6 results for author:"Hanamura I." in Literature citations
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| Frequent PVT1 rearrangement and novel chimeric genes PVT1-NBEA and PVT1-WWOX occur in multiple myeloma with 8q24 abnormality. Nagoshi H., Taki T., Hanamura I., Nitta M., Otsuki T., Nishida K., Okuda K., Sakamoto N., Kobayashi S., Yamamoto-Sugitani M. et al. Cancer Res. 72:4954-4962(2012) · Mapped (9) |
| ARK5 is transcriptionally regulated by the Large-MAF family and mediates IGF-1-induced cell invasion in multiple myeloma: ARK5 as a new molecular determinant of malignant multiple myeloma. Suzuki A., Iida S., Kato-Uranishi M., Tajima E., Zhan F., Hanamura I., Huang Y., Ogura T., Takahashi S., Ueda R. et al. Oncogene 24:6936-6944(2005) · UniProtKB (1) |
| Inactivation of the E3/LAPTm5 gene by chromosomal rearrangement and DNA methylation in human multiple myeloma. Hayami Y., Iida S., Nakazawa N., Hanamura I., Kato M., Komatsu H., Miura I., Dave B.J., Sanger W.G., Lim B. et al. Leukemia 17:1650-1657(2003) · Mapped (3) |
| Frequent occurrence of CCND1 deregulation in patients with early stages of plasma cell dyscrasia. Miura K., Iida S., Hanamura I., Kato M., Banno S., Ishida T., Kusumoto S., Takeuchi G., Miwa H., Nitta M. et al. Cancer Sci. 94:350-354(2003) · Mapped (5) |
| Possible dominant-negative mutation of the SHIP gene in acute myeloid leukemia. Luo J.-M., Yoshida H., Komura S., Ohishi N., Pan L., Shigeno K., Hanamura I., Miura K., Iida S., Ueda R. et al. Leukemia 17:1-8(2003) · UniProtKB (1) |
| Superior mesenteric venous thrombosis associated with a familial missense mutation (Pro626Leu) in the SHBG-like domain of the protein S molecule. Kato M., Iida S., Sato M., Hayami Y., Hanamura I., Miura K., Ito M., Harada S., Komatsu H., Wakita A. et al. Int. J. Hematol. 75:100-103(2002) · Mapped (28) |