|1.||Jones, Clinton: 4 articles (01/2013 - 12/2007)|
|2.||Miyakawa, Yuzo: 4 articles (04/2007 - 04/2002)|
|3.||Sinani, Devis: 3 articles (01/2013 - 03/2011)|
|4.||Moorman, Nathaniel J: 3 articles (08/2010 - 10/2003)|
|5.||Attoui, H: 3 articles (11/2009 - 11/2009)|
|6.||Maan, N: 3 articles (11/2009 - 11/2009)|
|7.||Anthony, S J: 3 articles (11/2009 - 11/2009)|
|8.||Maan, S: 3 articles (11/2009 - 11/2009)|
|9.||Sutton, G: 3 articles (11/2009 - 11/2009)|
|10.||Mertens, P P C: 3 articles (11/2009 - 11/2009)|
|1.||Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
06/01/2006 - "Readthrough strategies for stop codons in Duchenne muscular dystrophy."
01/01/2014 - "We presume that prednisolone has a read-through effect on the stop codons in the central nervous systems of Duchenne muscular dystrophy because intelligence quotient of point mutation case was improved significantly."
10/01/2007 - "A third study is evaluating efficacy and tolerability of a drug which induces read-through of stop codons in Duchenne muscular dystrophy patients carrying nonsense mutations. "
06/01/2010 - "Mutation suppression of stop codons, successfully achieved in the mdx mouse using gentamicin, represents an important evolving treatment strategy in Duchenne muscular dystrophy (DMD). "
06/01/2010 - "Gentamicin-induced readthrough of stop codons in Duchenne muscular dystrophy."
|2.||Contagious Ecthyma (Orf)
06/07/2015 - "The major stop codons of S-ORF were TAA (96.45%) and TGA (83.60%) in B2 and C2 subtype, respectively. "
06/01/2015 - "In contrast, mutant clones containing stop codons in either ORF decreased virus infectivity. "
08/01/2014 - "A C to T transition at position 99 of the rpoS ORF, which results in a premature amber stop codon often found in E. "
02/01/2014 - "The Nicotiana benthamiana plants infiltrated with the infectious clones harboring stop codons in the C2 ORF did not develop any symptoms unlike plants infiltrated with wild-type BYVMV. "
01/01/2013 - "Furthermore, selection analyses on the P3 cistron did not account for the existence of stop codons in the pipo ORF, but showed that positive selection was significant in the overlapping region for Potato virus Y (PVY) and TuMV. "
10/01/2012 - "This was convergent with previous results showing that introduction of stop codons in this region of ORF1 did not impair plant infection. "
02/20/2007 - "To investigate its role in HCV infection, we introduced four stop codons into the ARF of a genotype 1a H77 molecular clone. "
02/10/2001 - "The region immediately 3' of the nef termination codon, which exhibits clade-dependent specificity, was targeted by PCR to differentiate HIV-2 subtype A from subtype B infections, the two principal clinical HIV-2 subtypes. "
12/05/2000 - "Not only did nef fail to repair itself in vivo postinfection (p.i.), but instead, further mutations added additional stop codons with increasing time p.i. Infection of these animals was associated with minimal acute viral replication, followed by undetectable plasma viral loads and only intermittent PCR detection up to 5 years p.i. The three SIVhu infected and three control monkeys were then challenged with the heterologous highly pathogenic SHIV89.6p. "
03/01/1993 - "Point mutations that may result in the formation of stop codons and amino acid changes may affect the clinical picture of HBV infection and may be reflected in atypical serological patterns."
|4.||Mucopolysaccharidosis I (Hurler Syndrome)
04/30/2004 - "In an MPS I patient study, premature TGA stop codons were associated with a slightly attenuated clinical phenotype, when compared to classical Hurler syndrome (e.g. "
01/01/1994 - "A mutant stop codon (TAG) in the IDUA gene is used as an acceptor splice site in a patient with Hurler syndrome (MPS IH)."
03/01/2000 - "The Tyr433Phe polymorphism of mGluR7 and a novel polymorphism in the mGluR8 gene located 29 bp after the termination codon (2756C/T) were investigated in case control association studies performed on DNA from more than 100 patients with idiopathic generalised epilepsy (IGE). "
10/01/2012 - "The GABRG2 nonsense mutation, Q40X, is associated with the severe epilepsy syndrome, Dravet syndrome, and is predicted to generate a premature translation-termination codon (PTC) in the GABA(A) receptor γ2 subunit mRNA in a position that codes for the first amino acid of the mutant subunit. "
|3.||Nonsense Codon (Nonsense Mutation)
|4.||DNA (Deoxyribonucleic Acid)
|6.||Hepatitis delta Antigens (HDAg)
|7.||Chloramphenicol O-Acetyltransferase (Chloramphenicol Acetyltransferase)
|8.||Immunoglobulin E (IgE)
|9.||metabotropic glutamate receptor 8
|10.||metabotropic glutamate receptor 7