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Titlebook: Coronaviruses and their Diseases; David Cavanagh,T. David K. Brown Conference proceedings 1990 The Editor(s) (if applicable) and The Autho

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Joanna Fountain,Charlotte ThompsonFor mouse hepatitis virus, strain A59 (MHV-A59), a solid phase assay was developed to detect binding of virions to plasma membranes from normal target tissues of susceptible mice (1). Using a virus overlay protein blot assay, MHV-A59 was shown to bind specifically to a 100 to 110K protein from liver
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Jonathan Staggs,Matthew Brennerireceptor monoclonal antibody. Purified receptor was sequenced from the 1st to the 15th amino acids. Antiserum raised against a synthetic peptide having this sequence bound to the 110 K receptor from BALB/c intestine and a 58 K fragment of the receptor. SJL/J mice are resistant to MHV-A59 and their
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Joanna Fountain,Charlotte Thompsong the chemical mutagen, ethyl methane sulfonate (EMS), mouse fibroblast cell mutants were generated which were selected for resistance to cell-killing by MHV. These mutants were then screened for their susceptibility to MHV infection, ability to replicate MHV and relative sensitivity to MHV-induced
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Probabilistic Modelling and Optimization,gy of these ubiquitous pathogens. We have undertaken the molecular characterization of the prototype 229E strain of HCV. The virus grew to the highest titers on a human embryonic lung cell line (L132) at 33°C and purification was optimal on Renografin-60® gradients. Metabolic labeling with [.S]methi
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Anindita Roy,Santanu Bandyopadhyayral membrane protein (M), a large glycoprotein constituting the characteristic viral spikes (S), and an intermediate-sized glycoprotein (HE). This paper will summarize published knowledge on the properties and function of the small and the intermediate-sized membrane proteins. They will be referred
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