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7. Deletion mapping of a mouse hepatitis virus defective interfering RNA reveals the requirement of an internal and discontiguous sequence for replication. Lin YJ; Lai MM J Virol; 1993 Oct; 67(10):6110-8. PubMed ID: 8396672 [TBL] [Abstract][Full Text] [Related]
8. Analysis of cis-acting sequences essential for coronavirus defective interfering RNA replication. Kim YN; Jeong YS; Makino S Virology; 1993 Nov; 197(1):53-63. PubMed ID: 8212595 [TBL] [Abstract][Full Text] [Related]
10. Specific binding of host cellular proteins to multiple sites within the 3' end of mouse hepatitis virus genomic RNA. Yu W; Leibowitz JL J Virol; 1995 Apr; 69(4):2016-23. PubMed ID: 7884846 [TBL] [Abstract][Full Text] [Related]
11. A domain at the 3' end of the polymerase gene is essential for encapsidation of coronavirus defective interfering RNAs. van der Most RG; Bredenbeek PJ; Spaan WJ J Virol; 1991 Jun; 65(6):3219-26. PubMed ID: 2033672 [TBL] [Abstract][Full Text] [Related]
12. Two murine coronavirus genes suffice for viral RNA synthesis. Kim KH; Makino S J Virol; 1995 Apr; 69(4):2313-21. PubMed ID: 7884877 [TBL] [Abstract][Full Text] [Related]
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14. Recombinant genomic RNA of coronavirus MHV-A59 after coreplication with a DI RNA containing the MHV-RI spike gene. Zhang L; Homberger F; Spaan W; Luytjes W Virology; 1997 Mar; 230(1):93-102. PubMed ID: 9126265 [TBL] [Abstract][Full Text] [Related]
15. The 3' untranslated region of coronavirus RNA is required for subgenomic mRNA transcription from a defective interfering RNA. Lin YJ; Zhang X; Wu RC; Lai MM J Virol; 1996 Oct; 70(10):7236-40. PubMed ID: 8794374 [TBL] [Abstract][Full Text] [Related]
16. Identification of the cis-acting signal for minus-strand RNA synthesis of a murine coronavirus: implications for the role of minus-strand RNA in RNA replication and transcription. Lin YJ; Liao CL; Lai MM J Virol; 1994 Dec; 68(12):8131-40. PubMed ID: 7966604 [TBL] [Abstract][Full Text] [Related]
17. Common RNA replication signals exist among group 2 coronaviruses: evidence for in vivo recombination between animal and human coronavirus molecules. Wu HY; Guy JS; Yoo D; Vlasak R; Urbach E; Brian DA Virology; 2003 Oct; 315(1):174-83. PubMed ID: 14592769 [TBL] [Abstract][Full Text] [Related]
18. Natural evolution of coronavirus defective-interfering RNA involves RNA recombination. Furuya T; Macnaughton TB; La Monica N; Lai MM Virology; 1993 May; 194(1):408-13. PubMed ID: 8386886 [TBL] [Abstract][Full Text] [Related]
19. Using a defective-interfering RNA system to express the HE protein of mouse hepatitis virus for studying viral pathogenesis. Zhang X; Hinton D; Park S; Liao CL; Lai MM; Stohlman S Adv Exp Med Biol; 1998; 440():521-8. PubMed ID: 9782324 [TBL] [Abstract][Full Text] [Related]
20. A bulged stem-loop structure in the 3' untranslated region of the genome of the coronavirus mouse hepatitis virus is essential for replication. Hsue B; Masters PS J Virol; 1997 Oct; 71(10):7567-78. PubMed ID: 9311837 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]