Agematsu K - Search Results

1

Identification of Disease-Promoting HLA Class I and Protective Class II Modifiers in Japanese Patients with Familial Mediterranean Fever.

Yasunami M, Nakamura H, Agematsu K, Nakamura A, Yazaki M, Kishida D, Yachie A, Toma T, Masumoto J, Ida H, Koga T, Kawakami A, Eguchi K, Furukawa H, Nakamura T, Nakamura M, Migita K. Yasunami M, et al. Among authors: agematsu k. PLoS One. 2015 May 14;10(5):e0125938. doi: 10.1371/journal.pone.0125938. eCollection 2015. PLoS One. 2015. PMID: 25974247 Free PMC article.

2

CD27/CD70 interaction augments IgE secretion by promoting the differentiation of memory B cells into plasma cells.

Nagumo H, Agematsu K, Shinozaki K, Hokibara S, Ito S, Takamoto M, Nikaido T, Yasui K, Uehara Y, Yachie A, Komiyama A. Nagumo H, et al. Among authors: agematsu k. J Immunol. 1998 Dec 15;161(12):6496-502. J Immunol. 1998. PMID: 9862673

3

Familial Mediterranean fever in 2 Japanese families.

Shinozaki K, Agematsu K, Yasui K, Nagumo H, Naitoh H, Naganuma K, Komiyama A. Shinozaki K, et al. Among authors: agematsu k. J Rheumatol. 2002 Jun;29(6):1324-5. J Rheumatol. 2002. PMID: 12064853

4

Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families.

Kobayashi N, Agematsu K, Sugita K, Sako M, Nonoyama S, Yachie A, Kumaki S, Tsuchiya S, Ochs HD, Sugita K, Fukushima Y, Komiyama A. Kobayashi N, et al. Among authors: agematsu k. Hum Genet. 2003 Apr;112(4):348-52. doi: 10.1007/s00439-002-0897-x. Epub 2003 Feb 19. Hum Genet. 2003. PMID: 12592555

5

Expansion of clonotype-restricted HLA-identical maternal CD4+ T cells in a patient with severe combined immunodeficiency and a homozygous mutation in the Artemis gene.

Kobayashi N, Agematsu K, Nagumo H, Yasui K, Katsuyama Y, Yoshizawa K, Ota M, Yachie A, Komiyama A. Kobayashi N, et al. Among authors: agematsu k. Clin Immunol. 2003 Aug;108(2):159-66. doi: 10.1016/s1521-6616(03)00095-0. Clin Immunol. 2003. PMID: 12921762

6

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency.

Wada T, Toma T, Okamoto H, Kasahara Y, Koizumi S, Agematsu K, Kimura H, Shimada A, Hayashi Y, Kato M, Yachie A. Wada T, et al. Among authors: agematsu k. Blood. 2005 Sep 15;106(6):2099-101. doi: 10.1182/blood-2005-03-0936. Epub 2005 Apr 21. Blood. 2005. PMID: 15845893 Free article.

7

Anakinra improves sensory deafness in a Japanese patient with Muckle-Wells syndrome, possibly by inhibiting the cryopyrin inflammasome.

Yamazaki T, Masumoto J, Agematsu K, Sawai N, Kobayashi S, Shigemura T, Yasui K, Koike K. Yamazaki T, et al. Among authors: agematsu k. Arthritis Rheum. 2008 Mar;58(3):864-8. doi: 10.1002/art.23261. Arthritis Rheum. 2008. PMID: 18311804 Free article.

8

Adult onset X-linked chronic granulomatous disease in a woman patient caused by a de novo mutation in paternal-origin CYBB gene and skewed inactivation of normal maternal X chromosome.

Gono T, Yazaki M, Agematsu K, Matsuda M, Yasui K, Yamaura M, Hidaka F, Mizukami T, Nunoi H, Kubota T, Ikeda S. Gono T, et al. Among authors: agematsu k. Intern Med. 2008;47(11):1053-6. doi: 10.2169/internalmedicine.47.0919. Epub 2008 Jun 2. Intern Med. 2008. PMID: 18520120 Free article.

9

[Familial Mediterranean fever as representative autoinflammatory disease].

Yamazaki K, Yamazaki T, Masumoto J, Suzuki A, Yazaki M, Agematsu K. Yamazaki K, et al. Among authors: agematsu k. Rinsho Byori. 2009 Apr;57(4):371-81. Rinsho Byori. 2009. PMID: 19489440 Review. Japanese.

10

Clinical and genetic features of familial Mediterranean fever in Japan.

Tsuchiya-Suzuki A, Yazaki M, Nakamura A, Yamazaki K, Agematsu K, Matsuda M, Ikeda S. Tsuchiya-Suzuki A, et al. Among authors: agematsu k. J Rheumatol. 2009 Aug;36(8):1671-6. doi: 10.3899/jrheum.081278. Epub 2009 Jun 16. J Rheumatol. 2009. PMID: 19531756

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