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Found 36 results
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Journal Article
Strobl-Mazzulla PH, Moncaut NP, López GC, Miranda LA, Canario AVM, Somoza GM. Brain aromatase from pejerrey fish (Odontesthes bonariensis): cDNA cloning, tissue expression, and immunohistochemical localization. Gen Comp Endocrinol. 2005;143(1):21-32. doi:10.1016/j.ygcen.2005.02.026
Rotllant J, Redruello B, Guerreiro PM, Fernandes H, Canario AVM, Power DM. Calcium mobilization from fish scales is mediated by parathyroid hormone related protein via the parathyroid hormone type 1 receptor. Regul Pept. 2005;132(1-3):33-40. doi:10.1016/j.regpep.2005.08.004
Nowell MA, Power DM, Canario AVM, Llewellyn L, Sweeney GE. Characterization of a sea bream (Sparus aurata) thyroid hormone receptor-beta clone expressed during embryonic and larval development. Gen Comp Endocrinol. 2001;123(1):80-9. doi:10.1006/gcen.2001.7649
Santos CR, Ingleton PM, Cavaco JE, Kelly PA, Edery M, Power DM. Cloning, characterization, and tissue distribution of prolactin receptor in the sea bream (Sparus aurata). Gen Comp Endocrinol. 2001;121(1):32-47. doi:10.1006/gcen.2000.7553
Ortiz-Delgado JB, Simes DC, Viegas CSB, Schaff BJ, Sarasquete C, M. Cancela L. Cloning of matrix Gla protein in a marine cartilaginous fish, Prionace glauca: preferential protein accumulation in skeletal and vascular systems. Histochem Cell Biol. 2006;126(1):89-101. doi:10.1007/s00418-005-0125-6
Flanagan JA, Power DM, Bendell LA, et al. Cloning of the cDNA for sea bream (Sparus aurata) parathyroid hormone-related protein. Gen Comp Endocrinol. 2000;118(3):373-82. doi:10.1006/gcen.2000.7481
Flanagan JA, Bendell LA, Guerreiro PM, et al. Cloning of the cDNA for the putative calcium-sensing receptor and its tissue distribution in sea bream (Sparus aurata). Gen Comp Endocrinol. 2002;127(2):117-27.
Acerete L, Balasch JC, Castellana B, et al. Cloning of the glucocorticoid receptor (GR) in gilthead seabream (Sparus aurata). Differential expression of GR and immune genes in gilthead seabream after an immune challenge. Comp Biochem Physiol B Biochem Mol Biol. 2007;148(1):32-43. doi:10.1016/j.cbpb.2007.04.015
Campinho MA, Galay-Burgos M, Sweeney GE, Power DM. Coordination of deiodinase and thyroid hormone receptor expression during the larval to juvenile transition in sea bream (Sparus aurata, Linnaeus). Gen Comp Endocrinol. 2010;165(2):181-94. doi:10.1016/j.ygcen.2009.06.020
Ferraresso S, Vitulo N, Mininni AN, et al. Development and validation of a gene expression oligo microarray for the gilthead sea bream (Sparus aurata). BMC Genomics. 2008;9:580. doi:10.1186/1471-2164-9-580
Ferraresso S, Milan M, Pellizzari C, et al. Development of an oligo DNA microarray for the European sea bass and its application to expression profiling of jaw deformity. BMC Genomics. 2010;11:354. doi:10.1186/1471-2164-11-354
Pombinho AR, Laizé V, Molha DM, Marques SMP, M. Cancela L. Development of two bone-derived cell lines from the marine teleost Sparus aurata; evidence for extracellular matrix mineralization and cell-type-specific expression of matrix Gla protein and osteocalcin. Cell Tissue Res. 2004;315(3):393-406. doi:10.1007/s00441-003-0830-1
Bevelander GS, Guerreiro PM, Spanings T, Flik G. Differential expression of PTHrP and its receptor in pituitary gland and gills in estradiol-treated gilthead sea bream (Sparus auratus, L.). Gen Comp Endocrinol. 2011;173(1):199-204. doi:10.1016/j.ygcen.2011.05.017
Martins DAlves, Rocha F, Castanheira F, et al. Effects of dietary arachidonic acid on cortisol production and gene expression in stress response in Senegalese sole (Solea senegalensis) post-larvae. Fish Physiol Biochem. 2013;39(5):1223-38. doi:10.1007/s10695-013-9778-6
Liarte S, Chaves-Pozo E, Abellán E, et al. Estrogen-responsive genes in macrophages of the bony fish gilthead seabream: a transcriptomic approach. Dev Comp Immunol. 2011;35(8):840-9. doi:10.1016/j.dci.2011.03.015
Cardoso JCR, Pinto VC, Vieira FA, Clark MS, Power DM. Evolution of secretin family GPCR members in the metazoa. BMC Evol Biol. 2006;6:108. doi:10.1186/1471-2148-6-108
Pearson GA, Hoarau G, Lago-Lestón A, et al. An expressed sequence tag analysis of the intertidal brown seaweeds Fucus serratus (L.) and F. vesiculosus (L.) (Heterokontophyta, Phaeophyceae) in response to abiotic stressors. Mar Biotechnol (NY). 2010;12(2):195-213. doi:10.1007/s10126-009-9208-z
Moncaut N, Somoza G, Power DM, Canario AVM. Five gonadotrophin-releasing hormone receptors in a teleost fish: isolation, tissue distribution and phylogenetic relationships. J Mol Endocrinol. 2005;34(3):767-79. doi:10.1677/jme.1.01757
Gomes AS, Kamisaka Y, Harboe T, Power DM, Rønnestad I. Functional modifications associated with gastrointestinal tract organogenesis during metamorphosis in Atlantic halibut (Hippoglossus hippoglossus). BMC Dev Biol. 2014;14:11. doi:10.1186/1471-213X-14-11
Viegas CSB, Cavaco S, Neves PL, et al. Gla-rich protein is a novel vitamin K-dependent protein present in serum that accumulates at sites of pathological calcifications. Am J Pathol. 2009;175(6):2288-98. doi:10.2353/ajpath.2009.090474
Campinho MA, Power DM, Sweeney GE. Identification and analysis of teleost slow muscle troponin T (sTnT) and intronless TnT genes. Gene. 2005;361:67-79. doi:10.1016/j.gene.2005.07.003
Simões B, Conceição N, Viegas CSB, et al. Identification of a promoter element within the zebrafish colXalpha1 gene responsive to runx2 isoforms Osf2/Cbfa1 and til-1 but not to pebp2alphaA2. Calcif Tissue Int. 2006;79(4):230-44. doi:10.1007/s00223-006-0111-6
Laurentino SS, Pinto PIS, Tomás J, et al. Identification of androgen receptor variants in testis from humans and other vertebrates. Andrologia. 2013;45(3):187-94. doi:10.1111/j.1439-0272.2012.01333.x
Pinto PIS, Teodósio R, Galay-Burgos M, Power DM, Sweeney GE, Canario AVM. Identification of estrogen-responsive genes in the testis of sea bream (Sparus auratus) using suppression subtractive hybridization. Mol Reprod Dev. 2006;73(3):318-29. doi:10.1002/mrd.20402
Bal G, Futschik ME, Hartl D, et al. Identification of novel biomarkers in chronic immune thrombocytopenia (ITP) by microarray-based serum protein profiling. Br J Haematol. 2016;172(4):602-15. doi:10.1111/bjh.13861