RUNX1 Mutations in Myelodysplastic Syndrome

被引:0
|
作者
Quesada, Andres E. [1 ]
Routbort, Mark
Luthra, Rajyalakshmi [1 ]
Patel, Keyur [2 ]
Hidalgo-Lopez, Juliana E. [1 ]
Bueso-Ramos, Carlos [1 ]
Medeiros, L. Jeffrey [1 ]
Kanagal-Shamanna, Rashmi [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Sugar Land, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Bellaire, TX USA
关键词
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1531
引用
收藏
页码:545 / 546
页数:2
相关论文
共 50 条
  • [1] RUNX1 Mutations in Myelodysplastic Syndrome
    Quesada, Andres E.
    Routbort, Mark
    Luthra, Rajyalakshmi
    Patel, Keyur
    Hidalgo-Lopez, Juliana E.
    Bueso-Ramos, Carlos
    Medeiros, L. Jeffrey
    Kanagal-Shamanna, Rashmi
    MODERN PATHOLOGY, 2018, 31 : 545 - 546
  • [2] Point mutations in the AML1/RUNX1 gene associated with myelodysplastic syndrome
    Harada, H
    Harada, Y
    CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2005, 15 (03): : 183 - 196
  • [3] Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations
    H Niimi
    H Harada
    Y Harada
    Y Ding
    J Imagawa
    T Inaba
    T Kyo
    A Kimura
    Leukemia, 2006, 20 : 635 - 644
  • [4] Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations
    Niimi, H
    Harada, H
    Harada, Y
    Ding, Y
    Imagawa, J
    Inaba, T
    Kyo, T
    Kimura, A
    LEUKEMIA, 2006, 20 (04) : 635 - 644
  • [5] 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
  • [6] Overexpression of RUNX3 Represses RUNX1 to Drive Transformation of Myelodysplastic Syndrome
    Yokomizo-Nakano, Takako
    Kubota, Sho
    Bai, Jie
    Hamashima, Ai
    Morii, Mariko
    Sun, Yuqi
    Katagiri, Seiichiro
    Iimori, Mihoko
    Kanai, Akinori
    Tanaka, Daiki
    Oshima, Motohiko
    Harada, Yuka
    Ohyashiki, Kazuma
    Iwama, Atsushi
    Harada, Hironori
    Osato, Motomi
    Sashida, Goro
    CANCER RESEARCH, 2020, 80 (12) : 2523 - 2536
  • [7] 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
  • [8] Prognostic effect of RUNX1 mutations in myelodysplastic syndromes: a meta-analysis
    He, Wei
    Zhao, Caifang
    Hu, Huixian
    HEMATOLOGY, 2020, 25 (01) : 494 - 501
  • [9] Point mutations in the carboxy-terminal region of the AML1/RUNX1 gene associated with myelodysplastic syndrome.
    Harada, H
    Harada, Y
    Niimi, H
    Kimura, A
    Inaba, T
    BLOOD, 2003, 102 (11) : 913A - 914A
  • [10] Mutations in RUNX1 and TP53 Genes Predict Progression in Patients with Lower-Risk Myelodysplastic Syndrome
    Hruba, Monika
    Vesela, Jitka
    Votavova, Hana
    Merkerova, Michaela Dostalova
    Szikszai, Katarina
    Lauermannova, Marie
    Zemanova, Zuzana
    Jonasova, Anna
    Cermak, Jaroslav
    Belickova, Monika
    BLOOD, 2018, 132