A mouse model ofStreptococcus pneumoniaemeningitis mimicking several features of human disease
✍ Scribed by J. Gerber; G. Raivich; A. Wellmer; C. Noeske; T. Kunst; A. Werner; W. Brück; R. Nau
- Publisher
- Springer-Verlag
- Year
- 2001
- Tongue
- English
- Weight
- 326 KB
- Volume
- 101
- Category
- Article
- ISSN
- 0001-6322
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Glycogen storage disease type II (GSDII; Pompe's disease) is an autosomal recessive disease caused by lysosomal -glucosidase deficiency. Skeletal muscle weakness is the most conspicuous clinical symptom of patients suffering from GSDII and skeletal muscle also is prominently involved in the knockout
## Abstract ## Background Gene‐directed enzyme prodrug therapy (GDEPT) based on the __E. coli__ enzyme purine nucleoside phosphorylase (PNP) represents a new approach for treating slow growing tumours like prostate cancer (PCa). Expressed enzyme converts a systemically administered prodrug, fludar