Search Results

1 - 10 of 19 items :

  • "bovine leukaemia virus" x
Clear All

REFERENCES 1. Polat, M., Takeshima, Sh.N., Aida, Y. (2017). Epidemiology and genetic diversity of bovine leukemia virus. Virol J. 14(1): 209. https://doi.org/10.1186/s12985-017-0876-4 PMid:29096657 PMCid:PMC5669023 2. Hopkins, S.G., Digiacomo, R.F. (1997). Natural transmission of bovine leukemia virus in dairy and beef cattle. Vet Clin North Am Food Anim Pract. 13(1): 107-128. https://doi.org/10.1016/S0749-0720(15)30367-4 3. Panei, C.J., Larsen, A.E., Fuentealba, N.A., Metz, G.E., Echeverría, M.G., Galosi, C.M., Valera, A.R. (2019). Study of horn flies as

References 1. Adam E., Kerkhofs P., Mammerickx M., Kettmann R., Burny A, Droogmans L., Willems L.: Involvement of the cyclic AMPresponsive element binding protein in bovine leukemia virus expression in vivo. J Virol 1994, 68, 5845-5853. 2. Angelopoulou K., Brellou G.D., Greenland T., Vlemmas I.: A novel deletion in the LTR region of a Greek small ruminant lentivirus may be associated with low pathogenicity. Virus Res 2006,118, 178-184. 3. Calomme C., Nguyen T.L., de Launoit Y., Kiermer V., Droogmans L., Burny A., Van Lint C.: Upstream stimulatory factors binding

bovine leukemia virus proviral sequences in tissues of bovine, ovine and human origin, Ann Rech Vet 1978, 9, 837-844. 12. Klintevall K., Ballagi-Porda’ny A., Naslund K., Belák S.: Bovine leukemia virus: rapid detection of proviral DNA by nested PCR in blood and organs of experimentally infected calves. Vet Microbiol 1994, 42, 191-204. 13. Kubiś P., Szczotka M., Kuźmak J.: Detection of bovine leukaemia virus proviral DNA in paraffin sections, tissue smears, and peripheral blood leukocytes by in situ PCR. Bull Vet Inst 2007, 51, 337-342. 14. Lagarias D.M., Radke K

References 1. Bicka L., Rola M., Kozaczyńska B., Stec J., Kuźmak J.: Characteristics of genetic mutants of bovine leukaemia virus and their role in serodiagnosing BLV infections. Med Weter 2005, 61, 699–702. 2. Bruck C., Portetelle D., Burny A., Zavada J.: Topographical analysis by monoclonal antibodies of BLV-gp51 epitopes involved in viral functions. Virology 1982, 122, 353–362. 3. Bruck C., Mathot S., Portetelle D., Berte C., Franssen J.D., Herion P., Burny A.: Monoclonal antibodies define eight independent antigenic regions on the bovine leukemia virus (BLV

., Serpek B., NizamLıoğlu M., Başpınar N., Tiftik A.M., pp: 43–49. Faculty of Veterinary Medicine, Selcuk University Press, Konya, Turkey, 1998. 4. Bouzar A.B., Boxus M., Florins A., François C., Reichert M., Willems L.: Reduced levels of reactive oxygen species correlate with inhibition of apoptosis, rise in thioredoxin expression and increased bovine leukemia virus proviral loads. Retrovirology 2009, 6, 102–112. 5. Colombo J.P., Richterich R.: Zur bestimmung des caeruloplasmin im plasma. Schweiz Med Wschr 1964, 94, 715–720. 6. Fleming R.E., Whitman I.P., Gitlin J

References 1. Kabeya H, Ohashi K, Onuma M: Host immune responses in the course of bovine leukemia virus infection. J Vet Med Sci 2001, 63: 703-708. 2. Amills M, Ramiya V, Norimine J, Olmstead CA, Lewin HA: Reduced IL-2 and IL-4 mRNA expression in CD4+ T cells from bovine leukemia virus-infected cows with persistent lymphocytosis. Virology 2002, 304: 1-9. 3. Suzuki S, Konnai S, Okagawa T, Ikebuchi R, Shirai T, Sunden Y, Mingala CN, Murata S, Ohashi K: Expression analysis of Foxp3 in T-cells from bovine leukemia virus infected cattle. Microbiol Immunol 2013, 57

, 3, 755-758. 4. Altanerova V., Ban J., Kettmann R., Altaner C.: Induction of leukemia in chicken by bovine leukemia virus due to insertional mutagenesis. Arch Geschwulstforsch 1990, 60, 89-96. 5. Altanerova V., Holicova D., Kucerova L., Altaner A., Lairmore M.D., Boris-Lawrie K.: Long-term infection with retroviral structural gene vector provides protection against bovine leukemia virus disease in rabbits. Virology 2004, 329, 434-439. 6. Altanerova V., Portetelle D., Kettmann R., Altaner C.: Infection of rats with bovine leukaemia virus: establishment of a virus

., Majewski M.: Polymorphism of - lactalbumin gene and expression of the p24 protein in the B and T lymphocyte subpopulations in cows naturally infected with bovine leukaemia virus. Bull Vet Inst Pulawy 2008, 52 , 331-336. 12. Kaczmarczyk E., Bojarojć-Nosowicz B., Czarnik U., Strychalski J.: Prion protein gene polymorphism and blood lymphocyte profile in cows naturally infected with bovine leukemia virus. Pol J Vet 2010, 13 , 415-421. 13. Liu T., Li R., Wong B.S., Liu D., Pan T., Petersen R.B., Gambetti P., Sy M.S.: Normal cellular prion protein is preferentially

of bovine leukemia virus induced lymphosarcoma. Cancer Res 1993, 53, 429-437. 4. Balič D., Lojkič I., Perskič M., Bedekovič J.: Identification of a new genotype of bovine leukaemia virus. Arch Virol 2013, 157, 1281-1290. 5. Birkebak T.A., Palmer G.H., Davis W.C., Knowles D.P., McElwain T.F.: Association of gp51 expression and persistent CD5+ B-lymphocytes lymphocytosis in sheep infected with BLV. Leukemia 1994, 8, 1890-1899. 6. Cantor G.H., Pritchard S.M., Dequiedt F., Willems L., Kettmann R., Davis W.C.: CD5 is dissociated from the B-cell receptor in B- cells from

References 1. Aida Y., Murakami H., Takahashi M., Takeshima S.: Mechanisms of pathogenesis inducted by bovine leukemia virus as a model for human T-cell leukemia virus. Front Microbiol 2013, 4, 1–11. 2. Aspalter R.M., Eibl M.M., Wolf H.M.: Regulation of TCR-mediated T cell activation by TNF-RII. J Leukoc Biol 2003, 74, 572–582. 3. Bagshaw A.T.M.: Functional mechanisms of microsatellite DNA in eukaryotic genomes. Genome Biol Evol 2017, 9, 2428–2443. 4. Bojarojć-Nosowicz B., Kaczmarczyk E., Stachura A., Kubińska M.: Tumor necrosis factor-alpha (TNFα) gene