Nannya Y - Search Results

1

Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome.

Guzzi N, Muthukumar S, Cieśla M, Todisco G, Ngoc PCT, Madej M, Munita R, Fazio S, Ekström S, Mortera-Blanco T, Jansson M, Nannya Y, Cazzola M, Ogawa S, Malcovati L, Hellström-Lindberg E, Dimitriou M, Bellodi C. Guzzi N, et al. Among authors: nannya y. Nat Cell Biol. 2022 Mar;24(3):299-306. doi: 10.1038/s41556-022-00852-9. Epub 2022 Mar 15. Nat Cell Biol. 2022. PMID: 35292784 Free PMC article.

2

Molecular cytogenetic analyses of HIG, a novel human cell line carrying t(1;3)(p36.3;q25.3) established from a patient with chronic myelogenous leukemia in blastic crisis.

Hosoya N, Ogawa S, Motokura T, Hangaishi A, Wang L, Qiao Y, Nannya Y, Kogi M, Hirai H. Hosoya N, et al. Among authors: nannya y. Int J Hematol. 2003 Dec;78(5):432-8. doi: 10.1007/BF02983816. Int J Hematol. 2003. PMID: 14704036

3

Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation.

Hosoya N, Qiao Y, Hangaishi A, Wang L, Nannya Y, Sanada M, Kurokawa M, Chiba S, Hirai H, Ogawa S. Hosoya N, et al. Among authors: nannya y. Genes Chromosomes Cancer. 2005 Mar;42(3):269-79. doi: 10.1002/gcc.20147. Genes Chromosomes Cancer. 2005. PMID: 15611931

4

Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project.

Nannya Y, Taura K, Kurokawa M, Chiba S, Ogawa S. Nannya Y, et al. Hum Mol Genet. 2007 Oct 15;16(20):2494-505. doi: 10.1093/hmg/ddm205. Epub 2007 Jul 31. Hum Mol Genet. 2007. PMID: 17666406

5

Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype.

Akagi T, Ogawa S, Dugas M, Kawamata N, Yamamoto G, Nannya Y, Sanada M, Miller CW, Yung A, Schnittger S, Haferlach T, Haferlach C, Koeffler HP. Akagi T, et al. Among authors: nannya y. Haematologica. 2009 Feb;94(2):213-23. doi: 10.3324/haematol.13024. Epub 2009 Jan 14. Haematologica. 2009. PMID: 19144660 Free PMC article.

6

Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation.

Yoshizato T, Nannya Y, Atsuta Y, Shiozawa Y, Iijima-Yamashita Y, Yoshida K, Shiraishi Y, Suzuki H, Nagata Y, Sato Y, Kakiuchi N, Matsuo K, Onizuka M, Kataoka K, Chiba K, Tanaka H, Ueno H, Nakagawa MM, Przychodzen B, Haferlach C, Kern W, Aoki K, Itonaga H, Kanda Y, Sekeres MA, Maciejewski JP, Haferlach T, Miyazaki Y, Horibe K, Sanada M, Miyano S, Makishima H, Ogawa S. Yoshizato T, et al. Among authors: nannya y. Blood. 2017 Apr 27;129(17):2347-2358. doi: 10.1182/blood-2016-12-754796. Epub 2017 Feb 21. Blood. 2017. PMID: 28223278 Free PMC article.

7

Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice.

Kon A, Yamazaki S, Nannya Y, Kataoka K, Ota Y, Nakagawa MM, Yoshida K, Shiozawa Y, Morita M, Yoshizato T, Sanada M, Nakayama M, Koseki H, Nakauchi H, Ogawa S. Kon A, et al. Among authors: nannya y. Blood. 2018 Feb 8;131(6):621-635. doi: 10.1182/blood-2017-01-762393. Epub 2017 Nov 16. Blood. 2018. PMID: 29146882 Free PMC article.

8

Progression to polythythemia vera from familial thrombocytosis with germline JAK2 R867Q mutation.

Maie K, Yokoyama Y, Yano Y, Kato T, Nannya Y, Ogawa S, Noguchi M, Sakata-Yanagimoto M, Chiba S. Maie K, et al. Among authors: nannya y. Ann Hematol. 2018 Apr;97(4):737-739. doi: 10.1007/s00277-017-3209-1. Epub 2018 Jan 24. Ann Hematol. 2018. PMID: 29368262 No abstract available.

9

[Relationship between clinical features and somatic gene mutations in myelodysplastic syndrome].

Hirasawa N, Sakata-Yanagimoto M, Nannya Y, Hattori K, Suehara Y, Kato T, Yokoyama Y, Kurita N, Obara N, Ogawa S, Hasegawa Y, Chiba S. Hirasawa N, et al. Among authors: nannya y. Rinsho Ketsueki. 2018;59(1):80-83. doi: 10.11406/rinketsu.59.80. Rinsho Ketsueki. 2018. PMID: 29415943 Japanese.

10

Infection perturbs Bach2- and Bach1-dependent erythroid lineage 'choice' to cause anemia.

Kato H, Itoh-Nakadai A, Matsumoto M, Ishii Y, Watanabe-Matsui M, Ikeda M, Ebina-Shibuya R, Sato Y, Kobayashi M, Nishizawa H, Suzuki K, Muto A, Fujiwara T, Nannya Y, Malcovati L, Cazzola M, Ogawa S, Harigae H, Igarashi K. Kato H, et al. Among authors: nannya y. Nat Immunol. 2018 Oct;19(10):1059-1070. doi: 10.1038/s41590-018-0202-3. Epub 2018 Sep 24. Nat Immunol. 2018. PMID: 30250186

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