J Gen Virol Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 45 (1979), 1-13; DOI 10.1099/0022-1317-45-1-1
© 1979 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sangar, D. V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sangar, D. V.
Agricola
Right arrow Articles by Sangar, D. V.

The Replication of Picornaviruses

D. V. Sangar

Animal Virus Research Institute, Pirbright, Woking, Surrey, GU24 0NF, U.K.

Conclusions: The relatively simple structure of the picornaviruses has made them ideal subjects for study by molecular biologists and a great deal is now known concerning their replication. This does not mean, however, that all the fundamental questions have now been answered. The discovery of VPg opened completely new avenues of research and there is still a lot we do not know about this small protein; for example, the portion of the RNA that codes for it is still a mystery. The role of the poly(C) tract in FMDV and the cardioviruses is also difficult to explain since it is absent from both the entero- and the rhinoviruses. These are just a few of the questions which have arisen during the last 5 years and hopefully future work will provide some of the answers.




This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
M. F. Rosas, E. Martinez-Salas, and F. Sobrino
Stable expression of antisense RNAs targeted to the 5' non-coding region confers heterotypic inhibition to foot-and-mouth disease virus infection
J. Gen. Virol., January 1, 2003; 84(2): 393 - 402.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
M. Leippert and E. Pfaff
Foot-and-mouth disease virus can utilize the C-terminal extension of coxsackievirus A9 VP1 for cell infection
J. Gen. Virol., July 1, 2001; 82(7): 1703 - 1711.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1979 by the Society for General Microbiology.