Results 161 to 170 of about 11,544 (218)

Pseudorabies Virus UL41 Hijacks IFN Response via JAK/STAT Pathway While Cellular TRIM21 Blocks it Through K48 Ubiquitination. [PDF]

Transbound Emerg Dis
Li X, Zheng J, Zhang G, Li P, Dong M, Liu Q, Ren L.   +6 more
europepmc   +1 more source

<i>Pseudorabies Virus</i> IE180 Inhibits Virus Replication by Activating the Type I Interferon Pathway. [PDF]

Microorganisms
Zheng F, Song J, Chen X, Xing D, Bai R, Cheng C, Yuan J, Zhang R.   +7 more
europepmc   +1 more source

Vaccination of pigs with a DNA construct expressing an influenza virus M2-nucleoprotein fusion protein exacerbates disease after challenge with influenza A virus

, 2002
Heinen, P.P., Rijsewijk, F.A., Boer, L.E.A., de, Bianchi, A.T.J.   +3 more
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Characteristics of the Photoreactivation of Pseudorabies Virus

Journal of Bacteriology, 1966
Pfefferkorn, E. R. (Harvard Medical School, Boston, Mass.), Boyce W. Burge, and Helen M. Coady. Characteristics of the photoreactivation of pseudorabies virus. J. Bacteriol. 92:856-861. 1966.-Pseudorabies virus, killed with ultraviolet light and then allowed to adsorb to chick embryo tissue culture cells, can be photoreactivated by light of longer ...
E R, Pfefferkorn, B W, Burge, H M, Coady
openaire   +2 more sources

Survival of pseudorabies virus in aerosol

American Journal of Veterinary Research, 1990
SUMMARY The survival of pseudorabies virus in an aerosol was studied under different environmental conditions of temperature and relative humidity. Pseudorabies virus decayed logarithmically with mean half-lives of 17.4 (85% relative humidity, 22 C), 18.8 (25% relative humidity, 22 C), 27.3 (85% relative humidity, 4 C), 36.1 (55% relative humidity, 22 ...
M A, Schoenbaum, J J, Zimmerman, G W, Beran, D P, Murphy   +3 more
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Specificity of pseudorabies virus serotests

American Journal of Veterinary Research, 1984
SUMMARY Pigs experimentally inoculated with bovine herpesvirus-1 or equine herpesvirus-1 developed mild clinical disease signs. Regression of clinical disease was accompanied by development of specific virus-neutralizing antibodies. These antibodies did not react positively with pseudorabies antigens in the serumvirus neutralization test, an indirect ...
J D, Neill, C L, Kelling, M B, Rhodes
openaire   +2 more sources

Inactivation of the pseudorabies virus by dithiothreitol

Virology, 1971
Abstract The virucidal nature of reduced dithiothreitol (DTT) for the pseudorabies (PR) virus (PRV) is presented. The rate of decay of PRV in DTT increased exponentially as the pH rose from 6.5 to 8. Effective virucidal concentrations of DTT decreased in concentration as the pH was elevated.
J H, Gainer, J, Long, P, Hill, W I, Capps   +3 more
openaire   +2 more sources

Vaccines against pseudorabies virus (PrV)

Veterinary Microbiology, 2017
Aujeszkýs disease (AD, pseudorabies) is a notifiable herpesvirus infection of pigs causing substantial economic losses to swine producers. AD in pigs is controlled by the use of vaccination with inactivated and attenuated live vaccines. Starting with classically attenuated live vaccines derived from low virulent field isolates, AD vaccination has ...
Thomas F Müller, Thomas C Mettenleiter
exaly   +3 more sources

Hemagglutination with pseudorabies virus

Archives of Virology, 1989
Pseudorabies virus grown in CPK cell cultures was tested for hemagglutination (HA) with erythrocytes of a variety of species at 4°C, 25°C and 37°C. HA was observed at all temperatures with mouse erythrocytes but not with cattle, sheep, goat, swine, cat, rabbit, guinea pig, rat, mongolian gerbil, chicken, and goose erythrocytes.
N. Tetsu, Y. Inaba, M. Yukawa, K. Yoshiki, T. Hirahara, Y. Furuya, S. Ito, A. Yonemochi, H. Ishikawa   +8 more
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Effect of heparin on hemagglutination by pseudorabies virus

American Journal of Veterinary Research, 1993
SUMMARY Heparin inhibited hemagglutination (ha) by pseudorabies virus (prv), but not ha by Akabane virus, bovine adenovirus type 7, Fukuoka virus, Getah virus, Japanese encephalitis virus, and parainfluenza virus type 3 belonging to the families Bunyaviridae, Adenoviridae, Rhabdoviridae, Togaviridae, Flaviviidae, and Paramyxoviridae, respectively.
S, Ohashi, Y, Inaba, J, Kataoka, N, Tetsu, I, Shibata, M, Asagi   +5 more
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