Hayashi Y - Search Results

1

Low frequency of KIT gene mutation in pediatric acute myeloid leukemia with inv(16)(p13q22): a study of the Japanese Childhood AML Cooperative Study Group.

Shimada A, Ichikawa H, Taki T, Kubota C, Hongo T, Sako M, Morimoto A, Tawa A, Tsukimoto I, Hayashi Y. Shimada A, et al. Among authors: hayashi y. Int J Hematol. 2007 Oct;86(3):289-90. doi: 10.1532/IJH97.07098. Int J Hematol. 2007. PMID: 17989000 No abstract available.

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: hayashi y. Cancer Res. 2002 Jan 1;62(1):33-7. Cancer Res. 2002. PMID: 11782354

3

SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24.

Ono R, Taki T, Taketani T, Kawaguchi H, Taniwaki M, Okamura T, Kawa K, Hanada R, Kobayashi M, Hayashi Y. Ono R, et al. Among authors: hayashi y. Cancer Res. 2002 Jan 15;62(2):333-7. Cancer Res. 2002. PMID: 11809673

4

The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9.

Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y. Taketani T, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2002 Aug;34(4):437-43. doi: 10.1002/gcc.10077. Genes Chromosomes Cancer. 2002. PMID: 12112533

5

LCX, leukemia-associated protein with a CXXC domain, is fused to MLL in acute myeloid leukemia with trilineage dysplasia having t(10;11)(q22;q23).

Ono R, Taki T, Taketani T, Taniwaki M, Kobayashi H, Hayashi Y. Ono R, et al. Among authors: hayashi y. Cancer Res. 2002 Jul 15;62(14):4075-80. Cancer Res. 2002. PMID: 12124344

6

Novel NUP98-HOXC11 fusion gene resulted from a chromosomal break within exon 1 of HOXC11 in acute myeloid leukemia with t(11;12)(p15;q13).

Taketani T, Taki T, Shibuya N, Kikuchi A, Hanada R, Hayashi Y. Taketani T, et al. Among authors: hayashi y. Cancer Res. 2002 Aug 15;62(16):4571-4. Cancer Res. 2002. PMID: 12183408

7

Risk-directed treatment of infant acute lymphoblastic leukaemia based on early assessment of MLL gene status: results of the Japan Infant Leukaemia Study (MLL96).

Isoyama K, Eguchi M, Hibi S, Kinukawa N, Ohkawa H, Kawasaki H, Kosaka Y, Oda T, Oda M, Okamura T, Nishimura S, Hayashi Y, Mori T, Imaizumi M, Mizutani S, Tsukimoto I, Kamada N, Ishii E. Isoyama K, et al. Among authors: hayashi y. Br J Haematol. 2002 Sep;118(4):999-1010. doi: 10.1046/j.1365-2141.2002.03754.x. Br J Haematol. 2002. PMID: 12199778 Free article.

8

Translocation (8;12)(q13;p13) during disease progression in acute myelomonocytic leukemia with t(11;19)(q23;p13.1).

Yamamoto K, Nagata K, Tsurukubo Y, Inagaki K, Ono R, Taki T, Hayashi Y, Hamaguchi H. Yamamoto K, et al. Among authors: hayashi y. Cancer Genet Cytogenet. 2002 Aug;137(1):64-7. doi: 10.1016/s0165-4608(02)00555-1. Cancer Genet Cytogenet. 2002. PMID: 12377416

9

Fusion of an AF4-related gene, LAF4, to MLL in childhood acute lymphoblastic leukemia with t(2;11)(q11;q23).

Hiwatari M, Taki T, Taketani T, Taniwaki M, Sugita K, Okuya M, Eguchi M, Ida K, Hayashi Y. Hiwatari M, et al. Among authors: hayashi y. Oncogene. 2003 May 8;22(18):2851-5. doi: 10.1038/sj.onc.1206389. Oncogene. 2003. PMID: 12743608

10

AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.

Taketani T, Taki T, Takita J, Tsuchida M, Hanada R, Hongo T, Kaneko T, Manabe A, Ida K, Hayashi Y. Taketani T, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2003 Sep;38(1):1-7. doi: 10.1002/gcc.10246. Genes Chromosomes Cancer. 2003. PMID: 12874780

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