IDENTIFICATION OF NOVEL SOMATIC MUTATIONS IN PEDIATRIC ACUTE MYELOID LEUKEIMIA USING WHOLE-EXOME RESEQUENCING

被引:0
|
作者
Shiba, N. [1 ]
Yoshida, K. [2 ]
Okuno, Y. [2 ]
Shiraishi, Y. [2 ]
Kon, A. [2 ]
Nagata, Y. [2 ]
Ohki, K. [3 ]
Park, M. [3 ]
Kato, M. [4 ]
Kanazawa, T. [1 ]
Takita, J. [4 ]
Kudo, K. [5 ]
Arakawa, H. [1 ]
Ito, E. [6 ]
Sanada, M. [2 ]
Miyano, S. [7 ]
Ogawa, S. [2 ]
Hayashi, Y. [3 ]
机构
[1] Gunma Univ, Grad Sch Med, Maebashi, Gunma 371, Japan
[2] Univ Tokyo, Grad Sch Med, Canc Genom Project, Tokyo, Japan
[3] Gunma Childrens Med Ctr, Shibukawa, Japan
[4] Univ Tokyo, Grad Sch Med, Tokyo, Japan
[5] Shizuoka Childrens Hosp, Shizuoka, Japan
[6] Hirosaki Univ, Grad Sch Med, Hirosaki, Aomori, Japan
[7] Univ Tokyo, Inst Med Sci, Grad Sch Med, Lab DNA Informat Anal,Human Genome Ctr, Tokyo, Japan
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:6 / 6
页数:1
相关论文
共 50 条
  • [1] Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia
    Heo, Seong Gu
    Koh, Youngil
    Kim, Jong Kwang
    Jung, Jongsun
    Kim, Hyung-Lae
    Yoon, Sung-Soo
    Park, Ji Wan
    [J]. BMC MEDICAL GENETICS, 2017, 18
  • [2] Archiving of Somatic Novel Mutations Using Whole-Exome Sequencing in Pakistani Myeloid Leukemic Patients
    Khalil, Abdul Rehman
    Naz, Arshi
    Ujjan, Ikramdin
    Shamsi, Tahir S.
    [J]. BLOOD, 2019, 134
  • [3] Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing
    Cromer, M. Kyle
    Starker, Lee F.
    Choi, Murim
    Udelsman, Robert
    Nelson-Williams, Carol
    Lifton, Richard P.
    Carling, Tobias
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (09): : E1774 - E1781
  • [4] Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype
    Grossmann, Vera
    Tiacci, Enrico
    Holmes, Antony B.
    Kohlmann, Alexander
    Martelli, Maria Paola
    Kern, Wolfgang
    Spanhol-Rosseto, Ariele
    Klein, Hans-Ulrich
    Dugas, Martin
    Schindela, Sonja
    Trifonov, Vladimir
    Schnittger, Susanne
    Haferlach, Claudia
    Bassan, Renato
    Wells, Victoria A.
    Spinelli, Orietta
    Chan, Joseph
    Rossi, Roberta
    Baldoni, Stefano
    De Carolis, Luca
    Goetze, Katharina
    Serve, Hubert
    Peceny, Rudolf
    Kreuzer, Karl-Anton
    Oruzio, Daniel
    Specchia, Giorgina
    Di Raimondo, Francesco
    Fabbiano, Francesco
    Sborgia, Marco
    Liso, Arcangelo
    Farinelli, Laurent
    Rambaldi, Alessandro
    Pasqualucci, Laura
    Rabadan, Raul
    Haferlach, Torsten
    Falini, Brunangelo
    [J]. BLOOD, 2011, 118 (23) : 6153 - 6163
  • [5] Discovery of somatic mutations in the progression of chronic myeloid leukemia by whole-exome sequencing
    Huang, Y.
    Zheng, J.
    Hu, J. D.
    Wu, Y. A.
    Zheng, X. Y.
    Liu, T. B.
    Chen, F. L.
    [J]. GENETICS AND MOLECULAR RESEARCH, 2014, 13 (01) : 945 - 953
  • [6] Identification of novel mutations in endometrial cancer patients by whole-exome sequencing
    Chang, Ya-Sian
    Huang, Hsien-Da
    Yeh, Kun-Tu
    Chang, Jan-Gowth
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2017, 50 (05) : 1778 - 1784
  • [7] Identification of somatic mutations in non-small cell lung carcinomas using whole-exome sequencing
    Liu, Pengyuan
    Morrison, Carl
    Wang, Liang
    Xiong, Donghai
    Vedell, Peter
    Cui, Peng
    Hua, Xing
    Ding, Feng
    Lu, Yan
    James, Michael
    Ebben, John D.
    Xu, Haiming
    Adjei, Alex A.
    Head, Karen
    Andrae, JaimeW.
    Tschannen, Michael R.
    Jacob, Howard
    Pan, Jing
    Zhang, Qi
    Van den Bergh, Francoise
    Xiao, Haijie
    Lo, Ken C.
    Patel, Jigar
    Richmond, Todd
    Watt, Mary-Anne
    Albert, Thomas
    Selzer, Rebecca
    Anderson, Marshall
    Wang, Jiang
    Wang, Yian
    Starnes, Sandra
    Yang, Ping
    You, Ming
    [J]. CARCINOGENESIS, 2012, 33 (07) : 1270 - 1276
  • [8] SOMATIC MUTATIONS IN NEWLY-DIAGNOSED CHRONIC MYELOID LEUKEMIA DETECTED BY WHOLE-EXOME SEQUENCING
    Nakaseko, C.
    Takeda, J.
    Togasaki, E.
    Yoshida, K.
    Shiozawa, Y.
    Takeuchi, M.
    Oshima, M.
    Saraya, A.
    Iwama, A.
    Yokote, K.
    Sakaida, E.
    Hirase, C.
    Takeshita, A.
    Imai, K.
    Okumura, H.
    Morishita, Y.
    Usui, N.
    Takahashi, N.
    Fujisawa, S.
    Shiraishi, Y.
    Chiba, K.
    Tanaka, H.
    Kiyoi, H.
    Ohnishi, K.
    Ohtake, S.
    Asou, N.
    Kobayashi, Y.
    Miyazaki, Y.
    Miyano, S.
    Ogawa, S.
    Matsumura, I.
    Naoe, T.
    [J]. HAEMATOLOGICA, 2016, 101 : 232 - 233
  • [9] Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers
    Zheng, Cui-Xia
    Gu, Zhao-Hui
    Han, Bing
    Zhang, Rong-Xin
    Pan, Chun-Ming
    Xiang, Yi
    Rong, Xia-Jun
    Chen, Xia
    Li, Qing-Yun
    Wan, Huan-Ying
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2013, 43 (03) : 755 - 764
  • [10] WHOLE-EXOME SEQUENCING IDENTIFIES NOVEL RECURRENT SOMATIC MUTATIONS IN SPORADIC PARATHYROID ADENOMAS
    Zhang, Z. L.
    Wei, Z.
    [J]. OSTEOPOROSIS INTERNATIONAL, 2018, 29 : S242 - S242