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

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發(fā)表于 2025-3-21 16:43:38 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Ruminant Pestivirus Infections
副標(biāo)題Virology, Pathogenes
編輯B. Liess,V. Moennig,G. Trautwein
視頻videohttp://file.papertrans.cn/833/832096/832096.mp4
叢書名稱Archives of Virology. Supplementa
圖書封面Titlebook: Ruminant Pestivirus Infections; Virology, Pathogenes B. Liess,V. Moennig,G. Trautwein Conference proceedings 1991 Springer-Verlag/Wien 1991
描述Findings concerning various clinical manifestations in cattle and sheep have made it clear that pestivirus infections in ruminants have an economic impact similar to hog cholera. Early data justified the classification of pestiviruses as a genus of nonarthopod-borne togaviruses. Since pestiviruses are difficult to work with, progress in understanding the virus and disease gradually came to a standstill because conventional techniques failed to yield further insights. About ten years ago interest in pestivirology was revived by strong impulses of modern biotechnology and a breakthrough in pathogenesis research, i.e. in vitro translation of BVD viral proteins and the ex experimental reproduction of mucosal disease in cattle. In order to summarize and discuss these exciting developments, an international community of pestivirus researchers came together in June 1990 in Hannover (Federal Republic of Germany) for the Symposium "Ruminant Pestivirus Infections: Virology, Pathogenesis and Perspectives on Prophylaxis". This book is a selection of papers presented at this symposium.
出版日期Conference proceedings 1991
關(guān)鍵詞Antigen; Cholera; Monoclonal Antibodies; Pathogen; Viruses; Virusinfektion; infections; polymer; protein; pro
版次1
doihttps://doi.org/10.1007/978-3-7091-9153-8
isbn_softcover978-3-211-82279-1
isbn_ebook978-3-7091-9153-8Series ISSN 0939-1983
issn_series 0939-1983
copyrightSpringer-Verlag/Wien 1991
The information of publication is updating

書目名稱Ruminant Pestivirus Infections影響因子(影響力)




書目名稱Ruminant Pestivirus Infections影響因子(影響力)學(xué)科排名




書目名稱Ruminant Pestivirus Infections網(wǎng)絡(luò)公開度




書目名稱Ruminant Pestivirus Infections網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Ruminant Pestivirus Infections被引頻次




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Bovine viral diarrhea virus proteins and their antigenic analyses is present on the surface of the virion and carries neutralization epitopes. Antigenic analyses with the panel of MABs reveals extensive antigenic heterogeneity among BVDV field isolates. MABs were used to determine the frequency of neutralization escape mutants in stocks of BVDV. Plaque-purified B
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Correlation of bovine viral diarrhoea virus induced cytopathic effects with expression of a biotype-ll damage other than the typical cytopathic effect might be responsible for the BVD/C38 reactivity of cells infected with BVDV..In addition, it was analyzed whether the antigenic marker associated with cpBVDV was expressed in cells infected with viral isolates from 21 animals with clinical mucosal d
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Diaplacental infections with ruminant pestiviruses in retinal dysplasia and cerebellar hypoplasia. The lesions were attributed to direct viral cytopathology. Noncytopathic BDV (BD-31) in lambs caused weak lambs, with hairy fleece and tonic-clonic tremors. The lambs were of low birth weight, persistently viremic and immunologically tolerant. The lam
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The pathways for bovine virus diarrhoea virus biotypes in the pathogenesis of diseasegenic and cytopathogenic, are described. Their sequential role in the pathogenesis of mucosal disease arises from the initial foetal infection with the non-cytopathogenic virus and the subsequent production of persistently viraemic calves. These calves may later develop mucosal disease as a result o
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Identification and production of pestivirus proteins for diagnostic and vaccination purposesn the polyprotein encoded by the viral genome was refined by epitope scanning using synthetic hexameric peptides. This viral antigen was further expressed in E. coli, produced as inclusion bodies and used successfully as an ELISA antigen in both competitive and indirect assays for the detection of B
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