Metabolic phenotype, Microbiology, Physiology and Energy homeostasis in addition to Gut flora. His Microbiology research is multidisciplinary, relying on both T cell, Receptor, Toxicity and Lactobacillus. His Immune system study focuses on Peyer's patch in particular.
His primary scientific interests are in Immunology, Cell biology, Gut flora, Epithelium and Immune system. Koji Hase interconnects Metabolite and Metabolome in the investigation of issues within Immunology. He has researched Cell biology in several fields, including Gene silencing, Macrophage, Cellular differentiation and Transcription Factor Maf.
His Gut flora research incorporates elements of Offspring, Pregnancy, Embryonic stem cell, Embryonic Stage and Metabolic phenotype. The Epithelium study which covers Antigen that intersects with Secretion. Koji Hase works in the field of Immune system, namely Peyer's patch.
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Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
Yukihiro Furusawa;Yuuki Obata;Shinji Fukuda;Takaho A. Endo.
Nature (2013)
Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota
Koji Atarashi;Takeshi Tanoue;Kenshiro Oshima;Wataru Suda.
Nature (2013)
Bifidobacteria can protect from enteropathogenic infection through production of acetate
Shinji Fukuda;Hidehiro Toh;Koji Hase;Kenshiro Oshima.
Nature (2011)
The microbiota regulates type 2 immunity through RORγt+ T cells
Caspar Ohnmacht;Joo Hong Park;Sascha Cording;James B. Wing.
Science (2015)
Uptake through glycoprotein 2 of FimH(+) bacteria by M cells initiates mucosal immune response.
Koji Hase;Kazuya Kawano;Tomonori Nochi;Gemilson Soares Pontes.
Nature (2009)
Gut microbiota–generated metabolites in animal health and disease
Won Jae Lee;Koji Hase.
Nature Chemical Biology (2014)
Cell Differentiation Is a Key Determinant of Cathelicidin LL-37/Human Cationic Antimicrobial Protein 18 Expression by Human Colon Epithelium
Koji Hase;Lars Eckmann;John D. Leopard;Nissi Varki.
Infection and Immunity (2002)
A novel subset of mouse NKT cells bearing the IL-17 receptor B responds to IL-25 and contributes to airway hyperreactivity
Asuka Terashima;Hiroshi Watarai;Sayo Inoue;Etsuko Sekine.
Journal of Experimental Medicine (2008)
Four Di-O-caffeoyl Quinic Acid Derivatives from Propolis. Potent Hepatoprotective Activity in Experimental Liver Injury Models
Purusotam Basnet;Katsumichi Matsushige;Koji Hase;Shigetoshi Kadota.
Biological & Pharmaceutical Bulletin (1996)
Expression of LL-37 by human gastric epithelial cells as a potential host defense mechanism against Helicobacter pylori.
Koji Hase;Masamoto Murakami;Mitsutoshi Iimura;Sheri P Cole.
Gastroenterology (2003)
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