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Canine DLA diversity: 3. Disease studies
Presentation / Conference Contribution
Kennedy, L. J., Barnes, A., Short, A., Brown, J. J., Seddon, J., Fleeman, L., Brkljacic, M., Happ, G. M., Catchpole, B., & Ollier, W. E. R. Canine DLA diversity: 3. Disease studies

Characterization of the fine specificity of bovine CD8+ T cell responses to defined antigens from the protozoan parasite Theileria parva
Journal Article
Graham, S. P., Pellé, R., Yamage, M., Mwangi, D. M., Honda, Y., Mwakubambanya, R. S., De Villiers, E. P., Abuya, E., Awino, E., Gachanja, J., Mbwika, F., Muthiani, A. M., Muriuki, C., Nyanjui, J. K., Onono, F. O., Osaso, J., Riitho, V., Saya, R. M., Ellis, S. A., McKeever, D. J., …Taracha, E. L. N. Characterization of the fine specificity of bovine CD8+ T cell responses to defined antigens from the protozoan parasite Theileria parva. Infection and Immunity, 76(2), 685-694. https://doi.org/10.1128/IAI.01244-07

Proteomic comparison of four Eimeria tenella life-cycle stages: unsporulated oocyst, sporulated oocyst, sporozoite and second-generation merozoite
Journal Article
Lal, K., Bromley, E., Oakes, R. D., Prieto, J. H., Sanderson, S. J., Kurian, D., Hunt, L., Yates, J. R., Wastling, J. M., Sinden, R. E., & Tomley, F. M. Proteomic comparison of four Eimeria tenella life-cycle stages: unsporulated oocyst, sporulated oocyst, sporozoite and second-generation merozoite. Proteomics, 9(19), 4566-76. https://doi.org/10.1002/pmic.200900305

CD8+ T-cell responses to Theileria parva are preferentially directed to a single dominant antigen: Implications for parasite strain-specific immunity
Journal Article
MacHugh, N. D., Connelly, T., Graham, S. P., Pelle, R., Formisano, P., Taracha, E. L., Ellis, S. A., McKeever, D. J., Burrells, A., & Morrison, W. CD8+ T-cell responses to Theileria parva are preferentially directed to a single dominant antigen: Implications for parasite strain-specific immunity. European Journal of Immunology, 39(9), 1-11. https://doi.org/10.1002/eji.200939227

MORN1 has a conserved role in asexual and sexual development across the apicomplexa. Eukaryot Cell
Journal Article
Ferguson, D. J. P., Sahoo, N., Pinches, R. A., Bumstead, J. M., Tomley, F. M., & Gubbels, M. J. (in press). MORN1 has a conserved role in asexual and sexual development across the apicomplexa. Eukaryot Cell. https://doi.org/10.1128/EC.00021-08

The gene encoding the membrane occupation and recognition nexus protein MORN1 is conserved across the Apicomplexa. In Toxoplasma gondii, MORN1 is associated with the spindle poles, the anterior and posterior rings of the inner membrane complex (IMC).... Read More about MORN1 has a conserved role in asexual and sexual development across the apicomplexa. Eukaryot Cell.

Sequestration of free cholesterol in cell membranes by prions correlates with cytoplasmic phospholipase A(2) activation
Journal Article
Bate, C., Tayebi, M., & Williams, A. Sequestration of free cholesterol in cell membranes by prions correlates with cytoplasmic phospholipase A(2) activation. BMC Biology, 6, https://doi.org/10.1186/1741-7007-6-8

Background: The transmissible spongiform encephalopathies (TSEs), otherwise known as the prion diseases, occur following the conversion of the normal cellular prion protein ( PrPC) to an alternatively folded isoform ( PrPSc). The accumulation of PrPS... Read More about Sequestration of free cholesterol in cell membranes by prions correlates with cytoplasmic phospholipase A(2) activation.

Docosahexaenoic and eicosapentaenoic acids increase prion formation in neuronal cells
Journal Article
Bate, C., Tayebi, M., Diomede, L., Salmona, M., & Williams, A. Docosahexaenoic and eicosapentaenoic acids increase prion formation in neuronal cells. BMC Biology, 6, https://doi.org/10.1186/1741-7007-6-39

Background: The transmissible spongiform encephalopathies, otherwise known as prion diseases, occur following the conversion of the cellular prion protein (PrPC) to an alternatively folded, disease-associated isoform (PrPSc). Recent studies suggest t... Read More about Docosahexaenoic and eicosapentaenoic acids increase prion formation in neuronal cells.