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Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity.
Moriya K, Nakano T, Honda Y, Tsumura M, Ogishi M, Sonoda M, Nishitani-Isa M, Uchida T, Hbibi M, Mizoguchi Y, Ishimura M, Izawa K, Asano T, Kakuta F, Abukawa D, Rinchai D, Zhang P, Kambe N, Bousfiha A, Yasumi T, Boisson B, Puel A, Casanova JL, Nishikomori R, Ohga S, Okada S, Sasahara Y, Kure S. Moriya K, et al. Among authors: sasahara y. J Exp Med. 2023 Sep 4;220(9):e20212276. doi: 10.1084/jem.20212276. Epub 2023 Jun 5. J Exp Med. 2023. PMID: 37273177 Free PMC article.
Nationwide survey of patients with primary immunodeficiency diseases in Japan.
Ishimura M, Takada H, Doi T, Imai K, Sasahara Y, Kanegane H, Nishikomori R, Morio T, Heike T, Kobayashi M, Ariga T, Tsuchiya S, Nonoyama S, Miyawaki T, Hara T. Ishimura M, et al. Among authors: sasahara y. J Clin Immunol. 2011 Dec;31(6):968-76. doi: 10.1007/s10875-011-9594-7. Epub 2011 Sep 29. J Clin Immunol. 2011. PMID: 21956496 Free article.
Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemia.
Saito Y, Aoki Y, Muramatsu H, Makishima H, Maciejewski JP, Imaizumi M, Rikiishi T, Sasahara Y, Kure S, Niihori T, Tsuchiya S, Kojima S, Matsubara Y. Saito Y, et al. Among authors: sasahara y. Leuk Res. 2012 Aug;36(8):1009-15. doi: 10.1016/j.leukres.2012.04.018. Epub 2012 May 14. Leuk Res. 2012. PMID: 22591685 Free PMC article.
A case series of CAEBV of children and young adults treated with reduced-intensity conditioning and allogeneic bone marrow transplantation: a single-center study.
Watanabe Y, Sasahara Y, Satoh M, Looi CY, Katayama S, Suzuki T, Suzuki N, Ouchi M, Horino S, Moriya K, Nanjyo Y, Onuma M, Kitazawa H, Irie M, Niizuma H, Uchiyama T, Rikiishi T, Kumaki S, Minegishi M, Wada T, Yachie A, Tsuchiya S, Kure S. Watanabe Y, et al. Among authors: sasahara y. Eur J Haematol. 2013 Sep;91(3):242-248. doi: 10.1111/ejh.12151. Epub 2013 Jun 28. Eur J Haematol. 2013. PMID: 23734904
Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome.
Horino S, Sasahara Y, Sato M, Niizuma H, Kumaki S, Abukawa D, Sato A, Imaizumi M, Kanegane H, Kamachi Y, Sasaki S, Terui K, Ito E, Kobayashi I, Ariga T, Tsuchiya S, Kure S. Horino S, et al. Among authors: sasahara y. Pediatr Transplant. 2014 Feb;18(1):E25-30. doi: 10.1111/petr.12184. Epub 2013 Nov 7. Pediatr Transplant. 2014. PMID: 24224516
A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study.
Abe J, Nakamura K, Nishikomori R, Kato M, Mitsuiki N, Izawa K, Awaya T, Kawai T, Yasumi T, Toyoshima I, Hasegawa K, Ohshima Y, Hiragi T, Sasahara Y, Suzuki Y, Kikuchi M, Osaka H, Ohya T, Ninomiya S, Fujikawa S, Akasaka M, Iwata N, Kawakita A, Funatsuka M, Shintaku H, Ohara O, Ichinose H, Heike T. Abe J, et al. Among authors: sasahara y. Rheumatology (Oxford). 2014 Mar;53(3):448-58. doi: 10.1093/rheumatology/ket372. Epub 2013 Dec 3. Rheumatology (Oxford). 2014. PMID: 24300241
198 results