| 1997N |
| 1. Kong XT, Ida K, Ichikawa H, Shimizu K, Ohki M, Maseki N, Kaneko Y, Sako M, Kobayashi Y, Tojou A, Miura I, Kakuda H, Funabiki T, Horibe K, Hamaguchi H, Akiyama Y, Bessho F, Yanagisawa M, Hayashi Y: Consistent detection of TLS/FUS-ERG chimeric transcripts in acute myeloid leukemia with t(16;21)(p11;q22) and identification of a novel transcript. Blood 90:1192-1199, 1997 Abstract |
| 2. Takita J, Hayashi Y, Kohno T, Yamaguchi N, Hanada R, Yamamoto K, Yokota J: Deletion map of chromosome 9 and p16 (CDKN2A) gene alterations in neuroblastoma. Cancer Res 57:907-912, 1997 Abstract |
| 3. Takita J, Hayashi Y, Yokota J: Loss of heterozygosity in neuroblastomas -an overview. Eur J Cancer 33:1971-1973, 1997 Abstract |
| 4. Taki T, Sako M, Tsuchida M, Hayashi Y: The t(11;16)(q23;p13) translocation in myelodysplastic syndrome fuses the MLL gene to the CBP gene. Blood 89:3945-3950, 1997 Abstract |
| 5. Sheng XM, Kawamura M, Ohnishi H, Ida K, Hanada R, Kojima S, Kobayashi M, Bessho F, Yanagisawa M, Hayashi Y: Mutations of the RAS genes in childhood acute myeloid leukemia, myelodysplastic syndrome and juvenile chronic myelocytic leukemia. Leuk Res 21:697-701, 1997 Abstract |
| 6. Saitoh M, Sakakihara Y, Kobayashi S, Hayashi Y, Yanagisawa M: Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Japanese patients. Acta Paediatr Jpn 39:584-589, 1997 Abstract |
| 7. Kobayashi H, Arai Y, Hosoda F, Maseki N, Hayashi Y, Eguchi H, Ohki M, Kaneko Y: Inversion of chromosome 11 inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: identification of a P1 clone spanning the 11q22 breakpoint. Genes Chromosomes Cancer 19:150-155, 1997 Abstract |
| 8. Ohnishi H, Guo SX, Ida K, Taki T, Naritaka S, Bessho F, Yanagisawa M, Hanada R, Eguchi M, Kamada N, Kita K, Yamamori S, Hayashi Y: Alterations of p16 and p15 genes in acute leukemia with MLL gene rearrangements and their correlation with clinical features. Leukemia 11:2120-2124, 1997 Abstract |
| 9. Inoue A, Yokomori K, Tanabe H, Mizusawa H, Sofuni T, Hayashi Y, Tsuchida Y, Shimatake H: Extensive genetic heterogeneity in the neuroblastoma cell line NB(TU)1. Int J Cancer 72:1070-1077, 1997 Abstract |
| 10. Yamamoto K, Hanada R, Tanimura M, Aihara T, Hayashi Y: Natural history of neuroblastoma found by mass screening. Lancet 349:1102, 1997 |
| 11. Ida K, Taki T, Bessho F, Kobayashi M, Taira F, Hanada R, Yamamoto K, Okimoto Y, Seto M, Ueda R, Hayashi Y: Detection of chimeric mRNAs by reverse transcriptase-polymerase chain reaction for diagnosis and monitoring of acute leukemias with 11q23 abnormalities. Med Pediatr Oncol 28:325-332, 1997 Abstract |
| 12. Ida K, Kitabayashi I, Taki T, Taniwaki M, Noro K, Yamamoto M, Ohki M, Hayashi Y: Adenoviral E1A-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13). Blood 90:4699-4704, 1997 Abstract |
| 13. Arai Y, Hosoda F, Kobayashi H, Arai K, Hayashi Y, Kamada N, Kaneko Y, Ohki M: The inv(11)(p15q22) chromosome translocation of de novo and therapy- related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene, DDX10. Blood 89:3936-3944, 1997 Abstract |
| 14. Kong XT, Choi SH, Inoue A, Xu F, Chen T, Takita J, Yokota J, Bessho F, Yanagisawa M, Hanada R, Yamamoto K, Hayashi Y: Expression and mutational analysis of the DCC, DPC4, and MADR2/JV18-1 genes in neuroblastoma. Cancer Res 57:3772-3778, 1997 Abstract |
| 15. Kong XT, Choi SH, Inoue A, Takita J, Yokota J, Hanada R, Yamamoto K, Bessho F, Yanagisawa M, Hayashi Y: Alterations of the tumour suppressor gene DCC in neuroblastoma. Eur J Cancer 33:1962-1965, 1997 Abstract |
| 16. Kurachi Y, Kawahara H, Hatakeyama K, Yazawa K, Kubota M, Oka A, Kin S, Sakakihara Y, Yanagisawa M: [Acute necrotizing encephalopathy with horizontal gaze palsy]. No To Shinkei 49:753-758, 1997 Abstract |
@