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4. Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia

Author

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, RA, Powell, BL, Lübbert, M, Chng, WJ, Tien, H-F, Heuser, M, Ganser, A, Koren-Michowitz, M, Kornblau, SM, Kantarjian, HM, Nowak, D, Hofmann, W-K, Yang, H, Stock, W, Ghavamzadeh, A, Alimoghaddam, K, Haferlach, T, Ogawa, S, Shih, L-Y, Mathews, V, and Koeffler, HP

Subjects
Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Clinical Sciences, Oncology and Carcinogenesis, Cancer, Human Genome, Childhood Leukemia, Pediatric Cancer, Genetics, Rare Diseases, Hematology, Clinical Research, Pediatric, Cell Differentiation, DNA Mutational Analysis, DNA-Binding Proteins, Exome, Gene Expression Profiling, Humans, Leukemia, Promyelocytic, Acute, Nuclear Proteins, Recurrence, Transcription Factors, Immunology, Cardiovascular medicine and haematology, Clinical sciences, Oncology and carcinogenesis
Abstract

Acute promyelocytic leukemia (APL) is a subtype of myeloid leukemia characterized by differentiation block at the promyelocyte stage. Besides the presence of chromosomal rearrangement t(15;17), leading to the formation of PML-RARA (promyelocytic leukemia-retinoic acid receptor alpha) fusion, other genetic alterations have also been implicated in APL. Here, we performed comprehensive mutational analysis of primary and relapse APL to identify somatic alterations, which cooperate with PML-RARA in the pathogenesis of APL. We explored the mutational landscape using whole-exome (n=12) and subsequent targeted sequencing of 398 genes in 153 primary and 69 relapse APL. Both primary and relapse APL harbored an average of eight non-silent somatic mutations per exome. We observed recurrent alterations of FLT3, WT1, NRAS and KRAS in the newly diagnosed APL, whereas mutations in other genes commonly mutated in myeloid leukemia were rarely detected. The molecular signature of APL relapse was characterized by emergence of frequent mutations in PML and RARA genes. Our sequencing data also demonstrates incidence of loss-of-function mutations in previously unidentified genes, ARID1B and ARID1A, both of which encode for key components of the SWI/SNF complex. We show that knockdown of ARID1B in APL cell line, NB4, results in large-scale activation of gene expression and reduced in vitro differentiation potential.

Published
2016

7. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

Author

Haferlach, T, Nagata, Y, Grossmann, V, Okuno, Y, Bacher, U, Nagae, G, Schnittger, S, Sanada, M, Kon, A, Alpermann, T, Yoshida, K, Roller, A, Nadarajah, N, Shiraishi, Y, Shiozawa, Y, Chiba, K, Tanaka, H, Koeffler, HP, Klein, H-U, Dugas, M, Aburatani, H, Kohlmann, A, Miyano, S, Haferlach, C, Kern, W, and Ogawa, S

Subjects
Genetic Testing, Clinical Research, Rare Diseases, Human Genome, Genetics, Biotechnology, Cancer, Hematology, Adult, Aged, Aged, 80 and over, Female, Gene Frequency, Genetic Association Studies, Genetic Markers, High-Throughput Nucleotide Sequencing, Humans, Male, Middle Aged, Mutation, Mutation Rate, Myelodysplastic Syndromes, Polymorphism, Single Nucleotide, Prognosis, Proportional Hazards Models, Young Adult, next-generation sequencing, molecular markers, myelodysplastic syndromes, prognostic score, Clinical Sciences, Oncology and Carcinogenesis, Immunology
Abstract

High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patients with myelodysplastic syndromes (MDS). We determined the biological and prognostic significance of genetic aberrations in MDS. In total, 944 patients with various MDS subtypes were screened for known/putative mutations/deletions in 104 genes using targeted deep sequencing and array-based genomic hybridization. In total, 845/944 patients (89.5%) harbored at least one mutation (median, 3 per patient; range, 0-12). Forty-seven genes were significantly mutated with TET2, SF3B1, ASXL1, SRSF2, DNMT3A, and RUNX1 mutated in >10% of cases. Many mutations were associated with higher risk groups and/or blast elevation. Survival was investigated in 875 patients. By univariate analysis, 25/48 genes (resulting from 47 genes tested significantly plus PRPF8) affected survival (P

Published
2014

9. Topic: AS04-MDS Biology and Pathogenesis/AS04a-Normal, MDS, and leukemic stem cells: DER(1;7)(Q10;P10) DEFINES A DISTINCT SUBTYPE OF MYELODYSPLASIA

Author

Okuda, R., primary, Ochi, Y., additional, Saiki, R., additional, Chonabayashi, K., additional, Hiramoto, N., additional, Sanada, M., additional, Handa, H., additional, Kasahara, S., additional, Sato, S., additional, Kanemura, N., additional, Kitano, T., additional, Watanabe, M., additional, Kern, W., additional, Creignou, M., additional, Shiraishi, Y., additional, Usuki, K., additional, Imashuku, S., additional, Hellstrom-Lindberg, E., additional, Haferlach, T., additional, Chiba, S., additional, Sezaki, N., additional, Shih, L.-Y., additional, Miyazaki, Y., additional, Yoshida, Y., additional, Ishikawa, T., additional, Ohyashiki, K., additional, Atsuta, Y., additional, Shiozawa, Y., additional, Miyano, S., additional, Makishima, H., additional, Nannya, Y., additional, and Ogawa, S., additional

Published
2023
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10. Germ line DDX41 mutations define a unique subtype of myeloid neoplasms.

Author

Makishima, H., Saiki, R., Nannya, Y., Korotev, S., Gurnari, C., Takeda, J., Momozawa, Y., Best, S., Krishnamurthy, P., Yoshizato, T., Atsuta, Y., Shiozawa, Y., Iijima-Yamashita, Y., Yoshida, K., Shiraishi, Y., Nagata, Y., Kakiuchi, N., Onizuka, M., Chiba, K., Tanaka, H., Kon, A., Ochi, Y., Nakagawa, M.M., Okuda, R., Mori, T., Yoda, A., Itonaga, H., Miyazaki, Y., Sanada, M., Ishikawa, T., Chiba, S., Tsurumi, H., Kasahara, S., Müller-Tidow, C., Takaori-Kondo, A., Ohyashiki, K., Kiguchi, T., Matsuda, F., Jansen, J.H., Polprasert, C., Blombery, P., Kamatani, Y., Miyano, S., Malcovati, L., Haferlach, T, Kubo, M., Cazzola, M., Kulasekararaj, A.G., Godley, L.A., Maciejewski, J.P., Ogawa, S., Makishima, H., Saiki, R., Nannya, Y., Korotev, S., Gurnari, C., Takeda, J., Momozawa, Y., Best, S., Krishnamurthy, P., Yoshizato, T., Atsuta, Y., Shiozawa, Y., Iijima-Yamashita, Y., Yoshida, K., Shiraishi, Y., Nagata, Y., Kakiuchi, N., Onizuka, M., Chiba, K., Tanaka, H., Kon, A., Ochi, Y., Nakagawa, M.M., Okuda, R., Mori, T., Yoda, A., Itonaga, H., Miyazaki, Y., Sanada, M., Ishikawa, T., Chiba, S., Tsurumi, H., Kasahara, S., Müller-Tidow, C., Takaori-Kondo, A., Ohyashiki, K., Kiguchi, T., Matsuda, F., Jansen, J.H., Polprasert, C., Blombery, P., Kamatani, Y., Miyano, S., Malcovati, L., Haferlach, T, Kubo, M., Cazzola, M., Kulasekararaj, A.G., Godley, L.A., Maciejewski, J.P., and Ogawa, S.

Abstract

Item does not contain fulltext, Germ line DDX41 variants have been implicated in late-onset myeloid neoplasms (MNs). Despite an increasing number of publications, many important features of DDX41-mutated MNs remain to be elucidated. Here we performed a comprehensive characterization of DDX41-mutated MNs, enrolling a total of 346 patients with DDX41 pathogenic/likely-pathogenic (P/LP) germ line variants and/or somatic mutations from 9082 MN patients, together with 525 first-degree relatives of DDX41-mutated and wild-type (WT) patients. P/LP DDX41 germ line variants explained ∼80% of known germ line predisposition to MNs in adults. These risk variants were 10-fold more enriched in Japanese MN cases (n = 4461) compared with the general population of Japan (n = 20 238). This enrichment of DDX41 risk alleles was much more prominent in male than female (20.7 vs 5.0). P/LP DDX41 variants conferred a large risk of developing MNs, which was negligible until 40 years of age but rapidly increased to 49% by 90 years of age. Patients with myelodysplastic syndromes (MDS) along with a DDX41-mutation rapidly progressed to acute myeloid leukemia (AML), which was however, confined to those having truncating variants. Comutation patterns at diagnosis and at progression to AML were substantially different between DDX41-mutated and WT cases, in which none of the comutations affected clinical outcomes. Even TP53 mutations made no exceptions and their dismal effect, including multihit allelic status, on survival was almost completely mitigated by the presence of DDX41 mutations. Finally, outcomes were not affected by the conventional risk stratifications including the revised/molecular International Prognostic Scoring System. Our findings establish that MDS with DDX41-mutation defines a unique subtype of MNs that is distinct from other MNs.

Published
2023

12. P037 - Topic: AS04-MDS Biology and Pathogenesis/AS04a-Normal, MDS, and leukemic stem cells: DER(1;7)(Q10;P10) DEFINES A DISTINCT SUBTYPE OF MYELODYSPLASIA

Author

Okuda, R., Ochi, Y., Saiki, R., Chonabayashi, K., Hiramoto, N., Sanada, M., Handa, H., Kasahara, S., Sato, S., Kanemura, N., Kitano, T., Watanabe, M., Kern, W., Creignou, M., Shiraishi, Y., 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., and Ogawa, S.

Published
2023
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14. Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms

Author

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, and Yoshida, K

Published
2016
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15. Clinical characteristics and outcomes of B-ALL with ZNF384 rearrangements: a retrospective analysis by the Ponte di Legno Childhood ALL Working Group

Author

Hirabayashi, S, Butler, E, Ohki, K, Kiyokawa, N, Bergmann, A, Moricke, A, Boer, J, Cave, H, Cazzaniga, G, Yeoh, A, Sanada, M, Imamura, T, Inaba, H, Mullighan, C, Loh, M, Noren-Nystrom, U, Pastorczak, A, Shih, L, Zaliova, M, Pui, C, Haas, O, Harrison, C, Moorman, A, Manabe, A, Hirabayashi S., Butler E. R., Ohki K., Kiyokawa N., Bergmann A. K., Moricke A., Boer J. M., Cave H., Cazzaniga G., Yeoh A. E. J., Sanada M., Imamura T., Inaba H., Mullighan C., Loh M. L., Noren-Nystrom U., Pastorczak A., Shih L. -Y., Zaliova M., Pui C. -H., Haas O. A., Harrison C. J., Moorman A. V., Manabe A., Hirabayashi, S, Butler, E, Ohki, K, Kiyokawa, N, Bergmann, A, Moricke, A, Boer, J, Cave, H, Cazzaniga, G, Yeoh, A, Sanada, M, Imamura, T, Inaba, H, Mullighan, C, Loh, M, Noren-Nystrom, U, Pastorczak, A, Shih, L, Zaliova, M, Pui, C, Haas, O, Harrison, C, Moorman, A, Manabe, A, Hirabayashi S., Butler E. R., Ohki K., Kiyokawa N., Bergmann A. K., Moricke A., Boer J. M., Cave H., Cazzaniga G., Yeoh A. E. J., Sanada M., Imamura T., Inaba H., Mullighan C., Loh M. L., Noren-Nystrom U., Pastorczak A., Shih L. -Y., Zaliova M., Pui C. -H., Haas O. A., Harrison C. J., Moorman A. V., and Manabe A.

Published
2021

16. P741: DDX41 MUTATIONS DEFINE A UNIQUE SUBTYPE OF MYELOID NEOPLASMS.

Author

Makishima, H., primary, Saiki, R., additional, Nannya, Y., additional, Korotev, S., additional, Gurnari, C., additional, Takeda, J., additional, Momozawa, Y., additional, Best, S., additional, Krishnamurthy, P., additional, Yoshizato, T., additional, Atsuta, Y., additional, Shiozawa, Y., additional, Iijima-Yamashita, Y., additional, Yoshida, K., additional, Shiraishi, Y., additional, Nagata, Y., additional, Kakiuchi, N., additional, Onizuka, M., additional, Chiba, K., additional, Tanaka, H., additional, Kon, A., additional, Ochi, Y., additional, Nakagawa, M., additional, Okuda, R., additional, Mori, T., additional, Itonaga, H., additional, Miyazaki, Y., additional, Sanada, M., additional, Tsurumi, H., additional, Kasahara, S., additional, Müller-Tidow, C., additional, Takaori-Kondo, A., additional, Ohyashiki, K., additional, Kiguchi, T., additional, Matsuda, F., additional, Jansen, J., additional, Polprasert, C., additional, Miyano, S., additional, Malcovati, L., additional, Haferlach, T., additional, Kubo, M., additional, Cazzola, M., additional, Kulasekararaj, A., additional, Godley, L., additional, Maciejewski, J., additional, and Ogawa, S., additional

Published
2022
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17. P744: UNBALANCED TRANSLOCATION DER(1;7)(Q10;P10) AS A DISTINCT SUBTYPE IN MYELODYSPLASTIC SYNDROMES

Author

Okuda, R., primary, Ochi, Y., additional, Chonabayashi, K., additional, Hiramoto, N., additional, Sanada, M., additional, Handa, H., additional, Kasahara, S., additional, Sato, S., additional, Kanemura, N., additional, Kitano, T., additional, Watanabe, M., additional, Kern, W., additional, Creignou, M., additional, Shiraishi, Y., additional, Usuki, K., additional, Imashuku, S., additional, Hellstrom-Lindberg, E., additional, Haferlach, T., additional, Chiba, S., additional, Sezaki, N., additional, Shih, L.-Y., additional, Miyazaki, Y., additional, Yoshida, Y., additional, Ishikawa, T., additional, Ohyashiki, K., additional, Atsuta, Y., additional, Shiozawa, Y., additional, Miyano, S., additional, Makishima, H., additional, Nannya, Y., additional, and Ogawa, S., additional

Published
2022
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18. Monotonic and Nonmonotonic Reasoning in Zoom Reasoning Systems

Author

Murai, Tetsuya, Sanada, M., Kudo, Yasuo, Sato, Y., Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Dough, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Carbonell, Jaime G., editor, Siekmann, Jörg, editor, Negoita, Mircea Gh., editor, Howlett, Robert J., editor, and Jain, Lakhmi C., editor

Published
2004
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19. Long-Term Monitoring Study on Rain, Throughfall, and Stemflow Chemistry in Evergreen Coniforous Forests in Hokkaido, Northern Japan

Author

Matsuura, Y., Sanada, M., Takahashi, M., Sakai, Y., Tanaka, N., Satake, Kenichi, editor, Shindo, Junko, editor, Takamatsu, Takejiro, editor, Nakano, Takanori, editor, Aoki, Shigeru, editor, Fukuyama, Tsutomu, editor, Hatakeyama, Shiro, editor, Ikuta, Kazukamasa, editor, Kawashima, Munetsugu, editor, Kohno, Yoshihisa, editor, Kojima, Satoru, editor, Murano, Kentaro, editor, Okita, Toshiichi, editor, Taoda, Hiroshi, editor, Tsunoda, Kinichi, editor, and Tsurumi, Makoto, editor

Published
2001
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22. O09 - Topic: AS04-MDS Biology and Pathogenesis/AS04b-Clonal diversity & evolution: MYELOID NEOPLASMS WITH GERMLINE AND SOMATIC DDX41 MUTATIONS

Author

Makishima, H., Nannya, Y., Momozawa, Y., Gurnari, C., Kulasekararaj, A., Yoshizato, T., Takeda, J., Atsuta, Y., Shiozawa, Y., Iijima-Yamashita, Y., Saiki, R., Yoshida, K., Shiraishi, Y., Nagata, Y., Onizuka, M., Nakagawa, M., Itonaga, H., Kanda, Y., Miyazaki, Y., Sanada, M., Tsurumi, H., Kasahara, S., Kondo-Takaori, A., Ohyashiki, K., Kiguchi, T., Matsuda, F., Jansen, J., Papaemmanuil, E., Creignou, M., Tobiasson, M., Hellström-Lindberg, E., Polprasert, C., Malcovati, L., Cazzola, M., Haferlach, T., Maciejewski, J., Kamatani, Y., Miyano, S., and Ogawa, S.

Published
2021
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24. Topic: AS04-MDS Biology and Pathogenesis/AS04b-Clonal diversity & evolution

Author

Makishima, H., primary, Nannya, Y., additional, Momozawa, Y., additional, Gurnari, C., additional, Kulasekararaj, A., additional, Yoshizato, T., additional, Takeda, J., additional, Atsuta, Y., additional, Shiozawa, Y., additional, Iijima-Yamashita, Y., additional, Saiki, R., additional, Yoshida, K., additional, Shiraishi, Y., additional, Nagata, Y., additional, Onizuka, M., additional, Nakagawa, M., additional, Itonaga, H., additional, Kanda, Y., additional, Miyazaki, Y., additional, Sanada, M., additional, Tsurumi, H., additional, Kasahara, S., additional, Kondo-Takaori, A., additional, Ohyashiki, K., additional, Kiguchi, T., additional, Matsuda, F., additional, Jansen, J., additional, Papaemmanuil, E., additional, Creignou, M., additional, Tobiasson, M., additional, Hellström-Lindberg, E., additional, Polprasert, C., additional, Malcovati, L., additional, Cazzola, M., additional, Haferlach, T., additional, Maciejewski, J., additional, Kamatani, Y., additional, Miyano, S., additional, and Ogawa, S., additional

Published
2021
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29. Erratum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia

Author

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, and Koeffler, H P

Published
2016
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39. Fault diagnosis technology based on transistor behavior analysis for physical analysis

Author

Sanada, M, Yoshizawa, Y, Sanada, M, and Yoshizawa, Y

Abstract

The novel method has been developed to detect accuracy faultelements in transistor level circuit, analyzing the characteristics of circuitoperation influenced on leakage fault and being combined with diagnosissoftware, based on switching level simulation. This method is based on behaviorof CMOS transistor to which applied unstable voltage produced by leakage fault.Unsettled logic brings the transistor’s operation point to saturation area withmulti-impedance value and forms penetration current nets passing through it.Output value on the net is calculated with each element impedance value andmiss-logic signal is spread to output terminal. An evaluation of this technologycorroborates to be precise method by using the circuit in which embeddedarbitrary fault portions.

Published
2019

43. PS983 NOVEL MOLECULAR PATHOGENESIS AND THERAPEUTIC TARGET IN ACUTE ERYTHROID LEUKEMIA

Author

Takeda, J., primary, Shih, L.-Y., additional, Yoshida, K., additional, Makishima, H., additional, Yoshizato, T., additional, Shiozawa, Y., additional, Ochi, Y., additional, Kon, A., additional, Yoda, A., additional, Nakagawa, M., additional, Nannya, Y., additional, Kataoka, K., additional, Sanada, M., additional, Chiba, K., additional, Shiraishi, Y., additional, Miyano, S., additional, Hiramoto, N., additional, Chiba, S., additional, Miyazaki, Y., additional, Takaori-Kondo, A., additional, Ishikawa, T., additional, Kerr, C., additional, Maciejewski, J., additional, Ganser, A., additional, Heuser, M., additional, Thol, F., additional, and Ogawa, S., additional

Published
2019
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44. PS1367 COMPREHENSIVE GENETIC ANALYSIS OF MULTIPLE MYELOMA IN JAPAN

Author

Kanamori, T., primary, Sanada, M., additional, Ri, M., additional, Ueno, H., additional, Nishijima, D., additional, Yasuda, T., additional, Aoki, S., additional, Asano, A., additional, Tachita, T., additional, Kinoshita, S., additional, Narita, T., additional, Ito, A., additional, Kusumoto, S., additional, Masuda, Y., additional, Kobayashi, N., additional, Shiozawa, Y., additional, Yoshida, K., additional, Nakagawa, M., additional, Nannya, Y., additional, Shiraishi, Y., additional, Chiba, K., additional, Tanaka, H., additional, Komatsu, H., additional, Miyano, S., additional, Handa, H., additional, Ogawa, S., additional, and Iida, S., additional

Published
2019
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45. PF532 INTEGRATED PROFILING OF DNA METHYLATION AND MUTATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES

Author

Morimoto, S., primary, Makishima, H., additional, Nagata, Y., additional, Baer, C., additional, Nadarajah, N., additional, Nagae, G., additional, Nannya, Y., additional, Miyazaki, Y., additional, Yoshida, K., additional, Yoshizato, T., additional, Nakagawa, M., additional, Inagaki, R., additional, Takeda, J., additional, Fujii, Y., additional, Takeuchi, Y., additional, Ueno, H., additional, Shiraishi, Y., additional, Chiba, K., additional, Tanaka, H., additional, Sanada, M., additional, Miyano, S., additional, Haferlach, C., additional, Kern, W., additional, Aburatani, H., additional, Haferlach, T., additional, and Ogawa, S., additional

Published
2019
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46. INTEGRATED PROFILING OF DNA METHYLATION AND MUTATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES

Author

Morimoto, S., primary, Makishima, H., additional, Nagata, Y., additional, Baer, C., additional, Nadarajah, N., additional, Nagae, G., additional, Nannya, Y., additional, Miyazaki, Y., additional, Yoshida, K., additional, Yoshizato, T., additional, Nakagawa, M., additional, Inagaki, R., additional, Takeda, J., additional, Fujii, Y., additional, Takeuchi, Y., additional, Ueno, H., additional, Shiraishi, Y., additional, Chiba, K., additional, Tanaka, H., additional, Sanada, M., additional, Miyano, S., additional, Haferlach, C., additional, Kern, W., additional, Aburatani, H., additional, Haferlach, T., additional, and Ogawa, S., additional

Published
2019
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47. PF175 MULTICENTRE STANDARDIZATION OF MINIMAL RESIDUAL DISEASE DETECTION AND QUANTITATION USING THE EUROCLONALITY-NGS ASSAY

Author

Svaton, M., primary, Fronkova, E., additional, Kotrova, M., additional, Reigl, T., additional, Caye, A., additional, de Bie, M., additional, Genuardi, E., additional, Jelinkova, H., additional, Lim, E.H., additional, Nishijima, D., additional, Pal, K., additional, Salemi, D., additional, Sarasquete, M.E., additional, Songia, S., additional, Tosi, M., additional, Villarese, P., additional, Wakeman, S., additional, Cave, H., additional, Cazzaniga, G., additional, Ferrero, S., additional, Garcia Sanz, R., additional, Hancock, J., additional, Macintyre, E., additional, Plevova, K., additional, Sanada, M., additional, Santoro, A., additional, Spinelli, O., additional, van der Velden, V.H., additional, Yeoh, A.E. J., additional, Langerak, A.W., additional, Darzentas, N., additional, Brüggemann, M., additional, and Trka, J., additional

Published
2019
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48. S135 NGS-BASED COPY-NUMBER ANALYSIS IN MORE THAN 2,000 PATIENTS WITH MYELOID NEOPLASMS

Author

Saiki, R., primary, Shiozawa, Y., additional, Yoshizato, T., additional, Nanya, Y., additional, Takeda, J., additional, Yoshida, K., additional, Shiraishi, Y., additional, Tanaka, H., additional, Chiba, K., additional, Atsuta, Y., additional, Onizuka, M., additional, Itonaga, H., additional, Sanada, M., additional, Kanda, Y., additional, Przychodzen, B., additional, Sekeres, M.A., additional, Guinta, K.M., additional, Saunthararajah, Y., additional, Shih, L.-Y., additional, Miyawaki, S., additional, Nakamaki, T., additional, Taguchi, M., additional, Fuji, S., additional, Sasaki, N., additional, Uoshima, N., additional, Ueda, Y., additional, Miyazaki, Y., additional, Usuki, K., additional, Imada, K., additional, Takaori-Kondo, A., additional, Chiba, S., additional, Kasahara, S., additional, Kiguchi, T., additional, Tsurumi, H., additional, Malcovati, L., additional, Cazzola, M., additional, Ishikawa, T., additional, Miyano, S., additional, Maciejewski, J.P., additional, Makishima, H., additional, and Ogawa, S., additional

Published
2019
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50. Comprehensive genomic analysis of upper urinary tract urothelial carcinoma

Author

Fujii, Y., primary, Sato, Y., additional, Suzuki, H., additional, Tetsuichi, Y., additional, Yoshida, K., additional, Shiraishi, Y., additional, Kawai, T., additional, Nakagawa, T., additional, Nishimatsu, H., additional, Okaneya, T., additional, Sanada, M., additional, Makishima, H., additional, Miyano, S., additional, Ogawa, S., additional, and Kume, H., additional

Published
2019
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