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Evidence for a nonsense mutation at the niaD locus of Aspergillus nidulansMARTINELLI, S. D; ROBERTS, T. J; SEALY-LEWIS, H. M et al.Genetical research. 1984, Vol 43, Num 3, pp 241-248, issn 0016-6723Article

Omnipotent suppressors effective in ψ⁺ strains of Saccharomyces cerevisiae: recessiveness and dominanceONO, B.-I; MORIGA, N; ISHIMARA, K et al.Genetics. 1984, Vol 107, Num 2, pp 219-230, issn 0016-6731Article

PGC-1α/β upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutationsSRIVASTAVA, Sarika; BARRETT, John N; MORAES, Carlos T et al.Human molecular genetics (Print). 2007, Vol 16, Num 8, pp 993-1005, issn 0964-6906, 13 p.Article

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9COHEN, Jonathan; PERTSEMLIDIS, Alexander; KOTOWSKI, Ingrid K et al.Nature genetics. 2005, Vol 37, Num 2, pp 161-165, issn 1061-4036, 5 p.Article

Nonsense mutations affecting the lengths of the NSl nonstructural proteins of influenza A virus isolatesPARVIN, J. D; YOUNG, J. F; PALESE, P et al.Virology (New York, NY). 1983, Vol 128, Num 2, pp 512-517, issn 0042-6822Article

Readthrough of nonsense mutation W822X in the SCN5A gene can effectively restore expression of cardiac Na⁺ channelsSIYONG TENG; LIZHI GAO; PAAJANEN, Vesa et al.Cardiovascular research. 2009, Vol 83, Num 3, pp 473-480, issn 0008-6363, 8 p.Article

Translational readthrough induction of pathogenic nonsense mutationsKELLERMAYER, Richard.European journal of medical genetics. 2006, Vol 49, Num 6, pp 445-450, issn 1769-7212, 6 p.Article

Converting nonsense codons into sense codons by targeted pseudouridylationKARIJOLICH, John; YU, Yi-Tao.Nature (London). 2011, Vol 474, Num 7351, pp 395-398, issn 0028-0836, 4 p.Article

A Novel Homozygous Nonsense Mutation in CABP4 Causes Congenital Cone-Rod Synaptic DisorderLITTINK, Karin W; VAN GENDEREN, Maria M; DEN HOLLANDER, Anneke I et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 5, pp 2344-2350, issn 0146-0404, 7 p.Article

PYPAFf1 nonsense mutation in a patient with an unusual autoinflammatory syndrome : Role of PYPAF1 in inflammationJERU, I; HAYRAPETYAN, H; DUQUESNOY, P et al.Arthritis and rheumatism. 2006, Vol 54, Num 2, pp 508-514, issn 0004-3591, 7 p.Article

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Antisuppression of class I suppressors in an isopentenylated-transfer RNA deficient mutant of Saccharomyces cerevisiaeLATEN, H. M.Current genetics. 1984, Vol 8, Num 1, pp 29-32, issn 0172-8083Article

Isolation and characterization of chain-terminating nonsense mutations in a porin regulator gene, envZGARRETT, S; TAYLOR, R. K; SILHAVY, T. J et al.Journal of bacteriology. 1983, Vol 156, Num 1, pp 62-69, issn 0021-9193Article

Novel isoforms of the CARDS (TUCAN) gene evade a nonsense mutationBAGNALL, Richard D; ROBERTS, Roland G; MIRZA, Muddassar M et al.European journal of human genetics. 2008, Vol 16, Num 5, pp 619-625, issn 1018-4813, 7 p.Article

An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elementsDISSET, A; BOURGEOIS, C. F; BENMALEK, N et al.Human molecular genetics (Print). 2006, Vol 15, Num 6, pp 999-1013, issn 0964-6906, 15 p.Article

A novel nonsense mutation in kindler syndromeHAS, Cristina; BRUCKNER-TUDERMAN, Leena.Journal of investigative dermatology. 2004, Vol 122, Num 1, pp 84-86, issn 0022-202X, 3 p.Article

Nonsense mutations in the Chlamydomonas chloroplast gene that codes for the large subunit of ribulosebisphosphate carboxylase/oxygenaseSPREITZER, R. J; GOLDSCHMIDT-CLERMONT, M; RAHIRE, M et al.Proceedings of the National Academy of Sciences of the United States of America. 1985, Vol 82, Num 16, pp 5460-5464, issn 0027-8424Article

Identification of nonsense mutations in Neurospora: application to the complex arg-6 locusDAVIS, R. H; WEISS, R. L.MGG. Molecular & general genetics. 1983, Vol 192, Num 1-2, pp 46-50, issn 0026-8925Article

Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humansVALLEIX, Sophie; NIEL, Florence; NEDELEC, Brigitte et al.American journal of human genetics. 2006, Vol 79, Num 2, pp 358-364, issn 0002-9297, 7 p.Article

Human-specific nonsense mutations identified by genome sequence comparisonsHAHN, Yoonsoo; LEE, Byungkook.Human genetics. 2006, Vol 119, Num 1-2, pp 169-178, issn 0340-6717, 10 p.Article

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Homozygous Nonsense Mutations in TWIST2 Cause Setleis SyndromeTUKEL, Turgut; SOSIC, Dražen; AL-GAZALI, Lihadh I et al.American journal of human genetics. 2010, Vol 87, Num 2, pp 289-296, issn 0002-9297, 8 p.Article

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