120 related articles for article (PubMed ID: 8862433)
1. A murine and a porcine coronavirus are released from opposite surfaces of the same epithelial cells.
Rossen JW; Bekker CP; Strous GJ; Horzinek MC; Dveksler GS; Holmes KV; Rottier PJ
Virology; 1996 Oct; 224(1):345-51. PubMed ID: 8862433
[TBL] [Abstract][Full Text] [Related]
2. The viral spike protein is not involved in the polarized sorting of coronaviruses in epithelial cells.
Rossen JW; de Beer R; Godeke GJ; Raamsman MJ; Horzinek MC; Vennema H; Rottier PJ
J Virol; 1998 Jan; 72(1):497-503. PubMed ID: 9420251
[TBL] [Abstract][Full Text] [Related]
3. Coronaviruses in polarized epithelial cells.
Rossen JW; Bekker CP; Voorhout WF; Horzinek MC; Van der Ende A; Strous GJ; Rottier PJ
Adv Exp Med Biol; 1995; 380():135-8. PubMed ID: 8830469
[TBL] [Abstract][Full Text] [Related]
4. Mouse hepatitis virus strain A59 is released from opposite sides of different epithelial cell types.
Rossen JW; Strous GJ; Horzinek MC; Rottier PJ
J Gen Virol; 1997 Jan; 78 ( Pt 1)():61-9. PubMed ID: 9010286
[TBL] [Abstract][Full Text] [Related]
5. MHV-A59 enters polarized murine epithelial cells through the apical surface but is released basolaterally.
Rossen JW; Voorhout WF; Horzinek MC; van der Ende A; Strous GJ; Rottier PJ
Virology; 1995 Jun; 210(1):54-66. PubMed ID: 7793080
[TBL] [Abstract][Full Text] [Related]
6. Entry and release of transmissible gastroenteritis coronavirus are restricted to apical surfaces of polarized epithelial cells.
Rossen JW; Bekker CP; Voorhout WF; Strous GJ; van der Ende A; Rottier PJ
J Virol; 1994 Dec; 68(12):7966-73. PubMed ID: 7966587
[TBL] [Abstract][Full Text] [Related]
7. Feline and canine coronaviruses are released from the basolateral side of polarized epithelial LLC-PK1 cells expressing the recombinant feline aminopeptidase-N cDNA.
Rossen JW; Kouame J; Goedheer AJ; Vennema H; Rottier PJ
Arch Virol; 2001; 146(4):791-9. PubMed ID: 11402864
[TBL] [Abstract][Full Text] [Related]
8. Feline aminopeptidase N serves as a receptor for feline, canine, porcine, and human coronaviruses in serogroup I.
Tresnan DB; Levis R; Holmes KV
J Virol; 1996 Dec; 70(12):8669-74. PubMed ID: 8970993
[TBL] [Abstract][Full Text] [Related]
9. Porcine Deltacoronavirus Engages the Transmissible Gastroenteritis Virus Functional Receptor Porcine Aminopeptidase N for Infectious Cellular Entry.
Wang B; Liu Y; Ji CM; Yang YL; Liang QZ; Zhao P; Xu LD; Lei XM; Luo WT; Qin P; Zhou J; Huang YW
J Virol; 2018 Jun; 92(12):. PubMed ID: 29618640
[TBL] [Abstract][Full Text] [Related]
10. Feline aminopeptidase N is a receptor for all group I coronaviruses.
Tresnan DB; Holmes KV
Adv Exp Med Biol; 1998; 440():69-75. PubMed ID: 9782266
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Survival of surrogate coronaviruses in water.
Casanova L; Rutala WA; Weber DJ; Sobsey MD
Water Res; 2009 Apr; 43(7):1893-8. PubMed ID: 19246070
[TBL] [Abstract][Full Text] [Related]
13. An overview of immunological and genetic methods for detecting swine coronaviruses, transmissible gastroenteritis virus, and porcine respiratory coronavirus in tissues.
Sirinarumitr T; Paul PS; Halbur PG; Kluge JP
Adv Exp Med Biol; 1997; 412():37-46. PubMed ID: 9191988
[TBL] [Abstract][Full Text] [Related]
14. Coronavirus M proteins accumulate in the Golgi complex beyond the site of virion budding.
Klumperman J; Locker JK; Meijer A; Horzinek MC; Geuze HJ; Rottier PJ
J Virol; 1994 Oct; 68(10):6523-34. PubMed ID: 8083990
[TBL] [Abstract][Full Text] [Related]
15. The coronavirus transmissible gastroenteritis virus causes infection after receptor-mediated endocytosis and acid-dependent fusion with an intracellular compartment.
Hansen GH; Delmas B; Besnardeau L; Vogel LK; Laude H; Sjöström H; Norén O
J Virol; 1998 Jan; 72(1):527-34. PubMed ID: 9420255
[TBL] [Abstract][Full Text] [Related]
16. In situ hybridization technique for the detection of swine enteric and respiratory coronaviruses, transmissible gastroenteritis virus (TGEV) and porcine respiratory coronavirus (PRCV), in formalin-fixed paraffin-embedded tissues.
Sirinarumitr T; Paul PS; Kluge JP; Halbur PG
J Virol Methods; 1996 Feb; 56(2):149-60. PubMed ID: 8882645
[TBL] [Abstract][Full Text] [Related]
17. Further characterization of aminopeptidase-N as a receptor for coronaviruses.
Delmas B; Gelfi J; Sjöström H; Noren O; Laude H
Adv Exp Med Biol; 1993; 342():293-8. PubMed ID: 7911642
[TBL] [Abstract][Full Text] [Related]
18. Comparative in vivo analysis of the nsp15 endoribonuclease of murine, porcine and severe acute respiratory syndrome coronaviruses.
Cao J; Zhang X
Virus Res; 2012 Aug; 167(2):247-58. PubMed ID: 22617024
[TBL] [Abstract][Full Text] [Related]
19. Aminopeptidase N is not required for porcine epidemic diarrhea virus cell entry.
Li W; Luo R; He Q; van Kuppeveld FJM; Rottier PJM; Bosch BJ
Virus Res; 2017 May; 235():6-13. PubMed ID: 28363778
[TBL] [Abstract][Full Text] [Related]
20. Expression of the recombinant anchorless N-terminal domain of mouse hepatitis virus (MHV) receptor makes hamster of human cells susceptible to MHV infection.
Dveksler GS; Gagneten SE; Scanga CA; Cardellichio CB; Holmes KV
J Virol; 1996 Jun; 70(6):4142-5. PubMed ID: 8648757
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
