Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII
β Scribed by M. PINOTTI; L. RIZZOTTO; P. PINTON; P. FERRARESI; A. CHUANSUMRIT; P. CHAROENKWAN; G. MARCHETTI; R. RIZZUTO; G. MARIANI; F. BERNARDI; THE INTERNATIONAL FACTOR VII DEFICIENCY STUDY GROUP
- Book ID
- 109151510
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 308 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1538-7933
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Thirty-five percent of patients with Rett syndrome carry nonsense mutations in the __MECP2__ gene. We have recently shown in transfected HeLa cells that readthrough of nonsense mutations in the __MECP2__ gene can be achieved by treatment with gentamicin and geneticin. This study was performed to tes
We describe a polymorphism in the 5' region of the coagulation factor VII (FVII) gene, originating from a decanucleotide (CCTATATCCT) insert present in the less frequent allele. This marker can be detected by restriction analysis of polymerase chain reaction products.