318 related articles for article (PubMed ID: 25670774)
21. Mutations in the stalk region of the measles virus hemagglutinin inhibit syncytium formation but not virus entry.
Ennis MK; Hu C; Naik SK; Hallak LK; Peng KW; Russell SJ; Dingli D
J Virol; 2010 Oct; 84(20):10913-7. PubMed ID: 20702637
[TBL] [Abstract][Full Text] [Related]
22. Interaction of the Hemagglutinin Stalk Region with Cell Adhesion Molecule (CADM) 1 and CADM2 Mediates the Spread between Neurons and Neuropathogenicity of Measles Virus with a Hyperfusogenic Fusion Protein.
Takemoto R; Hirai Y; Watanabe S; Harada H; Suzuki T; Hashiguchi T; Yanagi Y; Shirogane Y
J Virol; 2023 May; 97(5):e0034023. PubMed ID: 37166307
[TBL] [Abstract][Full Text] [Related]
23. Structural characteristics of measles virus entry.
Fukuhara H; Mwaba MH; Maenaka K
Curr Opin Virol; 2020 Apr; 41():52-58. PubMed ID: 32413678
[TBL] [Abstract][Full Text] [Related]
24. Fatal measles virus infection prevented by brain-penetrant fusion inhibitors.
Welsch JC; Talekar A; Mathieu C; Pessi A; Moscona A; Horvat B; Porotto M
J Virol; 2013 Dec; 87(24):13785-94. PubMed ID: 24109233
[TBL] [Abstract][Full Text] [Related]
25. Previously unrecognized amino acid substitutions in the hemagglutinin and fusion proteins of measles virus modulate cell-cell fusion, hemadsorption, virus growth, and penetration rate.
Okada H; Itoh M; Nagata K; Takeuchi K
J Virol; 2009 Sep; 83(17):8713-21. PubMed ID: 19553316
[TBL] [Abstract][Full Text] [Related]
26. A single amino acid substitution in the measles virus F₂ protein reciprocally modulates membrane fusion activity in pathogenic and oncolytic strains.
Heidmeier S; Hanauer JR; Friedrich K; Prüfer S; Schneider IC; Buchholz CJ; Cichutek K; Mühlebach MD
Virus Res; 2014 Feb; 180():43-8. PubMed ID: 24368277
[TBL] [Abstract][Full Text] [Related]
27. Measles virus attachment proteins with impaired ability to bind CD46 interact more efficiently with the homologous fusion protein.
Corey EA; Iorio RM
Virology; 2009 Jan; 383(1):1-5. PubMed ID: 19013625
[TBL] [Abstract][Full Text] [Related]
28. Mutant fusion proteins with enhanced fusion activity promote measles virus spread in human neuronal cells and brains of suckling hamsters.
Watanabe S; Shirogane Y; Suzuki SO; Ikegame S; Koga R; Yanagi Y
J Virol; 2013 Mar; 87(5):2648-59. PubMed ID: 23255801
[TBL] [Abstract][Full Text] [Related]
29. Measles Virus Fusion Protein: Structure, Function and Inhibition.
Plattet P; Alves L; Herren M; Aguilar HC
Viruses; 2016 Apr; 8(4):112. PubMed ID: 27110811
[TBL] [Abstract][Full Text] [Related]
30. Mutations in the Fusion Protein of Measles Virus That Confer Resistance to the Membrane Fusion Inhibitors Carbobenzoxy-d-Phe-l-Phe-Gly and 4-Nitro-2-Phenylacetyl Amino-Benzamide.
Ha MN; Delpeut S; Noyce RS; Sisson G; Black KM; Lin LT; Bilimoria D; Plemper RK; Privé GG; Richardson CD
J Virol; 2017 Dec; 91(23):. PubMed ID: 28904193
[TBL] [Abstract][Full Text] [Related]
31. The hemagglutinin envelope protein of canine distemper virus (CDV) confers cell tropism as illustrated by CDV and measles virus complementation analysis.
Stern LB; Greenberg M; Gershoni JM; Rozenblatt S
J Virol; 1995 Mar; 69(3):1661-8. PubMed ID: 7853502
[TBL] [Abstract][Full Text] [Related]
32. Mutations in the putative dimer-dimer interfaces of the measles virus hemagglutinin head domain affect membrane fusion triggering.
Nakashima M; Shirogane Y; Hashiguchi T; Yanagi Y
J Biol Chem; 2013 Mar; 288(12):8085-8091. PubMed ID: 23362271
[TBL] [Abstract][Full Text] [Related]
33. Cell fusion by the envelope glycoproteins of persistent measles viruses which caused lethal human brain disease.
Cattaneo R; Rose JK
J Virol; 1993 Mar; 67(3):1493-502. PubMed ID: 8437226
[TBL] [Abstract][Full Text] [Related]
34. Importance of the cytoplasmic tails of the measles virus glycoproteins for fusogenic activity and the generation of recombinant measles viruses.
Moll M; Klenk HD; Maisner A
J Virol; 2002 Jul; 76(14):7174-86. PubMed ID: 12072517
[TBL] [Abstract][Full Text] [Related]
35. A recombinant measles vaccine virus expressing wild-type glycoproteins: consequences for viral spread and cell tropism.
Johnston IC; ter Meulen V; Schneider-Schaulies J; Schneider-Schaulies S
J Virol; 1999 Aug; 73(8):6903-15. PubMed ID: 10400788
[TBL] [Abstract][Full Text] [Related]
36. Targeted entry of enveloped viruses: measles and herpes simplex virus I.
Navaratnarajah CK; Miest TS; Carfi A; Cattaneo R
Curr Opin Virol; 2012 Feb; 2(1):43-9. PubMed ID: 22440965
[TBL] [Abstract][Full Text] [Related]
37. Development of measles virus-based shielded oncolytic vectors: suitability of other paramyxovirus glycoproteins.
Hudacek AW; Navaratnarajah CK; Cattaneo R
Cancer Gene Ther; 2013 Feb; 20(2):109-16. PubMed ID: 23306608
[TBL] [Abstract][Full Text] [Related]
38. Virus entry is a major determinant of cell tropism of Edmonston and wild-type strains of measles virus as revealed by vesicular stomatitis virus pseudotypes bearing their envelope proteins.
Tatsuo H; Okuma K; Tanaka K; Ono N; Minagawa H; Takade A; Matsuura Y; Yanagi Y
J Virol; 2000 May; 74(9):4139-45. PubMed ID: 10756026
[TBL] [Abstract][Full Text] [Related]
39. Structural and mechanistic studies of measles virus illuminate paramyxovirus entry.
Plemper RK; Brindley MA; Iorio RM
PLoS Pathog; 2011 Jun; 7(6):e1002058. PubMed ID: 21655106
[TBL] [Abstract][Full Text] [Related]
40. A novel amino acid position in hemagglutinin glycoprotein of measles virus is responsible for hemadsorption and CD46 binding.
Li L; Qi Y
Arch Virol; 2002 Apr; 147(4):775-86. PubMed ID: 12038687
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
