His scientific interests lie mostly in Pyrene, Carcinogen, Benzopyrene, Stereochemistry and Diol. His Pyrene research is multidisciplinary, incorporating perspectives in Medicinal chemistry, Mutagen, Phenols, Epoxy and Metabolism. His Carcinogen research incorporates elements of Metabolite, Toxicology and Chrysene.
His research integrates issues of Methylcholanthrene, Toxicity and Chinese hamster in his study of Benzopyrene. The Stereochemistry study combines topics in areas such as Benzophenanthrene, Mouse skin and DNA. His studies deal with areas such as Adduct, Enantiomer and Diastereomer as well as Diol.
Stereochemistry, Pyrene, Diol, Carcinogen and Benzopyrene are his primary areas of study. His study in Stereochemistry is interdisciplinary in nature, drawing from both Adduct, DNA, Deoxyadenosine and Benzophenanthrene. His Pyrene study combines topics in areas such as Medicinal chemistry, Molecular biology, Phenols, Microsome and Metabolism.
Diol is a subfield of Organic chemistry that Haruhiko Yagi explores. His work in Carcinogen addresses subjects such as Monooxygenase, which are connected to disciplines such as Cytochrome. He works in the field of Benzopyrene, focusing on Benzopyrene in particular.
Haruhiko Yagi focuses on Stereochemistry, Diol, Pyrene, Adduct and Benzopyrene. Haruhiko Yagi interconnects Deoxyguanosine, Oligonucleotide, DNA and Nucleotide in the investigation of issues within Stereochemistry. The Diol study which covers Benzophenanthrene that intersects with Mutagenesis.
His work carried out in the field of Pyrene brings together such families of science as Phenanthrene, Hydrolysis, Urine, Creatinine and A-DNA. Haruhiko Yagi combines subjects such as Chromatography, Polycyclic aromatic hydrocarbon and Carcinogen with his study of Phenanthrene. His Benzopyrene research is multidisciplinary, relying on both Yield and Group.
The scientist’s investigation covers issues in Stereochemistry, Pyrene, Adduct, Immune system and Cytotoxic T cell. His Stereochemistry research incorporates themes from DNA polymerase, Base pair and Benzopyrene. His research in Pyrene tackles topics such as Phenanthrene which are related to areas like Chromatography, Carcinogen and Biochemistry.
His Adduct study combines topics in areas such as Diol and Deoxyadenosine. His study with Diol involves better knowledge in Organic chemistry. His study focuses on the intersection of Immune system and fields such as Ovarian cancer with connections in the field of Antibody.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Foxp3+CD25+CD4+ natural regulatory T cells in dominant self-tolerance and autoimmune disease
Shimon Sakaguchi;Masahiro Ono;Ruka Setoguchi;Haruhiko Yagi.
Immunological Reviews (2006)
Programmed cell death 1 ligand 1 and tumor-infiltrating CD8+ T lymphocytes are prognostic factors of human ovarian cancer.
Junzo Hamanishi;Masaki Mandai;Masashi Iwasaki;Taku Okazaki.
Proceedings of the National Academy of Sciences of the United States of America (2007)
Crucial role of FOXP3 in the development and function of human CD25+CD4+ regulatory T cells
Haruhiko Yagi;Takashi Nomura;Kyoko Nakamura;Sayuri Yamazaki.
International Immunology (2004)
Tumorigenicity of the optical enantiomers of the diastereomeric benzo[a]pyrene 7,8-diol-9,10-epoxides in newborn mice: exceptional activity of (+)-7beta,8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene
M K Buening;P G Wislocki;W Levin;H Yagi.
Proceedings of the National Academy of Sciences of the United States of America (1978)
Metabolism of benzo(a)pyrene and benzo (a)pyrene derivatives to mutagenic products by highly purified hepatic microsomal enzymes.
A W Wood;W Levin;A Y Lu;H Yagi.
Journal of Biological Chemistry (1976)
Inhibition of the Mutagenicity of Bay-Region Diol Epoxides of Polycyclic Aromatic Hydrocarbons by Naturally Occurring Plant Phenols: Exceptional Activity of Ellagic Acid
Alexander W. Wood;Mou-Tuan Huang;Richard L. Chang;Harold L. Newmark.
Proceedings of the National Academy of Sciences of the United States of America (1982)
Marked Differences in the Skin Tumor-initiating Activities of the Optical Enantiomers of the Diastereomeric Benzo(a)pyrene 7,8-Diol-9,10-Epoxides
T. J. Slaga;W. J. Bracken;G. Gleason;W. Levin.
Cancer Research (1979)
Tumorigenicity studies with diol-epoxides of benzo(a)pyrene which indicate that (+/-)-trans-7beta,8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo(a)pyrene is an ultimate carcinogen in newborn mice.
Jaime Kapitulnik;Peter G. Wislocki;Wayne Levin;Haruhiko Yagi.
Cancer Research (1978)
Metabolism of benzo[a]pyrene: conversion of (+/-)-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene to highly mutagenic 7,8-diol-9,10-epoxides
D. R. Thakker;H. Yagi;A. Y.H. Lu;W. Levin.
Proceedings of the National Academy of Sciences of the United States of America (1976)
Metabolism of benzo[a]pyrene. VI. Stereoselective metabolism of benzo[a]pyrene and benzo[a]pyrene 7,8-dihydrodiol to diol epoxides.
D.R. Thakker;H. Yagi;H. Akagi;M. Koreeda.
Chemico-Biological Interactions (1977)
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