Whole-exome sequencing of chondroid hamartoma of lung identified no driver mutations

被引:0
|
作者
Choi, Su Hye [1 ,2 ]
Park, Hyeon-Chun [1 ,2 ]
Kim, Min Sung [3 ,4 ]
Chung, Yeun-Jun [2 ,5 ,6 ]
Lee, Sug Hyung [2 ,3 ,4 ]
机构
[1] Catholic Univ Korea, Dept Integrated Res, Ctr Genome Polymorphism, Seoul, South Korea
[2] Catholic Univ Korea, Dept Precis Med Res Ctr, Seoul, South Korea
[3] Catholic Univ Korea, Dept Pathol, Seoul, South Korea
[4] Catholic Univ Korea, Dept Canc Evolut Res Ctr, Seoul, South Korea
[5] Catholic Univ Korea, Dept Microbiol, Seoul, South Korea
[6] Catholic Univ Korea, Dept Integrated Res Ctr Genome Polymorphism, Seoul, South Korea
关键词
HIGH-FREQUENCY; GENES;
D O I
10.1016/j.prp.2017.12.013
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
引用
收藏
页码:459 / 462
页数:4
相关论文
共 50 条
  • [1] Novel mutations identified by whole-exome sequencing in acral melanoma
    Lim, Youngkyoung
    Yoon, Dokyoung
    Lee, Dong-Youn
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2020, 83 (06) : 1792 - 1794
  • [2] Novel mutations identified in patients with tooth agenesis by whole-exome sequencing
    Zhao, Kai
    Lian, Meifei
    Zou, Duohong
    Huang, Wei
    Zhou, Wenjie
    Shen, Yihan
    Wang, Feng
    Wu, Yiqun
    [J]. ORAL DISEASES, 2019, 25 (02) : 523 - 534
  • [3] Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing
    Kondo, Yukiko
    Saitsu, Hirotomo
    Miyamoto, Toshinobu
    Lee, Byung Joo
    Nishiyama, Kiyomi
    Nakashima, Mitsuko
    Tsurusaki, Yoshinori
    Doi, Hiroshi
    Miyake, Noriko
    Kim, Jeong Hun
    Yu, Young Suk
    Matsumoto, Naomichi
    [J]. MOLECULAR VISION, 2013, 19 : 384 - 389
  • [4] DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation
    Jones, Melanie A.
    Ng, Bobby G.
    Bhide, Shruti
    Chin, Ephrem
    Rhodenizer, Devin
    He, Ping
    Losfeld, Marie-Estelle
    He, Miao
    Raymond, Kimiyo
    Berry, Gerard
    Freeze, Hudson H.
    Hegdel, Madhuri R.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 90 (02) : 363 - 368
  • [5] PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
    C. Tzoulis
    Paweł Sztromwasser
    Stefan Johansson
    Ivar Otto Gjerde
    Per Knappskog
    L. A. Bindoff
    [J]. The Cerebellum, 2017, 16 : 272 - 275
  • [6] PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
    Tzoulis, C.
    Sztromwasser, Pawel
    Johansson, Stefan
    Gjerde, Ivar Otto
    Knappskog, Per
    Bindoff, L. A.
    [J]. CEREBELLUM, 2017, 16 (01): : 272 - 275
  • [7] Whole-exome sequencing identified novel mutations in FGA and FGG genes in the patients with decreased fibrinogen
    Cao, Zheng
    Dong, Ying
    Zeng, Jiazi
    Zhu, Hongyuan
    Xie, Xin
    Liu, Jingrui
    Zhai, Yanhong
    Li, Lin
    [J]. THROMBOSIS RESEARCH, 2019, 177 : 79 - 82
  • [8] Whole-exome sequencing identifies somatic mutations associated with lung cancer metastasis to the brain
    Liu, Zhenghao
    Zheng, Meiguang
    Lei, Bingxi
    Zhou, Zhiwei
    Huang, Yutao
    Li, Wenpeng
    Chen, Qinbiao
    Li, Pengcheng
    Deng, Yuefei
    [J]. ANNALS OF TRANSLATIONAL MEDICINE, 2021, 9 (08)
  • [9] 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
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2013, 43 (03) : 755 - 764
  • [10] Pathway Mutations in Breast Cancer Using Whole-Exome Sequencing
    Chang, Ya-Sian
    Chang, Chieh-Min
    Lin, Chien-Yu
    Chao, Dy-San
    Huang, Hsi-Yuan
    Chang, Jan-Gowth
    [J]. ONCOLOGY RESEARCH, 2020, 28 (02) : 107 - 116