Author

J. Ogawa

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 2 Immunology· 1 Plant Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:host-pathogen & immune response· 3 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Organism:E. coli· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

S. Kishino· 2 shared A. Ando· 1 shared A. L. Ryan (Firth)· 1 shared A. M. Poole· 1 shared A. M. Rickerby· 1 shared A. Shibata· 1 shared A. Sugiyama· 1 shared A. Yamamoto· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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Curved chords = mutual co-authorship

2 shared papersPlant Biology

S. Kishino

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Discovery of an isoflavone oxidative catabolic pathway in legume root microbiota

N. Aoki, T. Shimasaki, W. Yazaki, T. Sato, M. Nakayasu, A. Ando, S. Kishino, J. Ogawa, S. Masuda, A. Shibata, K. Shirasu, K. Yazaki, A. Sugiyama

The paper identifies an oxidative isoflavone catabolic pathway in legume root microbiota, revealing its role in detoxifying isoflavones and shaping microbiota interactions.

bioRxiv · Aug 7, 2023 · PreprintPlant Biology

The gut lactic acid bacteria metabolite, 10-oxo-cis-6,trans-11-octadecadienoic acid, suppresses inflammatory bowel disease in mice by modulating the NRF2 pathway and GPCR-signaling

M. Ando, K. Nagata, R. Takeshita, N. Ito, S. Noguchi, N. Minamikawa, N. Kodama, A. Yamamoto, T. Yashiro, M. Hachisu, G. Ichihara, S. Kishino, M. Yamamoto, J. Ogawa, C. Nishiyama

This study identifies 10-oxo-cis-6,trans-11-octadecadienoic acid as an anti-inflammatory metabolite that suppresses colitis in mice via NRF2 pathway activation and GPCR signaling.

bioRxiv · Feb 22, 2023Immunology

Characterisation of an Escherichia coli line that completely lacks ribonucleotide reduction yields insights into the evolution of obligate intracellularity.

S. D. M. Arras, N. Sibaeva, R. J. Catchpole, N. Horinouchi, D. Si, A. M. Rickerby, K. Deguchi, M. Hibi, K. Tanaka, M. Takeuchi, J. Ogawa, A. M. Poole

This paper creates an E. coli strain lacking ribonucleotide reduction and shows it adapts to depend on host-derived deoxyribonucleotides, mimicking evolutionary steps in obligate intracellular life.

bioRxiv · Sep 28, 2022Microbiology

The D614G mutation in the SARS-CoV2 Spike protein increases infectivity in an ACE2 receptor dependent manner

J. Ogawa, W. Zhu, N. Tonnu, O. Singer, T. Hunter, A. L. Ryan (Firth), G. M. Pao

The paper shows the D614G mutation in SARS-CoV-2 Spike protein increases infectivity via ACE2 receptor binding.

bioRxiv · Jul 21, 2020 · PreprintMicrobiology