These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 6093353)

  • 21. Inhibition of Sendai virus hemagglutinin neuraminidase by the fusion protein.
    Dallocchio F; Tomasi M; Bellini T
    Biochem Biophys Res Commun; 1994 Jun; 201(2):988-93. PubMed ID: 8003040
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Newcastle Disease Virus Establishes Persistent Infection in Tumor Cells
    Rangaswamy US; Wang W; Cheng X; McTamney P; Carroll D; Jin H
    J Virol; 2017 Aug; 91(16):. PubMed ID: 28592535
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Protective effects of monoclonal antibodies against parainfluenza virus type 3-induced brain infection in hamsters.
    Rydbeck R; Löve A; Norrby E
    J Gen Virol; 1988 May; 69 ( Pt 5)():1019-24. PubMed ID: 2836547
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Some physico-chemical and biological properties of egg-Sendai virus with altered haemagglutinin-neuraminidase protein.
    Popa LM; Repanovici R; Iliescu R; Mihalache O; Cajal N
    Acta Virol; 1985 Dec; 29(6):461-5. PubMed ID: 2869656
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Persistent infection with influenza A virus: evolution of virus mutants.
    Frielle DW; Huang DD; Youngner JS
    Virology; 1984 Oct; 138(1):103-17. PubMed ID: 6388147
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Human parainfluenza virus type 1 evolution combines cocirculation of strains and development of geographically restricted lineages.
    Hetherington SV; Watson AS; Scroggs RA; Portner A
    J Infect Dis; 1994 Feb; 169(2):248-52. PubMed ID: 7508966
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Homooligomerization of the hemagglutinin-neuraminidase glycoprotein of human parainfluenza virus type 3 occurs before the acquisition of correct intramolecular disulfide bonds and mature immunoreactivity.
    Collins PL; Mottet G
    J Virol; 1991 May; 65(5):2362-71. PubMed ID: 1707981
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evidence for different receptor sites in mouse spleen cells for the Sendai virus hemagglutinin-neuraminidase (HN) and fusion (F) glycoproteins.
    Peterhans E; Baechi T; Yewdell J
    Virology; 1983 Jul; 128(2):366-76. PubMed ID: 6310862
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Minimal features of efficient incorporation of the hemagglutinin-neuraminidase protein into sendai virus particles.
    Essaidi-Laziosi M; Shevtsova AS; Roux L
    J Virol; 2014 Jan; 88(1):303-13. PubMed ID: 24155372
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Elevated expression of the human parainfluenza virus type 1 F gene downregulates HN expression.
    Bousse T; Takimoto T; Murti KG; Portner A
    Virology; 1997 May; 232(1):44-52. PubMed ID: 9185587
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Expression of the HN, F, NP and M proteins of Sendai virus by recombinant vaccinia viruses and their contribution to protective immunity against Sendai virus infections in mice.
    Sakaguchi T; Takao S; Kiyotani K; Fujii Y; Nakayama T; Yoshida T
    J Gen Virol; 1993 Mar; 74 ( Pt 3)():479-84. PubMed ID: 8383180
    [TBL] [Abstract][Full Text] [Related]  

  • 32. An alternative route of infection for viruses: entry by means of the asialoglycoprotein receptor of a Sendai virus mutant lacking its attachment protein.
    Markwell MA; Portner A; Schwartz AL
    Proc Natl Acad Sci U S A; 1985 Feb; 82(4):978-82. PubMed ID: 2983337
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The fusion and hemagglutinin-neuraminidase glycoproteins of human parainfluenza virus 3 are both required for fusion.
    Ebata SN; Côté MJ; Kang CY; Dimock K
    Virology; 1991 Jul; 183(1):437-41. PubMed ID: 1647076
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Antigenic variation of HVJ (Sendai virus) HN glycoprotein detectable by monoclonal antibodies during persistent infection.
    Sato H; Ogura H; Tanaka J; Hatano M
    J Gen Virol; 1984 Jan; 65 ( Pt 1)():185-9. PubMed ID: 6198445
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The interaction of Sendai virus glycoprotein-bearing recombinant vesicles with cell surfaces.
    Al-Ahdal MN; Abidi TF; Flanagan TD
    Biochim Biophys Acta; 1986 Jan; 854(2):157-68. PubMed ID: 3002466
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fusion properties of cells persistently infected with human parainfluenza virus type 3: participation of hemagglutinin-neuraminidase in membrane fusion.
    Moscona A; Peluso RW
    J Virol; 1991 Jun; 65(6):2773-7. PubMed ID: 1851852
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Glycoproteins of Sendai virus (HVJ) have a critical ratio for fusion between virus envelopes and cell membranes.
    Nakanishi M; Uchida T; Kim J; Okada Y
    Exp Cell Res; 1982 Nov; 142(1):95-101. PubMed ID: 6291967
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Possible involvement of microtubule disruption in bipolar budding of a Sendai virus mutant, F1-R, in epithelial MDCK cells.
    Tashiro M; Seto JT; Klenk HD; Rott R
    J Virol; 1993 Oct; 67(10):5902-10. PubMed ID: 8396659
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Kinetics of interactions of sendai virus envelope glycoproteins, F and HN, with endoplasmic reticulum-resident molecular chaperones, BiP, calnexin, and calreticulin.
    Tomita Y; Yamashita T; Sato H; Taira H
    J Biochem; 1999 Dec; 126(6):1090-100. PubMed ID: 10578061
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Regions on the hemagglutinin-neuraminidase proteins of human parainfluenza virus type-1 and Sendai virus important for membrane fusion.
    Bousse T; Takimoto T; Gorman WL; Takahashi T; Portner A
    Virology; 1994 Nov; 204(2):506-14. PubMed ID: 7941317
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.