المؤلفون: Alves Farias, Inês

Thesis Advisors: Morales Nin, Beatriz

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Aphanopus carbo; black scabbardfish; benthopelagic; NE Atlantic; population dynamics; migration; fatty acids; stable isotopes; sex steroids; otolith; trace elements, Aphanopus carbo; peix sable negra; bentopelàgic; NE Atlàntic; dinàmica de la població; migració; àcids grassos; isòtops estables; esteroids sexuals; otòlit; elements traça, Aphanopus carbo; sable negro; bentopelágico; Atlántico NE; dinámica poblacional; migración; ácidos grasos; isotopos estables; esteroides sexuales; otolito; elementos traza, Ictiologia i Biologia Pesquera

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/673480

المؤلفون: Casals Gregori, Ferrer Costa Roser, Urgell Rull Eulàlia, Escobar-Morreale Héctor F., Argente Jesús, Sesmilo Gemma, Biagetti Betina

المصدر: Advances in Laboratory Medicine, Vol 4, Iss 1, Pp 61-69 (2023)

مصطلحات موضوعية: esteroides sexuales, testosterona, estradiol, inmunoensayo, espectrometría de masas, Medical technology, R855-855.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2628-491X

URL الوصول: https://doaj.org/article/f4c2fca091004ccfb54d1df0ac56806e

المؤلفون: Beltramone, F, Estofán, P, Piccinali, N, Torres, PJ, Ramírez, N, Cantarelli, V, Ponzio, MF, Motrich, R, Severgnini, M, Martini, AC

المصدر: Revista de la Facultad de Ciencias Médicas de Córdoba.; Vol. 79 No. Suplemento JIC XXIII (2022): Suplemento JIC XXIII ; Revista de la Facultad de Ciencias Médicas de Córdoba; Vol. 79 Núm. Suplemento JIC XXIII (2022): Suplemento JIC XXIII ; Revista da Faculdade de Ciências Médicas de Córdoba; v. 79 n. Suplemento JIC XXIII (2022): Suplemento JIC XXIII ; 1853-0605 ; 0014-6722

مصطلحات موضوعية: ghrelin, controlled ovarian hyperstimulation, reproductive immunology, spontaneous abortions, sexual steroids, ghrelina, hiperestimulación ovárica controlada, inmunología reproductiva, abortos espontáneos, esteroides sexuales

Relation: https://revistas.unc.edu.ar/index.php/med/article/view/39073

الاتاحة: https://revistas.unc.edu.ar/index.php/med/article/view/39073

المؤلفون: Arisha, Ahmed Hamed

Thesis Advisors: López Pérez, Miguel A., Diéguez González, Carlos, Universidade de Santiago de Compostela. Departamento de Fisioloxía

مصطلحات موضوعية: Metabolismo / Metabolism, Hipotálamo / Hypothalamus, Termogénesis / Thermogensis, Esteroides sexuales / Sex steroids

URL الوصول: http://hdl.handle.net/10347/14926

Thesis Advisors: López Pérez, Miguel A., Diéguez González, Carlos, Universidade de Santiago de Compostela. Departamento de Fisioloxía

مصطلحات موضوعية: Metabolismo / Metabolism, Hipotálamo / Hypothalamus, Termogénesis / Thermogensis, Esteroides sexuales / Sex steroids

URL الوصول: http://hdl.handle.net/10347/14926

المؤلفون: González Mira, Amparo

Thesis Advisors: Torreblanca Tamarit, Amparo, Varó Vaello, Inmaculada, Departament de Biologia Funcional i Antropologia Física

مصطلحات موضوعية: teleósteo marino, enzimas de biotransformación, enzimas antioxidantes, fármacos, osmorregulación, aclimatación a la temperatura, hsp70, ácidos grasos, esteroides sexuales, UNESCO::CIENCIAS DE LA VIDA::Biología animal (Zoología) ::Fisiología animal

URL الوصول: http://hdl.handle.net/10550/60004

المؤلفون: González Mira, Amparo

Thesis Advisors: Torreblanca Tamarit, Amparo, Varó Vaello, Inmaculada, Departament de Biologia Funcional i Antropologia Física

مصطلحات موضوعية: teleósteo marino, enzimas de biotransformación, enzimas antioxidantes, fármacos, osmorregulación, aclimatación a la temperatura, hsp70, ácidos grasos, esteroides sexuales, UNESCO::CIENCIAS DE LA VIDA::Biología animal (Zoología) ::Fisiología animal

URL الوصول: http://hdl.handle.net/10803/571579

المؤلفون: González Mira, Amparo

Thesis Advisors: Torreblanca Tamarit, Amparo, Varó Vaello, Inmaculada, Departament de Biologia Funcional i Antropologia Física

مصطلحات موضوعية: teleósteo marino, enzimas de biotransformación, enzimas antioxidantes, fármacos, osmorregulación, aclimatación a la temperatura, hsp70, ácidos grasos, esteroides sexuales, UNESCO::CIENCIAS DE LA VIDA::Biología animal (Zoología) ::Fisiología animal

URL الوصول: http://hdl.handle.net/10550/60004

المؤلفون: Nieto-Vera, Mónica T., Rodríguez-Pulido, José A., Góngora-Orjuela, Agustín

المصدر: https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/601.

مصطلحات موضوعية: Gonadotropin, sex steroid, gonadal maturation, fish reproduction, Gonadotropinas, esteroides sexuales, maduración gonadal, reproducción en peces, Gonadotrofinas, esteroides sexuais, maturação gonadal, reprodução em peixes

وصف الملف: application/pdf

Relation: Masafumi A, Shunsuke M, Masayuki L, Shoji K, Noriko A, Kunio Y, Kazuyoshi U, Kazuyoshi T. Novel fish hypothalamic neuropeptides stimulate the release of gonadotrophins and growth hormone from the pituitary of sockeye salmon. J Endocrinol, 2006;188(3):417-423. doi:10.1677/joe.1.06494.; Mohamed AA, Takeshi M, Chiemi M, Kohei Y. Involvement of Sex Steroid Hormones in the Early Stages of Spermatogenesis in Japanese Huchen (Hucho perryi )1. Biol Reprod, 2001; 65(4):1057-1066. doi:10.1095/biolreprod65.4.1057.; Ando H, Shahjahan M, Kitahashi T. Periodic regulation of expression of genes for kisspeptin, gonadotropin-inhibitory hormone and their receptors in the grass puffer: Implications in seasonal, daily and lunar rhythms of reproduction. Gen Comp Endocrinol, 2018;265:149-153. doi:10.1016/j.ygcen.2018.04.006.; Andreu-Vieyra CV, Buret AG, Habibi HR. Gronadotropin-releasing hormone induction of apoptosis in the testes of goldfish (Caraasius auratus). Endocrinology, 2005;146(3):1588-1596. doi:10.1210/en.2004-0818.; Barrero M, Small BC, D’Abramo LR, Hanson LA, Kelly AM. Comparison of estradiol, testosterone, vitellogenin and cathepsin profiles among young adult channel catfish (Ictalurus punctatus) females from four selectively bred strains. Aquaculture, 2007:264(1-4):390–397. doi:10.1016/j.aquaculture.2006.12.003.; Biran J, Golan M, Mizrahi N, Ogawa S, Parhar IS, Levavi-Sivan B. LPXRFa, the Piscine Ortholog of GnIH, and LPXRF Receptor Positively Regulate Gonadotropin Secretion in Tilapia (Oreochromis niloticus). Endocrinology, 2014;155(11):4391-4401. doi:10.1210/en.2013-2047.; Borg B. Androgens in teleost fishes. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1994;109(3):219-245. doi:10.1016/0742-8413(94)00063-G.; Breton B, Govoroun M, Mikolajczyk T. GTH I and GTH II Secretion Profiles during the Reproductive Cycle in Female Rainbow Trout : Relationship with Pituitary Responsiveness to GnRH-A Stimulation. Gen Comp Endocrinol, 1998;111(1):38-50. doi.org/10.1006/gcen.1998.7088; Burow S, Fontaine R, von Krogh K, Mayer I, Nourizadeh-Lillabadi R, Hollander-Cohen L, et al. Medaka follicle-stimulating hormone (Fsh) and luteinizing hormone (Lh): Developmental profiles of pituitary protein and gene expression levels. Gen Comp Endocrinol, 2018;272:93-108. doi:10.1016/j.ygcen.2018.12.006.; Cavaco JE, Bogerd J, Goos H, Schulz RW. Testosterone Inhibits 11-Ketotestosterone-Induced Spermatogenesis in African Catfish (Clarias gariepinus)1. Biol Reprod, 2001;65(6):1807-1812. doi:10.1095/biolreprod65.6.1807.; Chaube R, Mishra S, Singh RK. A comparison of steroid profiles in the testis and seminal vesicle of the catfish (Heteropneustes fossilis). Theriogenology, 2018; 105:90-96. doi:10.1016/j.theriogenology.2017.09.010.; Chowdhury VS, Ubuka T, Osugi T, Shimura T, Tsutsui K. Identification, localization and expression of LPXRFamide peptides, and melatonin-dependent induction of their precursor mRNA in the newt brain. J Endocrinol, 2011;209(2):211-220. doi:10.1530/JOE-10-0494.; Ciccone NA, Dunn IC, Boswell T, Tsutsui K, Ubuka T, Ukena K, Sharp PJ. Gonadotrophin Inhibitory Hormone Depresses Gonadotrophin alpha and Follicle-Stimulating Hormone beta Subunit Expression in the Pituitary of the Domestic Chicken”, J Neuroendocrinol, 2004;16(12):999-1006. doi:10.1111/j.1365-2826.2005.01260.x.; Devlin RH, Nagahama Y. Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences. Aquaculture, 2002;208(3-4):191-364. doi:10.1016/S0044-8486(02)00057-1.; Felip A, Zanuy S, Pineda R, Pinilla L, Carrillo M, Tena-Sempere M, Gómez A. Evidence for two distinct KiSS genes in non-placental vertebrates that encode kisspeptins with different gonadotropin-releasing activities in fish and mammals. Mol Cell Endocrinol, 2009;312(1-2):61-71. doi:10.1016/j.mce.2008.11.017.; Hollander-Cohen, L. et al. Characterization of carp gonadotropins: Structure, annual profile, and carp and zebrafish pituitary topographic organization. Gen Comp Endocrinol. 2018;264:28-38. doi:10.1016/j.ygcen.2017.11.022.; Honji RM, Caneppele D, Pandolfi M, Lo Nostro FL, Guimarães-Moreiraa R. Characterization of the gonadotropin-releasing hormone system in the Neotropical teleost, Steindachneridion parahybae during the annual reproductive cycle in captivity. Gen Comp Endocrinol, 2019;273:73-85.doi:10.1016/j.ygcen.2018.05.007.; Hoskins LJ, Xu M, Volkoff H. Interactions between gonadotropin-releasing hormone (GnRH) and orexin in the regulation of feeding and reproduction in goldfish (Carassius auratus). Horm Behav, 2008;54(3):379-385. doi:10.1016/j.yhbeh.2008.04.011.; Hou ZS, Wen HS, Li JF, He F, Li Y, Tao YX. Hypothalamus-pituitary-gonad axis of rainbow trout (Oncorhynchus mykiss) during early ovarian development and under dense rearing condition. Gen Comp Endocrinol, 2016;236:131-138. doi:10.1016/j.ygcen.2016.07.011.; de Jesus LWO, Bogerd J, Vieceli FM, Branco GS, Camargo MP, Cassel M, Moreira RG, et al. Gonadotropin subunits of the characiform Astyanax altiparanae: Molecular characterization, spatiotemporal expression and their possible role on female reproductive dysfunction in captivity. Gen Comp Endocrinol, 2017;246:150-163. doi:10.1016/j.ygcen.2016.12.004.; Kajimura S. et al. cDNA Cloning of Two Gonadotropin β Subunits (GTH-Iβ and -IIβ) and Their Expression Profiles during Gametogenesis in the Japanese Flounder (Paralichthys olivaceus). Gen Comp Endocrinol, 2001;122(2):117-129. doi:10.1006/GCEN.2000.7610.; Karigo T, Oka Y. Neurobiological Study of Fish Brains Gives Insights into the Nature of Gonadotropin-Releasing Hormone 1–3 Neurons. Front Endocrinol, 2013;4:177. doi:10.3389/fendo.2013.00177.; Landines MA, Prieto CA, Rodriguez L, Rosado R. Perfil de esteroides sexuales del capitán de la sabana (Eremophilus mutisii) durante un ciclo hidrológico completo. Rev udca Actual Divulg Cient, 2017;20(1):43-50.doi: .; Levavi-Sivan B, Bogerd J, Mananos EL, Gomez A, Lareyre JJ. Perspectives on fish gonadotropins and their receptors. Gen Comp Endocrinol, 2010;165(3):412-437. doi:10.1016/J.YGCEN.2009.07.019.; Lubzens E, Young G, Bobe J, Cerdà J. Oogenesis in teleosts: How fish eggs are formed. Gen Comp Endocrinol, 2010;165(3):367-389. doi:10.1016/J.YGCEN.2009.05.022.; Maitra SK, Hattoraj A, Mukherjee S, Moniruzzaman M. Melatonin: A potent candidate in the regulation of fish oocyte growth and maturation. Gen Comp Endocrinol, 2013;181(1):215-222. doi:10.1016/j.ygcen.2012.09.015.; Mateos J, Mañanósa E, Martínez-Rodríguez G, Carrillo M, Querat B, Zanuy S. Molecular characterization of sea bass gonadotropin subunits (α, FSHβ, and LHβ) and their expression during the reproductive cycle. Gen Comp Endocrinol, 2003;133(2):216-232. doi:10.1016/S0016-6480(03)00164-3.; Matsuda K, Nakamura K, Shimakura SI, Miura T, Kageyama H, Uchiyama M, Shioda S, Ando H. Inhibitory effect of chicken gonadotropin-releasing hormone II on food intake in the goldfish, Carassius auratus. Horm Behav, 2008;54(1):83-89. doi:10.1016/j.yhbeh.2008.01.011.; Melamed P, Sherwood N. (2005) Hormones and Their Receptors in Fish Reproduction. WORLD SCIENTIFIC (Molecular Aspects of Fish & Marine Biology). doi:10.1142/5533.; Melo MC, Dijk P, Andersson E, Nilsen T, Fjelldal P, Male R, et al. Androgens directly stimulate spermatogonial differentiation in juvenile Atlantic salmon (Salmo salar). Gen Comp Endocrinol, 2015;211:52-61. doi:10.1016/j.ygcen.2014.11.015.; Miranda LA, Chalde T, Elisio M, Strüssmann CA. Effects of global warming on fish reproductive endocrine axis, with special emphasis in pejerrey Odontesthes bonariensis. Gen Comp Endocrinol, 2013;192:45-54. doi:10.1016/j.ygcen.2013.02.034.; Miura T, Miura C, Ohta T, Nader MR, Todo T, Yamauchi K. Estradiol-17β Stimulates the Renewal of Spermatogonial Stem Cells in Males. Biochem Biophys Res Commun, 1999;264(1):230-234. doi:10.1006/BBRC.1999.1494.; Mommsen TP, Vijayan MM, Moon TW. Cortisol in teleosts: dynamics, mechanisms of action, and metabolic regulation. Rev Fish Biol Fisher, 1999;9(3):211–268. doi:10.1023/A:1008924418720.; Moreira RG, Honji RM, Melo RG, Narcizo AM, Amaral JS, Araújo RC, Hilsdorf AW. The involvement of gonadotropins and gonadal steroids in the ovulatory dysfunction of the potamodromous Salminus hilarii (Teleostei: Characidae) in captivity. Fish Physiol Biochem, 2015;41(6):1435-1447. doi:10.1007/s10695-015-0097-y.; Nagahama Y. 7 alpha, 20 beta-Dihydroxy-4-pregnen-3-one: A Teleost Maturation-Inducing Hormone. Dev Growth Differ. 1987;29:1–12.; Nagahama Y. Endocrine regulation of gametogenesis in fish. Int J Dev BioI, 1994;38(2):217-229. doi: doi=7981031.; Nagahama Y. 17α,20β-Dihydroxy-4-pregnen-3-one, a maturation-inducing hormone in fish oocytes: Mechanisms of synthesis and action. Steroids. Elsevier, 1997;62(1):190-196. doi:10.1016/S0039-128X(96)00180-8.; Nagahama Y, Yamashita M. Regulation of oocyte maturation in fish. Dev Growth Differ, 2008;50(suppl1):S195-219. doi:10.1111/j.1440-169X.2008.01019.x.; Nyuji M, Hamada K, Kazeto Y, Mekuchi M, Gen K, Soyano K, Okuzawa K. Photoperiodic regulation of plasma gonadotropin levels in previtellogenic greater amberjack (Seriola dumerili). Gen Comp Endocrinol, 2018;269:149-155. doi:10.1016/j.ygcen.2018.09.007.; Okubo K, Nagahama Y. Structural and functional evolution of gonadotropin-releasing hormone in vertebrates. Acta Physiologica, 2008;193(1):3-15. doi:10.1111/j.1748-1716.2008.01832.x.; Park JW, Jin YH, Oh SY, Kwon JY. Kisspeptin2 stimulates the HPG axis in immature Nile tilapia (Oreochromis niloticus). Comp Biochem Physiol Part B: Biochem Mol Biol, Biochemistry and Molecular Biology, 2016;202:31-38. doi:10.1016/j.cbpb.2016.07.009.; Passini G, Carvalho CVA, Carneiro-Sterzelecki F, Francisco-Baloia M, Ronzani-Cerqueira V. Spermatogenesis and steroid hormone profile in puberty of laboratory-reared common snook (Centropomus undecimalis). Aquaculture, 2019;500:622-630. doi:10.1016/j.aquaculture.2018.10.031.; Peng C, Chang JP, Yu KL, Wong AO, Van-Goor F, Peter RE, Rivier JE. Neuropeptide-Y stimulates growth hormone and gonadotropin-II secretion in the goldfish pituitary: involvement of both presynaptic and pituitary cell actions. Endocrinology, 1993;132(4):1820-1829. doi:10.1210/endo.132.4.8462479.; Peng W, Cao M, Chen J, Li Y, Wang Y, Zhu Z, Hu W. GnIH plays a negative role in regulating GtH expression in the common carp, Cyprinus carpio L. Gen Comp Endocrinol, 2016;235:18-28. doi:10.1016/j.ygcen.2016.06.001.; Planas JV, Swanson P. Maturation-Associated Changes in the Response of the Salmon Testis to the Steroidogenic Actions of Gonadotropins (GTH I and GTH II ) In Vitro. Biol Reprod, 1995;52(3):697-704. doi:10.1095/biolreprod52.3.697; Qi X, Zhou W, Li S, Lu D, Yi S, Xie R, Liu X, Zhang Y, Lin H. “Evidences for the regulation of GnRH and GTH expression by GnIH in the goldfish, Carassius auratus”, Mol Cell Endocrinol, 2013;366(1):9-20. doi:10.1016/j.mce.2012.11.001.; Rather MA, Bhat IA, Gireesh-Babu P, Chaudhari A, Sundaray JK, Sharma R. Molecular characterization of kisspeptin gene and effect of nano-encapsulted kisspeptin-10 on reproductive maturation in Catla catla. Domest Anim Endocrinol, 2016;56:36-47. doi:10.1016/j.domaniend.2016.01.005.; Rocha MJ, Arukwe A, Kapoor BG. (2008) Fish reproduction. 1st ed. Science Publishers. Pp.632.; Saborido-Rey F. (2008) Ecología de la reproducción y potencial reproductivo en las poblaciones de peces marinos. Instituto de Investigaciones Marinas (CSIC) Universidad de Vigo. Pp.71.; Sawada K, Ukena A, Satake H, Iwakoshi E, Minakata H, Tsutsui K. “Novel fish hypothalamic neuropeptide”. Eur J Biochem, 2002;269(24):6000-6008. doi:10.1046/j.1432-1033.2002.03351.x.; Schulz RW, de França LR, Lareyre JJ, Le Gac F, Chiarini-Garcia H, Nobrega RH, Miura T. Spermatogenesis in fish. Gen Comp Endocrinol, 2010;165(3):390-411. doi:10.1016/j.ygcen.2009.02.013.; Swanson P, Dickey JT, Campbell B. Biochemistry and physiology of fish gonadotropins. Fish Physiol Biochem, 2003;28:53-59.; Tena-Sempere M, Felip A, Gómez A, Zanuy S, Carrillo M. Comparative insights of the kisspeptin/kisspeptin receptor system: Lessons from non-mammalian vertebrates”. Gen Comp Endocrinol, 2012;175(2):234-243. doi:10.1016/j.ygcen.2011.11.015.; Thorson JF, Prezotto LD, Cardoso RC, Sharpton SM, Edwards JF, et al. (2014) “Hypothalamic Distribution, Adenohypophyseal Receptor Expression, and Ligand Functionality of RFamide-Related Peptide 3 in the Mare During the Breeding and Nonbreeding Seasons1”. Biology of Reproduction, 2014;90(2):1-9. doi:10.1095/biolreprod.113.112185.; Tokarz J, Möller G, de Angelis MH, Adamski J. “Zebrafish and steroids: What do we know and what do we need to know?”. J Steroid Biochem Mol Biol, 2013;137:165-173. doi:10.1016/j.jsbmb.2013.01.003.; Tokarz J, Möller G1, Hrabě de Angelis M, Adamski J. Steroids in teleost fishes: A functional point of view. Steroids, 2015;103:123-144. doi:10.1016/j.steroids.2015.06.011.; Tsutsui K, Saigoh E, Ukena K, Teranishi H, Fujisawa Y, Kikuchi M, et al. A Novel Avian Hypothalamic Peptide Inhibiting Gonadotropin Release. Biochem Biophys Res Commun, 2000;275(2):661-667. doi:10.1006/BBRC.2000.3350.; Tsutsui K. A new key neurohormone controlling reproduction, gonadotropin-inhibitory hormone (GnIH): Biosynthesis, mode of action and functional significance. Progress in Neurobiology, 2009;88(1):76-88. doi:10.1016/j.pneurobio.2009.02.003.; Tsutsui K, Osugi T, Son YL, Ubuka T. Review: Structure, function and evolution of GnIH. Gen Comp Endocrinol, 2018;264:48-57. doi:10.1016/j.ygcen.2017.07.024.; Ubuka T, Bentley GE, Ukena K, Wingfield JC, Tsutsui K. Melatonin induces the expression of gonadotropin-inhibitory hormone in the avian brain. Proc Natl Acad Sci USA, 2005;102(8):3052-3057. doi:10.1073/PNAS.0403840102.; Ubuka T, Morgan K, Pawson AJ, Osugi T, Chowdhury VS, Minakata H, et al. Identification of Human GnIH Homologs, RFRP-1 and RFRP-3, and the Cognate Receptor, GPR147 in the Human Hypothalamic Pituitary Axis. PLoS One, 2009;4(12):e8400. doi:10.1371/journal.pone.0008400.; Ubuka T, Son YL, Tsutsui K. Molecular, cellular, morphological, physiological and behavioral aspects of gonadotropin-inhibitory hormone. Gen Comp Endocrinol, 2016;227:27-50. doi:10.1016/j.ygcen.2015.09.009.; Ukena K, Iwakoshi-Ukena E, Osugi T, Tsutsui K. Identification and localization of gonadotropin-inhibitory hormone (GnIH) orthologs in the hypothalamus of the red-eared slider turtle, Trachemys scripta elegans. Gen Comp Endocrinol, 2016;227:69-76. doi:10.1016/j.ygcen.2015.06.009.; Valdebenito I, Paiva L, Berland M. Atresia folicular en peces teleósteos : una revisión. Arch Med Vet, 2011;43(1):11-25. doi.org/10.4067/S0301-732X2011000100003; Volkoff H. The Neuroendocrine Regulation of Food Intake in Fish: A Review of Current Knowledge. Front Neurosci, 2016;10:540. doi:10.3389/fnins.2016.00540.; Wu C, Patiño R, Davis KB, Chang X. Localization of estrogen receptor α and β RNA in germinal and nongerminal epithelia of the channel catfish testis. Gen Comp Endocrinol, 2001;124(1):12-20. doi:10.1006/gcen.2001.7668.; Wylie MJ, Setiawan AN, Irvine GW, Symonds JE, Elizur A, Lokman PM. Effects of neuropeptides and sex steroids on the pituitary-gonadal axis of pre-pubertal F1 wreckfish (hāpuku) Polyprion oxygeneios in vivo: Evidence of inhibitory effects of androgens. Gen Comp Endocrinol, 2018;257:113-121. doi:10.1016/j.ygcen.2017.08.018.; Yaron Z, Gur G, Melamed P, Rosenfeld H, Elizur A, Levavi-Sivan B. Regulation of fish gonadotropins. Int Rev Cytol, 2003;225:131-185. doi.org/10.1016/S0074-7696(05)25004-0; Yu KL, Peter RE. Alterations in gonadotropin-releasing hormone immunoactivities in discrete brain areas of male goldfish during spawning behavior. Brain Research, 1990;512(1):89-94. doi:10.1016/0006-8993(90)91174-F.; Yu KL, Rosenblum PM, Peter RE. In vitro release of gonadotropin-releasing hormone from the brain preoptic-anterior hypothalamic region and pituitary of female goldfish. Gen Comp Endocrinol, 1991;81(2):256-267. doi:10.1016/0016-6480(91)90010-4.; Zhang Y, Li S, Liu Y, Lu D, Chen H, Huang X, et al. Structural diversity of the gnih/gnih receptor system in teleost: Its involvement in early development and the negative control of LH release. Peptides, 2010;31(6):1034-1043. doi:10.1016/j.peptides.2010.03.003.; Zohar Y, Muñoz-Cueto JA, Elizur A, Kah O. Neuroendocrinology of reproduction in teleost fish. Gen Comp Endocrinol, 2010;165(3):438-455. doi:10.1016/j.ygcen.2009.04.017.; https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/download/601/pdf; 63; 52; 24; Orinoquia; https://repositorio.unillanos.edu.co/handle/001/3982; https://doi.org/10.22579/20112629.601

الاتاحة: https://repositorio.unillanos.edu.co/handle/001/3982
https://doi.org/10.22579/20112629.601

المؤلفون: Nieto Vera, Mónica T., Rodríguez Pulido, José A, Góngora Orjuela, Agustín

المصدر: Revista Orinoquia; Vol. 24 No. 1 (2020): Enero-Junio; 52-63 ; Revista Orinoquia; Vol. 24 Núm. 1 (2020): Enero-Junio; 52-63 ; 2011-2629 ; 0121-3709 ; 10.22579/issn.2011-2629

مصطلحات موضوعية: Gonadotropin, sex steroid, gonadal maturation, fish reproduction, Gonadotropinas, esteroides sexuales, maduración gonadal, reproducción en peces, Gonadotrofinas, esteroides sexuais, maturação gonadal, reprodução em peixes

وصف الملف: application/pdf

Relation: https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/281/257; Masafumi A, Shunsuke M, Masayuki L, Shoji K, Noriko A, Kunio Y, Kazuyoshi U, Kazuyoshi T. Novel fish hypothalamic neuropeptides stimulate the release of gonadotrophins and growth hormone from the pituitary of sockeye salmon. J Endocrinol, 2006;188(3):417-423. doi: https://doi.org/10.1677/joe.1.06494.; Mohamed AA, Takeshi M, Chiemi M, Kohei Y. Involvement of Sex Steroid Hormones in the Early Stages of Spermatogenesis in Japanese Huchen (Hucho perryi )1. Biol Reprod, 2001; 65(4):1057-1066. doi: https://doi.org/10.1095/biolreprod65.4.1057.; Ando H, Shahjahan M, Kitahashi T. Periodic regulation of expression of genes for kisspeptin, gonadotropin-inhibitory hormone and their receptors in the grass puffer: Implications in seasonal, daily and lunar rhythms of reproduction. Gen Comp Endocrinol, 2018;265:149-153. doi: https://doi.org/10.1016/j.ygcen.2018.04.006.; Andreu-Vieyra CV, Buret AG, Habibi HR. Gronadotropin-releasing hormone induction of apoptosis in the testes of goldfish (Caraasius auratus). Endocrinology, 2005;146(3):1588-1596. doi: https://doi.org/10.1210/en.2004-0818.; Barrero M, Small BC, D’Abramo LR, Hanson LA, Kelly AM. Comparison of estradiol, testosterone, vitellogenin and cathepsin profiles among young adult channel catfish (Ictalurus punctatus) females from four selectively bred strains. Aquaculture, 2007:264(1-4):390–397. doi: https://doi.org/10.1016/j.aquaculture.2006.12.003.; Biran J, Golan M, Mizrahi N, Ogawa S, Parhar IS, Levavi-Sivan B. LPXRFa, the Piscine Ortholog of GnIH, and LPXRF Receptor Positively Regulate Gonadotropin Secretion in Tilapia (Oreochromis niloticus). Endocrinology, 2014;155(11):4391-4401. doi: https://doi.org/10.1210/en.2013-2047.; Borg B. Androgens in teleost fishes. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1994;109(3):219-245. doi: https://doi.org/10.1016/0742-8413(94)00063-G.; Breton B, Govoroun M, Mikolajczyk T. GTH I and GTH II Secretion Profiles during the Reproductive Cycle in Female Rainbow Trout : Relationship with Pituitary Responsiveness to GnRH-A Stimulation. Gen Comp Endocrinol, 1998;111(1):38-50. https://doi.org/10.1006/gcen.1998.7088; Burow S, Fontaine R, von Krogh K, Mayer I, Nourizadeh-Lillabadi R, Hollander-Cohen L, et al. Medaka follicle-stimulating hormone (Fsh) and luteinizing hormone (Lh): Developmental profiles of pituitary protein and gene expression levels. Gen Comp Endocrinol, 2018;272:93-108. doi: https://doi.org/10.1016/j.ygcen.2018.12.006.; Cavaco JE, Bogerd J, Goos H, Schulz RW. Testosterone Inhibits 11-Ketotestosterone-Induced Spermatogenesis in African Catfish (Clarias gariepinus)1. Biol Reprod, 2001;65(6):1807-1812. doi: https://doi.org/10.1095/biolreprod65.6.1807.; Chaube R, Mishra S, Singh RK. A comparison of steroid profiles in the testis and seminal vesicle of the catfish (Heteropneustes fossilis). Theriogenology, 2018; 105:90-96. doi:10.1016/j.theriogenology.2017.09.010.; Chowdhury VS, Ubuka T, Osugi T, Shimura T, Tsutsui K. Identification, localization and expression of LPXRFamide peptides, and melatonin-dependent induction of their precursor mRNA in the newt brain. J Endocrinol, 2011;209(2):211-220. doi: https://doi.org/10.1530/JOE-10-0494.; Ciccone NA, Dunn IC, Boswell T, Tsutsui K, Ubuka T, Ukena K, Sharp PJ. Gonadotrophin Inhibitory Hormone Depresses Gonadotrophin alpha and Follicle-Stimulating Hormone beta Subunit Expression in the Pituitary of the Domestic Chicken”, J Neuroendocrinol, 2004;16(12):999-1006. doi: https://doi.org/10.1111/j.1365-2826.2005.01260.x.; Devlin RH, Nagahama Y. Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences. Aquaculture, 2002;208(3-4):191-364. doi:10.1016/S0044-8486(02)00057-1.; Felip A, Zanuy S, Pineda R, Pinilla L, Carrillo M, Tena-Sempere M, Gómez A. Evidence for two distinct KiSS genes in non-placental vertebrates that encode kisspeptins with different gonadotropin-releasing activities in fish and mammals. Mol Cell Endocrinol, 2009;312(1-2):61-71. doi: https://doi.org/10.1016/j.mce.2008.11.017.; Hollander-Cohen, L. et al. Characterization of carp gonadotropins: Structure, annual profile, and carp and zebrafish pituitary topographic organization. Gen Comp Endocrinol. 2018;264:28-38. doi: https://doi.org/10.1016/j.ygcen.2017.11.022.; Honji RM, Caneppele D, Pandolfi M, Lo Nostro FL, Guimarães-Moreiraa R. Characterization of the gonadotropin-releasing hormone system in the Neotropical teleost, Steindachneridion parahybae during the annual reproductive cycle in captivity. Gen Comp Endocrinol, 2019;273:73-85.doi: https://doi.org/10.1016/j.ygcen.2018.05.007.; Hoskins LJ, Xu M, Volkoff H. Interactions between gonadotropin-releasing hormone (GnRH) and orexin in the regulation of feeding and reproduction in goldfish (Carassius auratus). Horm Behav, 2008;54(3):379-385. doi: https://doi.org/10.1016/j.yhbeh.2008.04.011.; Hou ZS, Wen HS, Li JF, He F, Li Y, Tao YX. Hypothalamus-pituitary-gonad axis of rainbow trout (Oncorhynchus mykiss) during early ovarian development and under dense rearing condition. Gen Comp Endocrinol, 2016;236:131-138. doi: https://doi.org/10.1016/j.ygcen.2016.07.011.; de Jesus LWO, Bogerd J, Vieceli FM, Branco GS, Camargo MP, Cassel M, Moreira RG, et al. Gonadotropin subunits of the characiform Astyanax altiparanae: Molecular characterization, spatiotemporal expression and their possible role on female reproductive dysfunction in captivity. Gen Comp Endocrinol, 2017;246:150-163. doi: https://doi.org/10.1016/j.ygcen.2016.12.004.; Kajimura S. et al. cDNA Cloning of Two Gonadotropin β Subunits (GTH-Iβ and -IIβ) and Their Expression Profiles during Gametogenesis in the Japanese Flounder (Paralichthys olivaceus). Gen Comp Endocrinol, 2001;122(2):117-129. doi: https://doi.org/10.1006/GCEN.2000.7610.; Karigo T, Oka Y. Neurobiological Study of Fish Brains Gives Insights into the Nature of Gonadotropin-Releasing Hormone 1–3 Neurons. Front Endocrinol, 2013;4:177. doi: https://doi.org/10.3389/fendo.2013.00177.; Landines MA, Prieto CA, Rodriguez L, Rosado R. Perfil de esteroides sexuales del capitán de la sabana (Eremophilus mutisii) durante un ciclo hidrológico completo. Rev udca Actual Divulg Cient, 2017;20(1):43-50.doi: .; Levavi-Sivan B, Bogerd J, Mananos EL, Gomez A, Lareyre JJ. Perspectives on fish gonadotropins and their receptors. Gen Comp Endocrinol, 2010;165(3):412-437. doi: https://doi.org/10.1016/J.YGCEN.2009.07.019.; Lubzens E, Young G, Bobe J, Cerdà J. Oogenesis in teleosts: How fish eggs are formed. Gen Comp Endocrinol, 2010;165(3):367-389. doi: https://doi.org/10.1016/J.YGCEN.2009.05.022.; Maitra SK, Hattoraj A, Mukherjee S, Moniruzzaman M. Melatonin: A potent candidate in the regulation of fish oocyte growth and maturation. Gen Comp Endocrinol, 2013;181(1):215-222. doi: https://doi.org/10.1016/j.ygcen.2012.09.015.; Mateos J, Mañanósa E, Martínez-Rodríguez G, Carrillo M, Querat B, Zanuy S. Molecular characterization of sea bass gonadotropin subunits (α, FSHβ, and LHβ) and their expression during the reproductive cycle. Gen Comp Endocrinol, 2003;133(2):216-232. doi:10.1016/S0016-6480(03)00164-3.; Matsuda K, Nakamura K, Shimakura SI, Miura T, Kageyama H, Uchiyama M, Shioda S, Ando H. Inhibitory effect of chicken gonadotropin-releasing hormone II on food intake in the goldfish, Carassius auratus. Horm Behav, 2008;54(1):83-89. doi: https://doi.org/10.1016/j.yhbeh.2008.01.011.; Melamed P, Sherwood N. (2005) Hormones and Their Receptors in Fish Reproduction. WORLD SCIENTIFIC (Molecular Aspects of Fish & Marine Biology). doi: https://doi.org/10.1142/5533.; Melo MC, Dijk P, Andersson E, Nilsen T, Fjelldal P, Male R, et al. Androgens directly stimulate spermatogonial differentiation in juvenile Atlantic salmon (Salmo salar). Gen Comp Endocrinol, 2015;211:52-61. doi: https://doi.org/10.1016/j.ygcen.2014.11.015.; Miranda LA, Chalde T, Elisio M, Strüssmann CA. Effects of global warming on fish reproductive endocrine axis, with special emphasis in pejerrey Odontesthes bonariensis. Gen Comp Endocrinol, 2013;192:45-54. doi: https://doi.org/10.1016/j.ygcen.2013.02.034.; Miura T, Miura C, Ohta T, Nader MR, Todo T, Yamauchi K. Estradiol-17β Stimulates the Renewal of Spermatogonial Stem Cells in Males. Biochem Biophys Res Commun, 1999;264(1):230-234. doi: https://doi.org/10.1006/BBRC.1999.1494.; Mommsen TP, Vijayan MM, Moon TW. Cortisol in teleosts: dynamics, mechanisms of action, and metabolic regulation. Rev Fish Biol Fisher, 1999;9(3):211–268. doi: https://doi.org/10.1023/A:1008924418720.; Moreira RG, Honji RM, Melo RG, Narcizo AM, Amaral JS, Araújo RC, Hilsdorf AW. The involvement of gonadotropins and gonadal steroids in the ovulatory dysfunction of the potamodromous Salminus hilarii (Teleostei: Characidae) in captivity. Fish Physiol Biochem, 2015;41(6):1435-1447. doi: https://doi.org/10.1007/s10695-015-0097-y.; Nagahama Y. 7 alpha, 20 beta-Dihydroxy-4-pregnen-3-one: A Teleost Maturation-Inducing Hormone. Dev Growth Differ. 1987;29:1–12.; Nagahama Y. Endocrine regulation of gametogenesis in fish. Int J Dev BioI, 1994;38(2):217-229. doi: doi=7981031.; Nagahama Y. 17α,20β-Dihydroxy-4-pregnen-3-one, a maturation-inducing hormone in fish oocytes: Mechanisms of synthesis and action. Steroids. Elsevier, 1997;62(1):190-196. doi:10.1016/S0039-128X(96)00180-8.; Nagahama Y, Yamashita M. Regulation of oocyte maturation in fish. Dev Growth Differ, 2008;50(suppl1):S195-219. doi: https://doi.org/10.1111/j.1440-169X.2008.01019.x.; Nyuji M, Hamada K, Kazeto Y, Mekuchi M, Gen K, Soyano K, Okuzawa K. Photoperiodic regulation of plasma gonadotropin levels in previtellogenic greater amberjack (Seriola dumerili). Gen Comp Endocrinol, 2018;269:149-155. doi: https://doi.org/10.1016/j.ygcen.2018.09.007.; Okubo K, Nagahama Y. Structural and functional evolution of gonadotropin-releasing hormone in vertebrates. Acta Physiologica, 2008;193(1):3-15. doi: https://doi.org/10.1111/j.1748-1716.2008.01832.x.; Park JW, Jin YH, Oh SY, Kwon JY. Kisspeptin2 stimulates the HPG axis in immature Nile tilapia (Oreochromis niloticus). Comp Biochem Physiol Part B: Biochem Mol Biol, Biochemistry and Molecular Biology, 2016;202:31-38. doi: https://doi.org/10.1016/j.cbpb.2016.07.009.; Passini G, Carvalho CVA, Carneiro-Sterzelecki F, Francisco-Baloia M, Ronzani-Cerqueira V. Spermatogenesis and steroid hormone profile in puberty of laboratory-reared common snook (Centropomus undecimalis). Aquaculture, 2019;500:622-630. doi: https://doi.org/10.1016/j.aquaculture.2018.10.031.; Peng C, Chang JP, Yu KL, Wong AO, Van-Goor F, Peter RE, Rivier JE. Neuropeptide-Y stimulates growth hormone and gonadotropin-II secretion in the goldfish pituitary: involvement of both presynaptic and pituitary cell actions. Endocrinology, 1993;132(4):1820-1829. doi: https://doi.org/10.1210/endo.132.4.8462479.; Peng W, Cao M, Chen J, Li Y, Wang Y, Zhu Z, Hu W. GnIH plays a negative role in regulating GtH expression in the common carp, Cyprinus carpio L. Gen Comp Endocrinol, 2016;235:18-28. doi: https://doi.org/10.1016/j.ygcen.2016.06.001.; Planas JV, Swanson P. Maturation-Associated Changes in the Response of the Salmon Testis to the Steroidogenic Actions of Gonadotropins (GTH I and GTH II ) In Vitro. Biol Reprod, 1995;52(3):697-704. doi: https://doi.org/10.1095/biolreprod52.3.697; Qi X, Zhou W, Li S, Lu D, Yi S, Xie R, Liu X, Zhang Y, Lin H. “Evidences for the regulation of GnRH and GTH expression by GnIH in the goldfish, Carassius auratus”, Mol Cell Endocrinol, 2013;366(1):9-20. doi: https://doi.org/10.1016/j.mce.2012.11.001.; Rather MA, Bhat IA, Gireesh-Babu P, Chaudhari A, Sundaray JK, Sharma R. Molecular characterization of kisspeptin gene and effect of nano-encapsulted kisspeptin-10 on reproductive maturation in Catla catla. Domest Anim Endocrinol, 2016;56:36-47. doi: https://doi.org/10.1016/j.domaniend.2016.01.005.; Rocha MJ, Arukwe A, Kapoor BG. (2008) Fish reproduction. 1st ed. Science Publishers. Pp.632.; Saborido-Rey F. (2008) Ecología de la reproducción y potencial reproductivo en las poblaciones de peces marinos. Instituto de Investigaciones Marinas (CSIC) Universidad de Vigo. Pp.71.; Sawada K, Ukena A, Satake H, Iwakoshi E, Minakata H, Tsutsui K. “Novel fish hypothalamic neuropeptide”. Eur J Biochem, 2002;269(24):6000-6008. doi: https://doi.org/10.1046/j.1432-1033.2002.03351.x.; Schulz RW, de França LR, Lareyre JJ, Le Gac F, Chiarini-Garcia H, Nobrega RH, Miura T. Spermatogenesis in fish. Gen Comp Endocrinol, 2010;165(3):390-411. doi: https://doi.org/10.1016/j.ygcen.2009.02.013.; Swanson P, Dickey JT, Campbell B. Biochemistry and physiology of fish gonadotropins. Fish Physiol Biochem, 2003;28:53-59.; Tena-Sempere M, Felip A, Gómez A, Zanuy S, Carrillo M. Comparative insights of the kisspeptin/kisspeptin receptor system: Lessons from non-mammalian vertebrates”. Gen Comp Endocrinol, 2012;175(2):234-243. doi: https://doi.org/10.1016/j.ygcen.2011.11.015.; Thorson JF, Prezotto LD, Cardoso RC, Sharpton SM, Edwards JF, et al. (2014) “Hypothalamic Distribution, Adenohypophyseal Receptor Expression, and Ligand Functionality of RFamide-Related Peptide 3 in the Mare During the Breeding and Nonbreeding Seasons1”. Biology of Reproduction, 2014;90(2):1-9. doi: https://doi.org/10.1095/biolreprod.113.112185.; Tokarz J, Möller G, de Angelis MH, Adamski J. “Zebrafish and steroids: What do we know and what do we need to know?”. J Steroid Biochem Mol Biol, 2013;137:165-173. doi: https://doi.org/10.1016/j.jsbmb.2013.01.003.; Tokarz J, Möller G1, Hrabě de Angelis M, Adamski J. Steroids in teleost fishes: A functional point of view. Steroids, 2015;103:123-144. doi: https://doi.org/10.1016/j.steroids.2015.06.011.; Tsutsui K, Saigoh E, Ukena K, Teranishi H, Fujisawa Y, Kikuchi M, et al. A Novel Avian Hypothalamic Peptide Inhibiting Gonadotropin Release. Biochem Biophys Res Commun, 2000;275(2):661-667. doi: https://doi.org/10.1006/BBRC.2000.3350.; Tsutsui K. A new key neurohormone controlling reproduction, gonadotropin-inhibitory hormone (GnIH): Biosynthesis, mode of action and functional significance. Progress in Neurobiology, 2009;88(1):76-88. doi: https://doi.org/10.1016/j.pneurobio.2009.02.003.; Tsutsui K, Osugi T, Son YL, Ubuka T. Review: Structure, function and evolution of GnIH. Gen Comp Endocrinol, 2018;264:48-57. doi: https://doi.org/10.1016/j.ygcen.2017.07.024.; Ubuka T, Bentley GE, Ukena K, Wingfield JC, Tsutsui K. Melatonin induces the expression of gonadotropin-inhibitory hormone in the avian brain. Proc Natl Acad Sci USA, 2005;102(8):3052-3057. doi: https://doi.org/10.1073/PNAS.0403840102.; Ubuka T, Morgan K, Pawson AJ, Osugi T, Chowdhury VS, Minakata H, et al. Identification of Human GnIH Homologs, RFRP-1 and RFRP-3, and the Cognate Receptor, GPR147 in the Human Hypothalamic Pituitary Axis. PLoS One, 2009;4(12):e8400. doi: https://doi.org/10.1371/journal.pone.0008400.; Ubuka T, Son YL, Tsutsui K. Molecular, cellular, morphological, physiological and behavioral aspects of gonadotropin-inhibitory hormone. Gen Comp Endocrinol, 2016;227:27-50. doi: https://doi.org/10.1016/j.ygcen.2015.09.009.; Ukena K, Iwakoshi-Ukena E, Osugi T, Tsutsui K. Identification and localization of gonadotropin-inhibitory hormone (GnIH) orthologs in the hypothalamus of the red-eared slider turtle, Trachemys scripta elegans. Gen Comp Endocrinol, 2016;227:69-76. doi: https://doi.org/10.1016/j.ygcen.2015.06.009.; Valdebenito I, Paiva L, Berland M. Atresia folicular en peces teleósteos : una revisión. Arch Med Vet, 2011;43(1):11-25. https://doi.org/10.4067/S0301-732X2011000100003; Volkoff H. The Neuroendocrine Regulation of Food Intake in Fish: A Review of Current Knowledge. Front Neurosci, 2016;10:540. doi: https://doi.org/10.3389/fnins.2016.00540.; Wu C, Patiño R, Davis KB, Chang X. Localization of estrogen receptor α and β RNA in germinal and nongerminal epithelia of the channel catfish testis. Gen Comp Endocrinol, 2001;124(1):12-20. doi: https://doi.org/10.1006/gcen.2001.7668.; Wylie MJ, Setiawan AN, Irvine GW, Symonds JE, Elizur A, Lokman PM. Effects of neuropeptides and sex steroids on the pituitary-gonadal axis of pre-pubertal F1 wreckfish (hāpuku) Polyprion oxygeneios in vivo: Evidence of inhibitory effects of androgens. Gen Comp Endocrinol, 2018;257:113-121. doi: https://doi.org/10.1016/j.ygcen.2017.08.018.; Yaron Z, Gur G, Melamed P, Rosenfeld H, Elizur A, Levavi-Sivan B. Regulation of fish gonadotropins. Int Rev Cytol, 2003;225:131-185. https://doi.org/10.1016/S0074-7696(05)25004-0; Yu KL, Peter RE. Alterations in gonadotropin-releasing hormone immunoactivities in discrete brain areas of male goldfish during spawning behavior. Brain Research, 1990;512(1):89-94. doi: https://doi.org/10.1016/0006-8993(90)91174-F.; Yu KL, Rosenblum PM, Peter RE. In vitro release of gonadotropin-releasing hormone from the brain preoptic-anterior hypothalamic region and pituitary of female goldfish. Gen Comp Endocrinol, 1991;81(2):256-267. doi: https://doi.org/10.1016/0016-6480(91)90010-4.; Zhang Y, Li S, Liu Y, Lu D, Chen H, Huang X, et al. Structural diversity of the gnih/gnih receptor system in teleost: Its involvement in early development and the negative control of LH release. Peptides, 2010;31(6):1034-1043. doi: https://doi.org/10.1016/j.peptides.2010.03.003.; Zohar Y, Muñoz-Cueto JA, Elizur A, Kah O. Neuroendocrinology of reproduction in teleost fish. Gen Comp Endocrinol, 2010;165(3):438-455. doi: https://doi.org/10.1016/j.ygcen.2009.04.017.; https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/281

الاتاحة: https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/281

المؤلفون: Lopez-García, Gerardo, Gongora-Orjuela, Agustin, Díaz-González, Félix, Rojas-Rodríguez, Adriana

المصدر: https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/565.

مصطلحات موضوعية: Gonadotropins, sex steroids, gonadal maturation, fish reproduction, Gonadotropinas, esteroides sexuales, maduración gonadal, reproducción en peces

وصف الملف: application/pdf

Relation: Ahola JK. 2004. Copper, Zinc, and Manganese In Beef Cattle Production: Effects of supplementation and source on reproduction, mineral status, feedlot performance, immunity, and carcass characteristics. Tesis PhD. Colorado State University; Álvarez JL. 2008. Bioquímica nutricional y metabólica del bovino en el tropico. Ed. Universidad de Antioquia, Medellín. p.188; Barth K, Aulrich K, Haufe HC, Muller U, Schaub D, Schulz F. Metabolic status in early lactation dairy cows of two breeds kept under condition of organics farming- a case study. Landbauforschung. VTI agriculture and forestry Research. 2011;4: 61:307-316; Barrios M, Sandoval E, Sánchez D, Borges J, Bastardo Y, Márquez O, Dávila L. 2013. Valores de referencia de diferentes parámetros bioquímicos en vacunos mestizos de doble propósito del valle de aroa, estado Yaracuy. Mundo Pecuario 2013;9(1):25-30; Bell AW. Regulation of organic nutrient metabolism during transition from late pregnancy to early lactation. J Anim Sci. 1995;73:2804-2819; Bermes-Junior EW, Eeviti V, Forman DT. 1976. Statistics, normal values, and quality control. In: TIETY, N.W. (Ed.). Fundamentals of clinical chemistry. Philadelphia: W.B. Saunders Co.; Butler WR, Smith RD. Interrelationships between energy balance and postpartum reproductive function in dairy cows. J Dairy Sci. 1989;72:767-783; Calvo JJ, Allue JR, Eesudeso A, Garcia LJ. Plasma ferritin of sows during pregnancy and lactation. Cornell Vet. 1989;79:273-282; Campos R, Carreño ES, González FD. Perfil metabólico de vacas nativas colombianas. Orinoquia. 2004;8:32-41; Caton JS, Hess BW. 2010. Maternal plane of nutrition: Impacts on fetal outcomes and postnatal offspring responses. Invited Review. Pages 104-122 in Proc. 4th Grazing Livestock Nutrition Conference.; Ceballos A, Gómez PM, Vélez ML, Villa NA, López LF. Variación de los indicadores bioquímicos del balance de energía según el estado productivo en bovinos lecheros de Manizales. Rev Col de Cienc Pec. 2002;15(1):13-25; Chilliard Y, Bocquier F, Doreau M. Digestive and metabolic adaptations of ruminants to undernutrition and consequences on reproduction. Reprod Nutr Dev. 1998;38:131-152; Church TL, Brunner RR, Janzen ED. A partial metabolic profile in a beef cow herd in which clinical hypocalcemia occurred. Can Vet J. 1978;19(4):110-112; Contreras PA. 2000. Indicadores do metabolismo protéico utilizado nos perfis metabólicos de rebanhos. In: González, F. H. D., J. O. Barcellos, H. Ospina, L. A. O. Ribeiro. (Ed.) Perfil metabólico em ruminantes: seu uso em nutrição e doenças nutricionais. Porto Alegre, Brasil. Gráfica da UFRGS. Pp. 23-30; Conpes. 2014. Política para el desarrollo integral de la Orinoquia: Altillanura - Fase 1. Documento 3797. Consejo Nacional de Política Económica y Social (CONPES), Departamento Nacional de Planeación (DNP), República de Colombia, Bogotá, Colombia.; Coppo JA, Coppo NB, Slanac AL, Revidatti MA, Capellari A. 2000. Influencia del desarrollo, sexo y tipo de destete sobre algumas actividades enzimáticas em plasma de terneros cruza cebú. In: Comunicaciones Científicas y Tecnológicas. Universidad Nacional del Nordeste Argentina.; Corah LR, Dargatz DA, Peters CW. NAHMS Forage Survey: Trace mineral analysis o f 352 forage samples collected in 18 states. J Anim Sci. 1996; 74(Suppl. 1):202. (Abstr.); Cottin SC, Roussel G, Gambling L, Hayes HE, Currie VJ, McArdle HJ. The effect of maternal iron deficiency on zinc and copper levels and on genes of zinc and copper metabolism during pregnancy in the rat. Br J Nutr. 2019;121(2):121-129; Cutaia L, Brogliatti G, Chesta P, Moreno D, Bó G. 2003. Efecto del momento de la IATF sobre los porcentajes de preñez en vacas para carne sincronizadas con Dispositivos con Progesterona y Benzoato de Estradiol. V° Simposio Internacional de Reproducción Animal. Huerta Grande, Córdoba. 27 al 29 de junio. Abstr. 385.; Depablos L, Godoy S, Chicco, CF, Orodoñez J. Nutrición mineral en sistemas ganaderos de las sabanas centrales de Venezuela. Zootecnia Trop. 2009;27(1): 27-38; Edmonson AJ, Lean IJ, Weaver LD, Farver T, Webster G. A body condition scoring chart for Holstein dairy cows. J Dairy Sci. 1989;72:68-78; Fiorentin EL, Zanobello S, Gato A, Piovezan AL, Alves MV, Rocha RX, Gonzalez F. Ocurrence of subclinic metabolic disorders in dairy cows from western Santa catarina state, Brasil. Pesq Vet Bras. 2018;38(4):629-634; Fordyce F, Masara D, Appleton J. Stream sediment, soil and forage chemistry as indicators of cattle mineral status in northeast Zimbabwe. Geol Soc. Special Pub. 1996;113:23-37; Freetly HC, Ferrell CL, Jenkins TG. Timing of realimentation of mature cows that were feed- restricted during pregnancy influences calf birth weights and growth rates. J Anim Sci. 2000;78:2790-2796; Giraldo LF, Loaiza AM, Botero SA, Uribe-Velásquez LF. Parámetros metabólicos séricos y condición corporal durante el pre y posparto en vacas Brahman: Serum Metabolic Parameters and Body Condition During Pre and Postpartum in Brahman Cows. Rev Cient. 2009;19(4):350-355; Gómez JM, Laredo MA. Fluctuaciones minerales en pastos tropicales. II. Andropogon gayanus, en los Llanos orientales. Revista ICA. 1983;18:95-104; González FHD, Silva SC. 2006. Introduçao à bioquímica clínica veterinária. Segunda edição. Universidade Federal do Rio Grande do Sul. UFRGS Editora. p. 358; Graham TW. Trace element deficiencies in cattle. Vet Clin North Am: Food Anim Pract. 1991;7:153-215; Houghton PL, Lemanager RP, Horstman LA, Hendrix KS, Moss GE. Effects of body composition, pre- and postpartum energy level and early weaning on reproductive per- formance of beef cows and preweaning calf gain. J Anim Sci. 1990;68:1438-1446; Kaneko JJ. 1989. Clinical biochemistry of domestic animals. San Diego: Academic Press, p. 932; Kaneko JJ, Harvey JW, Bruss ML. 1997. Clinical biochemistry of domestic animals. San Diego: Academic Press p. 932; Kindahl H, Kornmatitsuk B, Königsson K, Gustafsson H. Endocrine changes in late bovine pregnancy with special emphasis on fetal well-being. Dom Anim Endocrinol. 2002; 23(1-2):321-328; Laredo MA, Gómez J. Fluctuaciones minerales en pastos tropicales. I. Brachiaria en los Llanos Orientales. Revista ICA. 1980;15:71-78; Noaman V, Rasti M, Ranjbari AR, Shirvani E. Copper, zinc, and iron concentrations in blood serum and diet of dairy cattle on semi-industrial farms in central Iran. Trop Anim Health Prod. 2012;44:407-411; Mejía GM. 1984. Orinoquia Colombiana: Sabanas de la Altillanura – Clima y Uso de la tierra. Fondo Colombiano de Investigaciones Científicas y Proyectos Especiales Francisco José de Caldas – Colciencias – Corporación Araracuara. Universidad Nacional de Colombia, Palmira; Mortiner RG, Dargatz DA, Corah LR. 1999. Forage analysis from cow/calf herds in 23 states. USDA:APHIS:VS, Centers for Epidemiology and Animal Health. Fort Collins, CO. #N303.499. April 1999; Morrison DG, Spitzer JC, Perkins JL. Influence of prepartum body condition score change on reproduction in multiparous beef cows calving in moderate body condition. J Anim Sci. 1999;77:1048-1054; Obeidat BS, Thomas MG, Hallford DM, Keisler DH, Petersen MK, Bryant WD, Garcia MD, Narro L, López R. Metabolic characteristic of multiparous Angus and Brahman cows grazing in the Chihuahuan Desert. J Anim Sci. 2002;80(9):2223-2333; Payne JM, Dew SM, Manston R. 1970. The use of a metabolic profile test in dairy herds. Vet Rec.1970;87:150-158; Pearson ES, Stephens MA. 1964.The ratio of range to standard deviation in the same normal sample. Biometrika. 1964;51:484-487; Rae DO, Kunkle WE, Chenoweth PJ, Sand RS, Tran T. 1996. Body condition: influences on beef cattle reproductive performance. AMMVEB (Ed.), XX Congreso Nacional de Buiatrı́a, Acapulco, Gro., México, Pp. 339–343; Rivas L. 2004. Convenio de Cooperación Técnica y Científica MADR – CIAT: Resultados, Adopción e Impacto 1999 - 2003. Documento de Trabajo No 194, Centro Internacional de Agricultura Tropical. Proyecto de Evaluación de Impacto, Cali, Colombia, Julio; Roy S, Roy M, Mishra S. Haematological and biochemical profile during gestation period in Sahiwal cows. Vet World. 2010;3:1:26-28; Singh R, Singha SPS, Singh R, Setia MS. Distribution of trace elements in blood, plasma and erythrocytes during different stages of gestation in buffalo (Bubalus Bubalis). Buffalo J. 1991;1:77-85; Smith GL, Friggens NC, Ashworth CJ, Chagunda MGGAssociation between body energy content in the dry period and post-calving production disease status in dairy cattle. Animal. 2017;11:9:1590-1598; Quintela A, Becerra JJ, Rey C, Díaz C, Cainzos J, Rivas F, Huanca W, Prieta A, Herradón PG. 2011. Perfiles metabólicos en preparto, parto y postparto en vacas de raza rubia gallega: estudio preliminar. Recursos Rurais. 2011;7:5-14; Romero-Treviño E M, Gutiérrez-Ornelas E, Bernal-Barragán H, Martínez-González J C, González-Muñoz M A y López-Pérez. Calidad nutricional de pastos, condición corporal y niveles de metabolitos sanguíneos de vacas de doble propósito a través del año en el norte de Veracruz. Liv Res Rural Develop. 2011;23:215; Roos TB, Vendramin L, Schwengler E, Goulart MA, Quevedo PS, Silva VM, Verde PML, Del Pino FAB, Timm CD, Gil-Turnes C, Correa MN. Avaliação de parâmetros do perfil metabólico e do leite em diferentes categorias de vacas leiteiras da raça Jersey em rebanhos do Sul do Rio Grande do Sul. Vet Foco. 2008;5:121-130; Said RAH, Zaky K, El Azab EA, Shaker M. Effect of age, pregnancy and certain pathological conditions on serum levels of calcium, phosphorus, total protein and protein bound polysaccharides in Fresian cattle. Zentralblatt für Veterinarmendinzin, Ser.A. 1964;11:685; Shope RE, Gowen JW. Cholesterol And Cholesterol Ester In The Blood Serum Of Cattle Late In Pregnancy And During The Early Lactation Period. J Exp Med. Jun 1928;30;48(1):25-30; Slavik P, Illek J, Zeleny T. Zinc and copper status of beef cattle in the Sumava region, Czech Republic, Acta Veterinaria Brno. 2006;75:485–488; Soca P, Carriquiry M, Claramun M, Gestido V, Meikle A. Metabolic and endocrine profiles of primiparous beef cows grazing native grassland. 1. Relationships between body condition score at calving and metabolic profiles during the transition period. Animal Production Science. http://dx.doi.org/10.1071/AN13250; Tabeleão VC, Goulart MA, Schwegler E, Weiser MA, Moura SV, Silva VM, Pereira VS, Pino FAB, Corrêa MN. Avaliação ruminal e metabólica de bovinos machos e fêmeas, mantidos em sistema de semi-confinamento. Arch Zootec. 2008;57(218):147-154; Taylor-Macallister C. Haematology and serum biochemistry evaluation in normal postpartum mares. Equine Vet J. 1997;29(3):234-235; Underwood EJ, Suttle NF. 1999. The Mineral Nutrition o f Livestock (3rd ed.). CABI Publishing, Wallingford, UK.; Vera RR, Tergas LE. 1986. Develoment of improved grazing system in the savannas of Tropical America. Proc. Second International Rangeland Congress, Adelaide, Australia. P.p. 107-111; Vera RR, Ramírez-Restrepo CA. Complementary use of neotropical savanna and grass-legume pastures for early weaning and effects on growth and metabolic status of weaners and inter-calving intervals of dams. Tropical Grasslands-Forrajes Tropicales. 2017;5(2):50-65; Villa NA, Osorio JM, Escobar D, Ceballos A. Indicadores bioquímicos del balance energético en el periparto de vacas Brahman en pastoreo en el trópico colombiano. Rev Cient. 2011;21(4):353-359; Ward G. Molybdenum toxicity and hypocuprosis in ruminants: A review. J Anim Sci. 1978;46:1078-1085; Weisbrot IM. 1985. Statistics for the clinical laboratory. Philadelphia: J.B. Lippincott Company, p. 198; Zambrano JW, Marques jr AP. Perfil metabólico de vacas mestiças leiteiras do pré-parto ao quinto mês da lactação. Zootecnia Trop. 2009;27(4):475-488; Zhang WC, Nakao T, Kida K, Moriyoshi M, Nakada K. Effect of nutrition during pregnancy on calf birth weights and viability and fetal membrane expulsion in dairy cattle. J Reprod Fertil. 2002;48:415-422; https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/download/565/pdf; Núm. 2 , Año 2019; 23; Orinoquia; https://repositorio.unillanos.edu.co/handle/001/2727; https://doi.org/10.22579/20112629.565

الاتاحة: https://repositorio.unillanos.edu.co/handle/001/2727
https://doi.org/10.22579/20112629.565

المؤلفون: Velásquez-Penagos, José G., Velásquez-Penagos, José H., Gutiérrez-Parrado, Sonia Lucía, Barajas-Pardo, Diana Patricia, Neira-Rivera, Eliana, Ortiz-Valdés, Ciro, Onofre-Rodríguez, Héctor G.

المصدر: https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/566.

مصطلحات موضوعية: Gonadotropin, sex steroid, gonadal maturation, fish reproduction, Gonadotropinas, esteroides sexuales, maduración gonadal, reproducción en peces

وصف الملف: application/pdf

Relation: Almansa E, Velásquez JG, Rodríguez GA. Efecto del uso de aguas provenientes de la producción petrolera en actividades agrícolas y pecuarias. Corpoica Cienc Tecnol Agropecu. 2018;19(2):403-420; Anchieta MC, Vale Filho VR, Colosimo E, Sampaio IBM, Andrade VJ. Descarte e congelabilidade do sêmen de touros de raças zebuínas e taurinas em central de inseminação artificial no Brasil. Arq Bras Med Vet Zootec. 2005;57(2):196-204; Barszcz K, Wiesetek D, Wasowick M, Kupczynska M. Bull semen collection and analysis for artificial insemination. J Agric Sci. 2012;4(3):1-10; Berg HF, Kommisrud E, Bai G, Gaustad ER, Klinkenberg G, Standerholen FB, et al. Comparison of sperm adenosine triphosphate content, motility and fertility of immobilized and conventionally cryopreserved Norwegian Red bull semen. Theriogenology. 2018:121:181-187; Burnett CR, Pratt SL, Long NM, Sell GS, Schrick FN. Assessment of semen quality and fertility in young growing beef bulls exposed to ergot alkaloids. Theriogenology 2018;118:219-224; Braundmeier AG, Demers J, Shanks R, Saacke R, Miller D. Examination of the binding ability of bovine spermatozoa to the zona pellucida as an indicador of fertility. J Androl. 2002;23(5):645-651; Blondin P, Beaulieu M, Fournier V, Morin M, Crawford L, Madan P, King WA. Analysis of bovine sexed sperm for IVF from sorting to the embryo. Theriogenology. 2009;71: 30-38; Brito L. A Multilaboratory study on the variability of bovine semen analysis. Theriogenology. 2016;85(2):254-266; Cabrera P, Pantoja C. Viabilidad espermática e integridade del acrosoma em sêmen congelado de toros nacionales. Rev Investig Vet Perú. 2012;23(2):192-200; Cardozo JA, Velásquez JG, Rodríguez G, Prieto E, Tarazona G, Espitia A. 2002. Evaluación reproductiva del macho bovino en condiciones tropicales. Plan de modernización tecnológica de la ganadería colombiana. Manual técnico.; Chenoweth PJ, McPherson FJ. Bull breeding soundness, semen evaluation and cattle productivity. Anim Reprod Sci. 2016;169:32-36; Contri A, Valorz C, Faustini M, Wegher L, Carluccio A. Effect of sperm preparation on CASA motility results in cryopreserved bull spermatozoa. Theriogenology. 2010;74: 424-435; Coy P, Romar R, Payton R, McCann L, Saxton A, Edwards L. Maintenance of meiotic arrest in bovine oocytes using the S-enantiomer of roscovitine: effects on maturation, fertilization and subsequent embryo development in vitro. Reproduction. 2005;129(1):19-26; Fair S, Lonergan P. Review: Understanding the causes of variation in reproductive wastage among bulls. Animal. 2018;12(s1):s53-s62. Doi:10.1017/S1751731118000964; Felipe-Pérez YE, Juárez ML, Hernández EO, Valencia JJ. Viability of fresh and frozen bull sperm compared by two staining techniques. Acta Vet Bras. 2008;2(4):123-130; Ferraz MAMM, Morató R, Yeste M, Arcarons N, Pena AI, Tamargo C, et al. 2014. Evaluation of sperm subpopulation structure in relation to in vitro sperm-oocyte interaction of frozen-thawed semen from Holstein bulls. Theriogenology. 2014;81:1067-1072; Flowers WL. Sperm characteristics that limit success of fertilization. J Anim Sci. 2013;9(7):3022-3029; Hidaka T, Fukumoto Y, Yamamoto S, Ogata Y, Horiuchi T. Variations in bovine embryo production between individual donors for OPU-IVF are closely related to glutathione concentrations in oocytes during in vitro maturation. Theriogenology. 2018;113:176-182; Kastelic JP, Thundathil JC. Breeding soundness evaluation and semen analysis for predicting bull fertility. Reprod Domest Anim. 2008;43(2):368-373; Khalil WA, El-Harairy MA, Zeidan AE, Hassan MA, Mohey-Elsaeed O. Evaluation of bull spermatozoa during and after cryopreservation: Structural and ultrastructural insights. International Journal of Veterinary Science and Medicine. 2018;6:s49-s56; Oliveira LZ, Paes de Arruda R, Cesar de Andrade AF, Carvalho Celeghini EC, Dos Santos RM, Beletti ME, et al. Assessment of field fertility and several in vitro sperm characteristics following the use of different Angus sires in a timed-AI program with suckled Nelore cows. Livest Sci. 2012;146:38-46; Orantes MA, Vilaboa J, Ortega E, Córdova V. Comportamiento de los comercializadores de ganado bovino en la región Centro del estado de Chiapas. Quehacer Científico en Chiapas. 2010;1(9):51-56; Páez EM, Corredor ES. Evaluación de la aptitud reproductiva del toro. Ciencia y Agricultura. 2014;11(2):49-59; Parkinson TJ. Evaluation of fertility and infertility in natural service bulls. Vet J. 2004;168(3):215-229. Doi:10.1016/j.tvjl.2003.10.017; Petherick JC. A review of some factors affecting the expression of libido in beef cattle, and individual bull and herd fertility. Appl Anim Behav Sci. 2004;90:185-205; Prinosilova P, Kopecká V, Hlavicová J, Kunetková M. Modified hypoosmotic swelling test for the assessment of boar and bull sperm sensitivity to cryopreservation. Acta Vet Brno. 2014;(83):313-319; Quintero MA, Mayorga JM, Cardona MW. El análisis seminal como herramienta para predecir el potencial reproductivo en toros. Journal of veterinary andrology (JVA). 2017;2(1):30-37; Restrepo BG, Úsuga SA, Rojano BA. Técnicas para el análisis de la fertilidad potencia del semen equino. CES Med Vet Zootec. 2013;8(1):69-81; Rosseto A. O uso de sondas fluorescentes na avaliação morfofuncional de espermatozóides bovinos. Rev Ciêne Agrár Belêm. 2005;43 junio/julio Suplemento; Ruiz SB, Ruiz HH, Mendoza NP, Oliva MA, Gutiérrez MF, Rojas MRI, et al. Caracterización reproductiva de toros Bos taurus y Bos indicus y sus cruzas en un sistema de monta natural y sin reposo sexual en el trópico mexicano. Revista científica UDO Agrícola. 2010;10(1):94-102; Thundathil JC, Dance AL, Kastelic JP. Fertility management of bulls to improve beef cattle productivity. Theriogenology. 2016;86(1):397-405; Vejarano OA, Sanabria RD, Trujillo GA. Diagnóstico de la capacidad reproductiva de toros en ganaderías de tres municipios del alto Magdalena. Rev MVZ Córdoba 2005;10(2):648-662; Velásquez JG, Canovas S, Barajas DP, Marcos J, Jiménes-Movilla M, Gutierrez R, et al. Role of Sialic Acid in Bovine Sperm–Zona Pellucida Binding. Mol Reprod Dev. 2007;74:617-628; Velho ALC, Menezes E, Dinh T, Kaya A, Topper E, Moura AA, Memili E. Metabolomic markers of fertility in bull seminal plasma. Plos One. 2018;13(4):e0195279. doi:10.1371 / journal.pone.0195279; Viana AGA, Martins AMA, Pontes AH, Fontes W, Castro MS, Ricart CAO, et al. Proteomic landscape of seminal plasma associated with dairy bull fertility. Nature. 2018(8):16323. Doi:10.1038/s41598-018-34152-w; Yániz JL, Palacín I, Vicente-Fiel S, Gosalvez J, López-Fernández C, Santolaria P. Evaluation of comercial kit base don acridine orange/propidium iodide to assess the plasma membrane integrity of ram sperm. Span J Agric Res. 2013;11(2):362-365; Yániz JL, Palacín I, Caycho KS, Soler C, Silvestre MA, Santolaria P. Determining the relationship between bull sperm kinematic subpopulations and fluorescence groups using an integrated sperm quality analysis technique. Reprod Fert Develop. 2018;(30):919-923; Youngquist RS, Threlfall WR. 2007. Current therapy in Large Animal Theriogenology. Second edition. Philadelphia, United States: Elsevier.; https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/download/566/pdf; Núm. 2 , Año 2019; 23; Orinoquia; https://repositorio.unillanos.edu.co/handle/001/2728; https://doi.org/10.22579/20112629.566

الاتاحة: https://repositorio.unillanos.edu.co/handle/001/2728
https://doi.org/10.22579/20112629.566

المؤلفون: Manuel Alvarado, Edison Serrano, Juan Carlos Sánchez, Luis Valladares

المصدر: Latin American Journal of Aquatic Research, Vol 43, Iss 4, Pp 632-640 (2015)

مصطلحات موضوعية: Merluccius australis, merluza austral, maduración gonadal, esteroides sexuales, sur de Chile, Aquaculture. Fisheries. Angling, SH1-691, Oceanography, GC1-1581, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-560X2015000400002&lng=en&tlng=en; https://doaj.org/toc/0718-560X

URL الوصول: https://doaj.org/article/80f650d55e614fe993b384c916c50602

المؤلفون: Quinzaños Ruiz, Cristina

المساهمون: García Unzueta, María Teresa, Ruiz Ochoa, David, Universidad de Cantabria

مصطلحات موضوعية: Biomarcador, SARS-CoV-2, Esteroides sexuales, Biomarker, Sex steroids

Relation: https://hdl.handle.net/10902/30588

الاتاحة: https://hdl.handle.net/10902/30588

المؤلفون: Casals, Gregori, Ferrer Costa, Roser, Urgell Rull, Eulàlia, Escobar-Morreale, Héctor F., Argente Oliver, Jesús, Sesmilo, Gemma, Biagetti, Betina

المساهمون: UAM. Departamento de Pediatría

مصطلحات موضوعية: esteroides sexuales, testosterona, estradiol, inmunoensayo, espectrometría de masas, Medicina

وصف الملف: application/pdf

Relation: Advances in Laboratory Medicine; https://doi.org/10.1515/almed-2022-0121; Advances in Laboratory Medicine 4.1 (2023): 61-69; 2628-491X (online); http://hdl.handle.net/10486/709133; 61; 69

الاتاحة: http://hdl.handle.net/10486/709133
https://doi.org/10.1515/almed-2023-0020

المؤلفون: Deborah Legorreta Peyton

المصدر: Avances en Psicología Latinoamericana, Vol 25, Iss 1, Pp 44-51 (2007)

مصطلحات موضوعية: climaterio, perimenopausia, esteroides sexuales, calidad de vida, síntomas psicológicos., Psychology, BF1-990

وصف الملف: electronic resource

Relation: http://redalyc.uaemex.mx/src/inicio/ArtPdfRed.jsp?iCve=79902505&iCveNum=7627; https://doaj.org/toc/1794-4724

URL الوصول: https://doaj.org/article/4bffdc1d1369413c946e893f3530b5a1

المؤلفون: Alves Farias, Inês

المساهمون: Morales Nin, Beatriz

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Aphanopus carbo, black scabbardfish, benthopelagic, NE Atlantic, population dynamics, migration, fatty acids, stable isotopes, sex steroids, otolith, trace elements, peix sable negra, bentopelàgic, NE Atlàntic, dinàmica de la població, migració, àcids grassos, isòtops estables, esteroids sexuals, otòlit, elements traça, sable negro, bentopelágico, Atlántico NE, dinámica poblacional, migración, ácidos grasos, isotopos estables, esteroides sexuales, otolito

Time: 57, 574

وصف الملف: 149 p.; application/pdf

Relation: http://hdl.handle.net/10803/673480

الاتاحة: http://hdl.handle.net/10803/673480

المؤلفون: Beatriz Helena Quinchía-R., Bernardo Agudelo-J., Jesús Alfredo Berdugo, Jorge Eliécer Ossal-L.

المصدر: Revista Facultad de Odontología Universidad de Antioquia, Vol 10, Iss 1, Pp 48-56 (1998)

مصطلحات موضوعية: sex asteroid hormones, lipopolysaccharide, prevotella intermedia, interleukin 1b, fibroblasts, hormonas esteroides sexuales, lipopolisacárido, prevottella intermedia, interleukina1b, fibroblastos, Dentistry, RK1-715

وصف الملف: electronic resource

Relation: https://revistas.udea.edu.co/index.php/odont/article/view/327024/20784249; https://doaj.org/toc/0121-246X; https://doaj.org/toc/2145-7670

URL الوصول: https://doaj.org/article/e6ca4ce575d549c18de4927deeba1210

المؤلفون: Nieto-Vera, Mónica T., Rodríguez-Pulido, José A., Góngora-Orjuela, Agustín

المصدر: ORINOQUIA, Volume: 24, Issue: 1, Pages: 52-63, Published: JUN 2020

مصطلحات موضوعية: Gonadotropin, sex steroid, gonadal maturation, reproducción en peces, esteroides sexuales, maturação gonadal, reprodução em peixes, esteroides sexuais, Gonadotropinas, fish reproduction, maduración gonadal, Gonadotrofinas

وصف الملف: text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_______618::f4768401e2a23265482558082b0cb054
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-37092020000100052&lng=en&tlng=en

المؤلفون: Deborah Legorreta Peyton

المصدر: Avances en Psicología Latinoamericana, Vol 25, Iss 1 (2010)

مصطلحات موضوعية: climaterio, perimenopausia, esteroides sexuales, calidad de vida, síntomas psicológicos, Psychology, BF1-990

وصف الملف: electronic resource

Relation: https://revistas.urosario.edu.co/index.php/apl/article/view/556; https://doaj.org/toc/1794-4724; https://doaj.org/toc/2145-4515

URL الوصول: https://doaj.org/article/ab996f43ff624c43a4bfb456d2226166