The role of RUNX1 DNA-Binding mutations in acute myeloid leukemia.

被引:0
|
作者
Cammenga, J
Putz, G
Niebuhr, B
Horn, S
Bergholz, U
Buchholz, F
Stocking, C
机构
[1] Heinrich Pette Inst, Hamburg, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, Dresden, Germany
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
1373
引用
收藏
页码:397A / 398A
页数:2
相关论文
共 50 条
  • [21] De Novo Acute Myeloid Leukemia (AML) with RUNX1 Mutations Shows Characteristic Clinicopathologic Features
    Quesada, Andres
    Luthra, Rajyalakshmi
    Patel, Keyur P.
    Singh, Rajesh
    Routbort, Mark
    Loghavi, Sanam
    Khoury, Joseph D.
    Medeiros, Jeffrey
    Bueso-Ramos, Carlos E.
    Kanagal-Shamanna, Rashmi
    MODERN PATHOLOGY, 2016, 29 : 371A - 371A
  • [22] Familial Acute Myeloid Leukemia/Myelodysplastic Syndrome with Germline RUNX1 Mutations: A Single Instituion Experience
    Hathuc, Vivian
    Walkovich, Kelly
    Bixby, Dale
    Shao, Lina
    Smith, Lauren
    LABORATORY INVESTIGATION, 2017, 97 : 467A - 467A
  • [23] Frequent RUNX1 and TP53 Mutations in Secondary Acute Myeloid Leukemia with Mixed Phenotype
    Galera, Pallavi
    Baik, Jeeyeon
    Famulare, Christopher
    Sigler, Allison
    Zhang, Yanming
    Arcila, Maria
    Dogan, Ahmet
    Tallman, Martin
    Levine, Ross
    Glass, Jacob
    Roshal, Mikhail
    Xiao, Wenbin
    LABORATORY INVESTIGATION, 2020, 100 (SUPPL 1) : 1293 - 1294
  • [24] RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis
    Yamato, Genki
    Shiba, Norio
    Yoshida, Kenichi
    Hara, Yusuke
    Shiraishi, Yuichi
    Ohki, Kentaro
    Okubo, Jun
    Park, Myoung-ja
    Sotomatsu, Manabu
    Arakawa, Hirokazu
    Kiyokawa, Nobutaka
    Tomizawa, Daisuke
    Adachi, Souichi
    Taga, Takashi
    Horibe, Keizo
    Miyano, Satoru
    Ogawa, Seishi
    Hayashi, Yasuhide
    BLOOD, 2018, 131 (20) : 2266 - 2270
  • [25] RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features
    V I Gaidzik
    V Teleanu
    E Papaemmanuil
    D Weber
    P Paschka
    J Hahn
    T Wallrabenstein
    B Kolbinger
    C H Köhne
    H A Horst
    P Brossart
    G Held
    A Kündgen
    M Ringhoffer
    K Götze
    M Rummel
    M Gerstung
    P Campbell
    J M Kraus
    H A Kestler
    F Thol
    M Heuser
    B Schlegelberger
    A Ganser
    L Bullinger
    R F Schlenk
    K Döhner
    H Döhner
    Leukemia, 2016, 30 : 2160 - 2168
  • [26] Frequency, Characteristics and Prognostic Significance of RUNX1 mutations in Patients with Acute Myeloid Leukemia, Not Otherwise Specified
    Bae, Mi-Hyun
    Cho, Young-Uk
    Kim, Bohyun
    Lee, Dong Hyun
    Jang, Seongsoo
    Seo, Eul-Ju
    Park, Chan-Jeoung
    Kim, Dae-Young
    Lee, Jung-Hee
    Lee, Je-Hwan
    Lee, Kyoo-Hyung
    Chang, Yoon Hwan
    Kim, In-Suk
    BLOOD, 2015, 126 (23)
  • [27] Differential prognostic impact of RUNX1 mutations according to frontline therapy in patients with acute myeloid leukemia
    Venugopal, Sangeetha
    DiNardo, Courtney D.
    Loghavi, Sanam
    Qiao, Wei
    Ravandi, Farhad
    Konopleva, Marina
    Kadia, Tapan
    Bhalla, Kapil
    Jabbour, Elias
    Issa, Ghayas C.
    Macaron, Walid
    Daver, Naval
    Borthakur, Gautam
    Montalban-Bravo, Guillermo
    Yilmaz, Musa
    Patel, Keyur P.
    Kanagal-Shamanna, Rashmi
    Chien, Kelly
    Maiti, Abhishek
    Kantarjian, Hagop
    Short, Nicholas J.
    AMERICAN JOURNAL OF HEMATOLOGY, 2022, 97 (12) : 1560 - 1567
  • [28] Familial Acute Myeloid Leukemia/Myelodysplastic Syndrome with Germline RUNX1 Mutations: A Single Instituion Experience
    Hathuc, Vivian
    Walkovich, Kelly
    Bixby, Dale
    Shao, Lina
    Smith, Lauren
    MODERN PATHOLOGY, 2017, 30 : 467A - 467A
  • [29] De Novo Acute Myeloid Leukemia (AML) with RUNX1 Mutations Shows Characteristic Clinicopathologic Features
    Quesada, Andres
    Luthra, Rajyalakshmi
    Patel, Keyur P.
    Singh, Rajesh
    Routbort, Mark
    Loghavi, Sanam
    Khoury, Joseph D.
    Medeiros, Jeffrey
    Bueso-Ramos, Carlos E.
    Kanagal-Shamanna, Rashmi
    LABORATORY INVESTIGATION, 2016, 96 : 371A - 371A
  • [30] RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features
    Gaidzik, V. I.
    Teleanu, V.
    Papaemmanuil, E.
    Weber, D.
    Paschka, P.
    Hahn, J.
    Wallrabenstein, T.
    Kolbinger, B.
    Koehne, C. H.
    Horst, H. A.
    Brossart, P.
    Held, G.
    Kuendgen, A.
    Ringhoffer, M.
    Goetze, K.
    Rummel, M.
    Gerstung, M.
    Campbell, P.
    Kraus, J. M.
    Kestler, H. A.
    Thol, F.
    Heuser, M.
    Schlegelberger, B.
    Ganser, A.
    Bullinger, L.
    Schlenk, R. F.
    Doehner, K.
    Doehner, H.
    LEUKEMIA, 2016, 30 (11) : 2160 - 2168