| 1998N |
| 1. Osaka H, Sekiguchi H, Inoue K, Ikuta K, Sakakihara Y, Oka A, Onishi H, Miyakawa T, Suzuki K, Kimura S, Kosaka K, Matsuyama S: A novel mutation found in an adrenoleukodystrophy patient who underwent bone marrow transplantation. J Inherit Metab Dis 21: 162-166, 1998 Abstract |
| 2. Yamamoto K, Hanada R, Kikuchi A, Ichikawa M, Aihara T, Oguma E, Moritani T, Shimanuki Y, Tanimura M, Hayashi Y: Spontaneous regression of localized neuroblastoma detected by mass screening. J Clin Oncol 16: 1265-1269, 1998 Abstract |
| 3. Kitabayashi I, Ida K, Morohoshi F, Yokoyama A, Mitsuhashi N, Shimizu K, Nomura N, Hayashi Y, Ohki M: The AML1-MTG8 leukemic fusion protein forms a complex with a novel member of
the MTG8(ETO/CDR) family, MTGR1. Mol Cell Biol 18: 846-858, 1998 Abstract |
| 4. Takita J, Hayashi Y, Nakajima T, Adachi J, Tanaka T, Yamaguchi N, Ogawa Y, Hanada R, Yamamoto K, Yokota J: The p16 (CDKN2A) gene is involved in the growth of neuroblastoma cells and its expression is associated with prognosis of neuroblastoma patients. Oncogene 17:3137-3143, 1998 Abstract |
| 5. Taki T, Shibuya N, Taniwaki M, Hanada R, Morishita K, Bessho F, Yanagisawa M, Hayashi Y: ABI-1, a human homolog to mouse abl-interactor 1, fuses the MLL gene in
acute myeloid leukemia with t(10;11). Blood 92: 1125-1130, 1998 Abstract |
| 6. Ishiguro A, Ishikita T, Shimbo T, Matsubara K, Baba K, Hayashi Y, Naritaka S, Nakahata T: Elevation of serum thrombopoietin precedes thrombocytosis in Kawasaki disease. Thromb Haemost 79: 1096-1100, 1998 Abstract |
| 7. Gamou T, Kitamura E, Hosoda F, Shimizu K, Shinohara K, Hayashi Y, Nagase T, Yokoyama Y, Ohki M: The partner gene of AML1 in t(16;21) myeloid malignancies is a novel membe of the MTG8(ETO) family. Blood 91: 4028-4037, 1998 Abstract |
| 8. Miyagawa K, Kent J, Moore A, Charlieu JP, Little MH, Williamson KA, Kelsey A, Brown KW, Hassam S, Briner J, Hayashi Y, Hirai H, Yazaki Y, van Heyningen V, Hastie ND: Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour. Nat Genet 18:15-17, 1998 |
| 9. Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, Hamano K, Sakakihara Y, Nonaka I, Nakagome Y, Kanazawa I, Nakamura Y, Tokunaga K, Toda T: An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 394: 388-392, 1998 Abstract |
| 10. Koike T, Ishida G, Taniguchi M, Higaki K, Ayaki Y, Saito M, Sakakihara Y, Iwamori M, Ohno K: Decreased membrane fluidity and unsaturated fatty acids in Niemann-Pick disease type C fibroblasts. Biochim Biophys Acta 1406: 327-335, 1998 Abstract |
| 11. Oka A, Kubota M, Sakakihara Y, Yanagisawa M: A case of parietal lobe epilepsy with distinctive clinical and neuroradiological features. Brain Dev 20: 179-182, 1998 Abstract |
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