BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 30224349)

  • 21. The splicing effect of variants at branchpoint elements in cancer genes.
    Canson DM; Dumenil T; Parsons MT; O'Mara TA; Davidson AL; Okano S; Signal B; Mercer TR; Glubb DM; Spurdle AB
    Genet Med; 2022 Feb; 24(2):398-409. PubMed ID: 34906448
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Splicing signals in Drosophila: intron size, information content, and consensus sequences.
    Mount SM; Burks C; Hertz G; Stormo GD; White O; Fields C
    Nucleic Acids Res; 1992 Aug; 20(16):4255-62. PubMed ID: 1508718
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites.
    Zhang P; Chaldebas M; Ogishi M; Al Qureshah F; Ponsin K; Feng Y; Rinchai D; Milisavljevic B; Han JE; Moncada-Vélez M; Keles S; Schröder B; Stenson PD; Cooper DN; Cobat A; Boisson B; Zhang Q; Boisson-Dupuis S; Abel L; Casanova JL
    Proc Natl Acad Sci U S A; 2023 Nov; 120(46):e2314225120. PubMed ID: 37931111
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The 5' end domain of U2 snRNA is required to establish the interaction of U2 snRNP with U2 auxiliary factor(s) during mammalian spliceosome assembly.
    Khellil S; Daugeron MC; Alibert C; Jeanteur P; Cathala G; Brunel C
    Nucleic Acids Res; 1991 Feb; 19(4):877-84. PubMed ID: 1850127
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutational analysis of the U12-dependent branch site consensus sequence.
    Brock JE; Dietrich RC; Padgett RA
    RNA; 2008 Nov; 14(11):2430-9. PubMed ID: 18824513
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Why Selection Might Be Stronger When Populations Are Small: Intron Size and Density Predict within and between-Species Usage of Exonic Splice Associated cis-Motifs.
    Wu X; Hurst LD
    Mol Biol Evol; 2015 Jul; 32(7):1847-61. PubMed ID: 25771198
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MutSpliceDB: A database of splice sites variants with RNA-seq based evidence on effects on splicing.
    Palmisano A; Vural S; Zhao Y; Sonkin D
    Hum Mutat; 2021 Apr; 42(4):342-345. PubMed ID: 33600011
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genome-wide evolution of wobble base-pairing nucleotides of branchpoint motifs with increasing organismal complexity.
    Nguyen H; Das U; Xie J
    RNA Biol; 2020 Mar; 17(3):311-324. PubMed ID: 31814500
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A role for branchpoints in splicing in vivo.
    Rautmann G; Breathnach R
    Nature; 1985 May 30-Jun 5; 315(6018):430-2. PubMed ID: 4000270
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Splicing Enhancers at Intron-Exon Borders Participate in Acceptor Splice Sites Recognition.
    Kováčová T; Souček P; Hujová P; Freiberger T; Grodecká L
    Int J Mol Sci; 2020 Sep; 21(18):. PubMed ID: 32911621
    [TBL] [Abstract][Full Text] [Related]  

  • 31. RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
    Xiong HY; Alipanahi B; Lee LJ; Bretschneider H; Merico D; Yuen RK; Hua Y; Gueroussov S; Najafabadi HS; Hughes TR; Morris Q; Barash Y; Krainer AR; Jojic N; Scherer SW; Blencowe BJ; Frey BJ
    Science; 2015 Jan; 347(6218):1254806. PubMed ID: 25525159
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hotspot exons are common targets of splicing perturbations.
    Glidden DT; Buerer JL; Saueressig CF; Fairbrother WG
    Nat Commun; 2021 May; 12(1):2756. PubMed ID: 33980843
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The U2AF35-related protein Urp contacts the 3' splice site to promote U12-type intron splicing and the second step of U2-type intron splicing.
    Shen H; Zheng X; Luecke S; Green MR
    Genes Dev; 2010 Nov; 24(21):2389-94. PubMed ID: 21041408
    [TBL] [Abstract][Full Text] [Related]  

  • 34. METTL4 catalyzes m6Am methylation in U2 snRNA to regulate pre-mRNA splicing.
    Goh YT; Koh CWQ; Sim DY; Roca X; Goh WSS
    Nucleic Acids Res; 2020 Sep; 48(16):9250-9261. PubMed ID: 32813009
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of the aberrant splicing of DVL2 induced by cancer-associated SF3B1 mutation.
    Zhao B; Hu X; Zhou Y; Shi Y; Qian R; Wan Y
    Biochem Biophys Res Commun; 2021 Mar; 546():21-28. PubMed ID: 33561744
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The effect of U1 snRNA binding free energy on the selection of 5' splice sites.
    Bi J; Xia H; Li F; Zhang X; Li Y
    Biochem Biophys Res Commun; 2005 Jul; 333(1):64-9. PubMed ID: 15936716
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The upstream 5' splice site remains associated to the transcription machinery during intron synthesis.
    Leader Y; Lev Maor G; Sorek M; Shayevitch R; Hussein M; Hameiri O; Tammer L; Zonszain J; Keydar I; Hollander D; Meshorer E; Ast G
    Nat Commun; 2021 Jul; 12(1):4545. PubMed ID: 34315864
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The U1, U2 and U5 snRNAs crosslink to the 5' exon during yeast pre-mRNA splicing.
    McGrail JC; O'Keefe RT
    Nucleic Acids Res; 2008 Feb; 36(3):814-25. PubMed ID: 18084028
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genomic variants in exons and introns: identifying the splicing spoilers.
    Pagani F; Baralle FE
    Nat Rev Genet; 2004 May; 5(5):389-96. PubMed ID: 15168696
    [No Abstract]   [Full Text] [Related]  

  • 40. Widespread use of non-productive alternative splice sites in Saccharomyces cerevisiae.
    Kawashima T; Douglass S; Gabunilas J; Pellegrini M; Chanfreau GF
    PLoS Genet; 2014 Apr; 10(4):e1004249. PubMed ID: 24722551
    [TBL] [Abstract][Full Text] [Related]  

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