Zobrazeno 1 - 8
of 8
pro vyhledávání: '"James C. Cohen"'
Publikováno v:
Intervirology. 9:276-285
The replication of equine herpesvirus type 1 (EHV-1) and type 3 (EHV-3) was unimpeded in three different cell types – equine epithelial cells, equine fibroblasts, and mouse fibroblasts – which had been blocked in their capacity to synthesize host
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761f58d2359136d98c98998cb70bc9a3
https://doi.org/10.1159/000148945
https://doi.org/10.1159/000148945
Publikováno v:
The Journal of Arthroplasty. 3:369-377
The management of an infected total knee implant is a major challenge to the orthopaedic surgeon. This article reviews the use of antibiotic-PMMA spacer block in two-stage reimplantation of septic total knee arthroplasties. In addition to serving as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f23f229811a1275c7ee95f1d8c65857
https://doi.org/10.1016/s0883-5403(88)80040-8
https://doi.org/10.1016/s0883-5403(88)80040-8
Publikováno v:
Virology. 74:194-208
Three distinct species of nucleocapsids of equine herpesvirus type-1, designated as either light (L), intermediate (I), or heavy (H) on the basis of their densities in Renografin-76 density gradients (Perdue et al. 1975), were characterized with resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ccc9a25ed9cd3ced738d8d67ffa00ba
https://doi.org/10.1016/0042-6822(76)90141-0
https://doi.org/10.1016/0042-6822(76)90141-0
Publikováno v:
Virology. 68(2)
Hamster hepatic cells infected in vivo with equine herpesvirus, type 1, were used for the preparation of isolated nuclei, which were assayed for RNA and DNA polymerases. An endogenous RNA polymerase II activity (sensitive to α-amanitin) was inhibite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7e98bcf4432da40a0c52a0782cea9a2
https://pubmed.ncbi.nlm.nih.gov/173079
https://pubmed.ncbi.nlm.nih.gov/173079
Publikováno v:
Virology. 67(1)
Hydroxyurea (HU) at concentrations that rapidly and completely inhibit mammalian cellular DNA synthesis does not prevent either equine herpesvirus type 1 (EHV-1) DNA synthesis or virus replication. Analysis by CsCl isopycnic centrifugation of DNA syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b076809ae530a5822acbfdd609c798b
https://pubmed.ncbi.nlm.nih.gov/170739
https://pubmed.ncbi.nlm.nih.gov/170739
Publikováno v:
Virology. 68(2)
Scatchard analysis of RNA-DNA hybridization saturation kinetics of viral RNA from equine herpesvirus type 1 (EHV-1)-infected cells revealed the synthesis of two classes of RNA's distinguishable by relative molar concentration. A relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d95fe3ac5eafe9b0ca26d4ad1a3582c
https://pubmed.ncbi.nlm.nih.gov/173082
https://pubmed.ncbi.nlm.nih.gov/173082
Autor:
Charles C. Randall, James C. Cohen, Dennis J. O'Callaghan, Michael L. Perdue, Maurice C. Kemp
Publikováno v:
Virology. 64(1)
Three distinct species of nucleocapsids of equine herpesvirus type-1 (EHV-1) were isolated from infected L-M cell nuclei. The particles were classified on the basis of their densities in Renografin gradients as Light (L; ϱ = 1.237 g/cc), Intermediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4becc570d3b5e361a4e28de407509516
https://pubmed.ncbi.nlm.nih.gov/1167720
https://pubmed.ncbi.nlm.nih.gov/1167720
Publikováno v:
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.). 155(3)
SummaryThe role of an altered ribonu-cleotide diphosphate reductase activity in the resistance of equine herpesvirus type 1 to hydroxyurea was demonstrated. A 28% increase in total CDP reductase was observed by 6 hr PI, and the enzyme activity of EHV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3b552e8120c2278aeca22c450b3af64
https://pubmed.ncbi.nlm.nih.gov/195286
https://pubmed.ncbi.nlm.nih.gov/195286