𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII

✍ 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.


πŸ“œ SIMILAR VOLUMES


Readthrough of nonsense mutations in Ret
✍ Cornelia Brendel; Valery Belakhov; Hauke Werner; Eike Wegener; Jutta GΓ€rtner; Ig πŸ“‚ Article πŸ“… 2010 πŸ› Springer 🌐 English βš– 763 KB

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

A polymorphism in the 5β€² region of coagu
✍ G. Marchetti; P. Patracchini; M. Papacchini; M. Ferrati; F. Bernardi πŸ“‚ Article πŸ“… 1993 πŸ› Springer 🌐 English βš– 230 KB

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.