Relevant bibliographies by topics / Canine adenovirus type 2

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Canine adenovirus type 2'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Canine adenovirus type 2"

1

Tsukiyama, T., R. Shibata, Y. Katayama, and M. Shinagawa. "Transforming Genes of Canine Adenovirus Type 2." Journal of General Virology 69, no. 10 (1988): 2471–82. http://dx.doi.org/10.1099/0022-1317-69-10-2471.

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Fernandes, P., C. Peixoto, V. M. Santiago, E. J. Kremer, A. S. Coroadinha, and P. M. Alves. "Bioprocess development for canine adenovirus type 2 vectors." Gene Therapy 20, no. 4 (2012): 353–60. http://dx.doi.org/10.1038/gt.2012.52.

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Kaczorek, Edyta, Patrycja Schulz, Joanna Małaczewska, et al. "Prevalence of respiratory pathogens detected in dogs with kennel cough in Poland." Acta Veterinaria Brno 85, no. 4 (2016): 329–36. http://dx.doi.org/10.2754/avb201685040329.

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Kennel cough is a multifactorial disease occurring all over the world; however, its epidemiology is still not fully understood. To the authors’ knowledge, no studies monitoring the occurrence of infectious agents responsible for kennel cough have been carried out in Poland. Therefore, the objective of our study was to determine which of the four pathogens most frequently isolated in other countries are predominant in north-eastern Poland. Swabs from the upper respiratory tract and tracheal lavage fluids from dogs (n = 40) exhibiting symptoms of this disease were analysed. Canine herpesvirus, c
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Hamir, A. N., N. Raju, and C. E. Rupprecht. "Experimental Oral Administration of Canine Adenovirus (Type 2) to Raccoons (Procyon lotor)." Veterinary Pathology 29, no. 6 (1992): 509–13. http://dx.doi.org/10.1177/030098589202900604.

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Canine adenovirus type 2 (CAV2) has been proposed for recombinant vaccines to control rabies in wild animals. To evaluate the suitability of CAV2 as a safe vector for the genetically engineered vaccines, seven wild-caught raccoons (three males and four females) were administered CAV2 per os. Two of the animals were euthanatized on each of post-infection days 3, 6, and 14, and one was euthanatized on day 21. Two other control raccoons (a male and a female) were also euthanatized on day 21. Microscopic pulmonary lesions of multifocal necrotizing bronchiolitis with basophilic intranuclear inclusi
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Bru, Thierry, Sara Salinas, and Eric J. Kremer. "An Update on Canine Adenovirus Type 2 and Its Vectors." Viruses 2, no. 9 (2010): 2134–53. http://dx.doi.org/10.3390/v2092134.

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Shibata, Riri, Morikazu Shinagawa, Yoichi Iida, and Toshio Tsukiyama. "Nucleotide sequence of E1 region of canine adenovirus type 2." Virology 172, no. 2 (1989): 460–67. http://dx.doi.org/10.1016/0042-6822(89)90188-8.

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7

Bulut, Oya, Orhan Yapici, Oguzhan Avci, et al. "The Serological and Virological Investigation of Canine Adenovirus Infection on the Dogs." Scientific World Journal 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/587024.

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Two types of Canine Adenovirus (CAVs), Canine Adenovirus type 1 (CAV-1), the virus which causes infectious canine hepatitis, and Canine Adenovirus type 2 (CAV-2), which causes canine infectious laryngotracheitis, have been found in dogs. In this study, blood samples taken from 111 dogs, which were admitted to the Internal Medicine Clinic of Selcuk University, Faculty of Veterinary Medicine, with clinical symptoms. Seventy-seven dogs were sampled from Isparta and Burdur dog shelters by random sampling, regardless of the clinical findings. Dogs showed a systemic disease, characterized by fever,
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Grad, Roni, Richard E. Sobonya, Mark L. Witten, et al. "Localization of Inflammation and Virions in Canine Adenovirus Type 2 Bronchiolitis." American Review of Respiratory Disease 142, no. 3 (1990): 691–99. http://dx.doi.org/10.1164/ajrccm/142.3.691.

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Benetka, V., H. Weissenbock, I. Kudielka, C. Pallan, G. Rothmuller, and K. Mostl. "Canine adenovirus type 2 infection in four puppies with neurological signs." Veterinary Record 158, no. 3 (2006): 91–94. http://dx.doi.org/10.1136/vr.158.3.91.

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10

Raja, P., V. Sachin, M. Parthiban, and P. Aishwarya Janaki. "Molecular characterization of canine adenovirus type 2 in dogs from India." VirusDisease 32, no. 2 (2021): 369–74. http://dx.doi.org/10.1007/s13337-021-00690-7.

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Dissertations / Theses on the topic "Canine adenovirus type 2"

1

Klonjkowski, Bernard. "Adenovirus canin type 2 et transfert de gene." Paris 6, 1997. http://www.theses.fr/1997PA066402.

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Un vecteur defectif pour la replication, exprimant le gene de la -galactosidase, a ete derive de l'adenovirus canin type 2 (cav2). Ce virus recombinant possede la capacite de transduire des cellules de mammiferes de diverses origines et en particulier des cellules primaires humaines. Malgre un systeme de production qu'il reste a optimiser, des experiences de transfert de gene in vivo dans l'embryon de poulet et dans le systeme nerveux central de rat ont ete conduites. Lors de l'infection de cellules humaines kb par l'adenovirus canin type 2, le cycle productif viral est bloque. Une reponse cel
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2

Zhou, Xiaocui. "Vaccin dérivé de l’adénovirus canin type 2 : application à la fièvre aphteuse." Thesis, Paris Est, 2013. http://www.theses.fr/2013PEST0123.

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La fièvre aphteuse (FMD pour Foot-and-mouth disease en anglais) est une maladie très contagieuse touchant les animaux biongulés. Elle provoque des dégâts économiques considérables sur toute la surface du globe. La fièvre aphteuse est provoquée par un virus, le FMDV. Il s'agit d'un virus à ARN simple brin, de polarité positive appartenant au genre Aphtovirus dans la famille Picornaviridae. Ce virus se réplique et se propage dans l'hôte très rapidement. Dans les zones infectées, les deux principales stratégies de contrôle utilisées sont l'abattage systématique des animaux infectés et la vaccinat
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Monteiro, Francielle Liz. "Detecção molecular de vírus respiratórios em cães." Universidade Federal de Santa Maria, 2015. http://repositorio.ufsm.br/handle/1/10238.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico<br>The respiratory viruses of dogs are associated with a disease called canine infectious respiratory disease (CIRD). The main etiological agents of CIRD are canine distemper virus (CDV), canine parainfluenza virus (cPIV), canine adenovirus type 2 and canid herpesvirus type 1 (CaHV-1), which may cause single or mixed infections. CIRD occurs most frequently in places with high animal density and constant movement. CDV, cPIV, CAdV-2 and CaHV-1 infections have been described worldwide, however, few reports of molecular identification o
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Copeland, Kathryn. "Studies on the tropism of canine adenovirus type 1." Thesis, University of Glasgow, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407718.

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Cabrita, Goncalo Jose Martins. "The mechanism of activation of the adenovirus type 2 protease." Thesis, University of St Andrews, 1997. http://hdl.handle.net/10023/14307.

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The adenovirus codes for a protease which is essential for virion infectivity. This protease requires the presence of a peptide cofactor in order to develop optimal activity. This peptide, GVQSLBCRRRCF, originates from the C-terminal of a viral protein, pVI, and some evidence regarding its specificity came from observations showing that neither of the peptides GVQSLKRRRAF or KRRRCF was able to activate the protease, indicating that both the cysteine and the N-terminal were important in the activation process. However, the mechanism by which the peptide activates the protease has never been elu
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Rodríguez, Eduardo. "Virion- and VAP-receptor recognition in the human adenovirus type 2 system." Lund : Lund University, 1998. http://catalog.hathitrust.org/api/volumes/oclc/68945080.html.

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McMullen, Jr Richard Joseph. "Equine keratitis and the possible involvement of equine adenovirus type 1 (EAdV1) and type 2 (EAdV2)." Diss., lmu, 2005. http://nbn-resolving.de/urn:nbn:de:bvb:19-34239.

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Blixt, Ylva. "Early interaction between adenovirus type 2 and HeLa cells significance of the plasma membrane constitution /." Lund : Dept. of Microbiology, University of Lund, 1992. http://books.google.com/books?id=DzhrAAAAMAAJ.

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Bosher, Julia. "Assembly of cellular and viral proteins into nucleoprotein complexes in adenovirus type 2 infected cells." Thesis, University of St Andrews, 1993. http://hdl.handle.net/10023/13947.

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The adenovirus type 2 origin of DNA replication is located within the terminal 51 bp of the viral genome and contains three recognisable domains: the minimal origin or 'core' and binding sites for the cellular transcription factors Nuclear Factor I and Nuclear Factor III. Initiation of Ad2 DNA replication is preceded by the assembly of a nucleoprotein complex at the viral origin of DNA replication. Recombinant baculoviruses were previously constructed which express full-length Nuclear Factor I (NFIFL) or its DNA binding domain (NFTDBD) for use in experiments. DNase I footprinting experiments w
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Pickel, Lara Michelle. "Study of the role of the Angiotensin II (Ang II) type 2 receptor (AT[subscript]2) in lung tumorigenesis." Thesis, Manhattan, Kan. : Kansas State University, 2008. http://hdl.handle.net/2097/788.

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Books on the topic "Canine adenovirus type 2"

1

Dobbs, Michael. Characterization of incomplete particles associated with canine adenovirus type I. National Library of Canada = Bibliothèque nationale du Canada, 1991.

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2

Peerbaye, Yousouf A. E3 gene expression in two strains of canine adenovirus type 1. National Library of Canada = Bibliothèque nationale du Canada, 1993.

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Ojkic, Davor. Development of a bovine adenovirus type 2-based gene delivery vector. Brock University, Dept. of Biological Sciences, 1997.

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4

Kremer, Eric J., Melissa R. Andrews, Iria Gonzalez Dopeso-Reyes, and Mathieu Wolff, eds. Tropism, Mapping, Modeling, or Therapy Using Canine Adenovirus Type 2 (CAV-2) Vectors in the CNS. Frontiers Media SA, 2021. http://dx.doi.org/10.3389/978-2-88966-634-8.

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5

Liu, Yuan-Ching *. Studies on the genome of a vaccine strain of canine adenovirus type 1. 1988.

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6

Sira, Serge. Canine adenovirus type I: a potential viral expression vector for the rabies glycoprotein gene? 1987.

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Sira, Serge. Development of canine adenovirus type I as an expression vector for the rabies glycoprotein gene. 1993.

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Book chapters on the topic "Canine adenovirus type 2"

1

Fernandes, Paulo, Virgínia Santiago, Núria Viana, Eric J. Kremer, Ana S. Coroadinha, and Paula M. Alves. "Development of a Manufacturing Process for the Production of a Canine Adenovirus Type 2 (CAV-2) Vector Using MDCK Cells." In Proceedings of the 21st Annual Meeting of the European Society for Animal Cell Technology (ESACT), Dublin, Ireland, June 7-10, 2009. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-0884-6_106.

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Lin, Chao-Nan, and Shu-Yun Chiang. "Canine Parvovirus Type 2." In Canine Medicine - Recent Topics and Advanced Research. InTech, 2016. http://dx.doi.org/10.5772/65801.

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Conference papers on the topic "Canine adenovirus type 2"

1

Cambier, P., F. van de werf, and D. collen. "CORONARY THROMBOLYSIS IN DOGS WITH A NONGLYCOSYLATED VARIANT OF HUMAN TISSUE-TYPE PLASMINOGEN ACTIVATOR LACKING THE FINGER AND GROWTH FACTOR DOMAINS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643794.

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A variant of human tissue-type plasminogen activator (t-PA-AΔFE3X), with deletion of the NH2-terminal fibronectin-like finger (F) and epidermal growth factor (E) domains, and with amino acid substitution of Gin for Asn at all known N-linked glycosylation sites was expressed in Chinese Hamster Ovary Cells and purified to homogeneity. The thrombolytic and pharmacokinetic properties of this variant were studied in a canine model with copper coil induced thrombosis of the left anterior descending coronary artery. Infusion of t PAΔFE3X at a rate of 5 pg/kg/min for 30 min in 3 dogs resulted in a pla
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2

Chen, Cuiye, and Robert B. Roemer. "Simulation of Empirical Correlations Between Temperatures and Blood Perfusion During Heating Using a Temperature-Dependent Blood Perfusion Model." In ASME 2004 International Mechanical Engineering Congress and Exposition. ASMEDC, 2004. http://dx.doi.org/10.1115/imece2004-62061.

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This study applies a recently developed temperature-dependent blood perfusion model (TDBPM) coupled with a modified, one-dimensional Pennes bioheat transfer equation to predict the blood perfusion and temperature responses to step function microwave heating applied in the in vivo experiments performed by Sekins’ et al. [1] on human thigh muscle. The TDBPM model links the perfusion increase to the tissue temperature elevation based on physiological mechanisms underlying this temperature-blood-perfusion change phenomenon, i.e., a pharmacokinetic compartmental model. This physiology-based model a
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