Uses of vaccinia virus as a vector for the production of live recombinant vaccines
✍ Scribed by Geoffrey L. Smith; Bernard Moss
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 685 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0265-9247
No coin nor oath required. For personal study only.
✦ Synopsis
Influence of ethanol on chromosome segregation during the first and second meiotic divisions in the mouse egg. J. exp. Zool. 230, 3 15-320. 18 KAUFMAN, M. H. & BAIN, I. M. (19846). The development potential of ethanol-induced monosomic and trisomic conceptuses in the mouse. J. exp. Zool. (In the Press.) 19 O'SHEA, K. S. & KAUFMAN, M. H. (1 980). Neural tube closure defects following in vitro exposure of mouse embryos to xylocaine.
📜 SIMILAR VOLUMES
## Abstract The use of mammalian cells as substrates for the production of various vaccines is a time‐honored procedure. With the advent of recombinant DNA technology, various investigators soon realized that these techniques could be applied to mammalian cells to convert them to reliable, safe pro
All living organisms are continuously exposed to a plethora of viruses. In general, viruses tend to be restricted to the natural host species which they infect. From time to time viruses cross the host-range barrier expanding their host range. However, in very rare cases cross-species transfer is fo
A live cold-recombinant influenza B virus vaccine (RB77) was given intranasally in a placebo-controlled, double blind study to volunteers in dosages of 10(7.9) EID50/ml, 10(7.25) EID50/ml, 10(5.7) EID50/ml. The tolerability, safety, and immunogenicity of the vaccine were investigated. No revertant v
## Abstract A temperature‐sensitive mutant virus unable to replicate at 38°C was recovered from passage 189 (IVpi‐189) of Madin‐Darby canine kidney cells infected persistently with influenza A. Immunofluorescent staining of the IVpi‐189 virus‐infected cells revealed disrupted transport of the matri
## Abstract A process scheme for the harvesting and concentration of cell culture‐derived human influenza A virus is presented. The scheme comprises two static filtration steps, chemical inactivation by β‐propiolactone and cross‐flow ultrafiltration. Human influenza A virus A/PR/8/34 (H1N1) was pro