These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 32973084)

  • 1. Chromothripsis in Human Breast Cancer.
    Bolkestein M; Wong JKL; Thewes V; Körber V; Hlevnjak M; Elgaafary S; Schulze M; Kommoss FKF; Sinn HP; Anzeneder T; Hirsch S; Devens F; Schröter P; Höfer T; Schneeweiss A; Lichter P; Zapatka M; Ernst A
    Cancer Res; 2020 Nov; 80(22):4918-4931. PubMed ID: 32973084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer.
    Lin CL; Tan X; Chen M; Kusi M; Hung CN; Chou CW; Hsu YT; Wang CM; Kirma N; Chen CL; Lin CH; Lathrop KI; Elledge R; Kaklamani VG; Mitsuya K; Huang TH
    BMC Med Genomics; 2020 May; 13(1):69. PubMed ID: 32408897
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The landscape of chromothripsis across adult cancer types.
    Voronina N; Wong JKL; Hübschmann D; Hlevnjak M; Uhrig S; Heilig CE; Horak P; Kreutzfeldt S; Mock A; Stenzinger A; Hutter B; Fröhlich M; Brors B; Jahn A; Klink B; Gieldon L; Sieverling L; Feuerbach L; Chudasama P; Beck K; Kroiss M; Heining C; Möhrmann L; Fischer A; Schröck E; Glimm H; Zapatka M; Lichter P; Fröhling S; Ernst A
    Nat Commun; 2020 May; 11(1):2320. PubMed ID: 32385320
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer.
    Kloosterman WP; Hoogstraat M; Paling O; Tavakoli-Yaraki M; Renkens I; Vermaat JS; van Roosmalen MJ; van Lieshout S; Nijman IJ; Roessingh W; van 't Slot R; van de Belt J; Guryev V; Koudijs M; Voest E; Cuppen E
    Genome Biol; 2011 Oct; 12(10):R103. PubMed ID: 22014273
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells.
    Hattori A; Okamura K; Terada Y; Tanaka R; Katoh-Fukui Y; Matsubara Y; Matsubara K; Kagami M; Horikawa R; Fukami M
    BMC Med Genomics; 2019 May; 12(1):77. PubMed ID: 31138192
    [TBL] [Abstract][Full Text] [Related]  

  • 6. APOBEC3-dependent kataegis and TREX1-driven chromothripsis during telomere crisis.
    Maciejowski J; Chatzipli A; Dananberg A; Chu K; Toufektchan E; Klimczak LJ; Gordenin DA; Campbell PJ; de Lange T
    Nat Genet; 2020 Sep; 52(9):884-890. PubMed ID: 32719516
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genomic profiling of Acute lymphoblastic leukemia in ataxia telangiectasia patients reveals tight link between ATM mutations and chromothripsis.
    Ratnaparkhe M; Hlevnjak M; Kolb T; Jauch A; Maass KK; Devens F; Rode A; Hovestadt V; Korshunov A; Pastorczak A; Mlynarski W; Sungalee S; Korbel J; Hoell J; Fischer U; Milde T; Kramm C; Nathrath M; Chrzanowska K; Tausch E; Takagi M; Taga T; Constantini S; Loeffen J; Meijerink J; Zielen S; Gohring G; Schlegelberger B; Maass E; Siebert R; Kunz J; Kulozik AE; Worst B; Jones DT; Pfister SM; Zapatka M; Lichter P; Ernst A
    Leukemia; 2017 Oct; 31(10):2048-2056. PubMed ID: 28196983
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational mechanisms of amplifications revealed by analysis of clustered rearrangements in breast cancers.
    Głodzik D; Purdie C; Rye IH; Simpson PT; Staaf J; Span PN; Russnes HG; Nik-Zainal S
    Ann Oncol; 2018 Nov; 29(11):2223-2231. PubMed ID: 30252041
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing.
    Cortés-Ciriano I; Lee JJ; Xi R; Jain D; Jung YL; Yang L; Gordenin D; Klimczak LJ; Zhang CZ; Pellman DS; ; Park PJ;
    Nat Genet; 2020 Mar; 52(3):331-341. PubMed ID: 32025003
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole-Genome Sequencing Reveals Diverse Models of Structural Variations in Esophageal Squamous Cell Carcinoma.
    Cheng C; Zhou Y; Li H; Xiong T; Li S; Bi Y; Kong P; Wang F; Cui H; Li Y; Fang X; Yan T; Li Y; Wang J; Yang B; Zhang L; Jia Z; Song B; Hu X; Yang J; Qiu H; Zhang G; Liu J; Xu E; Shi R; Zhang Y; Liu H; He C; Zhao Z; Qian Y; Rong R; Han Z; Zhang Y; Luo W; Wang J; Peng S; Yang X; Li X; Li L; Fang H; Liu X; Ma L; Chen Y; Guo S; Chen X; Xi Y; Li G; Liang J; Yang X; Guo J; Jia J; Li Q; Cheng X; Zhan Q; Cui Y
    Am J Hum Genet; 2016 Feb; 98(2):256-74. PubMed ID: 26833333
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2
    Vasmatzis G; Wang X; Smadbeck JB; Murphy SJ; Geiersbach KB; Johnson SH; Gaitatzes AG; Asmann YW; Kosari F; Borad MJ; Serie DJ; McLaughlin SA; Kachergus JM; Necela BM; Thompson EA
    BMC Cancer; 2018 Jul; 18(1):738. PubMed ID: 30005627
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal catastrophe is a frequent event in clinically insignificant prostate cancer.
    Kovtun IV; Murphy SJ; Johnson SH; Cheville JC; Vasmatzis G
    Oncotarget; 2015 Oct; 6(30):29087-96. PubMed ID: 26337081
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene fusions by chromothripsis of chromosome 5q in the VCaP prostate cancer cell line.
    Teles Alves I; Hiltemann S; Hartjes T; van der Spek P; Stubbs A; Trapman J; Jenster G
    Hum Genet; 2013 Jun; 132(6):709-13. PubMed ID: 23615946
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.
    Walsh T; Casadei S; Coats KH; Swisher E; Stray SM; Higgins J; Roach KC; Mandell J; Lee MK; Ciernikova S; Foretova L; Soucek P; King MC
    JAMA; 2006 Mar; 295(12):1379-88. PubMed ID: 16551709
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Remarkable similarities of chromosomal rearrangements between primary human breast cancers and matched distant metastases as revealed by whole-genome sequencing.
    Tang MH; Dahlgren M; Brueffer C; Tjitrowirjo T; Winter C; Chen Y; Olsson E; Wang K; Törngren T; Sjöström M; Grabau D; Bendahl PO; Rydén L; Niméus E; Saal LH; Borg Å; Gruvberger-Saal SK
    Oncotarget; 2015 Nov; 6(35):37169-84. PubMed ID: 26439695
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic hotspots but few recurrent fusion genes in breast cancer.
    Fimereli D; Fumagalli D; Brown D; Gacquer D; Rothé F; Salgado R; Larsimont D; Sotiriou C; Detours V
    Genes Chromosomes Cancer; 2018 Jul; 57(7):331-338. PubMed ID: 29436103
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutational game changer: Chromothripsis and its emerging relevance to cancer.
    Luijten MNH; Lee JXT; Crasta KC
    Mutat Res Rev Mutat Res; 2018; 777():29-51. PubMed ID: 30115429
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults.
    Arniani S; Pierini V; Pellanera F; Matteucci C; Di Giacomo D; Bardelli V; Quintini M; Mavridou E; Lema Fernandez AG; Nardelli C; Moretti M; Gorello P; Crescenzi B; Romoli S; Beacci D; Cerrano M; Fracchiolla N; Sica S; Forghieri F; Giglio F; Dargenio M; Elia L; La Starza R; Mecucci C
    Leukemia; 2022 Nov; 36(11):2577-2585. PubMed ID: 35974102
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome-breakage genomic instability and chromothripsis in breast cancer.
    Przybytkowski E; Lenkiewicz E; Barrett MT; Klein K; Nabavi S; Greenwood CM; Basik M
    BMC Genomics; 2014 Jul; 15(1):579. PubMed ID: 25011954
    [TBL] [Abstract][Full Text] [Related]  

  • 20. When Genome Maintenance Goes Badly Awry.
    Kass EM; Moynahan ME; Jasin M
    Mol Cell; 2016 Jun; 62(5):777-87. PubMed ID: 27259208
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.