✦ LIBER ✦

Effects of Premature Termination Codon Polymorphisms in theDrosophila pseudoobscuraSubclade

✍ Scribed by Kenneth B. Hoehn, Suzanne E. McGaugh, Mohamed A. F. Noor

Book ID: 120762969
Publisher: Springer
Year: 2012
Tongue: English
Weight: 351 KB
Volume: 75
Category: Article
ISSN: 0022-2844
DOI: 10.1007/s00239-012-9528-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Erratum to: Effects of Premature Termina

Erratum to: Effects of Premature Termination Codon Polymorphisms in theDrosophila pseudoobscuraSubclade

✍ Kenneth B. Hoehn, Suzanne E. McGaugh, Mohamed A. F. Noor 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 120 KB

Alternative Splicing of In-Frame Exon As

Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies

✍ Hinzpeter, Alexandre; Aissat, Abdel; de Becdelièvre, Alix; Bieth, Eric; Sondo, E 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 219 KB

Incidence of lipoprotein lipase genotype

Incidence of lipoprotein lipase genotype for premature termination codon (Ser447-Ter) in Japanese, and association with dyslipoproteinemia

✍ Takeyoshi Murano; Yoh Miyashita; Yoshiaki Itoh; Satoko Tsuzuki; Syunji Yamamori; 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 132 KB

Nucleosome deposition and DNA methylatio

Nucleosome deposition and DNA methylation may participate in the recognition of premature termination codon in nonsense-mediated mRNA decay

✍ Deng-Ke Niu; Jian-Li Cao 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 341 KB

Quantitative sequence analysis of FBN1 p

Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytes

✍ István Magyar; Dvora Colman; Eliane Arnold; Daniela Baumgartner; Armand Bottani; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 363 KB

We improved, evaluated, and used Sanger sequencing for quantification of single nucleotide polymorphism (SNP) variants in transcripts and gDNA samples. This improved assay resulted in highly reproducible relative allele frequencies (e.g., for a heterozygous gDNA 50.0+/-1.4%, and for a missense mutat

Variable expression of cerebral cavernou

Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene

✍ Miguel Lucas; Alzenire F Costa; José M García-Moreno; Francisca Solano; Miguel A 📂 Article 📅 2003 🏛 BioMed Central 🌐 English ⚖ 312 KB