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 *

125 related articles for article (PubMed ID: 30408273)

  • 1. Disease-causing variants of the conserved +2T of 5' splice sites can be rescued by engineered U1snRNAs.
    Scalet D; Maestri I; Branchini A; Bernardi F; Pinotti M; Balestra D
    Hum Mutat; 2019 Jan; 40(1):48-52. PubMed ID: 30408273
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regulation of a strong F9 cryptic 5'ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotides.
    Balestra D; Barbon E; Scalet D; Cavallari N; Perrone D; Zanibellato S; Bernardi F; Pinotti M
    Hum Mol Genet; 2015 Sep; 24(17):4809-16. PubMed ID: 26063760
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A.
    Balestra D; Maestri I; Branchini A; Ferrarese M; Bernardi F; Pinotti M
    Front Genet; 2019; 10():974. PubMed ID: 31649737
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An exon-specific U1 small nuclear RNA (snRNA) strategy to correct splicing defects.
    Fernandez Alanis E; Pinotti M; Dal Mas A; Balestra D; Cavallari N; Rogalska ME; Bernardi F; Pagani F
    Hum Mol Genet; 2012 Jun; 21(11):2389-98. PubMed ID: 22362925
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Determinants of the inherent strength of human 5' splice sites.
    Roca X; Sachidanandam R; Krainer AR
    RNA; 2005 May; 11(5):683-98. PubMed ID: 15840817
    [TBL] [Abstract][Full Text] [Related]  

  • 6. How to Design U1 snRNA Molecules for Splicing Rescue.
    Matos L; Santos JI; Coutinho MF; Alves S
    Methods Mol Biol; 2022; 2434():89-102. PubMed ID: 35213011
    [TBL] [Abstract][Full Text] [Related]  

  • 7. OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spf
    Sacchetto C; Peretto L; Baralle F; Maestri I; Tassi F; Bernardi F; van de Graaf SFJ; Pagani F; Pinotti M; Balestra D
    Mol Med; 2021 Dec; 27(1):157. PubMed ID: 34906067
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High-throughput analysis revealed mutations' diverging effects on
    Souček P; Réblová K; Kramárek M; Radová L; Grymová T; Hujová P; Kováčová T; Lexa M; Grodecká L; Freiberger T
    RNA Biol; 2019 Oct; 16(10):1364-1376. PubMed ID: 31213135
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An Exon-Specific Small Nuclear U1 RNA (ExSpeU1) Improves Hepatic OTC Expression in a Splicing-Defective
    Balestra D; Ferrarese M; Lombardi S; Ziliotto N; Branchini A; Petersen N; Bosma P; Pinotti M; van de Graaf SFJ
    Int J Mol Sci; 2020 Nov; 21(22):. PubMed ID: 33228018
    [No Abstract]   [Full Text] [Related]  

  • 10. Quantitative Activity Profile and Context Dependence of All Human 5' Splice Sites.
    Wong MS; Kinney JB; Krainer AR
    Mol Cell; 2018 Sep; 71(6):1012-1026.e3. PubMed ID: 30174293
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy.
    Scalet D; Balestra D; Rohban S; Bovolenta M; Perrone D; Bernardi F; Campaner S; Pinotti M
    Biochim Biophys Acta Mol Basis Dis; 2017 Jan; 1863(1):15-20. PubMed ID: 27639833
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Widespread recognition of 5' splice sites by noncanonical base-pairing to U1 snRNA involving bulged nucleotides.
    Roca X; Akerman M; Gaus H; Berdeja A; Bennett CF; Krainer AR
    Genes Dev; 2012 May; 26(10):1098-109. PubMed ID: 22588721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Informational Suppression to Probe RNA:RNA Interactions in the Context of Ribonucleoproteins: U1 and 5' Splice-Site Base-Pairing.
    Tan J; Roca X
    Methods Mol Biol; 2016; 1421():243-68. PubMed ID: 26965270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Modeling splicing outcome by combining 5'ss strength and splicing regulatory elements.
    Müller L; Ptok J; Nisar A; Antemann J; Grothmann R; Hillebrand F; Brillen AL; Ritchie A; Theiss S; Schaal H
    Nucleic Acids Res; 2022 Aug; 50(15):8834-8851. PubMed ID: 35947702
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intrinsic differences between authentic and cryptic 5' splice sites.
    Roca X; Sachidanandam R; Krainer AR
    Nucleic Acids Res; 2003 Nov; 31(21):6321-33. PubMed ID: 14576320
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pick one, but be quick: 5' splice sites and the problems of too many choices.
    Roca X; Krainer AR; Eperon IC
    Genes Dev; 2013 Jan; 27(2):129-44. PubMed ID: 23348838
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intronic PAH gene mutations cause a splicing defect by a novel mechanism involving U1snRNP binding downstream of the 5' splice site.
    Martínez-Pizarro A; Dembic M; Pérez B; Andresen BS; Desviat LR
    PLoS Genet; 2018 Apr; 14(4):e1007360. PubMed ID: 29684050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. U1-like snRNAs lacking complementarity to canonical 5' splice sites.
    Kyriakopoulou C; Larsson P; Liu L; Schuster J; Söderbom F; Kirsebom LA; Virtanen A
    RNA; 2006 Sep; 12(9):1603-11. PubMed ID: 16829670
    [TBL] [Abstract][Full Text] [Related]  

  • 19. First estimate of the scale of canonical 5' splice site GT>GC variants capable of generating wild-type transcripts.
    Lin JH; Tang XY; Boulling A; Zou WB; Masson E; Fichou Y; Raud L; Le Tertre M; Deng SJ; Berlivet I; Ka C; Mort M; Hayden M; Leman R; Houdayer C; Le Gac G; Cooper DN; Li ZS; Férec C; Liao Z; Chen JM
    Hum Mutat; 2019 Oct; 40(10):1856-1873. PubMed ID: 31131953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants.
    Balestra D; Scalet D; Pagani F; Rogalska ME; Mari R; Bernardi F; Pinotti M
    Mol Ther Nucleic Acids; 2016 Oct; 5(10):e370. PubMed ID: 27701399
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.