Ito E - Search Results

1

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: ito e. Nat Genet. 2013 Nov;45(11):1293-9. doi: 10.1038/ng.2759. Epub 2013 Sep 22. Nat Genet. 2013. PMID: 24056718

2

The HOXD11 gene is fused to the NUP98 gene in acute myeloid leukemia with t(2;11)(q31;p15).

Taketani T, Taki T, Shibuya N, Ito E, Kitazawa J, Terui K, Hayashi Y. Taketani T, et al. Among authors: ito e. Cancer Res. 2002 Jan 1;62(1):33-7. Cancer Res. 2002. PMID: 11782354

3

Successful treatment of acute myelomonocytic leukaemia with NUP98-HOXD11 fusion transcripts and monitoring of minimal residual disease.

Terui K, Kitazawa J, Takahashi Y, Tohno C, Hayashi Y, Taketani T, Taki T, Ito E. Terui K, et al. Among authors: ito e. Br J Haematol. 2003 Jan;120(2):274-6. doi: 10.1046/j.1365-2141.2003.04052.x. Br J Haematol. 2003. PMID: 12542486 Free article.

4

Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome.

Xu G, Nagano M, Kanezaki R, Toki T, Hayashi Y, Taketani T, Taki T, Mitui T, Koike K, Kato K, Imaizumi M, Sekine I, Ikeda Y, Hanada R, Sako M, Kudo K, Kojima S, Ohneda O, Yamamoto M, Ito E. Xu G, et al. Among authors: ito e. Blood. 2003 Oct 15;102(8):2960-8. doi: 10.1182/blood-2003-02-0390. Epub 2003 Jun 19. Blood. 2003. PMID: 12816863 Free article.

5

B-cell-specific transcription factor BACH2 modifies the cytotoxic effects of anticancer drugs.

Kamio T, Toki T, Kanezaki R, Sasaki S, Tandai S, Terui K, Ikebe D, Igarashi K, Ito E. Kamio T, et al. Among authors: ito e. Blood. 2003 Nov 1;102(9):3317-22. doi: 10.1182/blood-2002-12-3656. Epub 2003 Jun 26. Blood. 2003. PMID: 12829606 Free article.

6

Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome.

Shimada A, Xu G, Toki T, Kimura H, Hayashi Y, Ito E. Shimada A, et al. Among authors: ito e. Blood. 2004 Jan 1;103(1):366. doi: 10.1182/blood-2003-09-3219. Blood. 2004. PMID: 14684662 Free article. No abstract available.

7

The GATA1 mutation in an adult patient with acute megakaryoblastic leukemia not accompanying Down syndrome.

Harigae H, Xu G, Sugawara T, Ishikawa I, Toki T, Ito E. Harigae H, et al. Among authors: ito e. Blood. 2004 Apr 15;103(8):3242-3. doi: 10.1182/blood-2004-01-0016. Blood. 2004. PMID: 15070711 Free article. No abstract available.

8

Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients.

Uyeda T, Takahashi T, Eto S, Sato T, Xu G, Kanezaki R, Toki T, Yonesaka S, Ito E. Uyeda T, et al. Among authors: ito e. J Hum Genet. 2004;49(8):404-407. doi: 10.1007/s10038-004-0168-x. Epub 2004 Jun 23. J Hum Genet. 2004. PMID: 15221638

9

Transgenic expression of BACH1 transcription factor results in megakaryocytic impairment.

Toki T, Katsuoka F, Kanezaki R, Xu G, Kurotaki H, Sun J, Kamio T, Watanabe S, Tandai S, Terui K, Yagihashi S, Komatsu N, Igarashi K, Yamamoto M, Ito E. Toki T, et al. Among authors: ito e. Blood. 2005 Apr 15;105(8):3100-8. doi: 10.1182/blood-2004-07-2826. Epub 2004 Dec 21. Blood. 2005. PMID: 15613547 Free article.

10

The proto-oncogene ERG in megakaryoblastic leukemias.

Rainis L, Toki T, Pimanda JE, Rosenthal E, Machol K, Strehl S, Göttgens B, Ito E, Izraeli S. Rainis L, et al. Among authors: ito e. Cancer Res. 2005 Sep 1;65(17):7596-602. doi: 10.1158/0008-5472.CAN-05-0147. Cancer Res. 2005. PMID: 16140924

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