Clonal evolution in chronic myeloid leukemia revealed by whole-exome sequencing

被引:0
|
作者
Menezes, Juliane [1 ]
Acquadro, Francesco [1 ]
Gomez-Lopez, Gonzalo [2 ]
Alvarez, Sara [1 ]
Trujillo, Mercedes [3 ]
Garcia-Talavera, Juan [3 ]
Pisano, David G. [2 ]
Cigudosa, Juan C. [1 ]
机构
[1] Ctr Nacl Invest Oncol CNIO, Mol Cytogenet Grp, Madrid, Spain
[2] Ctr Nacl Invest Oncol CNIO, Bioinformat Unit, Madrid, Spain
[3] Hosp N Sra La Candelaria, Hematol Serv, Tenerife, Spain
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
O7
引用
收藏
页码:S25 / S26
页数:2
相关论文
共 50 条
  • [21] Whole-exome and whole-genome sequencing in chronic lymphocytic leukemia: new biomarkers to target
    Hobeika, Charbel
    Rached, Gaelle
    Chebly, Alain
    Chouery, Eliane
    Kourie, Hampig Raphael
    PHARMACOGENOMICS, 2020, 21 (13) : 957 - 962
  • [22] Mutational landscape of prostate tumors revealed by whole-exome sequencing
    I. R. Gilyazova
    M. A. Yankina
    G. B. Kunsbaeva
    E. A. Klimentova
    A. A. Izmaylov
    V. N. Pavlov
    E. K. Khusnutdinova
    Russian Journal of Genetics, 2016, 52 : 999 - 1003
  • [23] Neurogenetic syndromes with cerebellar abnormalities revealed by whole-exome sequencing
    Okamoto, Nobuhiko
    Nishi, Eriko
    Hasegawa, Yuiko
    Yanagi, Kumiko
    Kaname, Tadashi
    Miya, Fuyuki
    Kosaki, Kenjiro
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 480 - 481
  • [24] Mutational landscape of prostate tumors revealed by whole-exome sequencing
    Gilyazova, I. R.
    Yankina, M. A.
    Kunsbaeva, G. B.
    Klimentova, E. A.
    Izmaylov, A. A.
    Pavlov, V. N.
    Khusnutdinova, E. K.
    RUSSIAN JOURNAL OF GENETICS, 2016, 52 (09) : 999 - 1003
  • [25] 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
    BLOOD, 2011, 118 (23) : 6153 - 6163
  • [26] Whole-exome sequencing enhances prognostic classification of myeloid malignancies
    Ruffalo, Matthew
    Husseinzadeh, Holleh
    Makishima, Hideki
    Przychodzen, Bartlomiej
    Ashkar, Mohamed
    Koyutuerk, Mehmet
    Maciejewski, Jaroslaw P.
    LaFramboise, Thomas
    JOURNAL OF BIOMEDICAL INFORMATICS, 2015, 58 : 104 - 113
  • [27] WHOLE EXOME SEQUENCING REVEALS CLONAL EVOLUTION PATTERNS AND DRIVER GENETIC ALTERATIONS OF RELAPSED PEDIATRIC ACUTE MYELOID LEUKEMIA
    Yoshida, K.
    Shiba, N.
    Shimada, A.
    Terui, K.
    Kato, M.
    Shiraishi, Y.
    Okuno, Y.
    Nagata, Y.
    Kon, A.
    Kataoka, K.
    Yoshizato, T.
    Shiozawa, Y.
    Matsunawa, M.
    Chiba, K.
    Tanaka, H.
    Sanada, M.
    Miyano, S.
    Ito, E.
    Hayashi, Y.
    Ogawa, S.
    HAEMATOLOGICA, 2014, 99 : 16 - 17
  • [28] 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
    BMC MEDICAL GENETICS, 2017, 18
  • [29] Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia
    E K Engle
    D A C Fisher
    C A Miller
    M D McLellan
    R S Fulton
    D M Moore
    R K Wilson
    T J Ley
    S T Oh
    Leukemia, 2015, 29 : 869 - 876
  • [30] Clonal Evolution Revealed by Whole Genome Sequencing in a Case of Primary Myelofibrosis Transformed to Secondary Acute Myeloid Leukemia
    Fisher, Daniel A. C.
    Miller, Christopher A.
    McLellan, Michael D.
    Fulton, Robert S.
    Martin, Katherine L.
    Kaiwar, Charu
    Moore, Deborah M.
    Ley, Timothy J.
    Oh, Stephen T.
    BLOOD, 2012, 120 (21)