BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 8408296)

  • 1. Interaction of the human autoantigen p150 with splicing snRNPs.
    Blencowe BJ; Carmo-Fonseca M; Behrens SE; Lührmann R; Lamond AI
    J Cell Sci; 1993 Jul; 105 ( Pt 3)():685-97. PubMed ID: 8408296
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The nuclear cap-binding complex interacts with the U4/U6·U5 tri-snRNP and promotes spliceosome assembly in mammalian cells.
    Pabis M; Neufeld N; Steiner MC; Bojic T; Shav-Tal Y; Neugebauer KM
    RNA; 2013 Aug; 19(8):1054-63. PubMed ID: 23793891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The yeast Prp3 protein is a U4/U6 snRNP protein necessary for integrity of the U4/U6 snRNP and the U4/U6.U5 tri-snRNP.
    Anthony JG; Weidenhammer EM; Woolford JL
    RNA; 1997 Oct; 3(10):1143-52. PubMed ID: 9326489
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SPF30 is an essential human splicing factor required for assembly of the U4/U5/U6 tri-small nuclear ribonucleoprotein into the spliceosome.
    Rappsilber J; Ajuh P; Lamond AI; Mann M
    J Biol Chem; 2001 Aug; 276(33):31142-50. PubMed ID: 11331295
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Protein 61K, encoded by a gene (PRPF31) linked to autosomal dominant retinitis pigmentosa, is required for U4/U6*U5 tri-snRNP formation and pre-mRNA splicing.
    Makarova OV; Makarov EM; Liu S; Vornlocher HP; Lührmann R
    EMBO J; 2002 Mar; 21(5):1148-57. PubMed ID: 11867543
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The human homologue of the yeast splicing factor prp6p contains multiple TPR elements and is stably associated with the U5 snRNP via protein-protein interactions.
    Makarov EM; Makarova OV; Achsel T; Lührmann R
    J Mol Biol; 2000 May; 298(4):567-75. PubMed ID: 10788320
    [TBL] [Abstract][Full Text] [Related]  

  • 7. U4/U5/U6 snRNP recognizes the 5' splice site in the absence of U2 snRNP.
    Konforti BB; Konarska MM
    Genes Dev; 1994 Aug; 8(16):1962-73. PubMed ID: 7958870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The 65 and 110 kDa SR-related proteins of the U4/U6.U5 tri-snRNP are essential for the assembly of mature spliceosomes.
    Makarova OV; Makarov EM; Lührmann R
    EMBO J; 2001 May; 20(10):2553-63. PubMed ID: 11350945
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A U1/U4/U5 snRNP complex induced by a 2'-O-methyl-oligoribonucleotide complementary to U5 snRNA.
    Ast G; Weiner AM
    Science; 1996 May; 272(5263):881-4. PubMed ID: 8629024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The [U4/U6.U5] tri-snRNP-specific 27K protein is a novel SR protein that can be phosphorylated by the snRNP-associated protein kinase.
    Fetzer S; Lauber J; Will CL; Lührmann R
    RNA; 1997 Apr; 3(4):344-55. PubMed ID: 9085842
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The 20kD protein of human [U4/U6.U5] tri-snRNPs is a novel cyclophilin that forms a complex with the U4/U6-specific 60kD and 90kD proteins.
    Teigelkamp S; Achsel T; Mundt C; Göthel SF; Cronshagen U; Lane WS; Marahiel M; Lührmann R
    RNA; 1998 Feb; 4(2):127-41. PubMed ID: 9570313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The biochemical defects of prp4-1 and prp6-1 yeast splicing mutants reveal that the PRP6 protein is required for the accumulation of the [U4/U6.U5] tri-snRNP.
    Galisson F; Legrain P
    Nucleic Acids Res; 1993 Apr; 21(7):1555-62. PubMed ID: 8479905
    [TBL] [Abstract][Full Text] [Related]  

  • 13. In vivo kinetics of U4/U6·U5 tri-snRNP formation in Cajal bodies.
    Novotný I; Blažíková M; Staněk D; Herman P; Malinsky J
    Mol Biol Cell; 2011 Feb; 22(4):513-23. PubMed ID: 21177826
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human U4/U6.U5 and U4atac/U6atac.U5 tri-snRNPs exhibit similar protein compositions.
    Schneider C; Will CL; Makarova OV; Makarov EM; Lührmann R
    Mol Cell Biol; 2002 May; 22(10):3219-29. PubMed ID: 11971955
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Direct probing of RNA structure and RNA-protein interactions in purified HeLa cell's and yeast spliceosomal U4/U6.U5 tri-snRNP particles.
    Mougin A; Gottschalk A; Fabrizio P; Lührmann R; Branlant C
    J Mol Biol; 2002 Apr; 317(5):631-49. PubMed ID: 11955014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biochemical and genetic analyses of the U5, U6, and U4/U6 x U5 small nuclear ribonucleoproteins from Saccharomyces cerevisiae.
    Stevens SW; Barta I; Ge HY; Moore RE; Young MK; Lee TD; Abelson J
    RNA; 2001 Nov; 7(11):1543-53. PubMed ID: 11720284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The splicing factor Prp17 interacts with the U2, U5 and U6 snRNPs and associates with the spliceosome pre- and post-catalysis.
    Sapra AK; Khandelia P; Vijayraghavan U
    Biochem J; 2008 Dec; 416(3):365-74. PubMed ID: 18691155
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies.
    Schaffert N; Hossbach M; Heintzmann R; Achsel T; Lührmann R
    EMBO J; 2004 Aug; 23(15):3000-9. PubMed ID: 15257298
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reassembly and protection of small nuclear ribonucleoprotein particles by heat shock proteins in yeast cells.
    Bracken AP; Bond U
    RNA; 1999 Dec; 5(12):1586-96. PubMed ID: 10606269
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In vitro reconstitution of mammalian U2 and U5 snRNPs active in splicing: Sm proteins are functionally interchangeable and are essential for the formation of functional U2 and U5 snRNPs.
    Ségault V; Will CL; Sproat BS; Lührmann R
    EMBO J; 1995 Aug; 14(16):4010-21. PubMed ID: 7664740
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.