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Armesto P, Campinho MA, Rodríguez-Rúa A, et al. Molecular characterization and transcriptional regulation of the Na +/K+ ATPase α subunit isoforms during development and salinity challenge in a teleost fish, the Senegalese sole (Solea senegalensis). Comp Biochem Physiol B Biochem Mol Biol. 2014;175:23-38. doi:10.1016/j.cbpb.2014.06.004
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Calado R, Vitorino A, Dinis MTeresa. Bopyrid isopods do not castrate the simultaneously hermaphroditic shrimp Lysmata amboinensis (Decapoda: Hippolytidae). Dis Aquat Organ. 2006;73(1):73-6. doi:10.3354/dao073073
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
Campinho MA, Silva N, Sweeney GE, Power DM. Molecular, cellular and histological changes in skin from a larval to an adult phenotype during bony fish metamorphosis. Cell Tissue Res. 2007;327(2):267-84. doi:10.1007/s00441-006-0262-9
Correia AT, Gomes P, Gonçalves JMS, Erzini K, Hamer PA. Population structure of the black seabream Spondyliosoma cantharus along the south-west Portuguese coast inferred from otolith chemistry. J Fish Biol. 2012;80(2):427-43. doi:10.1111/j.1095-8649.2011.03186.x
Cunha ME, Ré P, Quental-Ferreira H, Gavaia P, Pousão-Ferreira P. Larval and juvenile development of dusky grouper Epinephelus marginatus reared in mesocosms. J Fish Biol. 2013;83(3):448-65. doi:10.1111/jfb.12180
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M Estêvão D, Silva N, Redruello B, et al. Cellular morphology and markers of cartilage and bone in the marine teleost Sparus auratus. Cell Tissue Res. 2011;343(3):619-35. doi:10.1007/s00441-010-1109-y
Estêvão MD, Redruello B, Canario AVM, Power DM. Ontogeny of osteonectin expression in embryos and larvae of sea bream (Sparus auratus). Gen Comp Endocrinol. 2005;142(1-2):155-62. doi:10.1016/j.ygcen.2004.11.018
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Faria AM, Borges R, Gonçalves EJ. Critical swimming speeds of wild-caught sand-smelt Atherina presbyter larvae. J Fish Biol. 2014;85(3):953-9. doi:10.1111/jfb.12456
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Gavaia P, Simes DC, Ortiz-Delgado JB, et al. Osteocalcin and matrix Gla protein in zebrafish (Danio rerio) and Senegal sole (Solea senegalensis): comparative gene and protein expression during larval development through adulthood. Gene Expr Patterns. 2006;6(6):637-52. doi:10.1016/j.modgep.2005.11.010
Gomes AS, Jordal A-EOlderbakk, Olsen K, Harboe T, Power DM, Rønnestad I. Neuroendocrine control of appetite in Atlantic halibut (Hippoglossus hippoglossus): changes during metamorphosis and effects of feeding. Comp Biochem Physiol A Mol Integr Physiol. 2015;183:116-25. doi:10.1016/j.cbpa.2015.01.009
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
Guerreiro PM, Fuentes J, Power DM, Ingleton PM, Flik G, Canario AVM. Parathyroid hormone-related protein: a calcium regulatory factor in sea bream (Sparus aurata L.) larvae. Am J Physiol Regul Integr Comp Physiol. 2001;281(3):R855-60.
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Iwai S, Takeda M. Expression analysis of two types of transcripts from circadian output gene lark in Bombyx mori. Comp Biochem Physiol B Biochem Mol Biol. 2007;146(4):470-6. doi:10.1016/j.cbpb.2006.11.015
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Martins DAlves, Rocha F, Martínez-Rodríguez G, et al. Teleost fish larvae adapt to dietary arachidonic acid supply through modulation of the expression of lipid metabolism and stress response genes. Br J Nutr. 2012;108(5):864-74. doi:10.1017/S0007114511006143
Morais S, Conceição LEC. A new method for the study of essential fatty acid requirements in fish larvae. Br J Nutr. 2009;101(10):1564-8. doi:10.1017/S0007114508111436
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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
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Pérez-Cerezales S, Gutiérrez-Adán A, Martínez-Páramo S, Beirão J, Herráez MP. Altered gene transcription and telomere length in trout embryo and larvae obtained with DNA cryodamaged sperm. Theriogenology. 2011;76(7):1234-45. doi:10.1016/j.theriogenology.2011.05.028
Power DM. Developmental ontogeny of prolactin and its receptor in fish. Gen Comp Endocrinol. 2005;142(1-2):25-33. doi:10.1016/j.ygcen.2004.10.003
Power DM, Canario AVM. Immunocytochemistry of somatotrophs, gonadotrophs, prolactin and adrenocorticotropin cells in larval sea bream (Sparus auratus) pituitaries. Cell Tissue Res. 1992;269(2):341-6.
Power DM, Llewellyn L, Faustino M, et al. Thyroid hormones in growth and development of fish. Comp Biochem Physiol C Toxicol Pharmacol. 2001;130(4):447-59.
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Ribeiro ARA, Ribeiro L, Sæle O, Dinis MT, Moren M. Iodine and selenium supplementation increased survival and changed thyroid hormone status in Senegalese sole (Solea senegalensis) larvae reared in a recirculation system. Fish Physiol Biochem. 2012;38(3):725-34. doi:10.1007/s10695-011-9554-4
Richard N, Fernández I, Wulff T, et al. Dietary supplementation with vitamin k affects transcriptome and proteome of Senegalese sole, improving larval performance and quality. Mar Biotechnol (NY). 2014;16(5):522-37. doi:10.1007/s10126-014-9571-2
Rocha F, Dias J, Engrola S, et al. Glucose overload in yolk has little effect on the long-term modulation of carbohydrate metabolic genes in zebrafish (Danio rerio). J Exp Biol. 2014;217(Pt 7):1139-49. doi:10.1242/jeb.095463
Rojas-García CR, Morais S, Rønnestad I. Cholecystokinin (CCK) in Atlantic herring (Clupea harengus L.) - ontogeny and effects of feeding and diurnal rhythms. Comp Biochem Physiol A Mol Integr Physiol. 2011;158(4):455-60. doi:10.1016/j.cbpa.2010.12.006