Zobrazeno 1 - 10
of 120
pro vyhledávání: '"C. Cruciere"'
Autor:
F. Rosenthal, G. Chenut, A.-F. Saintilan, V. Bruyere, M. Picard, Emmanuel Albina, C. Burger, C. Cruciere
Publikováno v:
Veterinary Microbiology. 64:265-276
Seven experiments including a total of 47 pigs, 11 wild boars, 26 rabbits, 10 hares and 16 sheep were carried out to assess the efficacy, safety and transmission of the Chinese vaccine strain of the classical swine fever virus (CSFV) administrated by
Publikováno v:
Veterinary Microbiology. 47:365-375
This paper describes a single tube reverse transcription-polymerase chain reaction (RT-PCR) method for detection of African horse sickness virus (AHSV). The genomic segments 10 of viruses of the 9 AHSV serotypes were amplified. The 758bp products wer
Publikováno v:
Journal of Veterinary Medicine, Series B. 40:501-507
Summary The equine herpes viruses strains (EHV) isolated from organs of aborted foetuses or from nasal swabs have been analysed by comparison of their restriction endonucleases patterns using two enzymes, Bam HI and Pst I. The majority of the clinica
Publikováno v:
Molecular and cellular probes. 16(3)
For the detection of African swine fever virus (ASFV) by polymerase chain reaction (PCR) in clinical samples, an internal control was constructed to identify false negative results in each reaction. The internal control was designed in such a way tha
Autor:
F. M. Cancellotti, M Marault, Stéphan Zientara, C Cruciere, Matthew M. Binns, Nicholas Davis-Poynter, L. Ceglie, L Taylor, J. A. Mumford, S Ryder, G. Koptopoulos, Duncan Hannant, Ian Birch-Machin, P Iniguez
Publikováno v:
Journal of virological methods. 88(1)
Three filamentous phage random peptide display libraries were used in biopanning experiments with purified IgG from the serum of a gnotobiotic foal infected with equine herpesvirus-1 (EHV-1) to enrich for epitopes binding to anti-EHV-1 antibodies. Th
Autor:
José Manuel Sánchez-Vizcaíno, M. A. Cubillo, Stéphan Zientara, M. Diaz-Laviada, C. Cruciere, E. Plateau, C. Rubio, C. Hamblin, H. Hooghuis
Publikováno v:
African Horse Sickness ISBN: 9783211831328
The mortality rate in susceptible populations of horses during an epizootic of African horse sickness (AHS) may be in excess of 90%. Rapid and reliable assays are therefore essential for the confirmation of clinical diagnoses and to enable control st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a761c054cbc336d7fb766096d8200cc
https://doi.org/10.1007/978-3-7091-6823-3_27
https://doi.org/10.1007/978-3-7091-6823-3_27
Publikováno v:
African Horse Sickness ISBN: 9783211831328
This paper describes a method to rapidly identify African horse sickness virus (AHSV), using a single tube reverse transcription polymerase chain reaction (PCR). This method was used to amplify cDNA copies of genome segments 7 and 10 from several dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8896afb0ee6ecfdee6142e7f514e7977
https://doi.org/10.1007/978-3-7091-6823-3_20
https://doi.org/10.1007/978-3-7091-6823-3_20
Autor:
S. Moulay, M. El-Harrak, Corinne Sailleau, C. Hamblin, Stéphan Zientara, C. Cruciere, W. W. Laegreid
Publikováno v:
African Horse Sickness ISBN: 9783211831328
A coupled reverse transcriptase-polymerase chain reaction assay (RT-PCR) for the detection of African horse sickness virus (AHSV) dsRNA, has been developed using genome segment 7 as the target template for primers. RNA from isolates of all nine AHSV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::476800abd860e59a14974366163207ab
https://doi.org/10.1007/978-3-7091-6823-3_28
https://doi.org/10.1007/978-3-7091-6823-3_28
Publikováno v:
Research in veterinary science. 62(3)
A reverse transcription-polymerase chain reaction (RT-PCR) assay followed by dot-blot hybridisation was used to detect African horse sickness virus (AHSV); the primers employed amplified the S7 gene that encodes the VP7 protein. The RT-PCR assay was
Publikováno v:
Journal of virological methods. 53(1)
The development of a coupled reverse transcriptase-polymerase chain reaction assay (RT-PCR) is described for the detection of African horse sickness virus (AHSV) double-stranded RNA. Genome segments 7 and 10 were chosen as target templates for primer