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Kumon, K
Kobayashi, H
Namiki, T
Tsunematsu, Y
Miyauchi, J
Kikuta, A
Horikoshi, Y
Komada, Y
Hatae, Y
Eguchi, H
Kaneko, Y
Citation: K. Kumon et al., Frequent increase of DNA copy number in the 2q24 chromosomal region and its association with a poor clinical outcome in hepatoblastoma: Cytogenetic and comparative genomic hybridization analysis, JPN J CANC, 92(8), 2001, pp. 854-862
Authors:
Manabe, A
Tsuchida, M
Hanada, R
Ikuta, K
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Okimoto, Y
Ishimoto, K
Okawa, H
Ohara, A
Kaneko, T
Koike, K
Sato, T
Sugita, K
Bessho, F
Hoshi, Y
Maeda, M
Kinoshita, A
Saito, T
Tsunematsu, Y
Nakazawa, S
Citation: A. Manabe et al., Delay of the diagnostic lumbar puncture and intrathecal chemotherapy in children with acute lymphoblastic leukemia who undergo routine corticosteroidtesting: Tokyo Children's Cancer Study Group study L89-12, J CL ONCOL, 19(13), 2001, pp. 3182-3187
Authors:
Nakadate, H
Yokomori, K
Watanabe, N
Tsuchiya, T
Namiki, T
Kobayshi, H
Suita, S
Tsunematsu, Y
Horikoshi, Y
Hatae, Y
Endo, M
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Eguchi, H
Toyoda, Y
Kikuta, A
Kobayashi, R
Kaneko, Y
Citation: H. Nakadate et al., Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan, INT J CANC, 94(3), 2001, pp. 396-400
Authors:
Shen, LS
Tsuchida, R
Miyauchi, J
Saeki, M
Honna, T
Tsunematsu, Y
Kato, J
Mizutani, S
Citation: Ls. Shen et al., Differentiation-associated expression and intracellular localization of cyclin-dependent kinase inhibitor p27(KIP1) and c-Jun co-activator JAB1 in neuroblastoma, INT J ONCOL, 17(4), 2000, pp. 749-754
Authors:
Tsuchida, M
Ikuta, K
Hanada, R
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Sugita, K
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Manabe, A
Koike, K
Kinoshita, A
Maeda, M
Ishimoto, K
Sato, T
Okimoto, Y
Kaneko, T
Kajiwara, M
Sotomatsu, M
Hayashi, Y
Yabe, H
Hosoya, R
Hoshi, Y
Ohira, M
Bessho, F
Tsunematsu, Y
Tsukimoto, I
Nakazawa, S
Citation: M. Tsuchida et al., Long-term follow-up of childhood acute lymphoblastic leukemia in Tokyo Children's Cancer Study Group 1981-1995, LEUKEMIA, 14(12), 2000, pp. 2295-2306
Authors:
Toyoda, Y
Manabe, A
Tsuchida, M
Hanada, R
Ikuta, K
Okimoto, Y
Ohara, A
Ohkawa, Y
Mori, T
Ishimoto, K
Sato, T
Kaneko, T
Maeda, M
Koike, K
Shitara, T
Hoshi, Y
Hosoya, R
Tsunematsu, Y
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Saito, T
Citation: Y. Toyoda et al., Six months of maintenance chemotherapy after intensified treatment for acute lymphoblastic leukemia of childhood, J CL ONCOL, 18(7), 2000, pp. 1508-1516
Authors:
Horikoshi, Y
Mimaya, J
Amano, K
Kawano, Y
Watanabe, A
Watanabe, T
Sekine, I
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Tsunematsu, Y
Endo, M
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Kawakami, K
Oka, T
Matsushita, T
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Fujimoto, T
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Citation: Y. Horikoshi et al., Feasibility study of autologous peripheral blood stem cell transplantationfor the treatment of childhood acute myelogenous leukemia, JPN J CLIN, 30(3), 2000, pp. 137-145
Authors:
Tsunematsu, Y
Yoshizawa, Y
Miyauchi, J
Iijima, T
Konishi, M
Miyaki, M
Citation: Y. Tsunematsu et al., A novel case of Wilms' tumor followed by colon cancer, both showing microsatellite instability, ONCOL-BASEL, 58(2), 2000, pp. 159-160
Authors:
Imashuku, S
Hibi, S
Sako, M
Lin, YW
Ikuta, K
Nakata, Y
Mori, T
Iizuka, S
Horibe, K
Tsunematsu, Y
Citation: S. Imashuku et al., Hemophagocytosis by leukemic blasts in 7 acute myeloid leukemia cases witht(16;21)(p11;q22) - Common morphologic characteristics for this type of leukemia, CANCER, 88(8), 2000, pp. 1970-1975
Authors:
Tachibana, A
Kato, T
Ejima, Y
Yamada, T
Shimizu, T
Yang, LC
Tsunematsu, Y
Sasaki, MS
Citation: A. Tachibana et al., The FANCA gene in Japanese Fanconi anemia: Report of eight novel mutationsand analysis of sequence variability, HUM MUTAT, 13(3), 1999, pp. 237-244
Authors:
Nishiyama, M
Arai, Y
Tsunematsu, Y
Kobayashi, H
Asami, K
Yabe, M
Kato, S
Oda, M
Eguchi, H
Ohki, M
Kaneko, Y
Citation: M. Nishiyama et al., 11p15 translocations involving the NUP98 gene in childhood therapy-relatedacute myeloid leukemia/myelodysplastic syndrome, GENE CHROM, 26(3), 1999, pp. 215-220
Authors:
Nakadate, H
Tsuchiya, T
Maseki, N
Hatae, Y
Tsunematsu, Y
Horikoshi, Y
Ishida, Y
Kikuta, A
Eguchi, H
Endo, M
Miyake, M
Sakurai, M
Kaneko, Y
Citation: H. Nakadate et al., Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor, GENE CHROM, 25(1), 1999, pp. 26-32