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Evidence for the role of cell protein phosphorylation in human cytomegalovirus/host cell fusion.
Keay S, Baldwin BR. Keay S, et al. J Gen Virol. 1996 Oct;77 ( Pt 10):2597-604. doi: 10.1099/0022-1317-77-10-2597. J Gen Virol. 1996. PMID: 8887496
These data indicate that increased phosphorylation of a 92.5 kDa putative cell membrane protein receptor for gH is an early event in response to HCMV, and that cell protein phosphorylation by tyrosine kinase(s) and PKC may facilitate HCMV/cell membrane fusion....
These data indicate that increased phosphorylation of a 92.5 kDa putative cell membrane protein receptor for gH is an early event in respons …
Update on the 92.5 kDa putative HCMV fusion receptor.
Keay S, Baldwin B. Keay S, et al. Scand J Infect Dis Suppl. 1995;99:32-3. Scand J Infect Dis Suppl. 1995. PMID: 8668940 No abstract available.
The human cytomegalovirus UL55 (gB) and UL75 (gH) glycoprotein ligands initiate the rapid activation of Sp1 and NF-kappaB during infection.
Yurochko AD, Hwang ES, Rasmussen L, Keay S, Pereira L, Huang ES. Yurochko AD, et al. J Virol. 1997 Jul;71(7):5051-9. doi: 10.1128/JVI.71.7.5051-5059.1997. J Virol. 1997. PMID: 9188570 Free PMC article.
These results support our hypothesis that HCMV glycoproteins mediate an initial signal transduction pathway which leads to the upregulation of host cell transcription factors and suggests a model wherein the orderly sequence of virus-mediated changes in cellular activation initia …
These results support our hypothesis that HCMV glycoproteins mediate an initial signal transduction pathway which leads to the upregulation …
Molecular cloning and expression of receptor peptides that block human cytomegalovirus/cell fusion.
Baldwin BR, Kleinberg M, Keay S. Baldwin BR, et al. Biochem Biophys Res Commun. 1996 Feb 15;219(2):668-73. doi: 10.1006/bbrc.1996.0291. Biochem Biophys Res Commun. 1996. PMID: 8605045
Clones expressing a partial human cytomegalovirus putative fusion receptor were selected by binding specifically to monoclonal anti-idiotypic antibodies that mimic glycoprotein H. cDNA was isolated from 2 of the clones (131 and 611) and fused in frame with the glutathione S
Clones expressing a partial human cytomegalovirus putative fusion receptor were selected by binding specifically to monoclonal anti-idiotypi …
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