Titlebook: Ruminant Pestivirus Infections; Virology, Pathogenes B. Liess,V. Moennig,G. Trautwein Conference proceedings 1991 Springer-Verlag/Wien 1991

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P. Qvist,H. Houe,B. Aasted,A. Meyling,L. R?nsholt,B. Blochd sichtbares Licht k?nnen verschiedene Strukturen des Auges sch?digen, ja sogar zerst?ren, wenn eine hohe Lichtdosis auf das Auge trifft. Neuere experimentelle und epidemiologische Studien zeigen, dass sozio?konomisch wichtige Augenerkrankungen wie der graue Star und verschiedene Formen der Netzhaut

Myofibrils

Pestiviruses—taxonomic perspectivesiruses, and recent nucleotide sequence data have confirmed this resemblance at the level of genome organization. For other enveloped positive stranded RNA viruses with ikosahedral nucleocapsids e.g. equine arteritis and lactate dehydrogenase virus of mice a taxonomic dilemma is encountered; while vi

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Tincture

Bovine viral diarrhea virus genomic organizationIn order to refine this genetic map and to further elucidate the gene products and expression strategy of this virus, we have generated a broad panel of sequence-specific antibody reagents. Use of these reagents not only allowed the identification of several previously undescribed viral polypeptides

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GULF

A “zinc finger-like” domain in the 54 KDA protein of several pestiviruses cytopathic (cp) or non-cytopathic (ncp) pestiviral strains. Except for the previously described insertions in two cp strains of the Bovine Viral Diarrhea virus (BVDV), we did not find comparable insertions in this gene. The predicted amino acid sequences of this 54 KDa protein portion contain a con

蠟燭

BVD monoclonal antibodies: relationship between viral protein specificity and viral strain specificisults. Seven monoclonal antibodies precipitated a polypeptide of 80kD and defined four domains, all of which showed considerable conservation amongst the 180 pestivirus strains and isolates examined. Nine monoclonal antibodies, including six with virus neutralizing activity, precipitated a 53kD poly

杠桿

Correlation of bovine viral diarrhoea virus induced cytopathic effects with expression of a biotype-es (BVDV). Cells infected with 19 strains of each viral biotype were analyzed for reactivity with the monoclonal antibody (mab) BVD/C38. Reactivity was examined using an enzyme immunoassay on fixed infected monolayers of fetal calf kidney cells. In the majority of cases, the mab discriminated betwee

CESS

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