Inohara, Naohiro

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature

Inflammatory Bowel DiseaseImmune Response and Inflammation

Cited by 5,030

Control of pathogens and pathobionts by the gut microbiota

Kamada, N., Chen, G. Y., Inohara, N., & Núñez, G. (2013) · Nature Immunology

Gut microbiota and healthClostridium difficile and Clostridium perfringens research

Cited by 1,625

Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1β in salmonella-infected macrophages

Franchi, L., Amer, A., Body-Malapel, M., Kanneganti, T.-D., Özören, N., Jagirdar, R., Inohara, N., Vandenabeele, P., Bertin, J., Coyle, A., et al. (2006) · Nature Immunology

Immune Response and InflammationInflammasome and immune disorders

Cited by 1,131

NOD1 and NOD2: Signaling, Host Defense, and Inflammatory Disease

Caruso, R., Warner, N., Inohara, N., & Núñez, G. (2014) · Immunity

Immune Response and InflammationInflammasome and immune disorders

Cited by 830

Nod1, an Apaf-1-like Activator of Caspase-9 and Nuclear Factor-κB

Inohara, N., Koseki, T., del Peso, L., Hu, Y., Yee, C., Chen, S., Carrio, R., Merino, J., Liu, D., Ni, J., et al. (1999) · Journal of Biological Chemistry

Cell death mechanisms and regulationNF-κB Signaling Pathways

Cited by 742

Staphylococcus δ-toxin induces allergic skin disease by activating mast cells

Nakamura, Y., Oscherwitz, J., Cease, K. B., Chan, S. M., Muñoz-Planillo, R., Hasegawa, M., Villaruz, A. E., Cheung, G. Y. C., McGavin, M. J., Travers, J. B., et al. (2013) · Nature

Dermatology and Skin DiseasesMast cells and histamine

Cited by 558

Gut Microbiota-Induced Immunoglobulin G Controls Systemic Infection by Symbiotic Bacteria and Pathogens

Zeng, M. Y., Cisalpino, D., Varadarajan, S., Hellman, J., Warren, H. S., Cascalho, M., Inohara, N., & Núñez, G. (2016) · Immunity

Gut microbiota and healthImmune Response and Inflammation

Cited by 417

Microbial Metabolite Signaling Is Required for Systemic Iron Homeostasis

Das, N. K., Schwartz, A. J., Barthel, G., Inohara, N., Liu, Q., Sankar, A., Hill, D. R., Ma, X., Lamberg, O., Schnizlein, M. K., et al. (2020) · Cell Metabolism

Iron Metabolism and DisordersGut microbiota and health

Cited by 331

Distinct Commensals Induce Interleukin-1β via NLRP3 Inflammasome in Inflammatory Monocytes to Promote Intestinal Inflammation in Response to Injury

Seo, S.-U., Kamada, N., Muñoz-Planillo, R., Kim, Y.-G., Kim, D., Koizumi, Y., Hasegawa, M., Himpsl, S. D., Browne, H. P., Lawley, T. D., et al. (2015) · Immunity

Inflammasome and immune disordersImmune Response and Inflammation

Cited by 318

A specific gene-microbe interaction drives the development of Crohn’s disease–like colitis in mice

Caruso, R., Mathes, T., Martens, E. C., Kamada, N., Nusrat, A., Inohara, N., & Núñez, G. (2019) · Science Immunology

Inflammatory Bowel DiseaseGut microbiota and health

Cited by 185

IL-22 controls iron-dependent nutritional immunity against systemic bacterial infections

Sakamoto, K., Kim, Y.-G., Hara, H., Kamada, N., Caballero-Flores, G., Tolosano, E., Soares, M. P., Puente, J. L., Inohara, N., & Núñez, G. (2017) · Science Immunology

Hemoglobin structure and functionImmune Response and Inflammation

Cited by 127

Maternal Immunization Confers Protection to the Offspring against an Attaching and Effacing Pathogen through Delivery of IgG in Breast Milk

Caballero-Flores, G., Sakamoto, K., Zeng, M. Y., Wang, Y., Hakim, J., Matus-Acuña, V., Inohara, N., & Núñez, G. (2019) · Cell Host & Microbe

Escherichia coli research studiesInfant Nutrition and Health

Cited by 111