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Page 1
Novel mutations in a Japanese patient with CD19 deficiency.
Kanegane H, Agematsu K, Futatani T, Sira MM, Suga K, Sekiguchi T, van Zelm MC, Miyawaki T. Kanegane H, et al. Among authors: agematsu k. Genes Immun. 2007 Dec;8(8):663-70. doi: 10.1038/sj.gene.6364431. Epub 2007 Sep 20. Genes Immun. 2007. PMID: 17882224
Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry.
Kanegane H, Tsukada S, Iwata T, Futatani T, Nomura K, Yamamoto J, Yoshida T, Agematsu K, Komiyama A, Miyawaki T. Kanegane H, et al. Among authors: agematsu k. Clin Exp Immunol. 2000 Jun;120(3):512-7. doi: 10.1046/j.1365-2249.2000.01244.x. Clin Exp Immunol. 2000. PMID: 10844531 Free PMC article.
X-linked agammaglobulinemia diagnosed in adulthood: a case report.
Mitsui T, Tsukamoto N, Kanegane H, Agematsu K, Sekigami T, Irisawa H, Saitoh T, Uchiumi H, Handa H, Matsushima T, Karasawa M, Murakami H, Miyawaki T, Nojima Y. Mitsui T, et al. Among authors: agematsu k. Int J Hematol. 2006 Aug;84(2):154-7. doi: 10.1532/IJH97.06095. Int J Hematol. 2006. PMID: 16926138
Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity.
Minegishi Y, Saito M, Morio T, Watanabe K, Agematsu K, Tsuchiya S, Takada H, Hara T, Kawamura N, Ariga T, Kaneko H, Kondo N, Tsuge I, Yachie A, Sakiyama Y, Iwata T, Bessho F, Ohishi T, Joh K, Imai K, Kogawa K, Shinohara M, Fujieda M, Wakiguchi H, Pasic S, Abinun M, Ochs HD, Renner ED, Jansson A, Belohradsky BH, Metin A, Shimizu N, Mizutani S, Miyawaki T, Nonoyama S, Karasuyama H. Minegishi Y, et al. Among authors: agematsu k. Immunity. 2006 Nov;25(5):745-55. doi: 10.1016/j.immuni.2006.09.009. Immunity. 2006. PMID: 17088085 Free article.
Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway.
Nomura K, Kanegane H, Karasuyama H, Tsukada S, Agematsu K, Murakami G, Sakazume S, Sako M, Tanaka R, Kuniya Y, Komeno T, Ishihara S, Hayashi K, Kishimoto T, Miyawaki T. Nomura K, et al. Among authors: agematsu k. Blood. 2000 Jul 15;96(2):610-7. Blood. 2000. PMID: 10887125 Free article.
Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia.
Cho K, Yamada M, Agematsu K, Kanegane H, Miyake N, Ueki M, Akimoto T, Kobayashi N, Ikemoto S, Tanino M, Fujita A, Hayasaka I, Miyamoto S, Tanaka-Kubota M, Nakata K, Shiina M, Ogata K, Minakami H, Matsumoto N, Ariga T. Cho K, et al. Among authors: agematsu k. Am J Hum Genet. 2018 Mar 1;102(3):480-486. doi: 10.1016/j.ajhg.2018.01.019. Epub 2018 Feb 15. Am J Hum Genet. 2018. PMID: 29455859 Free PMC article.
188 results