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 *

123 related articles for article (PubMed ID: 18835837)

  • 1. Nonsense-mediated mRNA decay in the ADAMTS13 gene caused by a 29-nucleotide deletion.
    Garagiola I; Valsecchi C; Lavoretano S; Oren H; Bohm M; Peyvandi F
    Haematologica; 2008 Nov; 93(11):1678-85. PubMed ID: 18835837
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nonsense mutations in close proximity to the initiation codon fail to trigger full nonsense-mediated mRNA decay.
    Inácio A; Silva AL; Pinto J; Ji X; Morgado A; Almeida F; Faustino P; Lavinha J; Liebhaber SA; Romão L
    J Biol Chem; 2004 Jul; 279(31):32170-80. PubMed ID: 15161914
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT.
    Forster L; Ardakani RM; Qadah T; Finlayson J; Ghassemifar R
    Hemoglobin; 2015; 39(5):334-9. PubMed ID: 26207313
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nonsense-mediated mRNA decay (NMD) silences the accumulation of aberrant trypsin proteinase inhibitor mRNA in Nicotiana attenuata.
    Wu J; Kang JH; Hettenhausen C; Baldwin IT
    Plant J; 2007 Aug; 51(4):693-706. PubMed ID: 17587303
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay.
    Luan CJ; Shen W; Yu Z; Chen L; Gu Y; Tang LY; Wang ZG; Dai L; Gu MM
    Thromb Res; 2015 Apr; 135(4):733-8. PubMed ID: 25648792
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon.
    Musante L; Kunde SA; Sulistio TO; Fischer U; Grimme A; Frints SG; Schwartz CE; Martínez F; Romano C; Ropers HH; Kalscheuer VM
    Hum Mutat; 2010 Jan; 31(1):90-8. PubMed ID: 19847789
    [TBL] [Abstract][Full Text] [Related]  

  • 7. At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation.
    Zhang J; Sun X; Qian Y; LaDuca JP; Maquat LE
    Mol Cell Biol; 1998 Sep; 18(9):5272-83. PubMed ID: 9710612
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript.
    De Rosa M; Morelli G; Cesaro E; Duraturo F; Turano M; Rossi GB; Delrio P; Izzo P
    Gene; 2007 Jun; 395(1-2):8-14. PubMed ID: 17360132
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon.
    Maillet P; Dalla Venezia N; Lorenzo F; Morinière M; Bozon M; Noël B; Delaunay J; Baklouti F
    Hum Mutat; 1999; 14(2):145-55. PubMed ID: 10425037
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.
    Hurtado B; Muñoz X; Mulero MC; Navarro G; Domènech P; García de Frutos P; Pérez-Riba M; Sala N
    Haematologica; 2008 Apr; 93(4):574-80. PubMed ID: 18322254
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of nine new IDS alleles in mucopolysaccharidosis II. Quantitative evaluation by real-time RT-PCR of mRNAs sensitive to nonsense-mediated and nonstop decay mechanisms.
    Lualdi S; Di Rocco M; Corsolini F; Spada M; Bembi B; Cotugno G; Battini R; Stroppiano M; Gabriela Pittis M; Filocamo M
    Biochim Biophys Acta; 2006 Apr; 1762(4):478-84. PubMed ID: 16495038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal alpha-N-acetyl-neuraminidase (sialidase) gene.
    Sergi C; Penzel R; Uhl J; Zoubaa S; Dietrich H; Decker N; Rieger P; Kopitz J; Otto HF; Kiessling M; Cantz M
    Hum Genet; 2001 Oct; 109(4):421-8. PubMed ID: 11702224
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.
    Dall'Osso C; Guella I; Duga S; Locatelli N; Paraboschi EM; Spreafico M; Afrasiabi A; Pechlaner C; Peyvandi F; Tenchini ML; Asselta R
    Haematologica; 2008 Oct; 93(10):1505-13. PubMed ID: 18728029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human alpha2-globin nonsense-mediated mRNA decay induced by a novel alpha-thalassaemia frameshift mutation at codon 22.
    Pereira FJ; do Céu Silva M; Picanço I; Seixas MT; Ferrão A; Faustino P; Romão L
    Br J Haematol; 2006 Apr; 133(1):98-102. PubMed ID: 16512835
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Binary specification of nonsense codons by splicing and cytoplasmic translation.
    Thermann R; Neu-Yilik G; Deters A; Frede U; Wehr K; Hagemeier C; Hentze MW; Kulozik AE
    EMBO J; 1998 Jun; 17(12):3484-94. PubMed ID: 9628884
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay.
    Harries LW; Bingham C; Bellanne-Chantelot C; Hattersley AT; Ellard S
    Hum Genet; 2005 Nov; 118(2):214-24. PubMed ID: 16133182
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nonsense mediated decay downregulates conserved alternatively spliced ABCC4 transcripts bearing nonsense codons.
    Lamba JK; Adachi M; Sun D; Tammur J; Schuetz EG; Allikmets R; Schuetz JD
    Hum Mol Genet; 2003 Jan; 12(2):99-109. PubMed ID: 12499391
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes.
    Liu HX; Cartegni L; Zhang MQ; Krainer AR
    Nat Genet; 2001 Jan; 27(1):55-8. PubMed ID: 11137998
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic.
    Wieland I; Makarov R; Reardon W; Tinschert S; Goldenberg A; Thierry P; Wieacker P
    Eur J Hum Genet; 2008 Feb; 16(2):184-91. PubMed ID: 18043713
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A minor alternative transcript of the fumarylacetoacetate hydrolase gene produces a protein despite being likely subjected to nonsense-mediated mRNA decay.
    Dreumont N; Maresca A; Boisclair-Lachance JF; Bergeron A; Tanguay RM
    BMC Mol Biol; 2005 Jan; 6():1. PubMed ID: 15638932
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.