Carlson College of Veterinary Medicine

M. A. Boin, Austin, M. J., and Häse, C. C., “Chemotaxis in Vibrio cholerae.”, FEMS microbiology letters, vol. 239, no. 1, pp. 1-8, 2004.

D. D. Rockey, Grosenbach, D., Hruby, D. E., Peacock, M. G., Heinzen, R. A., and Hackstadt, T., “Chlamydia psittaci IncA is phosphorylated by the host cell and is exposed on the cytoplasmic face of the developing inclusion.”, Mol Microbiol, vol. 24, no. 1, pp. 217-28, 1997.

D. D. Rockey, Grosenbach, D., Hruby, D. E., Peacock, M. G., Heinzen, R. A., and Hackstadt, T., “Chlamydia psittaci IncA is phosphorylated by the host cell and is exposed on the cytoplasmic face of the developing inclusion.”, Molecular microbiology, vol. 24, no. 1, pp. 217-28, 1997.

E. D. Cram, Rockey, D. D., and Dolan, B. P., “Chlamydia spp. development is differentially altered by treatment with the LpxC inhibitor LPC-011.”, BMC Microbiol, vol. 17, no. 1, p. 98, 2017.

J. P. Bannantine, Stamm, W. E., Suchland, R. J., and Rockey, D. D., “Chlamydia trachomatis IncA is localized to the inclusion membrane and is recognized by antisera from infected humans and primates.”, Infect Immun, vol. 66, no. 12, pp. 6017-21, 1998.

J. P. Bannantine, Stamm, W. E., Suchland, R. J., and Rockey, D. D., “Chlamydia trachomatis IncA is localized to the inclusion membrane and is recognized by antisera from infected humans and primates.”, Infection and immunity, vol. 66, no. 12, pp. 6017-21, 1998.

T. Hackstadt, Rockey, D. D., Heinzen, R. A., and Scidmore, M. A., “Chlamydia trachomatis interrupts an exocytic pathway to acquire endogenously synthesized sphingomyelin in transit from the Golgi apparatus to the plasma membrane.”, EMBO J, vol. 15, no. 5, pp. 964-77, 1996.

T. Hackstadt, Rockey, D. D., Heinzen, R. A., and Scidmore, M. A., “Chlamydia trachomatis interrupts an exocytic pathway to acquire endogenously synthesized sphingomyelin in transit from the Golgi apparatus to the plasma membrane.”, The EMBO journal, vol. 15, no. 5, pp. 964-77, 1996.

M. Xia, Suchland, R. J., Bumgarner, R. E., Peng, T., Rockey, D. D., and Stamm, W. E., “Chlamydia trachomatis variant with nonfusing inclusions: growth dynamic and host-cell transcriptional response.”, The Journal of infectious diseases, vol. 192, no. 7, pp. 1229-36, 2005.

M. Xia, Suchland, R. J., Bumgarner, R. E., Peng, T., Rockey, D. D., and Stamm, W. E., “Chlamydia trachomatis variant with nonfusing inclusions: growth dynamic and host-cell transcriptional response.”, J Infect Dis, vol. 192, no. 7, pp. 1229-36, 2005.

D. D. Rockey, Wang, J., Lei, L., and Zhong, G., “Chlamydia vaccine candidates and tools for chlamydial antigen discovery.”, Expert review of vaccines, vol. 8, no. 10, pp. 1365-77, 2009.

D. D. Rockey, Wang, J., Lei, L., and Zhong, G., “Chlamydia vaccine candidates and tools for chlamydial antigen discovery.”, Expert Rev Vaccines, vol. 8, no. 10, pp. 1365-77, 2009.

N. Borel, Leonard, C., Slade, J., and Schoborg, R. V., “Chlamydial Antibiotic Resistance and Treatment Failure in Veterinary and Human Medicine.”, Curr Clin Microbiol Rep, vol. 3, pp. 10-18, 2016.

W. J. Brown, Skeiky, Y. A. W., Probst, P., and Rockey, D. D., “Chlamydial antigens colocalize within IncA-laden fibers extending from the inclusion membrane into the host cytosol.”, Infection and immunity, vol. 70, no. 10, pp. 5860-4, 2002.

W. J. Brown, Skeiky, Y. A. W., Probst, P., and Rockey, D. D., “Chlamydial antigens colocalize within IncA-laden fibers extending from the inclusion membrane into the host cytosol.”, Infect Immun, vol. 70, no. 10, pp. 5860-4, 2002.

D. Alzhanov, Barnes, J., Hruby, D. E., and Rockey, D. D., “Chlamydial development is blocked in host cells transfected with Chlamydophila caviae incA.”, BMC microbiology, vol. 4, p. 24, 2004.

D. Alzhanov, Barnes, J., Hruby, D. E., and Rockey, D. D., “Chlamydial development is blocked in host cells transfected with Chlamydophila caviae incA.”, BMC Microbiol, vol. 4, p. 24, 2004.

A. W. Biondo and de Morais, H. Autran, “Chloride: a quick reference.”, The Veterinary clinics of North America. Small animal practice, vol. 38, no. 3, pp. 459-65, viii, 2008.

Y. Vengrenyuk, Nishi, H., Long, X., Ouimet, M., Savji, N., Martinez, F. O., Cassella, C. P., Moore, K. J., Ramsey, S. A., Miano, J. M., and Fisher, E. A., “Cholesterol loading reprograms the microRNA-143/145-myocardin axis to convert aortic smooth muscle cells to a dysfunctional macrophage-like phenotype.”, Arterioscler Thromb Vasc Biol, vol. 35, no. 3, pp. 535-46, 2015.

R. J. Suchland, Carrell, S. J., Wang, Y., Hybiske, K., Kim, D. B., Dimond, Z. E., P Hefty, S., and Rockey, D. D., “Chromosomal Recombination Targets in Interspecies Lateral Gene Transfer.”, J Bacteriol, vol. 201, no. 23, 2019.

L. L. Blythe, Schmitz, J. A., Roelke, M., and Skinner, S., “Chronic encephalomyelitis caused by canine distemper virus in a Bengal tiger.”, Journal of the American Veterinary Medical Association, vol. 183, no. 11, pp. 1159-62, 1983.

L. L. Blythe and Craig, A. M., “A chronic in vivo liver perfusion technique in ruminants.”, Veterinary and human toxicology, vol. 28, no. 3, pp. 201-4, 1986.

J. A. Hall, Jackson, M. I., Jewell, D. E., and Ephraim, E., “Chronic kidney disease in cats alters response of the plasma metabolome and fecal microbiome to dietary fiber.”, PLoS One, vol. 15, no. 7, p. e0235480, 2020.

G. W. Broussard, Norris, M. B., Schwindt, A. R., Fournie, J. W., Winn, R. N., Kent, M. L., and Ennis, D. G., “Chronic Mycobacterium marinum infection acts as a tumor promoter in Japanese Medaka (Oryzias latipes).”, Comp Biochem Physiol C Toxicol Pharmacol, vol. 149, no. 2, pp. 152-60, 2009.

M. McDougall, Choi, J., Magnusson, K., Truong, L., Tanguay, R., and Traber, M. G., “Chronic vitamin E deficiency impairs cognitive function in adult zebrafish via dysregulation of brain lipids and energy metabolism.”, Free Radic Biol Med, vol. 112, pp. 308-317, 2017.