Osato M - Search Results

1

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: osato m. 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.

2

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.

3

TEL/AML1 fusion gene resulting from a cryptic t(12;21) is uncommon in adult patients with B-cell lineage ALL and CML lymphoblastic transformation.

Hoshino K, Asou N, Suzushima H, Osato M, Yamasaki H, Okubo T, Nishimura S, Kiyokawa T, Kawano F, Takatsuki K. Hoshino K, et al. Among authors: osato m. Int J Hematol. 1997 Aug;66(2):213-8. doi: 10.1016/s0925-5710(97)00036-4. Int J Hematol. 1997. PMID: 9277052

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

5

[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.

6

Requirement of Runx1/AML1/PEBP2alphaB for the generation of haematopoietic cells from endothelial cells.

Yokomizo T, Ogawa M, Osato M, Kanno T, Yoshida H, Fujimoto T, Fraser S, Nishikawa S, Okada H, Satake M, Noda T, Nishikawa S, Ito Y. Yokomizo T, et al. Among authors: osato m. Genes Cells. 2001 Jan;6(1):13-23. doi: 10.1046/j.1365-2443.2001.00393.x. Genes Cells. 2001. PMID: 11168593 Free article.

7

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.

8

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.

9

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.

10

Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.

Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K. Yoshida T, et al. Among authors: osato m. Am J Hum Genet. 2002 Oct;71(4):724-38. doi: 10.1086/342717. Epub 2002 Aug 26. Am J Hum Genet. 2002. PMID: 12196916 Free PMC article.

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