MULTIPLE RECURRENT GENOMIC REARRANGEMENTS AND FRAGILE SITES IN HUMAN CANCER

被引：36
|
作者：
YUNIS, JJ
机构：
来源：
SOMATIC CELL AND MOLECULAR GENETICS | 1987年 / 13卷 / 04期
关键词：
D O I：
10.1007/BF01534938
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：397 / 403
页数：7
相关论文
共 50 条
  • [31] Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
    Akdemir, Kadir C.
    Le, Victoria T.
    Chandran, Sahaana
    Li, Yilong
    Verhaak, Roel G.
    Beroukhim, Rameen
    Campbell, Peter J.
    Chin, Lynda
    Dixon, Jesse R.
    Futreal, P. Andrew
    Alvarez, Eva G.
    Baez-Ortega, Adrian
    Beroukhim, Rameen
    Boutros, Paul C.
    Bowtell, David D. L.
    Brors, Benedikt
    Burns, Kathleen H.
    Chan, Kin
    Chen, Ken
    Cortes-Ciriano, Isidro
    Dueso-Barroso, Ana
    Dunford, Andrew J.
    Edwards, Paul A.
    Estivill, Xavier
    Etemadmoghadam, Dariush
    Feuerbach, Lars
    Fink, J. Lynn
    Frenkel-Morgenstern, Milana
    Garsed, Dale W.
    Gerstein, Mark
    Gordenin, Dmitry A.
    Haan, David
    Haber, James E.
    Hess, Julian M.
    Hutter, Barbara
    Imielinski, Marcin
    Jones, David T. W.
    Ju, Young Seok
    Kazanov, Marat D.
    Klimczak, Leszek J.
    Koh, Youngil
    Korbel, Jan O.
    Kumar, Kiran
    Lee, Eunjung Alice
    Lee, Jake June-Koo
    Lynch, Andy G.
    Macintyre, Geoff
    Markowetz, Florian
    Martincorena, Inigo
    Martinez-Fundichely, Alexander
    NATURE GENETICS, 2020, 52 (03) : 294 - +
  • [32] FRAGILE SITES AND CHROMOSOME BREAKPOINTS IN CONSTITUTIONAL REARRANGEMENTS .1. AMNIOCENTESIS
    HECHT, F
    HECHT, BK
    CLINICAL GENETICS, 1984, 26 (03) : 169 - 173
  • [33] Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites
    Burrow, Allison A.
    Williams, Laura E.
    Pierce, Levi C. T.
    Wang, Yuh-Hwa
    BMC GENOMICS, 2009, 10
  • [34] Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites
    Allison A Burrow
    Laura E Williams
    Levi CT Pierce
    Yuh-Hwa Wang
    BMC Genomics, 10
  • [35] Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series
    Shwan, Nzar A. A.
    Louzada, Sandra
    Yang, Fengtang
    Armour, John A. L.
    HUMAN MUTATION, 2017, 38 (05) : 532 - 539
  • [36] Complex human chromosomal and genomic rearrangements
    Zhang, Feng
    Carvalho, Claudia M. B.
    Lupski, James R.
    TRENDS IN GENETICS, 2009, 25 (07) : 298 - 307
  • [37] Structural genomic rearrangements in colorectal cancer
    van den Broek, E.
    Haan, J. C.
    Carvalho, B.
    de Wiel, M. A. van
    Nagtegaal, I. D.
    Punt, C. J. A.
    Ylstra, B.
    Meijer, G. A.
    Fijneman, R. J. A.
    CELLULAR ONCOLOGY, 2012, 35 : S19 - S19
  • [38] Genomic rearrangements in inherited disease and cancer
    Chen, Jian-Min
    Cooper, David N.
    Ferec, Claude
    Kehrer-Sawatzki, Hildegard
    Patrinos, George P.
    SEMINARS IN CANCER BIOLOGY, 2010, 20 (04) : 222 - 233
  • [39] Genomic rearrangements of PTEN in prostate cancer
    Phin, Sopheap
    Moore, Mathew W.
    Cotter, Philip D.
    FRONTIERS IN ONCOLOGY, 2013, 3
  • [40] HYBRIDIZATION OF TELOMERIC DNA TO INTERSTITIAL CHROMOSOMAL SITES - CORRELATION WITH FRAGILE SITES AND BREAKPOINTS OF CHROMOSOMAL REARRANGEMENTS
    ADEKUNLE, S
    MILUNSKY, A
    WYANDT, HE
    CYTOGENETICS AND CELL GENETICS, 1992, 60 (3-4): : 265 - 265
12345