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210 results

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Page 1
Assessment of type I interferon signatures in undifferentiated inflammatory diseases: A Japanese multicenter experience.
Miyamoto T, Honda Y, Izawa K, Kanazawa N, Kadowaki S, Ohnishi H, Fujimoto M, Kambe N, Kase N, Shiba T, Nakagishi Y, Akizuki S, Murakami K, Bamba M, Nishida Y, Inui A, Fujisawa T, Nishida D, Iwata N, Otsubo Y, Ishimori S, Nishikori M, Tanizawa K, Nakamura T, Ueda T, Ohwada Y, Tsuyusaki Y, Shimizu M, Ebato T, Iwao K, Kubo A, Kawai T, Matsubayashi T, Miyazaki T, Kanayama T, Nishitani-Isa M, Nihira H, Abe J, Tanaka T, Hiejima E, Okada S, Ohara O, Saito MK, Takita J, Nishikomori R, Yasumi T. Miyamoto T, et al. Among authors: matsubayashi t. Front Immunol. 2022 Sep 23;13:905960. doi: 10.3389/fimmu.2022.905960. eCollection 2022. Front Immunol. 2022. PMID: 36211342 Free PMC article.
Disease-associated CIAS1 mutations induce monocyte death, revealing low-level mosaicism in mutation-negative cryopyrin-associated periodic syndrome patients.
Saito M, Nishikomori R, Kambe N, Fujisawa A, Tanizaki H, Takeichi K, Imagawa T, Iehara T, Takada H, Matsubayashi T, Tanaka H, Kawashima H, Kawakami K, Kagami S, Okafuji I, Yoshioka T, Adachi S, Heike T, Miyachi Y, Nakahata T. Saito M, et al. Among authors: matsubayashi t. Blood. 2008 Feb 15;111(4):2132-41. doi: 10.1182/blood-2007-06-094201. Epub 2007 Dec 6. Blood. 2008. PMID: 18063752 Free article.
Febrile attacks triggered by milk allergy in an infant with mevalonate kinase deficiency.
Nakashimai H, Miyake F, Ohki S, Hattori S, Matsubayashi T, Izawa K, Nishikomori R, Heike T, Honda Y, Shigematsu Y. Nakashimai H, et al. Among authors: matsubayashi t. Rheumatol Int. 2016 Oct;36(10):1477-8. doi: 10.1007/s00296-016-3522-3. Epub 2016 Jul 7. Rheumatol Int. 2016. PMID: 27387687 Free PMC article. No abstract available.
Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry.
Kadowaki T, Ohnishi H, Kawamoto N, Kadowaki S, Hori T, Nishimura K, Kobayashi C, Shigemura T, Ogata S, Inoue Y, Hiejima E, Izawa K, Matsubayashi T, Matsumoto K, Imai K, Nishikomori R, Ito S, Kanegane H, Fukao T. Kadowaki T, et al. Among authors: matsubayashi t. Clin Immunol. 2020 Jul;216:108441. doi: 10.1016/j.clim.2020.108441. Epub 2020 Apr 23. Clin Immunol. 2020. PMID: 32335289
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations.
Sakata S, Tsumura M, Matsubayashi T, Karakawa S, Kimura S, Tamaura M, Okano T, Naruto T, Mizoguchi Y, Kagawa R, Nishimura S, Imai K, Le Voyer T, Casanova JL, Bustamante J, Morio T, Ohara O, Kobayashi M, Okada S. Sakata S, et al. Among authors: matsubayashi t. Int Immunol. 2020 Sep 30;32(10):663-671. doi: 10.1093/intimm/dxaa043. Int Immunol. 2020. PMID: 32603428
Augmentation of Stimulator of Interferon Genes-Induced Type I Interferon Production in COPA Syndrome.
Kato T, Yamamoto M, Honda Y, Orimo T, Sasaki I, Murakami K, Hemmi H, Fukuda-Ohta Y, Isono K, Takayama S, Nakamura H, Otsuki Y, Miyamoto T, Takita J, Yasumi T, Nishikomori R, Matsubayashi T, Izawa K, Kaisho T. Kato T, et al. Among authors: matsubayashi t. Arthritis Rheumatol. 2021 Nov;73(11):2105-2115. doi: 10.1002/art.41790. Arthritis Rheumatol. 2021. PMID: 33982886
Increased levels of cytokines and high-mobility group box 1 are associated with the development of severe pneumonia, but not acute encephalopathy, in 2009 H1N1 influenza-infected children.
Ito Y, Torii Y, Ohta R, Imai M, Hara S, Kawano Y, Matsubayashi T, Inui A, Yoshikawa T, Nishimura N, Ozaki T, Morishima T, Kimura H. Ito Y, et al. Among authors: matsubayashi t. Cytokine. 2011 Nov;56(2):180-7. doi: 10.1016/j.cyto.2011.07.016. Epub 2011 Sep 8. Cytokine. 2011. PMID: 21862344
210 results