Archiving of Somatic Novel Mutations Using Whole-Exome Sequencing in Pakistani Myeloid Leukemic Patients

被引:0
|
作者
Khalil, Abdul Rehman [1 ]
Naz, Arshi [2 ]
Ujjan, Ikramdin [1 ]
Shamsi, Tahir S. [3 ]
机构
[1] Liaquat Univ Med & Hlth Sci, Jamshoro, Pakistan
[2] NIBD, Karachi, Pakistan
[3] Natl Inst Blood Dis & Bone Marrow Transplantat, Dept Clin Hematol, Karachi, Pakistan
关键词
Acute myeloid leukemia; Gene ontology; Pathway analysis; Somatic mutation; Subtype-specific; mutation; Whole-exome sequencing;
D O I
10.1182/blood-2019-131688
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
5167
引用
收藏
页数:3
相关论文
共 50 条
  • [1] 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
  • [2] Discovery of somatic mutations in the progression of chronic myeloid leukemia by whole-exome sequencing
    Huang, Y.
    Zheng, J.
    Hu, J. D.
    Wu, Y. A.
    Zheng, X. Y.
    Liu, T. B.
    Chen, F. L.
    GENETICS AND MOLECULAR RESEARCH, 2014, 13 (01) : 945 - 953
  • [3] Whole-Exome Sequencing Identifies Small Mutations in Pakistani Muscular Dystrophy Patients
    Zehravi, Mehwish
    Wahid, Mohsin
    Ashraf, Junaid
    Fatima, Tehseen
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2021, 25 (03) : 218 - 226
  • [4] Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing
    Cromer, M. Kyle
    Starker, Lee F.
    Choi, Murim
    Udelsman, Robert
    Nelson-Williams, Carol
    Lifton, Richard P.
    Carling, Tobias
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (09): : E1774 - E1781
  • [5] IDENTIFICATION OF NOVEL SOMATIC MUTATIONS IN PEDIATRIC ACUTE MYELOID LEUKEIMIA USING WHOLE-EXOME RESEQUENCING
    Shiba, N.
    Yoshida, K.
    Okuno, Y.
    Shiraishi, Y.
    Kon, A.
    Nagata, Y.
    Ohki, K.
    Park, M.
    Kato, M.
    Kanazawa, T.
    Takita, J.
    Kudo, K.
    Arakawa, H.
    Ito, E.
    Sanada, M.
    Miyano, S.
    Ogawa, S.
    Hayashi, Y.
    PEDIATRIC BLOOD & CANCER, 2013, 60 : 6 - 6
  • [6] Genomic Studies of Brazilian Patients with Hepatoblastoma: Insight Into Somatic Mutations Using Whole-Exome Sequencing
    Aguiar, T.
    Rodrigues, T.
    Rivas, M.
    Aparecida, F.
    Fernandes, G.
    Valieris, R.
    Lima da Costa, C. M.
    Werneck, I.
    Cypriano, M.
    Caminada de Toledo, S.
    Odone, V.
    Tojal, I.
    Carraro, D.
    Rosenberg, C.
    Krepischi, A.
    PEDIATRIC BLOOD & CANCER, 2018, 65 : S354 - S354
  • [7] Genomic studies of Brazilian patients with hepatoblastoma: Insight into somatic mutations using whole-exome sequencing
    Aguiar, Talita F.
    Rodrigues, Tatiane
    Prates, Maria
    dos Santos, Fernanda Aparecida
    Fernandes, Gustavo
    Lima da Costa, Cecilia Maria
    da Cunha, Isabela Werneck
    Cypriano, Monica
    Caminada de Toledo, Silvia Regina
    de Souza, Jorge Estefano S.
    Valadares, Eugenia
    Borges, Raquel
    Odone, Vicente
    Tojal, Israel
    Carraro, Dirce
    Rosenberg, Carla
    Krepischi, Ana C. V.
    CANCER RESEARCH, 2018, 78 (13)
  • [8] 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
  • [9] SOMATIC MUTATIONS IN NEWLY-DIAGNOSED CHRONIC MYELOID LEUKEMIA DETECTED BY WHOLE-EXOME SEQUENCING
    Nakaseko, C.
    Takeda, J.
    Togasaki, E.
    Yoshida, K.
    Shiozawa, Y.
    Takeuchi, M.
    Oshima, M.
    Saraya, A.
    Iwama, A.
    Yokote, K.
    Sakaida, E.
    Hirase, C.
    Takeshita, A.
    Imai, K.
    Okumura, H.
    Morishita, Y.
    Usui, N.
    Takahashi, N.
    Fujisawa, S.
    Shiraishi, Y.
    Chiba, K.
    Tanaka, H.
    Kiyoi, H.
    Ohnishi, K.
    Ohtake, S.
    Asou, N.
    Kobayashi, Y.
    Miyazaki, Y.
    Miyano, S.
    Ogawa, S.
    Matsumura, I.
    Naoe, T.
    HAEMATOLOGICA, 2016, 101 : 232 - 233
  • [10] Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers
    Zheng, Cui-Xia
    Gu, Zhao-Hui
    Han, Bing
    Zhang, Rong-Xin
    Pan, Chun-Ming
    Xiang, Yi
    Rong, Xia-Jun
    Chen, Xia
    Li, Qing-Yun
    Wan, Huan-Ying
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2013, 43 (03) : 755 - 764