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The landscape of somatic mutations in Down syndrome-related myeloid disorders.
Yoshida K, Toki T, Okuno Y, Kanezaki R, Shiraishi Y, Sato-Otsubo A, Sanada M, Park MJ, Terui K, Suzuki H, Kon A, Nagata Y, Sato Y, Wang R, Shiba N, Chiba K, Tanaka H, Hama A, Muramatsu H, Hasegawa D, Nakamura K, Kanegane H, Tsukamoto K, Adachi S, Kawakami K, Kato K, Nishimura R, Izraeli S, Hayashi Y, Miyano S, Kojima S, Ito E, Ogawa S. Yoshida K, et al. Among authors: kato k. Nat Genet. 2013 Nov;45(11):1293-9. doi: 10.1038/ng.2759. Epub 2013 Sep 22. Nat Genet. 2013. PMID: 24056718
Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.
Furuta T, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sugiura M, Sone M, Hiramatsu M, Sugiura S, Ando F, Shimokata H, Nakashima T. Furuta T, et al. Among authors: kato k. Int J Immunogenet. 2011 Jun;38(3):249-54. doi: 10.1111/j.1744-313X.2011.01004.x. Epub 2011 Mar 9. Int J Immunogenet. 2011. PMID: 21385326
PBSCT is associated with poorer survival and increased chronic GvHD than BMT in Japanese paediatric patients with acute leukaemia and an HLA-matched sibling donor.
Shinzato A, Tabuchi K, Atsuta Y, Inoue M, Inagaki J, Yabe H, Koh K, Kato K, Ohta H, Kigasawa H, Kitoh T, Ogawa A, Takahashi Y, Sasahara Y, Kato S, Adachi S. Shinzato A, et al. Among authors: kato s, kato k. Pediatr Blood Cancer. 2013 Sep;60(9):1513-9. doi: 10.1002/pbc.24524. Epub 2013 Mar 19. Pediatr Blood Cancer. 2013. PMID: 23512888
9,694 results