BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 37198482)

  • 21. 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]  

  • 22. Palindromic amplification of the ERBB2 oncogene in primary HER2-positive breast tumors.
    Marotta M; Onodera T; Johnson J; Budd GT; Watanabe T; Cui X; Giuliano AE; Niida A; Tanaka H
    Sci Rep; 2017 Feb; 7():41921. PubMed ID: 28211519
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Inverted DNA repeats channel repair of distant double-strand breaks into chromatid fusions and chromosomal rearrangements.
    VanHulle K; Lemoine FJ; Narayanan V; Downing B; Hull K; McCullough C; Bellinger M; Lobachev K; Petes TD; Malkova A
    Mol Cell Biol; 2007 Apr; 27(7):2601-14. PubMed ID: 17242181
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Extrachromosomal DNA is associated with oncogene amplification and poor outcome across multiple cancers.
    Kim H; Nguyen NP; Turner K; Wu S; Gujar AD; Luebeck J; Liu J; Deshpande V; Rajkumar U; Namburi S; Amin SB; Yi E; Menghi F; Schulte JH; Henssen AG; Chang HY; Beck CR; Mischel PS; Bafna V; Verhaak RGW
    Nat Genet; 2020 Sep; 52(9):891-897. PubMed ID: 32807987
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Intrachromosomal gene amplification triggered by hairpin-capped breaks requires homologous recombination and is independent of nonhomologous end-joining.
    Narayanan V; Lobachev KS
    Cell Cycle; 2007 Aug; 6(15):1814-8. PubMed ID: 17671429
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Focal amplification and oncogene dependency of GAB2 in breast cancer.
    Bocanegra M; Bergamaschi A; Kim YH; Miller MA; Rajput AB; Kao J; Langerød A; Han W; Noh DY; Jeffrey SS; Huntsman DG; Børresen-Dale AL; Pollack JR
    Oncogene; 2010 Feb; 29(5):774-9. PubMed ID: 19881546
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MYEOV: a candidate gene for DNA amplification events occurring centromeric to CCND1 in breast cancer.
    Janssen JW; Cuny M; Orsetti B; Rodriguez C; Vallés H; Bartram CR; Schuuring E; Theillet C
    Int J Cancer; 2002 Dec; 102(6):608-14. PubMed ID: 12448002
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Marked contribution of alternative end-joining to chromosome-translocation-formation by stochastically induced DNA double-strand-breaks in G2-phase human cells.
    Soni A; Siemann M; Pantelias GE; Iliakis G
    Mutat Res Genet Toxicol Environ Mutagen; 2015 Nov; 793():2-8. PubMed ID: 26520366
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular profiling of invasive breast cancer by multiplex ligation-dependent probe amplification-based copy number analysis of tumor suppressor and oncogenes.
    Moelans CB; de Weger RA; Monsuur HN; Vijzelaar R; van Diest PJ
    Mod Pathol; 2010 Jul; 23(7):1029-39. PubMed ID: 20473280
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mode of ATM-dependent suppression of chromosome translocation.
    Yamauchi M; Suzuki K; Oka Y; Suzuki M; Kondo H; Yamashita S
    Biochem Biophys Res Commun; 2011 Dec; 416(1-2):111-8. PubMed ID: 22093823
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line.
    Nattestad M; Goodwin S; Ng K; Baslan T; Sedlazeck FJ; Rescheneder P; Garvin T; Fang H; Gurtowski J; Hutton E; Tseng E; Chin CS; Beck T; Sundaravadanam Y; Kramer M; Antoniou E; McPherson JD; Hicks J; McCombie WR; Schatz MC
    Genome Res; 2018 Aug; 28(8):1126-1135. PubMed ID: 29954844
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Polymerase chain reaction amplification of long DNA targets: application to analysis of chromosomal translocations in human B-cell tumors (review).
    Akasaka T; Akasaka H; Ohno H
    Int J Oncol; 1998 Jan; 12(1):113-21. PubMed ID: 9454894
    [TBL] [Abstract][Full Text] [Related]  

  • 33. When, where and how the bridge breaks: anaphase bridge breakage plays a crucial role in gene amplification and HSR generation.
    Shimizu N; Shingaki K; Kaneko-Sasaguri Y; Hashizume T; Kanda T
    Exp Cell Res; 2005 Jan; 302(2):233-43. PubMed ID: 15561104
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers.
    Blumrich A; Zapatka M; Brueckner LM; Zheglo D; Schwab M; Savelyeva L
    Hum Mol Genet; 2011 Apr; 20(8):1488-501. PubMed ID: 21258086
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mechanisms that promote and suppress chromosomal translocations in lymphocytes.
    Gostissa M; Alt FW; Chiarle R
    Annu Rev Immunol; 2011; 29():319-50. PubMed ID: 21219174
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Telomere dysfunction and chromosome instability.
    Murnane JP
    Mutat Res; 2012 Feb; 730(1-2):28-36. PubMed ID: 21575645
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Assessment of palindromes as platforms for DNA amplification in breast cancer.
    Guenthoer J; Diede SJ; Tanaka H; Chai X; Hsu L; Tapscott SJ; Porter PL
    Genome Res; 2012 Feb; 22(2):232-45. PubMed ID: 21752925
    [TBL] [Abstract][Full Text] [Related]  

  • 38. ATM-deficient thymic lymphoma is associated with aberrant tcrd rearrangement and gene amplification.
    Zha S; Bassing CH; Sanda T; Brush JW; Patel H; Goff PH; Murphy MM; Tepsuporn S; Gatti RA; Look AT; Alt FW
    J Exp Med; 2010 Jul; 207(7):1369-80. PubMed ID: 20566716
    [TBL] [Abstract][Full Text] [Related]  

  • 39. DNA amplifications in breast cancer: genotypic-phenotypic correlations.
    Shiu KK; Natrajan R; Geyer FC; Ashworth A; Reis-Filho JS
    Future Oncol; 2010 Jun; 6(6):967-84. PubMed ID: 20528234
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sequence analysis of mutations and translocations across breast cancer subtypes.
    Banerji S; Cibulskis K; Rangel-Escareno C; Brown KK; Carter SL; Frederick AM; Lawrence MS; Sivachenko AY; Sougnez C; Zou L; Cortes ML; Fernandez-Lopez JC; Peng S; Ardlie KG; Auclair D; Bautista-Piña V; Duke F; Francis J; Jung J; Maffuz-Aziz A; Onofrio RC; Parkin M; Pho NH; Quintanar-Jurado V; Ramos AH; Rebollar-Vega R; Rodriguez-Cuevas S; Romero-Cordoba SL; Schumacher SE; Stransky N; Thompson KM; Uribe-Figueroa L; Baselga J; Beroukhim R; Polyak K; Sgroi DC; Richardson AL; Jimenez-Sanchez G; Lander ES; Gabriel SB; Garraway LA; Golub TR; Melendez-Zajgla J; Toker A; Getz G; Hidalgo-Miranda A; Meyerson M
    Nature; 2012 Jun; 486(7403):405-9. PubMed ID: 22722202
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.