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  • 1
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A highly pathogenic avian influenza virus, H5N1, caused disease outbreaks in poultry in China and seven other east Asian countries between late 2003 and early 2004; the same virus was fatal to humans in Thailand and Vietnam. Here we demonstrate a series of genetic reassortment events traceable ...
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-7284
    Keywords: Influenza A viruses ; Genetic reassortment ; Interspecies transmission ; Pandemic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The human influenza pandemics of 1957 and 1968 were caused by reassortant viruses that possessed internal gene segments from avian and human strains. Whether genetic reassortment of human and avian influenza viruses occurs during interpandemic periods and how often humans are infected with such reassortants is not known. To provide this information, we used dot-blot hybridization, partial nucleotide sequencing and subsequent phylogenetic analysis to examine the 6 internal genes of 122 viruses isolated in humans between 1933 and 1992 primarily from Asia, Europe, and the Americas. The internal genes of A/New Jersey/11/76 isolated from a human fatality at Fort Dix, New Jersey in 1976 were found to be of porcine origin. Although none of the geographically and temporally diverse collection of 122 viruses was an avian-human or other reassortant, cognizance was made of the fact that there were two isolates from children from amongst 546 influenza A isolates obtained from The Netherlands from 1989–1994 which were influenza reassortants containing genes of avian origin, viruses which have infected European pigs since 1983–1985. Thus, genetic reassortment between avian and human influenza strains does occur in the emergence of pandemic and interpandemic influenza A viruses. However, in the interpandemic periods the reassortants have no survival advantage, and the circulating interpandemic influenza viruses in humans do not appear to accumulate avian influenza virus genes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 25 (1968), S. 148-159 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In this paper evidence is presented to show that the non-specific inhibitor of adenovirus type 5 haemagglutination is associated with a very labile, low molecular weight α1-globulin. This inhibitor flocculates the whole particle and a mixture of its soluble antigens. The data suggest that the inhibitor attaches directly to the haemagglutination sites on the virus and electron microscope evidence is produced to support this idea. Electron microscopy of the flocculated virus revealed that the particles appeared to be joined at the vertex projections. It is hoped that the study of the interaction of serum inhibitors and viruses could serve as a means of elucidating the nature of the virus surface.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 30 (1970), S. 238-244 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In this paper evidence is presented to show that the non-specific inhibitor of adenovirus haemagglutination combines with hexons (soluble and viral) as well as with the haemagglutinating entities to produce flocculation. Therefore the haemagglutination inhibition test is best performed using either penton or fibre antigen as indicator and because of its stability the fibre is preferred. Of the hexons, the inhibitor appears to combine specifically with the hexons proper. It is concluded that the adjacent hexons and/or peripentons are responsible for attachment of virus to the host cell. The nature of these interactions is discussed. These results underline the importance of the use of serum inhibitors in the elucidation of the nature of the viral surface and the relationship of that surface to red blood cell and host cell systems. It is hoped that chemical identification of the active groupings involved will shed light on the fundamentals of the infective process.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 32 (1970), S. 286-290 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Newcastle disease virus vaccine strain (La Sota) specific monoclonal antibody (La-1) was produced by immunizing mice with isolated glycoproteins of strain La Sota. This antibody was recognized only in the ELISA test in which it bound exclusively to La Sota strain out of a range of over 300 lentogenic, mesogenic and velogenic strains examined.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 29 (1970), S. 1-24 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Adenovirus type 5 was degraded by 8m urea to release three readily identifiable internal components and three species of surface hexon component each of which appeared to be associated with minor constituents which were lacking in the “soluble” hexon antigens. The vertex projection was destroyed. All components were recognized serologically. Whole virus antiserum appeared to contain antibody to both external and internal components. Any breakdown product that reacted with this antiserum and not “soluble” hexon antiserum was regarded as an internal component. The major internal component was estimated to be 170Å×23Å and of molecular weight (MW) 280,000. Two minor internal components were of approximate MW 5,000. The individual hexons, as well as “soluble” hexons were estimated to be 160Å×33Å and of MW 380,000. The three species were ascribed various positions in the virus particle. 1. Hexons surrounding the vertex capsomere — peripentons. 2. Hexons that lie along the adjacent sides — adjacent hexons. 3. Hexons occurring in triangular facets of six lying in the one plane — hexons proper. It is suggested that the central hole of the hexons plays a role in attaching them to the virus particle. This attachment may be mediated by the major internal component which could occur as a radial array around the DNA base structure.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 60 (1979), S. 105-113 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The morphological, bio-physical and growth properties of the isolate duck/Hong Kong/D3/75 (D3/75) were consistent with this virus being a member of the paramyxovirus group. Using haemagglutination inhibition and neuraminidase inhibition tests no serological relationships between D3/75 and other paramyxoviruses could be demonstrated. The structural polypeptides of D3/75 were also typical of paramyxoviruses, consisting of 6–7 polypeptides ranging in molecular weight from 46,000–200,000 under reduced conditions. Two polypeptides were glycosylated.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 52 (1976), S. 181-186 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Trypsinization rendered human group 0 erythrocytes highly susceptible to agglutination by chagres virus possibly due to the exposure of underlying lipid receptor groups to give rise to haemagglutination patterns firmer than those observed with gander cells.
    Type of Medium: Electronic Resource
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