✦ LIBER ✦

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

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

Book ID: 120762973
Publisher: Springer
Year: 2012
Tongue: English
Weight: 120 KB
Volume: 76
Category: Article
ISSN: 0022-2844
DOI: 10.1007/s00239-012-9537-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Effects of Premature Termination Codon P

Effects of Premature Termination Codon Polymorphisms in theDrosophila pseudoobscuraSubclade

✍ Kenneth B. Hoehn, Suzanne E. McGaugh, Mohamed A. F. Noor 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 351 KB

The position of premature termination co

The position of premature termination codons in the hepatocyte nuclear factor −1 beta gene determines susceptibility to nonsense-mediated decay

✍ L. W. Harries; Coralie Bingham; Christine Bellanne-Chantelot; A. T. Hattersley; 📂 Article 📅 2005 🏛 Springer 🌐 English ⚖ 455 KB

An activated 5′ cryptic splice site in t

An activated 5′ cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id)

✍ Jonas Denecke; Christian Kranz; Dirk Kemming; Hans-Georg Koch; Thorsten Marquard 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 305 KB

A defect of the dolichyl-P-Man:Man5GlcNAc2-PP-dolichyl mannosyltransferase encoded by the ALG3 gene (alias NOT56L) causes congenital disorder of glycosylation type Id (CDG-Id). In this work, a new mutation in the ALG3 gene causing atypical splicing is described with characterization of expression le

Erratum to: Cellular isoform of the prio

Erratum to: Cellular isoform of the prion protein PrPc in human intestinalcell lines: Genetic polymorphism at codon 129, mRNA quantification and protein detection in lipid rafts [30 (6) 559–567]

✍ Nicolas Garmy; Xiao-Jun Guo; Nadira Taïeb; Christian Tourrès; Catherine Tamalet; 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 62 KB

Erratum to Genetic effect of single-nucl

Erratum to Genetic effect of single-nucleotide polymorphisms in the PPARGC1B gene on airway hyperreactivity in asthmatic patients

✍ Park, Jong-Sook; Kim, Myung-Sin; Park, Sung-Woo; Jang, An-Soo; Park, Choon-Sik 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 53 KB

A polymorphic variation of serine to tyr

A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population

✍ Jun-ichi Satoh; Yasuo Kuroda 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 98 KB