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R. Roy MacGregor, Hafner, R., Wu, J. W., Murphy, R. L., Perlman, D. C., Bermudez, L. E., Inderlied, C. B., Picker, L. J., Wallis, R. S., Andersen, J. W., Mahon, L. F., Koletar, S. L., and Peterson, D. M., Clinical, microbiological, and immunological characteristics in HIV-infected subjects at risk for disseminated Mycobacterium avium complex disease: an AACTG study., AIDS research and human retroviruses, vol. 21, no. 8, pp. 689-95, 2005.
A. J. Mathers, Poulter, M., Dirks, D., Carroll, J., Sifri, D. D., and Hazen, K. C., Clinical Microbiology Costs for Methods of Active Surveillance for Klebsiella pneumoniae Carbapenemase-Producing Enterobacteriaceae, Infection Control and Hospital Epidemiology, vol. 35, no. No. 4, pp. 350-355, 2014.
E. D. Rout, Labadie, J. D., Yoshimoto, J. A., Avery, P. R., Curran, K. M., and Avery, A. C., Clinical outcome and prognostic factors in dogs with B-cell chronic lymphocytic leukemia: A retrospective study., J Vet Intern Med, 2021.
M. Latifi, Tuohy, J. L., Coutermarsh-Ott, S. L., Klahn, S. L., Leeper, H., and Dervisis, N., Clinical outcomes in dogs with localized splenic histiocytic sarcoma treated with splenectomy with or without adjuvant chemotherapy., J Vet Intern Med, vol. 34, no. 6, pp. 2645-2650, 2020.
M. R. Cook, Gasparini, M., Cianciolo, R. E., Brown, M. E., Moore, A. S., Curran, K. M., Maxwell, E. A., Gasson, S., Wustefeld-Janssenss, B. G., Veluvolu, S. M., Keepman, S., Wouda, R., Griffin, L. R., and Selmic, L. E., Clinical outcomes of thyroid tumours with concurrent epithelial and mesenchymal components in 14 dogs (2006-2020)., Vet Med Sci, vol. 8, no. 2, pp. 509-516, 2022.
S. J. Tornquist, Clinical pathology of llamas and alpacas., The Veterinary clinics of North America. Food animal practice, vol. 25, no. 2, pp. 311-22, 2009.
K. P. Sears, Knowles, D. P., and Fry, L. M., Clinical Progression of in Splenectomized Horses Reveals Decreased Virulence Compared to ., Pathogens, vol. 11, no. 2, 2022.
D. M. Mulrooney, Johnson, M. R., Smith, B. B., and Zimmerman, G. L., Clinical reference values for serum protein electrophoresis for the llama (Lama glama)., American journal of veterinary research, vol. 50, no. 11, pp. 1889-92, 1989.
I. Yankin, Nemanic, S., Funes, S., de Morais, H. Autran, M Gorman, E., and Ruaux, C., Clinical relevance of splenic nodules or heterogeneous splenic parenchyma assessed by cytologic evaluation of fine-needle samples in 125 dogs (2011-2015)., J Vet Intern Med, vol. 34, no. 1, pp. 125-131, 2020.
R. V. Shawley and Mandsager, R. E., Clinical use of positive-pressure ventilation in the horse., The Veterinary clinics of North America. Equine practice, vol. 6, no. 3, pp. 575-85, 1990.
L. L. Blythe, Hultgren, B. D., Craig, A. M., Appell, L. H., Lassen, E. D., Mattson, D. E., and Duffield, D., Clinical, viral, and genetic evaluation of equine degenerative myeloencephalopathy in a family of Appaloosas., Journal of the American Veterinary Medical Association, vol. 198, no. 6, pp. 1005-13, 1991.
J. A. Hall, Clinically evaluating gastric diseases in dogs and cats, Veterinary Medicine, vol. 95, no. 1, pp. 450-465, 2000.
M. M. Garner, Ramsell, K., Morera, N., Juan-Sallés, C., Jiménez, J., Ardiaca, M., Montesinos, A., Teifke, J. P., Löhr, C. V., Evermann, J. F., Baszler, T. V., Nordhausen, R. W., Wise, A. G., Maes, R. K., and Kiupel, M., Clinicopathologic features of a systemic coronavirus-associated disease resembling feline infectious peritonitis in the domestic ferret (Mustela putorius)., Veterinary pathology, vol. 45, no. 2, pp. 236-46, 2008.
P. E. Chappell, Clocks and the black box: circadian influences on gonadotropin-releasing hormone secretion., Journal of neuroendocrinology, vol. 17, no. 2, pp. 119-30, 2005.
K. J. Tonsfeldt and Chappell, P. E., Clocks on top: the role of the circadian clock in the hypothalamic and pituitary regulation of endocrine physiology., Molecular and cellular endocrinology, vol. 349, no. 1, pp. 3-12, 2012.
D. T. Alzhanov, Suchland, R. J., Bakke, A. C., Stamm, W. E., and Rockey, D. D., Clonal isolation of chlamydia-infected cells using flow cytometry., J Microbiol Methods, vol. 68, no. 1, pp. 201-8, 2007.
D. T. Alzhanov, Suchland, R. J., Bakke, A. C., Stamm, W. E., and Rockey, D. D., Clonal isolation of chlamydia-infected cells using flow cytometry., Journal of microbiological methods, vol. 68, no. 1, pp. 201-8, 2007.
D. D. Rockey, Heinzen, R. A., and Hackstadt, T., Cloning and characterization of a Chlamydia psittaci gene coding for a protein localized in the inclusion membrane of infected cells., Molecular microbiology, vol. 15, no. 4, pp. 617-26, 1995.
D. D. Rockey, Heinzen, R. A., and Hackstadt, T., Cloning and characterization of a Chlamydia psittaci gene coding for a protein localized in the inclusion membrane of infected cells., Mol Microbiol, vol. 15, no. 4, pp. 617-26, 1995.
J. Barra-Carrasco, Olguín-Araneda, V., Plaza-Garrido, A., Miranda-Cárdenas, C., Cofré-Araneda, G., Pizarro-Guajardo, M., Sarker, M. R., and Paredes-Sabja, D., The Clostridium difficile exosporium cysteine (CdeC)-rich protein is required for exosporium morphogenesis and coat assembly., Journal of bacteriology, vol. 195, no. 17, pp. 3863-75, 2013.
S. Banawas, Paredes-Sabja, D., Korza, G., Li, Y., Hao, B., Setlow, P., and Sarker, M. R., The Clostridium perfringens germinant receptor protein GerKC is located in the spore inner membrane and is crucial for spore germination., Journal of bacteriology, vol. 195, no. 22, pp. 5084-91, 2013.
D. Paredes-Sabja, J Torres, A., Setlow, P., and Sarker, M. R., Clostridium perfringens spore germination: characterization of germinants and their receptors., Journal of bacteriology, vol. 190, no. 4, pp. 1190-201, 2008.
D. Paredes-Sabja and Sarker, M. R., Clostridium perfringens sporulation and its relevance to pathogenesis., Future microbiology, vol. 4, no. 5, pp. 519-25, 2009.
D. Paredes-Sabja, Sarker, N., and Sarker, M. R., Clostridium perfringens tpeL is expressed during sporulation., Microbial pathogenesis, vol. 51, no. 5, pp. 384-8, 2011.
S. J. Billington, Wieckowski, E. U., Sarker, M. R., Bueschel, D., Songer, J. G., and McClane, B. A., Clostridium perfringens type E animal enteritis isolates with highly conserved, silent enterotoxin gene sequences., Infection and immunity, vol. 66, no. 9, pp. 4531-6, 1998.

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