Osato M - Search Results

1

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: osato m. Blood. 2002 Aug 1;100(3):998-1007. doi: 10.1182/blood.v100.3.998. Blood. 2002. PMID: 12130514 Free article.

2

Lack of the expression of EBNA-2 and LMP-1 in T-cell neoplasms possessing Epstein-Barr virus.

Suzushima H, Asou N, Fujimoto T, Nishimura S, Okubo T, Yamasaki H, Osato M, Matsuoka M, Tsukamoto A, Takai K, et al. Suzushima H, et al. Among authors: osato m. Blood. 1995 Jan 15;85(2):480-6. Blood. 1995. PMID: 7812002 Free article.

3

CD4+ CD8+ granular lymphocytic leukemia arising in a patient with acute myeloblastic leukemia.

Suzushima H, Asou N, Eto K, Nishimura S, Okubo T, Fujimoto T, Yamasaki H, Osato M, Takeya M, Takatsuki K. Suzushima H, et al. Among authors: osato m. Leukemia. 1994 Nov;8(11):1884-9. Leukemia. 1994. PMID: 7967733

4

Myelomonoblastic leukaemia cells carrying the PEBP2beta/MYH11 fusion gene are CD34, c-KIT+ immature cells.

Osato M, Asou N, Okubo T, Nishimura S, Yamasaki H, Era T, Suzushima H, Kawano F, Matsuoka R, Oka H, Bae SC, Ito Y, Takatsuki K. Osato M, et al. Br J Haematol. 1997 Jun;97(3):656-8. doi: 10.1046/j.1365-2141.1997.1012917.x. Br J Haematol. 1997. PMID: 9207416 Free article.

5

Detection of the PEBP2beta/MYH11 fusion transcript in acute myelomonoblastic leukemia (M4Eo) supervening in a patient with adult T-cell leukemia.

Osato M, Asou N, Takata N, Suzushima H, Takatsuki K, Kawano F. Osato M, et al. Am J Hematol. 1997 Aug;55(4):216-7. doi: 10.1002/(sici)1096-8652(199707)55:4<216::aid-ajh10>3.0.co;2-9. Am J Hematol. 1997. PMID: 9257884 Free article. No abstract available.

6

Acute myelomonoblastic leukemia carrying the PEBP2beta/MYH11 fusion gene.

Asou N, Osato M, Okubo T, Yamasaki H, Hoshino K, Nishimura S, Era T, Suzushima H, Takatsuki K. Asou N, et al. Among authors: osato m. Leuk Lymphoma. 1998 Sep;31(1-2):81-91. doi: 10.3109/10428199809057587. Leuk Lymphoma. 1998. PMID: 9720717 Review.

7

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. Blood. 1999 Mar 15;93(6):1817-24. Blood. 1999. PMID: 10068652 Free article.

8

[Loss-of-function of AML1/PEBP2 alpha B and leukemogenesis].

Osato M, Ito Y, Asou N. Osato M, et al. Tanpakushitsu Kakusan Koso. 2000 Jan;45(1):40-7. Tanpakushitsu Kakusan Koso. 2000. PMID: 10643334 Review. Japanese. No abstract available.

9

Point mutations of the RUNx1/AML1 gene in sporadic and familial myeloid leukemias.

Osato M, Yanagida M, Shigesada K, Ito Y. Osato M, et al. Int J Hematol. 2001 Oct;74(3):245-51. doi: 10.1007/BF02982056. Int J Hematol. 2001. PMID: 11721958 Review.

10

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: osato m. Blood. 2002 Feb 15;99(4):1364-72. doi: 10.1182/blood.v99.4.1364. Blood. 2002. PMID: 11830488 Free article.

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