BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

423 related articles for article (PubMed ID: 29617666)

  • 1. Systematic Analysis of Splice-Site-Creating Mutations in Cancer.
    Jayasinghe RG; Cao S; Gao Q; Wendl MC; Vo NS; Reynolds SM; Zhao Y; Climente-González H; Chai S; Wang F; Varghese R; Huang M; Liang WW; Wyczalkowski MA; Sengupta S; Li Z; Payne SH; Fenyö D; Miner JH; Walter MJ; ; Vincent B; Eyras E; Chen K; Shmulevich I; Chen F; Ding L
    Cell Rep; 2018 Apr; 23(1):270-281.e3. PubMed ID: 29617666
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Discovery of driver non-coding splice-site-creating mutations in cancer.
    Cao S; Zhou DC; Oh C; Jayasinghe RG; Zhao Y; Yoon CJ; Wyczalkowski MA; Bailey MH; Tsou T; Gao Q; Malone A; Reynolds S; Shmulevich I; Wendl MC; Chen F; Ding L
    Nat Commun; 2020 Nov; 11(1):5573. PubMed ID: 33149122
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of somatic TP53 splice site mutations in diffuse astrocytomas.
    Uno M; Oba-Shinjo SM; de Aguiar PH; Leite CC; Rosemberg S; Miura FK; Junior RM; Scaff M; Nagahashi Marie SK
    Cancer Lett; 2005 Jun; 224(2):321-7. PubMed ID: 15914282
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PARP1 expression and its correlation with survival is tumour molecular subtype dependent in glioblastoma.
    Murnyák B; Kouhsari MC; Hershkovitch R; Kálmán B; Marko-Varga G; Klekner Á; Hortobágyi T
    Oncotarget; 2017 Jul; 8(28):46348-46362. PubMed ID: 28654422
    [TBL] [Abstract][Full Text] [Related]  

  • 5. BAP1 missense mutation c.2054 A>T (p.E685V) completely disrupts normal splicing through creation of a novel 5' splice site in a human mesothelioma cell line.
    Morrison A; Chekaluk Y; Bacares R; Ladanyi M; Zhang L
    PLoS One; 2015; 10(4):e0119224. PubMed ID: 25830670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. High incidence of protein-truncating TP53 mutations in BRCA1-related breast cancer.
    Holstege H; Joosse SA; van Oostrom CT; Nederlof PM; de Vries A; Jonkers J
    Cancer Res; 2009 Apr; 69(8):3625-33. PubMed ID: 19336573
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association and prognostic significance of BRCA1/2-mutation status with neoantigen load, number of tumor-infiltrating lymphocytes and expression of PD-1/PD-L1 in high grade serous ovarian cancer.
    Strickland KC; Howitt BE; Shukla SA; Rodig S; Ritterhouse LL; Liu JF; Garber JE; Chowdhury D; Wu CJ; D'Andrea AD; Matulonis UA; Konstantinopoulos PA
    Oncotarget; 2016 Mar; 7(12):13587-98. PubMed ID: 26871470
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Aberrant splicing induced by missense mutations in BRCA1: clues from a humanized mouse model.
    Yang Y; Swaminathan S; Martin BK; Sharan SK
    Hum Mol Genet; 2003 Sep; 12(17):2121-31. PubMed ID: 12915465
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of two novel BRCA1 germ-line mutations involving splice donor sites.
    Brose MS; Volpe P; Paul K; Stopfer JE; Colligon TA; Calzone KA; Weber BL
    Genet Test; 2004; 8(2):133-8. PubMed ID: 15345110
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Potential Predictive Value of
    Dong ZY; Zhong WZ; Zhang XC; Su J; Xie Z; Liu SY; Tu HY; Chen HJ; Sun YL; Zhou Q; Yang JJ; Yang XN; Lin JX; Yan HH; Zhai HR; Yan LX; Liao RQ; Wu SP; Wu YL
    Clin Cancer Res; 2017 Jun; 23(12):3012-3024. PubMed ID: 28039262
    [No Abstract]   [Full Text] [Related]  

  • 11. RNA analysis reveals splicing mutations and loss of expression defects in MLH1 and BRCA1.
    Sharp A; Pichert G; Lucassen A; Eccles D
    Hum Mutat; 2004 Sep; 24(3):272. PubMed ID: 15300854
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Systematic discovery of complex insertions and deletions in human cancers.
    Ye K; Wang J; Jayasinghe R; Lameijer EW; McMichael JF; Ning J; McLellan MD; Xie M; Cao S; Yellapantula V; Huang KL; Scott A; Foltz S; Niu B; Johnson KJ; Moed M; Slagboom PE; Chen F; Wendl MC; Ding L
    Nat Med; 2016 Jan; 22(1):97-104. PubMed ID: 26657142
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A specific GFP expression assay, penetrance estimate, and histological assessment for a putative splice site mutation in BRCA1.
    Southey MC; Tesoriero A; Young MA; Holloway AJ; Jenkins MA; Whitty J; Misfud S; kConFab ; McLachlan SA; Venter DJ; Armes JE
    Hum Mutat; 2003 Jul; 22(1):86-91. PubMed ID: 12815598
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin.
    Krivokuca A; Dragos VS; Stamatovic L; Blatnik A; Boljevic I; Stegel V; Rakobradovic J; Skerl P; Jovandic S; Krajc M; Magic MB; Novakovic S
    Fam Cancer; 2018 Apr; 17(2):179-185. PubMed ID: 28685474
    [TBL] [Abstract][Full Text] [Related]  

  • 15. UG repeats/TDP-43 interactions near 5' splice sites exert unpredictable effects on splicing modulation.
    Passoni M; De Conti L; Baralle M; Buratti E
    J Mol Biol; 2012 Jan; 415(1):46-60. PubMed ID: 22100394
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation landscape of germline and somatic BRCA1/2 in patients with high-grade serous ovarian cancer.
    Eoh KJ; Kim HM; Lee JY; Kim S; Kim SW; Kim YT; Nam EJ
    BMC Cancer; 2020 Mar; 20(1):204. PubMed ID: 32164585
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Somatic mutations in the BRCA1 gene in Chinese women with sporadic breast cancer.
    Zhang M; Xu Y; Ouyang T; Li J; Wang T; Fan Z; Fan T; Lin B; Xie Y
    Breast Cancer Res Treat; 2012 Feb; 132(1):335-40. PubMed ID: 22116506
    [TBL] [Abstract][Full Text] [Related]  

  • 18. K120R mutation inactivates p53 by creating an aberrant splice site leading to nonsense-mediated mRNA decay.
    Lee SY; Park JH; Jeong S; Kim BY; Kang YK; Xu Y; Chung SK
    Oncogene; 2019 Mar; 38(10):1597-1610. PubMed ID: 30348990
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel crosstalk between BRCA1 and poly (ADP-ribose) polymerase 1 in breast cancer.
    Li D; Bi FF; Chen NN; Cao JM; Sun WP; Zhou YM; Li CY; Yang Q
    Cell Cycle; 2014; 13(21):3442-9. PubMed ID: 25485588
    [TBL] [Abstract][Full Text] [Related]  

  • 20. RNA analysis of eight BRCA1 and BRCA2 unclassified variants identified in breast/ovarian cancer families from Spain.
    Campos B; Díez O; Domènech M; Baena M; Balmaña J; Sanz J; Ramírez A; Alonso C; Baiget M
    Hum Mutat; 2003 Oct; 22(4):337. PubMed ID: 12955719
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.