RUNX1 mutations are frequent in chronic myelomonocytic leukemia and mutations at the C-terminal region might predict acute myeloid leukemia transformation von Kuo, M-C, Liang, D-C, Huang, C-F, Shih, Y-S, Wu, J-H, Lin, T-L, Shih, L-Y

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Cadmium-induced autophagy and apoptosis are mediated by a calcium signaling pathway von Wang, S. H, Shih, Y. L, Ko, W. C, Wei, Y. H, Shih, C. M

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Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia von Madan, V, Shyamsunder, P, Han, L, Mayakonda, A, Nagata, Y, Sundaresan, J, Kanojia, D, Yoshida, K, Ganesan, S, Hattori, N, Fulton, N, Tan, K-T, Alpermann, T, Kuo, M-C, Rostami, S, Matthews, J, Sanada, M, Liu, L-Z, Shiraishi, Y, Miyano, S, Chendamarai, E, Hou, H-A, Malnassy, G, Ma, T, Garg, M, Ding, L-W, Sun, Q-Y, Chien, W, Ikezoe, T, Lill, M, Biondi, A, Larson, R A, Powell, B L, Lübbert, M, Chng, W J, Tien, H-F, Heuser, M, Ganser, A, Koren-Michowitz, M, Kornblau, S M, Kantarjian, H M, Nowak, D, Hofmann, W-K, Yang, H, Stock, W, Ghavamzadeh, A, Alimoghaddam, K, Haferlach, T, Ogawa, S, Shih, L-Y, Mathews, V, Koeffler, H P

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Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms von Mori, T, Nagata, Y, Makishima, H, Sanada, M, Shiozawa, Y, Kon, A, Yoshizato, T, Sato-Otsubo, A, Kataoka, K, Shiraishi, Y, Chiba, K, Tanaka, H, Ishiyama, K, Miyawaki, S, Mori, H, Nakamaki, T, Kihara, R, Kiyoi, H, Koeffler, H P, Shih, L-Y, Miyano, S, Naoe, T, Haferlach, C, Kern, W, Haferlach, T, Ogawa, S, Yoshida, K

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EED mutants impair polycomb repressive complex 2 in myelodysplastic syndrome and related neoplasms von Ueda, T, Sanada, M, Matsui, H, Yamasaki, N, Honda, Z-i, Shih, L-Y, Mori, H, Inaba, T, Ogawa, S, Honda, H

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Antiplatelet autoantibodies elicited by dengue virus non‐structural protein 1 cause thrombocytopenia and mortality in mice von SUN, D.‐S., KING, C.‐C., HUANG, H.‐S., SHIH, Y.‐L., LEE, C.‐C., TSAI, W.‐J., YU, C.‐C., CHANG, H.‐H.

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Diagnosis and relapse: cytogenetically normal acute myelogenous leukemia without FLT3-ITD or MLL-PTD von Chien, W, Sun, Q-Y, Ding, L-W, Mayakonda, A, Takao, S, Liu, L, Lim, S L, Tan, K T, Garg, M, De Sousa Maria Varela, A, Xiao, J, Jacob, N, Behrens, K, Stocking, C, Lill, M, Madan, V, Hattori, N, Gery, S, Ogawa, S, Wakita, S, Ikezoe, T, Shih, L-Y, Alpermann, T, Haferlach, T, Yang, H, Koeffler, H P

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Characterization of fusion partner genes in 114 patients with de novo acute myeloid leukemia and MLL rearrangement von SHIH, L.-Y, LIANG, D.-C, LAI, C.-L, FU, J.-F, WU, J.-H, WANG, P.-N, LIN, T.-L, DUNN, P, KUO, M.-C, TANG, T.-C, LIN, T.-H

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Effectiveness of national cervical cancer screening programme in Taiwan: 12-year experiences von Chen, Y-Y, You, S-L, Chen, C-A, Shih, L-Y, Koong, S-L, Chao, K-Y, Hsiao, M-L, Hsieh, C-Y, Chen, C-J

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Cooperating mutations of receptor tyrosine kinases and Ras genes in childhood core-binding factor acute myeloid leukemia and a comparative analysis on paired diagnosis and relapse... von Shih, L-Y, Liang, D-C, Huang, C-F, Chang, Y-T, Lai, C-L, Lin, T-H, Yang, C-P, Hung, I-J, Liu, H-C, Jaing, T-H, Wang, L-Y, Yeh, T-C

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Acquisition of FLT3 or N-ras mutations is frequently associated with progression of myelodysplastic syndrome to acute myeloid leukemia von SHIN, L-Y, HUANG, C-F, WANG, P-N, WU, J-H, LIN, T-L, DUNN, P, KUO, M-C

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Dlk1 in normal and abnormal hematopoiesis von SAKAJIRI, S, O'KELLY, J, TEISNER, B, KAWAMATA, N, KOEFFLER, H. P, YIN, D, MILLER, C. W, HOFMANN, W. K, OSHIMI, K, SHIH, L.-Y, KIM, K.-H, SUL, H. S, JENSEN, C. H

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P744: UNBALANCED TRANSLOCATION DER(1;7)(Q10;P10) AS A DISTINCT SUBTYPE IN MYELODYSPLASTIC SYNDROMES von Okuda, R., Ochi, Y., Chonabayashi, K., Hiramoto, N., Sanada, M., Handa, H., Kasahara, S., Sato, S., Kanemura, N., Kitano, T., Watanabe, M., Kern, W., Creignou, M., Shiraishi, Y., Watanabe, M., Usuki, K., Imashuku, S., Hellstrom‐Lindberg, E., Haferlach, T., Chiba, S., Sezaki, N., Shih, L.‐Y., Miyazaki, Y., Yoshida, Y., Ishikawa, T., Ohyashiki, K., Atsuta, Y., Shiozawa, Y., Miyano, S., Makishima, H., Nannya, Y., Ogawa, S.

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Rubella seroepidemiology and estimations of the catch‐up immunisation rate and persistence of antibody titers in pregnant women in Taiwan von Lin, C‐C, Yang, C‐Y, Shih, Y‐L, Hsu, H‐W, Yang, T‐H, Cheng, Y‐W, Chang, C‐F, Hsieh, L‐C, Chen, B‐H, Lee, C‐H, Huang, Y‐L

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P466: AMPLIFIED EPOR/JAK2 GENES DEFINE A UNIQUE SUBTYPE OF ACUTE ERYTHROID LEUKEMIA von Takeda, J., Yoshida, K., Nakagawa, M., Nannya, Y., Yoda, A., Saiki, R., Ochi, Y., Zhao, L., Okuda, R., Qi, X., Mori, T., Kon, A., Chiba, K., Tanaka, H., Shiraishi, Y., Kuo, M.‐C., Kerr, C., Nagata, Y., Morishita, D., Hiramoto, N., Hangaishi, A., Nakazawa, H., Ishiyama, K., Miyano, S., Chiba, S., Miyazaki, Y., Kitano, T., Usuki, K., Sezaki, N., Tsurumi, H., Miyawaki, S., Maciejewski, J., Ishikawa, T., Ohyashiki, K., Ganser, A., Heuser, M., Thol, F., Shih, L.‐Y., Takaori−Kondo, A., Makishima, H., Ogawa, S.

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A nonsense mutation of IDH1 in myelodysplastic syndromes and related disorders von Yoshida, K, Sanada, M, Kato, M, Kawahata, R, Matsubara, A, Takita, J, Shih, L-Y, Mori, H, Koeffler, H P, Ogawa, S

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CEBPα mutations in childhood acute myeloid leukemia von LIANG, D.-C, SHIH, L.-Y, HUANG, C.-F, HUNG, I.-J, YANG, C.-P, LIU, H.-C, JAING, T.-H, WANG, L.-Y, CHANG, W.-H

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FLT3-TKD mutation in childhood acute myeloid leukemia von LIANG, D.-C, SHIH, L.-Y, HUNG, I.-J, YANG, C.-P, CHEN, S.-H, JAING, T.-H, LIU, H.-C, WANG, L.-Y, CHANG, W.-H

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Aml patients with CEBPα mutations mostly retain identical mutant patterns but frequently change in allelic distribution at relapse : a comparative analysis on paired diagnosis and... von SHIH, L.-Y, LIANG, D.-C, HUANG, C.-F, WU, J.-H, LIN, T.-L, WANG, P.-N, DUNN, P, KUO, M.-C, TANG, T.-C

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Cholesterol-3-beta, 5-alpha, 6-beta-triol induced genotoxicity through reactive oxygen species formation von Cheng, Y.W., Kang, J.J., Shih, Y.L., Lo, Y.L., Wang, C.F.

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