論文・総説 - 今井　耕輔

281. 今井 耕輔. WASPの異常と免疫不全症 免疫Immunology Frontier. 2000.10; 10 (5): 335-341.

282. 瀧本浩幸, 今井耕輔, 浅野貴子, 亀井宏一, 小林克樹, 水沢慵一, 下田益弘, 竹田篤, 大川洋二, 矢田純一, 新村文男. 重症全身性エリテマトーデスに対する自己末梢血幹細胞移植時に急性腎不全を合併した1例 日本小児腎不全学会雑誌. 2000.08; 20 187-190.

283. 今井 耕輔. 【期待される開発途上の診断法・治療法】自己免疫疾患に対する造血幹細胞移植療法 小児科. 1999.09; 40 (10): 1327-1331.

284. 今井 耕輔. 【先天性免疫不全症の分子機構】WASP(Wiskott-Aldrich syndrome protein)の分子機構 医学のあゆみ. 1997.09; 182 (10): 731-735.

285. 今井耕輔, 山本 貴子, 伊東 祐之, 吉田 邦枝, 前田 浩利, 梶原 道子, 高木 秀二, 大川 洋二, 平井 莞二, 矢田 純一. 骨髄移植後にEpstein-Barr virusに関連したlymphoproliferative disorderを発症したWiskott-Aldrich症候群の1例 日本小児血液学会雑誌. 1996.06; 10 (3): 210-215.

286. Kracker S, Imai K, Gardes P, Ochs HD, Fischer A, Durandy A. Impaired induction of DNA lesions during immunoglobulin class-switch recombination in humans influences end-joining repair Proc Natl Acad Sci U S A. 2010.12; 107 (51): 22225-22230. ( PubMed, DOI )

287. Albert MH, Bittner TC, Nonoyama S, Notarangelo LD, Burns S, Imai K, Espanol T, Fasth A, Pellier I, Strauss G, Morio T, Gathmann B, Noordzij JG, Fillat C, Hoenig M, Nathrath M, Meindl A, Pagel P, Wintergerst U, Fischer A, Thrasher AJ, Belohradsky BH, Ochs HD. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options Blood. 2010.04; 115 (16): 3231-3238. ( PubMed, DOI )

288. Morinishi Y, Imai K, Nakagawa N, Sato H, Horiuchi K, Ohtsuka Y, Kaneda Y, Taga T, Hisakawa H, Miyaji R, Endo M, Oh-Ishi T, Kamachi Y, Akahane K, Kobayashi C, Tsuchida M, Morio T, Sasahara Y, Kumaki S, Ishigaki K, Yoshida M, Urabe T, Kobayashi N, Okimoto Y, Reichenbach J, Hashii Y, Tsuji Y, Kogawa K, Yamaguchi S, Kanegane H, Miyawaki T, Yamada M, Ariga T, Nonoyama S. Identification of severe combined immunodeficiency by T-cell receptor excision circles quantification using neonatal guthrie cards J Pediatr. 2009.12; 155 (6): 829.

289. Imai K, Shimadzu M, Kubota T, Morio T, Matsunaga T, Park YD, Yoshioka A, Nonoyama S.. Female hyper IgM syndrome type 1 with a chromosomal translocation disrupting CD40LG Biochim Biophys Acta. 2006.03; 1762 (3): 335-340.

290. Imai K, Zhu Y, Revy P, Morio T, Mizutani S, Fischer A, Nonoyama S, Durandy A. Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2 Clin Immunol. 2005.06; 115 (3): 277-285.

291. Imai K, Morio T, Zhu Y, Jin Y, Itoh S, Kajiwara M, Yata J, Mizutani S, Ochs HD, Nonoyama S. Clinical course of patients with WASP gene mutations Blood. 2004.01; 103 (2): 456-464.

292. Imai K, Nonoyama S, Ochs HD.. WASP (Wiskott-Aldrich syndrome protein) gene mutations and phenotype Curr Opin Allergy Clin Immunol.. 2003.12; 3 (6): 427-436.

293. Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, Yel L, Forveille M, Kavli B, Krokan HE, Ochs HD, Fischer A, Durandy A. . Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination Nature Immunology. 2003.10; 4 (10): 1023-1028. ( PubMed, DOI )

294. Imai K, Catalan N, Plebani A, Marodi L, Sanal O, Kumaki S, Nagendran V, Wood P, Glastre C, Sarrot-Reynauld F, Hermine O, Forveille M, Revy P, Fischer A, Durandy A.. Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination J Clin Invest. 2003.07; 112 (1): 136-42.

295. Nadia Catalan, Kohsuke Imai, Patrick Revy, Alain Fischer, Anne Durandy. [Two years after, activation-induced cytidine deaminase has not revealed all of its secrets]. Med Sci (Paris). 2003.02; 19 (2): 139-141. ( PubMed, DOI )

296. Imai K, Nonoyama S, Miki H, Morio T, Fukami K, Zhu Q, Aruffo A, Ochs HD, Yata J, Takenawa T.. The pleckstrin homology domain of the Wiskott-Aldrich syndrome protein is involved in the organization of actin cytoskeleton. Clin Immunol. 1999.08; 92 (2): 128-137.