2023 - Research.com Medicine in Japan Leader Award
2023 - Research.com Molecular Biology in Japan Leader Award
2022 - Research.com Best Scientist Award
2022 - Research.com Genetics and Molecular Biology in Japan Leader Award
Masayuki Yamamoto mainly focuses on Transcription factor, Biochemistry, Cell biology, Molecular biology and KEAP1. The concepts of his Transcription factor study are interwoven with issues in Regulation of gene expression and Transcription. His studies in Cell biology integrate themes in fields like Kelch-Like ECH-Associated Protein 1, Receptor, Oxidative phosphorylation and Autophagy.
The various areas that he examines in his Molecular biology study include Maf Transcription Factors, Gene expression, Transgene, Cellular differentiation and GCLM. His work focuses on many connections between KEAP1 and other disciplines, such as Cancer cell, that overlap with his field of interest in Cancer research. His Glutathione research focuses on Oxidative stress and how it connects with Immunology, Pathogenesis and Inflammation.
His scientific interests lie mostly in Cell biology, Molecular biology, Internal medicine, Transcription factor and Gene. His Cell biology research integrates issues from Schizosaccharomyces pombe, KEAP1, Biochemistry and Meiosis. His Molecular biology research is multidisciplinary, incorporating elements of Gene expression, Transgene, Cellular differentiation, Mutant and Regulation of gene expression.
His work deals with themes such as Gastroenterology, Endocrinology and Oncology, which intersect with Internal medicine. Gene is a subfield of Genetics that Masayuki Yamamoto investigates. His Oxidative stress research incorporates elements of Reactive oxygen species, Glutathione and Immunology.
Cell biology, Internal medicine, Cancer research, Genetics and KEAP1 are his primary areas of study. His Cell biology study combines topics from a wide range of disciplines, such as Schizosaccharomyces pombe, Mutant, Transcription factor, Downregulation and upregulation and Regulation of gene expression. His Schizosaccharomyces pombe study integrates concerns from other disciplines, such as Meiosis and Ploidy.
Internal medicine is frequently linked to Endocrinology in his study. His Cancer research research incorporates themes from Carcinogenesis, Cell culture and Haematopoiesis, GATA2. His Genetics study frequently draws parallels with other fields, such as Disease.
His main research concerns Cell biology, Oxidative stress, Transcription factor, KEAP1 and Cancer research. His work carried out in the field of Cell biology brings together such families of science as Inflammation, Schizosaccharomyces pombe, Regulation of gene expression and Oxidative phosphorylation. His research in Regulation of gene expression intersects with topics in Promoter and Molecular biology.
His research integrates issues of Autophagy, Reactive oxygen species and Pathology in his study of Oxidative stress. His Transcription factor research includes elements of Cancer cell, Ubiquitin, Ubiquitin ligase and Detoxification. His research investigates the connection between KEAP1 and topics such as Activator that intersect with issues in Osteoclast.
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.
AN NRF2/SMALL MAF HETERODIMER MEDIATES THE INDUCTION OF PHASE II DETOXIFYING ENZYME GENES THROUGH ANTIOXIDANT RESPONSE ELEMENTS
Ken Itoh;Tomoki Chiba;Satoru Takahashi;Tetsuro Ishii.
Biochemical and Biophysical Research Communications (1997)
Keap1 represses nuclear activation of antioxidant responsive elements by Nrf2 through binding to the amino-terminal Neh2 domain
Ken Itoh;Nobunao Wakabayashi;Yasutake Katoh;Tetsuro Ishii.
Genes & Development (1999)
Homeostatic Levels of p62 Control Cytoplasmic Inclusion Body Formation in Autophagy-Deficient Mice
Masaaki Komatsu;Satoshi Waguri;Masato Koike;Yu shin Sou;Yu shin Sou.
Cell (2007)
Oxidative Stress Sensor Keap1 Functions as an Adaptor for Cul3-Based E3 Ligase To Regulate Proteasomal Degradation of Nrf2
Akira Kobayashi;Moon Il Kang;Hiromi Okawa;Makiko Ohtsuji.
Molecular and Cellular Biology (2004)
Transcription Factor Nrf2 Coordinately Regulates a Group of Oxidative Stress-inducible Genes in Macrophages
Tetsuro Ishii;Ken Itoh;Satoru Takahashi;Hideyo Sato.
Journal of Biological Chemistry (2000)
The selective autophagy substrate p62 activates the stress responsive transcription factor Nrf2 through inactivation of Keap1
Masaaki Komatsu;Hirofumi Kurokawa;Satoshi Waguri;Keiko Taguchi.
Nature Cell Biology (2010)
Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants
Albena T. Dinkova-Kostova;W. David Holtzclaw;Robert N. Cole;Ken Itoh.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Nrf2-Keap1 defines a physiologically important stress response mechanism.
Hozumi Motohashi;Masayuki Yamamoto.
Trends in Molecular Medicine (2004)
Essential Bacillus subtilis genes
K. Kobayashi;S.D. Ehrlich;A. Albertini;G. Amati.
Proceedings of the National Academy of Sciences of the United States of America (2003)
A promoter-level mammalian expression atlas
Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Nature (2014)
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