Asou N - Search Results

1

Concurrent transcriptional deregulation of AML1/RUNX1 and GATA factors by the AML1-TRPS1 chimeric gene in t(8;21)(q24;q22) acute myeloid leukemia.

Asou N, Yanagida M, Huang L, Yamamoto M, Shigesada K, Mitsuya H, Ito Y, Osato M. Asou N, et al. Blood. 2007 May 1;109(9):4023-7. doi: 10.1182/blood-2006-01-031781. Epub 2007 Jan 23. Blood. 2007. PMID: 17244685 Free article.

2

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.

Michaud J, Wu F, Osato M, Cottles GM, Yanagida M, Asou N, Shigesada K, Ito Y, Benson KF, Raskind WH, Rossier C, Antonarakis SE, Israels S, McNicol A, Weiss H, Horwitz M, Scott HS. Michaud J, et al. Among authors: asou n. Blood. 2002 Feb 15;99(4):1364-72. doi: 10.1182/blood.v99.4.1364. Blood. 2002. PMID: 11830488 Free article.

3

Hematopoietic stem cells acquire survival advantage by loss of RUNX1 methylation identified in familial leukemia.

Matsumura T, Nakamura-Ishizu A, Muddineni SSNA, Tan DQ, Wang CQ, Tokunaga K, Tirado-Magallanes R, Sian S, Benoukraf T, Okuda T, Asou N, Matsuoka M, Osato M, Suda T. Matsumura T, et al. Among authors: asou n. Blood. 2020 Oct 22;136(17):1919-1932. doi: 10.1182/blood.2019004292. Blood. 2020. PMID: 32573733 Free article.

4

Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias.

Osato M, Asou N, Abdalla E, Hoshino K, Yamasaki H, Okubo T, Suzushima H, Takatsuki K, Kanno T, Shigesada K, Ito Y. Osato M, et al. Among authors: asou n. Blood. 1999 Mar 15;93(6):1817-24. Blood. 1999. PMID: 10068652 Free article.

5

Dual mutations in the AML1 and FLT3 genes are associated with leukemogenesis in acute myeloblastic leukemia of the M0 subtype.

Matsuno N, Osato M, Yamashita N, Yanagida M, Nanri T, Fukushima T, Motoji T, Kusumoto S, Towatari M, Suzuki R, Naoe T, Nishii K, Shigesada K, Ohno R, Mitsuya H, Ito Y, Asou N. Matsuno N, et al. Among authors: asou n. Leukemia. 2003 Dec;17(12):2492-9. doi: 10.1038/sj.leu.2403160. Leukemia. 2003. PMID: 14562119

6

Heterozygous PU.1 mutations are associated with acute myeloid leukemia.

Mueller BU, Pabst T, Osato M, Asou N, Johansen LM, Minden MD, Behre G, Hiddemann W, Ito Y, Tenen DG. Mueller BU, et al. Among authors: asou n. Blood. 2002 Aug 1;100(3):998-1007. doi: 10.1182/blood.v100.3.998. Blood. 2002. PMID: 12130514 Free article.

7

Heterozygous PU.1 mutations are associated with acute myeloid leukemia.

Mueller BU, Pabst T, Osato M, Asou N, Johansen LM, Minden MD, Behre G, Hiddemann W, Ito Y, Tenen DG. Mueller BU, et al. Among authors: asou n. Blood. 2003 Mar 1;101(5):2074. doi: 10.1182/blood-2002-12-3903. Blood. 2003. PMID: 12584148 Free article. No abstract available.

8

Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice.

Yamashita N, Osato M, Huang L, Yanagida M, Kogan SC, Iwasaki M, Nakamura T, Shigesada K, Asou N, Ito Y. Yamashita N, et al. Among authors: asou n. Br J Haematol. 2005 Nov;131(4):495-507. doi: 10.1111/j.1365-2141.2005.05793.x. Br J Haematol. 2005. PMID: 16281942 Free article.

9

A family harboring a germ-line N-terminal C/EBPalpha mutation and development of acute myeloid leukemia with an additional somatic C-terminal C/EBPalpha mutation.

Nanri T, Uike N, Kawakita T, Iwanaga E, Mitsuya H, Asou N. Nanri T, et al. Among authors: asou n. Genes Chromosomes Cancer. 2010 Mar;49(3):237-41. doi: 10.1002/gcc.20734. Genes Chromosomes Cancer. 2010. PMID: 19953636

10

Stem cell exhaustion due to Runx1 deficiency is prevented by Evi5 activation in leukemogenesis.

Jacob B, Osato M, Yamashita N, Wang CQ, Taniuchi I, Littman DR, Asou N, Ito Y. Jacob B, et al. Among authors: asou n. Blood. 2010 Feb 25;115(8):1610-20. doi: 10.1182/blood-2009-07-232249. Epub 2009 Dec 14. Blood. 2010. PMID: 20008790 Free PMC article.

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