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 *

142 related articles for article (PubMed ID: 19293337)

  • 1. A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs.
    Huranová M; Hnilicová J; Fleischer B; Cvacková Z; Stanek D
    Hum Mol Genet; 2009 Jun; 18(11):2014-23. PubMed ID: 19293337
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Human RBM28 protein is a specific nucleolar component of the spliceosomal snRNPs.
    Damianov A; Kann M; Lane WS; Bindereif A
    Biol Chem; 2006; 387(10-11):1455-60. PubMed ID: 17081119
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of PAP-1 and Prp3p, the products of causative genes of dominant retinitis pigmentosa, in the tri-snRNP complex.
    Maita H; Kitaura H; Ariga H; Iguchi-Ariga SM
    Exp Cell Res; 2005 Jan; 302(1):61-8. PubMed ID: 15541726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Binding of the human Prp31 Nop domain to a composite RNA-protein platform in U4 snRNP.
    Liu S; Li P; Dybkov O; Nottrott S; Hartmuth K; Lührmann R; Carlomagno T; Wahl MC
    Science; 2007 Apr; 316(5821):115-20. PubMed ID: 17412961
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The assembly of a spliceosomal small nuclear ribonucleoprotein particle.
    Patel SB; Bellini M
    Nucleic Acids Res; 2008 Nov; 36(20):6482-93. PubMed ID: 18854356
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Cajal body: a meeting place for spliceosomal snRNPs in the nuclear maze.
    Stanek D; Neugebauer KM
    Chromosoma; 2006 Oct; 115(5):343-54. PubMed ID: 16575476
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 tri-snRNP integration and is associated with retinitis pigmentosa.
    Linder B; Hirmer A; Gal A; Rüther K; Bolz HJ; Winkler C; Laggerbauer B; Fischer U
    PLoS One; 2014; 9(11):e111754. PubMed ID: 25383878
    [TBL] [Abstract][Full Text] [Related]  

  • 11. RNA structural requirements for the association of the spliceosomal hPrp31 protein with the U4 and U4atac small nuclear ribonucleoproteins.
    Schultz A; Nottrott S; Hartmuth K; Lührmann R
    J Biol Chem; 2006 Sep; 281(38):28278-86. PubMed ID: 16857676
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in spliceosomal proteins and retina degeneration.
    Růžičková Š; Staněk D
    RNA Biol; 2017 May; 14(5):544-552. PubMed ID: 27302685
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sm core variation in spliceosomal small nuclear ribonucleoproteins from Trypanosoma brucei.
    Wang P; Palfi Z; Preusser C; Lücke S; Lane WS; Kambach C; Bindereif A
    EMBO J; 2006 Oct; 25(19):4513-23. PubMed ID: 16977313
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel missense RP1 mutation in retinitis pigmentosa.
    Chiang SW; Wang DY; Chan WM; Tam PO; Chong KK; Lam DS; Pang CP
    Eye (Lond); 2006 May; 20(5):602-5. PubMed ID: 15933747
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Roles of the U5 snRNP in spliceosome dynamics and catalysis.
    Turner IA; Norman CM; Churcher MJ; Newman AJ
    Biochem Soc Trans; 2004 Dec; 32(Pt 6):928-31. PubMed ID: 15506927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A role for Cajal bodies in the final steps of U2 snRNP biogenesis.
    Nesic D; Tanackovic G; Krämer A
    J Cell Sci; 2004 Sep; 117(Pt 19):4423-33. PubMed ID: 15316075
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cajal bodies and snRNPs - friends with benefits.
    Staněk D
    RNA Biol; 2017 Jun; 14(6):671-679. PubMed ID: 27627834
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Retinitis pigmentosa mutations of SNRNP200 enhance cryptic splice-site recognition.
    Cvačková Z; Matějů D; Staněk D
    Hum Mutat; 2014 Mar; 35(3):308-17. PubMed ID: 24302620
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosa.
    Tanackovic G; Ransijn A; Ayuso C; Harper S; Berson EL; Rivolta C
    Am J Hum Genet; 2011 May; 88(5):643-9. PubMed ID: 21549338
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcriptional co-activator protein p100 interacts with snRNP proteins and facilitates the assembly of the spliceosome.
    Yang J; Välineva T; Hong J; Bu T; Yao Z; Jensen ON; Frilander MJ; Silvennoinen O
    Nucleic Acids Res; 2007; 35(13):4485-94. PubMed ID: 17576664
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.