Whole Exome Sequencing Reveals Acquired SF3B1 Mutations Defining Patients with Acquired Idiopathic Sideroblastic Anaemia

被引：0
|
作者：
Smith, Alexander E. [1 ]
Mian, Syed A. [1 ]
Kulasekararaj, Austin G. [1 ]
Mohamedali, Azim M. [1 ]
Mufti, Ghulam J. [1 ]
机构：
[1] Kings Coll Hosp London, Dept Haematol Med, London, England
来源：
BLOOD | 2011年 / 118卷 / 21期
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：
引用
收藏
页码：1204 / 1204
页数：1
相关论文
共 50 条
  • [31] Analysis of SF3B1 mutations in monoclonal B-cell lymphocytosis
    Greco, Mariangela
    Capello, Daniela
    Bruscaggin, Alessio
    Spina, Valeria
    Rasi, Silvia
    Monti, Sara
    Ciardullo, Carmela
    Cresta, Stefania
    Fangazio, Marco
    Gaidano, Gianluca
    Foa, Robin
    Rossi, Davide
    HEMATOLOGICAL ONCOLOGY, 2013, 31 (01) : 54 - 55
  • [32] SF3B1 MUTATIONS AND THEIR IMPACT ON CELLULAR BIOENERGETICS IN MYELODYSPLASTIC SYNDROMES
    Hrustincova, A.
    Trsova, I.
    Krejcik, Z.
    Kundrat, D.
    Belickova, M.
    Kaisrlikova, M.
    Vesela, J.
    Klema, J.
    Rysavy, P.
    Suttnar, J.
    Hlavackova, A.
    Jonasova, A.
    Cermak, J.
    Merkerova, M. Dostalova
    LEUKEMIA RESEARCH, 2023, 128
  • [33] SF3B1 Mutations Are Associated with Alternative Splicing in Uveal Melanoma
    Furney, Simon J.
    Pedersen, Malin
    Gentien, David
    Dumont, Amaury G.
    Rapinat, Audrey
    Desjardins, Laurence
    Turajlic, Samra
    Piperno-Neumann, Sophie
    de la Grange, Pierre
    Roman-Roman, Sergio
    Stern, Marc-Henri
    Marais, Richard
    CANCER DISCOVERY, 2013, 3 (10) : 1122 - 1129
  • [34] SF3B1 and EIF1AX mutations in uveal melanoma
    Verdijk, R. M.
    Yavuzyigitoglu, S.
    Koopmans, A.
    Smit, K.
    Vaarwater, J.
    Paridaens, D.
    Kilic, E.
    de Klein, A.
    VIRCHOWS ARCHIV, 2016, 469 : S10 - S11
  • [35] The biological function and clinical significance of SF3B1 mutations in cancer
    Zhou, Zhixia
    Gong, Qi
    Wang, Yin
    Li, Mengkun
    Wang, Lu
    Ding, Hongfei
    Li, Peifeng
    BIOMARKER RESEARCH, 2020, 8 (01)
  • [36] SF3B1 and BAP1 Mutations in malignant blue Nevus
    Griewank, K.
    Mueller, H.
    Jackett, L.
    Emberger, M.
    Moeller, I
    van de Nes, J.
    Zimmer, L.
    Livingstone, E.
    Wiesner, T.
    Scholz, S.
    Cosgarea, I
    Sucker, A.
    Schimming, T.
    Hillen, U.
    Schilling, B.
    Paschen, A.
    Reis, H.
    Mentzel, T.
    Kutzner, H.
    Ruetten, A.
    Murali, R.
    Scolyer, R.
    Schadendorf, D.
    JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2017, 15 : 2 - 2
  • [37] The biological function and clinical significance of SF3B1 mutations in cancer
    Zhixia Zhou
    Qi Gong
    Yin Wang
    Mengkun Li
    Lu Wang
    Hongfei Ding
    Peifeng Li
    Biomarker Research, 8
  • [38] SF3B1 Mutations Frequently Occur With Both ATM Mutations and TP53 Mutations In CLL Patients
    Navrkalova, Veronika
    Malcikova, Jitka
    Kantorova, Barbara
    Sebejova, Ludmila
    Plevova, Karla
    Mraz, Marek
    Doubek, Michael
    Brychtova, Yvona
    Smardova, Jana
    Mayer, Jiri
    Pospisilova, Sarka
    Trbusek, Martin
    BLOOD, 2013, 122 (21)
  • [39] Modeling SF3B1 Mutations in Cancer: Advances, Challenges, and Opportunities
    Inoue, Daichi
    Abdel-Wahab, Omar
    CANCER CELL, 2016, 30 (03) : 371 - 373
  • [40] Whole Exome Sequencing in Thai Patients With Retinitis Pigmentosa Reveals Novel Mutations in Six Genes
    Jinda, Worapoj
    Taylor, Todd D.
    Suzuki, Yutaka
    Thongnoppakhun, Wanna
    Limwongse, Chanin
    Lertrit, Patcharee
    Suriyaphol, Prapat
    Trinavarat, Adisak
    Atchaneeyasakul, La-ongsri
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (04) : 2259 - 2268
12345