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On JM: Dual function of fish hepcidin: response to experimental iron overload and bacterial infection in sea bass (Dicentrarchus labrax). Dev Comp Immunol 2006, 30(12):1156?167. 63. Hammer ND, Skaar EP: Molecular mechanisms of Staphylococcus aureus iron acquisition. Annu Rev Microbiol 2011, 65:129?47. 64. Hood MI, Skaar EP: Nutritional immunity: transition metals at the pathogen-host interface. Na
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On JM: Dual function of fish hepcidin: response to experimental iron overload and bacterial infection in sea bass (Dicentrarchus labrax). Dev Comp Immunol 2006, 30(12):1156?167. 63. Hammer ND, Skaar EP: Molecular mechanisms of Staphylococcus aureus iron acquisition. Annu Rev Microbiol 2011, 65:129?47. 64. Hood MI, Skaar EP: Nutritional immunity: transition metals at the pathogen-host interface. Na
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Obial Peptide and Iron Regulatory Hormone. In Proceedings of The Third Bilateral Conference Between the United States and Russia: Aquatic Animal Health: 12?0 July 2009; Sheperdstown, WV. USA: Michigan State University; 2011:284?92. 60. Barnes AC, Trewin B, Snape N, Kvennefors ECE, Baiano JCF: Two hepcidin-like antimicrobial peptides in barramundi Lates calcarifer exhibit differing tissue tropism a
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A lice on juvenile Pacific salmon in the Gulf Islands area of British Columbia, Canada. Aquaculture 2009, 297(1?):31?7. Wagner GN, Fast MD, Johnson SC: Physiology and immunology of Lepeophtheirus salmonis infections of salmonids. Trends Parasitol 2008, 24(4):176?83. Jones SRM, Kim E, Bennett W: Early development of resistance to the salmon louse, Lepeophtheirus salmonis (Kr er), in juvenile pink s
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Vel interaction partner of FGF-7, FGF-10 and FGF-22 and regulates FGF activity: implications for epithelial repair. Oncogene 2005, 24(34):5269?277. 44. Nurminsky D, Magee C, Faverman L, Nurminskaya M: Regulation of chondrocyte differentiation by actin-severing protein adseverin. Dev Biol 2007, 302(2):427?37. 45. Vairapandi M, Balliet AG, Hoffman B, Liebermann DA: GADD45b and GADD45g are cdc2/cycli
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Ne expression analyses of immune responses in Atlantic salmon during early stages of infection by salmon louse (Lepeophtheirus salmonis) revealed bi-phasic responses coinciding with the copepod-chalimus transition. BMC Genomics 2011, 12:141.Sutherland et al. BMC Genomics 2014, 15:200 http://www.biomedcentral.com/1471-2164/15/Page 16 of25. Rolff J, Siva-Jothy MT: Invertebrate ecological immunology.
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Control in the anterior kidney of all three species early in the infection. Boxplot displays median and interquartile range, and circles are outliers. *denotes p < 0.05; **denotes p < 0.001. Competing interests The authors declare that they have no competing interests. Authors' contributions BJGS contributed to experimental design, performed microarray, immunoassay and qPCR work and statistical an
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T direction of fold change. Primers were designed to ensure equal amplification for all species to ensure correct estimates of expression levels, as shown for collagenase-3 log2(qPCR) against log2 (microarray) shown for (B) Atlantic and (C) pink salmon. chm = chum; pnk = pink; atl = Atlantic; AK = anterior kidney; S = skin; gene acronyms are as per the primer table (Additional file 4: Table S2). A