Yamamoto, Masahiro
Center for Infectious Disease Education and Research, The University of Osaka · Immunology Frontier Research Center, The University of Osaka · Research Institute for Microbial Diseases, The University of Osaka · The University of Osaka
17 papers on CoChatORCID 0000-0002-6821-2785
Most cited papers
- Verified
Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses
Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K. J., et al. (2006) · Nature
interferon and immune responsesImmune Response and Inflammation
Cited by 3,888
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Cell Type-Specific Involvement of RIG-I in Antiviral Response
Kato, H., Sato, S., Yoneyama, M., Yamamoto, M., Uematsu, S., Matsui, K., Tsujimura, T., Takeda, K., Fujita, T., Takeuchi, O., et al. (2005) · Immunity
interferon and immune responsesImmune Response and Inflammation
Cited by 1,368
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ATP drives lamina propria TH17 cell differentiation
Atarashi, K., Nishimura, J., Shima, T., Umesaki, Y., Yamamoto, M., Onoue, M., Yagita, H., Ishii, N., Evans, R., Honda, K., et al. (2008) · Nature
Psoriasis: Treatment and PathogenesisT-cell and B-cell Immunology
Cited by 1,089
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Caspase-11 activation requires lysis of pathogen-containing vacuoles by IFN-induced GTPases
Meunier, E., Dick, M. S., Dreier, R. F., Schürmann, N., Broz, D. K., Warming, S., Roose-Girma, M., Bumann, D., Kayagaki, N., Takeda, K., et al. (2014) · Nature
Inflammasome and immune disordersImmune Response and Inflammation
Cited by 485
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The transcription factor IRF1 and guanylate-binding proteins target activation of the AIM2 inflammasome by Francisella infection
Man, S. M., Karki, R., Malireddi, R. K. S., Neale, G., Vogel, P., Yamamoto, M., Lamkanfi, M., & Kanneganti, T.-D. (2015) · Nature Immunology
Inflammasome and immune disordersinterferon and immune responses
Cited by 380
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Guanylate binding proteins promote caspase-11–dependent pyroptosis in response to cytoplasmic LPS
Pilla, D. M., Hagar, J. A., Haldar, A. K., Mason, A. K., Degrandi, D., Pfeffer, K., Ernst, R. K., Yamamoto, M., Miao, E. A., & Coers, J. (2014) · Proceedings of the National Academy of Sciences
Inflammasome and immune disordersinterferon and immune responses
Cited by 357
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IRGB10 Liberates Bacterial Ligands for Sensing by the AIM2 and Caspase-11-NLRP3 Inflammasomes
Man, S. M., Karki, R., Sasai, M., Place, D. E., Kesavardhana, S., Temirov, J., Frase, S., Zhu, Q., Malireddi, R. K. S., Kuriakose, T., et al. (2016) · Cell
Inflammasome and immune disordersImmune Response and Inflammation
Cited by 312
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LC3 lipidation is essential for TFEB activation during the lysosomal damage response to kidney injury
Nakamura, S., Shigeyama, S., Minami, S., Shima, T., Akayama, S., Matsuda, T., Esposito, A., Napolitano, G., Kuma, A., Namba-Hamano, T., et al. (2020) · Nature Cell Biology
Autophagy in Disease and TherapyCalcium signaling and nucleotide metabolism
Cited by 235
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Host immune responses to Toxoplasma gondii
Sasai, M., Pradipta, A., & Yamamoto, M. (2018) · International Immunology
Toxoplasma gondii Research StudiesImmune Response and Inflammation
Cited by 202
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The Nuclear IκB Protein IκBNS Selectively Inhibits Lipopolysaccharide-Induced IL-6 Production in Macrophages of the Colonic Lamina Propria
Hirotani, T., Lee, P. Y., Kuwata, H., Yamamoto, M., Matsumoto, M., Kawase, I., Akira, S., & Takeda, K. (2005) · The Journal of Immunology
NF-κB Signaling PathwaysImmune Response and Inflammation
Cited by 167
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Regulation of lipopolysaccharide-inducible genes by MyD88 and Toll/IL-1 domain containing adaptor inducing IFN-β
Hirotani, T., Yamamoto, M., Kumagai, Y., Uematsu, S., Kawase, I., Takeuchi, O., & Akira, S. (2005) · Biochemical and Biophysical Research Communications
Immune Response and InflammationInflammasome and immune disorders
Cited by 135
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Lipocalin 2-Dependent Inhibition of Mycobacterial Growth in Alveolar Epithelium
Saiga, H., Nishimura, J., Kuwata, H., Okuyama, M., Matsumoto, S., Sato, S., Matsumoto, M., Akira, S., Yoshikai, Y., Honda, K., et al. (2008) · The Journal of Immunology
Tuberculosis Research and EpidemiologyImmune Response and Inflammation
Cited by 133
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Notch restricts lymphatic vessel sprouting induced by vascular endothelial growth factor
Zheng, W., Tammela, T., Yamamoto, M., Anisimov, A., Holopainen, T., Kaijalainen, S., Karpanen, T., Lehti, K., Ylä-Herttuala, S., & Alitalo, K. (2011) · Blood
Lymphatic System and DiseasesAngiogenesis and VEGF in Cancer
Cited by 132
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SARS-CoV-2 infection triggers paracrine senescence and leads to a sustained senescence-associated inflammatory response
Tsuji, S., Minami, S., Hashimoto, R., Konishi, Y., Suzuki, T., Kondo, T., Sasai, M., Torii, S., Ono, C., Shichinohe, S., et al. (2022) · Nature Aging
Telomeres, Telomerase, and SenescenceCOVID-19 Clinical Research Studies
Cited by 84
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Ecto-nucleoside triphosphate diphosphohydrolase 7 controls Th17 cell responses through regulation of luminal ATP in the small intestine
Kusu, T., Kayama, H., Kinoshita, M., Jeon, S. G., Ueda, Y., Goto, Y., Okumura, R., Saiga, H., Kurakawa, T., Ikeda, K., et al. (2013) · The Journal of Immunology
Adenosine and Purinergic SignalingBiochemical and Molecular Research
Cited by 73
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Phospholipase C‐β1 potentiates glucose‐stimulated insulin secretion
Hwang, H.-J., Yang, Y. R., Kim, H. Y., Choi, Y., Park, K.-S., Lee, H., Ma, J. S., Yamamoto, M., Kim, J., Chae, Y. C., et al. (2019) · The FASEB Journal
Pancreatic function and diabetesDiabetes Treatment and Management
Cited by 20
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Mortalin is a novel mediator of erythropoietin signaling
Ohtsuka, R., Abe, Y., Fujii, T., Yamamoto, M., Nishimura, J., Takayanagi, R., & Muta, K. (2007) · European Journal of Haematology
Erythropoietin and Anemia TreatmentHeat shock proteins research
Cited by 14
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