RUNX1 MUTATIONS IN LEUKEMIAS DEVELOPED IN PATIENTS WITH CONGENITAL NEUTROPENIAS

被引:0
|
作者
Steinemann, J. [1 ]
Skokowa, J. [1 ]
Zeidler, C. [1 ]
Goehring, G. [1 ]
Schlegelberger, B. [1 ]
Welte, K. [1 ]
机构
[1] Hannover Med Sch, Hannover, 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
0893
引用
收藏
页码:369 / 369
页数:1
相关论文
共 50 条
  • [41] Novel RUNX1 targeted therapy for AML expressing mutant RUNX1
    Mill, Christopher P.
    DiNardo, Courtney D.
    Fiskus, Warren
    Saenz, Dyana T.
    Nowak, Agnieszka J.
    Sun, Baohua
    Saenz, David N.
    Kornblau, Steven M.
    Bhalla, Kapil N.
    CANCER RESEARCH, 2018, 78 (13)
  • [42] Incidence of Secondary Leukemias in Patients With Severe Chronic Neutropenias
    C Zeidler
    M A Bonilla
    L Boxer
    S Brown
    D C Dale
    B Cham
    C Fier
    M Freedman
    G Kannourakis
    S E Kinsey
    P Mori
    K Welte
    Pediatric Research, 1999, 45 : 752 - 752
  • [43] Germline RUNX1 mutations/deletions and genetic predisposition to hematological malignancies
    Antony-Debre, Ileana
    Duployez, Nicolas
    HEMATOLOGIE, 2021, 27 (01): : 19 - 31
  • [44] The landscape of RUNX1 mutations in breast cancer and its therapeutic potential
    Ariffin, N. S.
    ANNALS OF ONCOLOGY, 2022, 33 : S235 - S235
  • [45] RUNX1 Mutations Reduce the Expression of CEBPA in Acute Myeloid Leukemia
    Grossmann, Vera
    Kohlmann, Alexander
    Dicker, Frank
    Butschalowski, Katrin
    Kern, Wolfgang
    Schnittger, Susanne
    Haferlach, Torsten
    Haferlach, Claudia
    BLOOD, 2011, 118 (21) : 1040 - 1040
  • [46] SCL and RUNX1 regulate RUNX1 gene expression by association to RUNX1-P1 promoter
    Gutierrez, S.
    Martinez, M.
    FEBS JOURNAL, 2014, 281 : 689 - 689
  • [47] ANALYSIS OF THE FUNCTIONAL IMPACT OF RUNX1 MUTATIONS IN MDS STEM CELLS
    Langer, S.
    Kiljan, M.
    Horn, P. A.
    Heinrichs, S.
    LEUKEMIA RESEARCH, 2017, 55 : S123 - S123
  • [48] Spectrum of Abnormalities and Clonal Transformation in Germline RUNX1 Familial Platelet Disorder and a Comparative Analysis with Somatic RUNX1 Mutations in Myeloid Neoplasms
    Difilippo, Emma
    Coltro, Giacomo
    Carr, Ryan M.
    Mangaonkar, Abhishek A.
    Binder, Moritz
    Khan, Shakila P.
    Rodriguez, Vilmarie
    Gangat, Naseema
    Wolanskyj, Alexandra
    Pruthi, Rajiv K.
    Chen, Dong
    He, Rong
    Viswanatha, David S.
    Lasho, Terra
    Finke, Christy
    Tefferi, Ayalew
    Pardanani, Animesh
    Litzow, Mark
    Patnaik, Mrinal M.
    BLOOD, 2019, 134
  • [49] Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis
    Skokowa, Julia
    Steinemann, Doris
    Katsman-Kuipers, Jenny E.
    Zeidler, Cornelia
    Klimenkova, Olga
    Klimiankou, Maksim
    Uenalan, Murat
    Kandabarau, Siarhei
    Makaryan, Vahagn
    Beekman, Renee
    Behrens, Kira
    Stocking, Carol
    Obenauer, Julia
    Schnittger, Susanne
    Kohlmann, Alexander
    Valkhof, Marijke G.
    Hoogenboezem, Remco
    Goehring, Gudrun
    Reinhardt, Dirk
    Schlegelberger, Brigitte
    Stanulla, Martin
    Vandenberghe, Peter
    Donadieu, Jean
    Zwaan, C. Michel
    Touw, Ivo P.
    van den Heuvel-Eibrink, Marry M.
    Dale, David C.
    Welte, Karl
    BLOOD, 2014, 123 (14) : 2229 - 2237
  • [50] Functional characterization of cooperating MGA mutations in RUNX1::RUNX1T1 acute myeloid leukemia
    Thomas, Melvin E.
    Qi, Wenqing
    Walsh, Michael P.
    Ma, Jing
    Westover, Tamara
    Abdelhamed, Sherif
    Ezzell, Lauren J.
    Rolle, Chandra
    Xiong, Emily
    Rosikiewicz, Wojciech
    Xu, Beisi
    Loughran, Allister J.
    Pruett-Miller, Shondra M.
    Janke, Laura J.
    Klco, Jeffery M.
    LEUKEMIA, 2024, 38 (05) : 991 - 1002