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3. The spike but not the hemagglutinin/esterase protein of bovine coronavirus is necessary and sufficient for viral infection. Popova R; Zhang X Virology; 2002 Mar; 294(1):222-36. PubMed ID: 11886280 [TBL] [Abstract][Full Text] [Related]
4. Recognition of N-acetyl-9-O-acetylneuraminic acid by bovine coronavirus and hemagglutinating encephalomyelitis virus. Schultze B; Herrler G Adv Exp Med Biol; 1993; 342():299-304. PubMed ID: 8209746 [TBL] [Abstract][Full Text] [Related]
5. Characterization of the coronavirus M protein and nucleocapsid interaction in infected cells. Narayanan K; Maeda A; Maeda J; Makino S J Virol; 2000 Sep; 74(17):8127-34. PubMed ID: 10933723 [TBL] [Abstract][Full Text] [Related]
7. Complex formation between the spike protein and the membrane protein during mouse hepatitis virus assembly. Opstelten DJ; Horzinek MC; Rottier PJ Adv Exp Med Biol; 1993; 342():189-95. PubMed ID: 8209729 [TBL] [Abstract][Full Text] [Related]
8. Interaction of mouse hepatitis virus (MHV) spike glycoprotein with receptor glycoprotein MHVR is required for infection with an MHV strain that expresses the hemagglutinin-esterase glycoprotein. Gagneten S; Gout O; Dubois-Dalcq M; Rottier P; Rossen J; Holmes KV J Virol; 1995 Feb; 69(2):889-95. PubMed ID: 7815557 [TBL] [Abstract][Full Text] [Related]
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10. Folding of the mouse hepatitis virus spike protein and its association with the membrane protein. Opstelten DJ; de Groote P; Horzinek MC; Rottier PJ Arch Virol Suppl; 1994; 9():319-28. PubMed ID: 8032264 [TBL] [Abstract][Full Text] [Related]
11. Neuropathogenicity of mouse hepatitis virus JHM isolates differing in hemagglutinin-esterase protein expression. Yokomori K; Asanaka M; Stohlman SA; Makino S; Shubin RA; Gilmore W; Weiner LP; Wang FI; Lai MM J Neurovirol; 1995 Dec; 1(5-6):330-9. PubMed ID: 9222375 [TBL] [Abstract][Full Text] [Related]
12. Coexpression and association of the spike protein and the membrane protein of mouse hepatitis virus. Opstelten DJ; Raamsman MJ; Wolfs K; Horzinek MC; Rottier PJ Adv Exp Med Biol; 1995; 380():291-7. PubMed ID: 8830496 [TBL] [Abstract][Full Text] [Related]
13. The mouse hepatitis virus A59 spike protein is not cleaved in primary hepatocyte and glial cell cultures. Hingley ST; Leparc-Goffart I; Weiss SR Adv Exp Med Biol; 1998; 440():529-35. PubMed ID: 9782325 [TBL] [Abstract][Full Text] [Related]
14. Communication between S1N330 and a region in S2 of murine coronavirus spike protein is important for virus entry into cells expressing CEACAM1b receptor. Matsuyama S; Taguchi F Virology; 2002 Mar; 295(1):160-71. PubMed ID: 12033774 [TBL] [Abstract][Full Text] [Related]
15. Molecular mimicry between S peplomer proteins of coronaviruses (MHV, BCV, TGEV and IBV) and Fc receptor. Oleszak EL; Perlman S; Parr R; Collisson EW; Leibowitz JL Adv Exp Med Biol; 1993; 342():183-8. PubMed ID: 8209728 [TBL] [Abstract][Full Text] [Related]
16. Heterogeneity of gene expression of the hemagglutinin-esterase (HE) protein of murine coronaviruses. Yokomori K; Banner LR; Lai MM Virology; 1991 Aug; 183(2):647-57. PubMed ID: 1649505 [TBL] [Abstract][Full Text] [Related]
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19. Assembly of spikes into coronavirus particles is mediated by the carboxy-terminal domain of the spike protein. Godeke GJ; de Haan CA; Rossen JW; Vennema H; Rottier PJ J Virol; 2000 Feb; 74(3):1566-71. PubMed ID: 10627571 [TBL] [Abstract][Full Text] [Related]
20. Primary structures of hemagglutinin-esterase and spike glycoproteins of murine coronavirus DVIM. Morita E; Ebina H; Muto A; Himeno H; Hatakeyama K; Sugiyama K Virus Genes; 1998; 17(2):123-8. PubMed ID: 9857985 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]