BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 2992976)

  • 1. Infection of AtT20 murine pituitary tumour cells by mouse hepatitis virus strain A59: virus budding is restricted to the Golgi region.
    Tooze J; Tooze SA
    Eur J Cell Biol; 1985 May; 37():203-12. PubMed ID: 2992976
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Replication of coronavirus MHV-A59 in sac- cells: determination of the first site of budding of progeny virions.
    Tooze J; Tooze S; Warren G
    Eur J Cell Biol; 1984 Mar; 33(2):281-93. PubMed ID: 6325194
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Laminated cisternae of the rough endoplasmic reticulum induced by coronavirus MHV-A59 infection.
    Tooze J; Tooze SA; Warren G
    Eur J Cell Biol; 1985 Jan; 36(1):108-15. PubMed ID: 2983995
    [TBL] [Abstract][Full Text] [Related]  

  • 4. AtT20 pituitary tumour cells contain mouse mammary tumour virus and intracisternal A-type particles in addition to murine leukemia virus.
    Tooze J; Tooze S; Haisma H; Hilgers J
    Eur J Cell Biol; 1985 Nov; 39(1):224-31. PubMed ID: 2417843
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Host-derived intracellular immunization against mouse hepatitis virus infection.
    Chen W; Madden VJ; Bagnell CR; Baric RS
    Virology; 1997 Feb; 228(2):318-32. PubMed ID: 9123839
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sorting of progeny coronavirus from condensed secretory proteins at the exit from the trans-Golgi network of AtT20 cells.
    Tooze J; Tooze SA; Fuller SD
    J Cell Biol; 1987 Sep; 105(3):1215-26. PubMed ID: 2821011
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Post-translational glycosylation of coronavirus glycoprotein E1: inhibition by monensin.
    Niemann H; Boschek B; Evans D; Rosing M; Tamura T; Klenk HD
    EMBO J; 1982; 1(12):1499-504. PubMed ID: 6327272
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A spike protein-dependent cellular factor other than the viral receptor is required for mouse hepatitis virus entry.
    Yokomori K; Asanaka M; Stohlman SA; Lai MM
    Virology; 1993 Sep; 196(1):45-56. PubMed ID: 8395126
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spike glycoprotein-mediated fusion in biliary glycoprotein-independent cell-associated spread of mouse hepatitis virus infection.
    Nash TC; Buchmeier MJ
    Virology; 1996 Sep; 223(1):68-78. PubMed ID: 8806541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The murine coronavirus mouse hepatitis virus strain A59 from persistently infected murine cells exhibits an extended host range.
    Schickli JH; Zelus BD; Wentworth DE; Sawicki SG; Holmes KV
    J Virol; 1997 Dec; 71(12):9499-507. PubMed ID: 9371612
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tissue and cellular distribution of an adhesion molecule in the carcinoembryonic antigen family that serves as a receptor for mouse hepatitis virus.
    Godfraind C; Langreth SG; Cardellichio CB; Knobler R; Coutelier JP; Dubois-Dalcq M; Holmes KV
    Lab Invest; 1995 Nov; 73(5):615-27. PubMed ID: 7474935
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Selection in persistently infected murine cells of an MHV-A59 variant with extended host range.
    Schickli JH; Wentworth DE; Zelus BD; Holmes KV; Sawicki SG
    Adv Exp Med Biol; 1998; 440():735-41. PubMed ID: 9782352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Identification of H209 as Essential for pH 8-Triggered Receptor-Independent Syncytium Formation by S Protein of Mouse Hepatitis Virus A59.
    Li P; Shan Y; Zheng W; Ou X; Mi D; Mu Z; Holmes KV; Qian Z
    J Virol; 2018 Jun; 92(11):. PubMed ID: 29514915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Natural cytotoxicity against mouse hepatitis virus-infected target cells. I. Correlation of cytotoxicity with virus binding to leukocytes.
    Holmes KV; Welsh RM; Haspel MV
    J Immunol; 1986 Feb; 136(4):1446-53. PubMed ID: 3003198
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Restricted replication of mouse hepatitis virus A59 in primary mouse brain astrocytes correlates with reduced pathogenicity.
    van Berlo MF; Wolswijk G; Calafat J; Koolen MJ; Horzinek MC; van der Zeijst BA
    J Virol; 1986 May; 58(2):426-33. PubMed ID: 3009857
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Assembly and maturation of the flavivirus Kunjin virus appear to occur in the rough endoplasmic reticulum and along the secretory pathway, respectively.
    Mackenzie JM; Westaway EG
    J Virol; 2001 Nov; 75(22):10787-99. PubMed ID: 11602720
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Site of addition of N-acetyl-galactosamine to the E1 glycoprotein of mouse hepatitis virus-A59.
    Tooze SA; Tooze J; Warren G
    J Cell Biol; 1988 May; 106(5):1475-87. PubMed ID: 2836431
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Predominance of MHC class II-restricted CD4+ cytotoxic T cells against mouse hepatitis virus A59.
    Heemskerk MH; Schoemaker HM; Spaan WJ; Boog CJ
    Immunology; 1995 Apr; 84(4):521-7. PubMed ID: 7790024
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of the coronavirus mouse hepatitis virus strain A59 small membrane protein E.
    Raamsman MJ; Locker JK; de Hooge A; de Vries AA; Griffiths G; Vennema H; Rottier PJ
    J Virol; 2000 Mar; 74(5):2333-42. PubMed ID: 10666264
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.