References
- Pistol GC, Gras MA, Marin DE, et al. Natural feed contaminant zearalenone decreases the expressions of important pro- and anti-inflammatory mediators and mitogen-activated protein kinase/NF-kappaB signalling molecules in pigs. Br J Nutr 2014;111:452-64.
- Oswald iP, Comera C. Immunotoxicity of mycotoxins. Rev Med Vet 1998;149:585-90.
- Danicke S, Doll S, Goyarts T, et al. On the evolution of the occurrence of the Fusarium-toxins deoxynivalenol (DON) und zearalenon (ZEN) and their metabolites in physiological substrates of the pig. Tierarztl Praxis 2008;36:35-47.
- Basso K, Gomes F, Bracarense APL. Deoxynivanelol and fumonisin, alone or in combination, induce changes on intestinal junction complexes and in e-cadherin expression. Toxins 2013;5:2341-52. https://doi.org/10.3390/toxins5122341
- Pinton P, Oswald iP. Effect of deoxynivalenol and other type B trichothecenes on the intestine: A review. Toxins 2014;6: 1615-43. https://doi.org/10.3390/toxins6051615
- Accensi F, Pinton P, Callu P, et al. Ingestion of low doses of deoxynivalenol does not affect hematological, biochemical, or immune responses of piglets. J Anim Sci 2006;84:1935-42. https://doi.org/10.2527/jas.2005-355
- Alexopoulos C. Association of Fusarium mycotoxicosis with failure in applying an induction of parturition program with PGF2alpha and oxytocin in sows. Theriogenology 2001;55: 1745-57. https://doi.org/10.1016/S0093-691X(01)00517-9
- Marin DE, Taranu i, Burlacum R, et al. Effects of zearalenone and its derivatives on porcine immune response. Toxicol in Vitro 2011;25:1981-8. https://doi.org/10.1016/j.tiv.2011.06.022
- Brzuzan P, Wozny M, Wolinska-Niziol L, et al. MicroRNA expression profiles in liver and colon of sexually immature gilts after exposure to Fusarium mycotoxins. Pol J Vet Sci 2015; 18:29-38.
- National Research Council (NRC). Nutrition requirements of swine. 11th edition. Washington, DC, USA: National Academy Press; 2012.
- Robinson MD, McCarthy DJ, Smyth GK. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 2010;26:139-40. https://doi.org/10.1093/bioinformatics/btp616
- Reddy KE, Jeong JY, Lee SD, et al. Effect of different early weaning regimens for calves on adipogenic gene expression in Hanwoo loin at the fattening stage. Livest Sci 2017;195: 87-98.
- Dennis G, Jr Sherman BT, Hosack DA, et al. DAViD: database for annotation, visualization, and integrated discovery. Genom Biol 2003;4:R60. https://doi.org/10.1186/gb-2003-4-9-r60
- Brzuzan P, Wozny M, Wolinska-NiziolL, et al. MicroRNA expression profiles in liver and colon of sexually immature gilts after exposure to Fusarium mycotoxins. Pol J Vet Sci 2015; 18:29-38.
- Lee SK, Moon J, Park SW, et al. Loss of the tight junction protein claudin 4 correlates with histological growth-pattern and differentiation in advanced gastric adenocarcinoma. Oncol Rep 2005;13:193-9.
- Alizadeh A, Braber S, Akbari P, Garssen J, Gremmels JF. Deoxynivalenol impairs weight gain and affects markers of gut health after low-dose, short-term exposure of growing pigs. Toxins 2015;7:2071-95. https://doi.org/10.3390/toxins7062071
-
Hochepied T, Berger FG, Baumann H, Libert C.
${\alpha}1$ -Acid glycoprotein: an acute phase protein with inflammatory and immunomodulating properties. Cytokine Growth Factor Rev 2003; 14:25-34. https://doi.org/10.1016/S1359-6101(02)00054-0 - Lee CG, Ren J, Cheong IS, et al. Expression of the FAT10 gene is highly upregulated in hepatocellular carcinoma and other gastrointestinal and gynecological cancers. Oncogene 2003;22: 2592-603. https://doi.org/10.1038/sj.onc.1206337
- Carter AM, Kingston MJ, Han KK, et al. Altered expression of IGFs and IGF-binding proteins during intrauterine growth restriction in guinea pigs. J Endocrinol 2005;184:179-89. https://doi.org/10.1677/joe.1.05781
- Blair iP, Dawkins JL, Nicholson GA. Fine mapping of the hereditary sensory neuropathy type i locus on chromosome 9q22.1-->q22.3: exclusion of GAS1 and XPA. Cytogenet Cell Genet 1997;78:140-4. https://doi.org/10.1159/000134649
- Sacilotto N, Castillo J, Riffo-Campos AL, et al. Growth arrest specific 1 (Gas1) gene overexpression in liver reduces the in vivo progression of murine hepatocellular carcinoma and partially restores gene expression levels. PLoS ONE 2015;10: e0132477. https://doi.org/10.1371/journal.pone.0132477
- Ross KR, Corey DA, Dunn JM, Kelley TJ. SMAD3 expression is regulated by mitogen-activated protein kinase kinase-1 in epithelial and smooth muscle cells. Cell Signal 2007;19:923-31.
- Marton N, Baricza E, Ersek B, Buzas EI, Nagy G. The emerging and diverse roles of src-like adaptor proteins in health and disease. Mediators inflamm 2015;2015:Article iD:952536.
- Feldhahn N, Schwering I, Lee S, et al. Silencing of B cell receptor signals in human naive B cells. J Exp Med 2002;196: 1291-305. https://doi.org/10.1084/jem.20020881
- Lawrence CB. Galanin-like peptide modulates energy balance by affecting inflammatory mediators? Physiol Behav 2009;97: 515-9. https://doi.org/10.1016/j.physbeh.2009.02.041
- Hikami K, Ehara Y, Hasegawa M, et al. Association of IL-10 receptor 2 (IL10RB) SNP with systemic sclerosis. Biochem Biophys Res Commun 2008;373:403-7. https://doi.org/10.1016/j.bbrc.2008.06.054
- Szakacs G, Annereau JP, Lababidi S, et al. Predicting drug sensitivity and resistance: profiling ABC transporter genes in cancer cells. Cancer Cell 2004;6:129-37. https://doi.org/10.1016/j.ccr.2004.06.026
- Yakar S, Rosen CJ, Beamer WG, et al. Circulating levels of iGF-1 directly regulate bone growth and density. J Clin invest 2002;110:771-81. https://doi.org/10.1172/JCI0215463
- Mousseau DD, Banville D, L'Abbe D, Bouchard P, Shen SH. PiLR-alpha, a novel immunoreceptor tyrosine-based inhibitory motif-bearing protein, recruits SHP-1 upon tyrosine phosphorylation and is paired with the truncated counterpart PiLRbeta. J Biol Chem 2000;275:4467-74. https://doi.org/10.1074/jbc.275.6.4467
- Altara R, Manca M, Hessel MH, et al. CXCL10 is a Circulating inflammatory Marker in Patients with Advanced Heart Failure: a Pilot Study. J Cardiovasc Transl Res 2016;9:302-14. https://doi.org/10.1007/s12265-016-9703-3
- Wu Q, Dohnal V, Huang L, Kuca K, Yuan Z, Metabolic pathways of trichothecenes. Drug Metab Rev 2010;42:250-67. https://doi.org/10.3109/03602530903125807
- Le Moine A, Goldman M, Abramowicz D. Multiple pathways to allograft rejection. Transplantation 2002;73:1373-81. https://doi.org/10.1097/00007890-200205150-00001
- Choi SW, Levine JE, Ferrara JL. Pathogenesis and management of graft-versus-host disease. Immunol Allergy Clin North Am 2010;30:75-101. https://doi.org/10.1016/j.iac.2009.10.001
- Ruwhof C, Drexhage HA. iodine and thyroid autoimmune disease in animal models. Thyroid 2001;11:427-36. https://doi.org/10.1089/105072501300176381
- Crawford JM, Watanabe K. Cell adhesion molecules in inflammation and immunity: relevance to periodontal diseases. Crit Rev Oral Biol Med 1994;5:91-123. https://doi.org/10.1177/10454411940050020301
- Weiss RA. Viral mechanisms of carcinogenesis. IARC Sci Publ 1982;39:307-16.
- Matsumori A, Kawai, C. Experimental animal models of viral myocarditis. Eur Heart J 1987;8 (suppl_J):383-8. https://doi.org/10.1093/eurheartj/8.suppl_J.383
- Chatterjee B, Leung CS, Munz C. Animal models of Epstein Barr virus infection. J Immunol Methods 2014;410:80-7. https://doi.org/10.1016/j.jim.2014.04.009
- Pistol GC, Braicu C, Motiu M, et al. Zearalenone mycotoxin affects immune mediators, MAPK signalling molecules, nuclear receptors and genome-wide gene expression in pig spleen. PLoS ONE 2015;10:e0127503. https://doi.org/10.1371/journal.pone.0127503
- Stoeker L, Nordone S, Gunderson S, et al. Assessment of Lactobacillus gasseri as a candidate oral vaccine vector. Clin Vaccine Immunol 2011;18:1834-44. https://doi.org/10.1128/CVI.05277-11
- Pestka JJ, Amuzie CJ. Tissue distribution and proinflammatory cytokine gene expression following acute oral exposure to deoxynivalenol: comparison of weanling and adult mice. Food Chem Toxicol 2008;46:2826-31.
- Li M, Cuff CF, Pestka J. Modulation of murine host response to enteric reovirus infection by the trichothecenedeoxynivalenol. Toxicol Sci 2005;87:134-45. https://doi.org/10.1093/toxsci/kfi225
- Fink-Gremmels J, Malekinejad H. Clinical effects and biochemical mechanisms associated with exposure to the mycoestrogen zearalenone. Anim Feed Sci Technol 2007;137;326-41. https://doi.org/10.1016/j.anifeedsci.2007.06.008
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