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American Journal of Human Genetics
Volumn 59, Issue 2, 1996, Pages 279-286
Defects in RNA splicing and the consequence of shortened translational reading frames
Author keywords

[No Author keywords available]
Indexed keywords

MESSENGER RNA; MESSENGER RNA PRECURSOR; RNA PRECURSOR;
EID: 0029835707     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial
Times cited : (237)
References (6)
  • 1
    • 15844406352 scopus 로고    scopus 로고
    • Nonsense mutations inhibit RNA splicing in a cell free system: Recognition of mutant codon is independent of protein synthesis and tissue specific
    • Aoufouchi S, Yélamos J, Milstein C (1996) Nonsense mutations inhibit RNA splicing in a cell free system: recognition of mutant codon is independent of protein synthesis and tissue specific. Cell 85:415-422
    • (1996) Cell , vol.85 , pp. 415-422
    • Aoufouchi, S.1    Yélamos, J.2    Milstein, C.3
  • 2
    • 0027379866 scopus 로고
    • Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: Multiple allelic mutations of the IDUA gene in a small geographic area
    • Bach G, Moskowitz SM, Tieu PT, Matynia A, Neufeld EF (1993) Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic area. Am J Hum Genet 53:330-338
    • (1993) Am J Hum Genet , vol.53 , pp. 330-338
    • Bach, G.1    Moskowitz, S.M.2    Tieu, P.T.3    Matynia, A.4    Neufeld, E.F.5
  • 3
    • 0027388887 scopus 로고
    • Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA
    • Belgrader P, Cheng J, Maquat LE (1993) Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA. Proc Natl Acad Sci USA 90:482-486
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 482-486
    • Belgrader, P.1    Cheng, J.2    Maquat, L.E.3
  • 4
    • 0027487938 scopus 로고
    • Exon skipping and translation in patients with frameshift deletions in the dystrophin gene
    • Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN (1993) Exon skipping and translation in patients with frameshift deletions in the dystrophin gene. Am J Hum Genet 53:1007-1015
    • (1993) Am J Hum Genet , vol.53 , pp. 1007-1015
    • Sherratt, T.G.1    Vulliamy, T.2    Dubowitz, V.3    Sewry, C.A.4    Strong, P.N.5
  • 5
    • 0028833771 scopus 로고
    • Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: Mechanisms of dystrophin production
    • Winnard AV, Mendell JR, Prior TW, Florence J, Burghes AHM (1995) Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production. Am J Hum Genet 56:158-166
    • (1995) Am J Hum Genet , vol.56 , pp. 158-166
    • Winnard, A.V.1    Mendell, J.R.2    Prior, T.W.3    Florence, J.4    Burghes, A.H.M.5
  • 6
    • 0029845144 scopus 로고    scopus 로고
    • Evidence that the decay of nucleus-associated nonsense mRNA for human triosephosphate isomerase involves nonsense codon recognition after splicing
    • Zhang J, Maquat LE (1996) Evidence that the decay of nucleus-associated nonsense mRNA for human triosephosphate isomerase involves nonsense codon recognition after splicing. RNA 2:235-243
    • (1996) RNA , vol.2 , pp. 235-243
    • Zhang, J.1    Maquat, L.E.2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.