- -

Managing Sexual Receptivity and Ovulation Induction in Rabbit Does: Evidence from Recent Research

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

Managing Sexual Receptivity and Ovulation Induction in Rabbit Does: Evidence from Recent Research

Mostrar el registro sencillo del ítem

Ficheros en el ítem

dc.contributor.author Rebollar, Pilar G. es_ES
dc.contributor.author Arias-Álvarez, María es_ES
dc.contributor.author Lorenzo, Pedro L. es_ES
dc.contributor.author García-García, Rosa M. es_ES
dc.date.accessioned 2023-07-13T12:05:52Z
dc.date.available 2023-07-13T12:05:52Z
dc.date.issued 2023-06-30
dc.identifier.issn 1257-5011
dc.identifier.uri http://hdl.handle.net/10251/194892
dc.description.abstract [EN] The sexual receptivity and ovulation induction of the reproductive rabbit are key points determining their success in productive life. Adequate synchronisation of the sexual receptivity methods of inseminated rabbit does unquestionably favours fertility and prolificacy outcomes. This review aims to bring together the different methods applied in synchronising primiparous rabbits and the consequences at metabolic, endocrine and ovarian levels, as well as in the embryonic, foetal and post-natal development that our research group has studied over the years. Likewise, the latest advances regarding ovulation induction in the rabbit are described, as well as the search for alternatives to the intramuscular injection of synthetic analogues of gonadotropins and seminal plasma components that could be involved in this process. Different experiments performed with a physiological basis confirm that nerve stimulation during artificial insemination or coitus is especially important in the ovulation induction reflex in rabbit females. es_ES
dc.language Inglés es_ES
dc.publisher Universitat Politècnica de València es_ES
dc.relation.ispartof World Rabbit Science es_ES
dc.rights Reconocimiento - No comercial - Compartir igual (by-nc-sa) es_ES
dc.subject Synchronization es_ES
dc.subject Oocyte es_ES
dc.subject Embryo es_ES
dc.subject Spermatozoa es_ES
dc.subject Semen es_ES
dc.subject Rabbit es_ES
dc.title Managing Sexual Receptivity and Ovulation Induction in Rabbit Does: Evidence from Recent Research es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.4995/wrs.2023.18762
dc.rights.accessRights Abierto es_ES
dc.description.bibliographicCitation Rebollar, PG.; Arias-Álvarez, M.; Lorenzo, PL.; García-García, RM. (2023). Managing Sexual Receptivity and Ovulation Induction in Rabbit Does: Evidence from Recent Research. World Rabbit Science. 31(2):77-92. https://doi.org/10.4995/wrs.2023.18762 es_ES
dc.description.accrualMethod OJS es_ES
dc.relation.publisherversion https://doi.org/10.4995/wrs.2023.18762 es_ES
dc.description.upvformatpinicio 77 es_ES
dc.description.upvformatpfin 92 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 31 es_ES
dc.description.issue 2 es_ES
dc.identifier.eissn 1989-8886
dc.relation.pasarela OJS\18762 es_ES
dc.description.references Abir R., Fisch B., Jin S., Barnnet M., Ben-Haroush A., Felz, C., Kessler-Icekson D., Feldberg D., Ao A. 2005. Presence of NGF and its receptors in ovaries from human fetuses and adults. Mol. Hum. Reprod., 11: 229-236. https://doi.org/10.1093/molehr/gah164 es_ES
dc.description.references Adams G.P., Ratto M.H., Huanca W., Singh J. 2005. Ovulation-inducing factor in the seminal plasma of alpacas and llamas. Biol. Reprod., 73: 452-457. https://doi.org/10.1095/biolreprod.105.040097 es_ES
dc.description.references Arias-Álvarez M., García-García M.R., Rebollar P.G., Revuelta L., Millán P., Lorenzo P.L. 2009a. Influence of metabolic status on oocyte quality and follicular characteristics at different postpartum periods in primiparous rabbit does. Theriogenol., 72: 612-623. https://doi.org/10.1016/j.theriogenology.2009.04.017 es_ES
dc.description.references Arias-Álvarez M., García-García M.R., Rebollar P.G., Nicodemus N., Revuelta L., Millán P., Lorenzo P.L. 2009b. Effects of a lignin-rich fibre diets on productive, reproductive and endocrine parameters in nulliparous rabbit does. Livest. Sci., 123: 107-115. https://doi.org/10.1016/j.livsci.2008.10.013 es_ES
dc.description.references Arias-Álvarez M., García-García R.M., Torres-Rovira L., González-Bulnes A., Rebollar P.G., Lorenzo, P.L. 2010a. Influence of hormonal and non-hormonal estrus synchronization methods on follicular and oocyte quality in primiparous lactating does at early postpartum period. Theriogenol., 73: 26-35. https://doi.org/10.1016/j.theriogenology.2009.07.017 es_ES
dc.description.references Arias-Álvarez M., García-García R.M., Torres-Rovira L., González-Bulnes A., Rebollar P.G., Lorenzo P.L. 2010b. Influence of leptin on in vitro maturation and steroidogenic secretion of cumulus-oocyte complexes through JAK2/STAT3 and MEK 1/2 pathways in the rabbit model. Reproduction, 139: 23-32. https://doi.org/10.1530/rep-09-0309 es_ES
dc.description.references Arias-Álvarez M., García-García R.M., Rebollar P.G., Nicodemus N., Millán P. Revuelta L., Lorenzo P.L. 2010c. Follicular, Oocyte and Embryo Features Related to Metabolic Status in Primiparous Lactating does Fed with High-Fibre Rearing Diets. Reprod. Dom. Anim., 45: e91-e100. https://doi.org/10.1111/j.1439-0531.2009.01528.x es_ES
dc.description.references Arias-Álvarez M., García-García R.M., Rebollar P.G., Gutiérrez-Adán A., López-Béjar M., Lorenzo P.L. 2013. Ovarian response and embryo gene expression patterns after nonsuperovulatory gonadotropin stimulation in primiparous rabbits does. Theriogenol., 79: 323-330. https://doi.org/10.1016/j.theriogenology.2012.09.019 es_ES
dc.description.references Arias-Álvarez M., Pericuesta E., Gutiérrez-Adán A., Rebollar P.G.,vLorenzo P.L., Garcia-Garcia R.M. 2022. Gene expression patterns of NGF- TrKA- p75 system in cumulus- oocyte complexes and early embryos in rabbit. In Proc.: 16th International Congress of the Spanish Society for Animal es_ES
dc.description.references Reproduction (AERA), León, España, 20-22 October 2022. es_ES
dc.description.references Ayer-LeLievre C., Olson L., Ebendal T., Hallböök F., Persson H. 1988. Nerve growth factor mRNA and protein in the testis and epididymis of mouse and rat. Proc. Nat. Acad. Sci., 85: 2628-2632. https://doi.org/10.1073/pnas.85.8.2628 es_ES
dc.description.references Barboni B., Mattioli M., Gioia L., Turriani M., Capacchietti G., Berardinelli P., Bernabò N. 2002. Preovulatory rise of NGF in ovine follicular fluid: possible involvement in the control of oocyte maturation. Microsc. Res. Tech., 59: 516-521. https://doi.org/10.1002/jemt.10230 es_ES
dc.description.references Bogle O.A., Ratto, M.H., Adams, G.P. 2011. Evidence for the conservation of biological activity of ovulation-inducing factor (OIF) in seminal plasma. Reproduction, 142: 277-283. https://doi.org/10.1530/rep-11-0042 es_ES
dc.description.references Bolet G., Brun J.M., Lechevestrier S., López M., Boucher, S. 2004. Evaluation of reproductive performance of eight rabbit breeds on experimental farms. Anim. Res., EDP Sciences, 53: 59-65. https://doi.org/10.1051/animres:2003043 es_ES
dc.description.references Calzà L., Giardino L., Giuliani A., Aloe L., Levi-Montalcini, R. 2001. Nerve growth factor control of neuronal expression of angiogenetic and vasoactive factors. Proc. Nat. Acad. Sci., 98: 4160-4165. https://doi.org/10.1073%2Fpnas.051626998 es_ES
dc.description.references Cardinali R., Dal Bosco A., Bonanno A., Di Grigoli A., Rebollar P.G., Lorenzo P.L., Castellini C. 2008. Connection between body condition score, chemical characteristics of body and reproductive traits of rabbit does. Livest. Sci., 116: 209-215. https://doi.org/10.1016/j.livsci.2007.10.004 es_ES
dc.description.references Carrasco R.A., Singh J., Adams G.P. 2016. The dynamics of TrKA expression in the bovine ovary are associated with a luteotrophic effect of ovulation-inducing factor/nerve growth factor (OIF/NGF). Reprod. Biol. Endocrinol., 14: 47. https://doi.org/10.1186%2Fs12958-016-0182-9 es_ES
dc.description.references Castellini C. 1996. Recent advances in rabbit artificial insemination. In Proc.: 6th World Rabbit Congress, 9-12 July, 1996. Toulouse. France, 2: 13-26. es_ES
dc.description.references Castellini C. 2007. Reproductive activity and welfare of rabbit does. It. J. Anim. ScI., 6: 743-747. https://doi.org/10.4081/ijas.2007.1s.743 es_ES
dc.description.references Castellini C., Brecchia G., Canali C., Boiti C. 2000. Effect of different percentages of sucrose in drinking water on reproductive performance and energy balance of primiparous lactating rabbit does. In Proc.: 7th World Rabbit Congress, 4-7 July, 2000, Valencia, Spain, vol C.: 161-166. es_ES
dc.description.references Castellini C., Dal Bosco A., Mugnai C. 2003. Comparison of different reproduction protocols for rabbit does: effect of litter size and mating interval. Livest. Prod. Sci., 83: 131-139. https://doi.org/10.1016/S0301-6226(03)00070-8 es_ES
dc.description.references Castellini C., Dal Bosco A., Cardinali R. 2006. Long effect of postweaning rhythm on the body fat and performance of rabbit doe. Reprod. Nutr. Develop., EDP Sciences, 46: 195-204. https://doi.org/10.1051/rnd:2006009 es_ES
dc.description.references Castellini C., Dal Bosco A., Arias-Álvarez M., Lorenzo P.L., Cardinali R., Rebollar, PG. 2010. The main factors affecting the reproductive performance of rabbit does, a review. Anim. Reprod. Sci., 122: 174-182. https://doi.org/10.1016/j.anireprosci.2010.10.003 es_ES
dc.description.references Castellini C., Mattioli S., Dal Bosco A., Collodel G., Pistilli A., Stabile A.M., Macchioni L., Mancuso F., Luca G., Rende M. 2019. In vitro effect of nerve growth factor on the main traits of rabbit sperm. Reprod. Biol. Endocrinol., 17: 93. https://doi.org/10.1186%2Fs12958-019-0533-4 es_ES
dc.description.references Castellini C., Mattioli S., Dal Bosco A., Cotozzolo E., Mancinelli A.C., Rende M., Stabile A.M., Pistilli A. 2020. Nerve growth factor receptor role on rabbit sperm storage. Theriogenol., 153: 54-61. https://doi.org/10.1016/j.theriogenology.2020.04.042 es_ES
dc.description.references Cervantes M.P., Palomino J.M., Adams G.P. 2015. In vivo imaging in the rabbit as a model for the study of ovulation-inducing factors. Lab. Anim., 49: 1-9. https://doi.org/10.1177/0023677214547406 es_ES
dc.description.references Cervera C., Costera A., Moya J., Fernández-Carmona J., Pascual J.J. 2001. Utilización de piensos de alfalfa en la recría de conejas reproductoras. In Proc.: XXVI Symposium de ASESCU. 23-24 May, 2001. 1st Iberic Rabbit Congress. Aveiro, Portugal., 156-163. es_ES
dc.description.references Chao M.V., Hempstead B.L. 1995. p75 and Trk: a tworeceptor system. Trends Neurosci., 18: 321-326. https://doi.org/10.1016/0166-236(95)93922-K es_ES
dc.description.references Chaves R.N., Alves A.M.C.V., Duarte A.B.G., Araújo V.R., Celestino J.J.H., Matos M.H.T., Lopes C.A.P., Campello C.C, Nam K.P.O. Báo S.N., Figueiredo J.R. 2010. Nerve growth factor promotes the survival of goat preantral follicles cultured in vitro. Cells Tissues Organs, 192: 272-282. https://doi.org/10.1159/000317133 es_ES
dc.description.references Chen Y., Dicou E., Djakiew D. 1997. Characterization of nerve growth factor precursor protein expression in rat round spermatids and the trophic effects of nerve growth factor in the maintenance of Sertoli cell viability. Mol. Cell. Endocrinol., 127: 129-136. https://doi.org/10.1016/s0303-7207(96)04001-4 es_ES
dc.description.references Clegg D.O., Large T.H., Bodary S.C., Reichardt L.F. 1989. Regulation of nerve growth factor mRNA levels in developing rat heart ventricle is not altered by sympathectomy. Develop. Biol., 134: 30-37. https://doi.org/10.1016/0012-1606(89)90075-4 es_ES
dc.description.references Cohen S., Levi-Montalcini R. 1956. A nerve growth-stimulating factor isolated from snake venom. Proc. Nat. Acad. Sci., 42: 571-574. https://doi.org/10.1073%2Fpnas.42.9.571 es_ES
dc.description.references Crispo M., dos Santos-Neto P.C., Vilariño M., Mulet A P., de León A., Barbeito L. Menchaca A. 2016. Rapid Communication: Nerve growth factor influences cleavage rate and embryo development in sheep. J. Anim. Sci., 94: 4447-4451. https://doi.org/10.2527/jas.2016-0736 es_ES
dc.description.references Cupp A.S., Kim G.H., Skinner M.K. 2000. Expression and action of neurotropin-3 and nerve growth factor in embryonic and early postnatal rat testis development. Biol. Reprod., 63: 1617-1628. https://doi.org/10.1095/biolreprod63.6.1617 es_ES
dc.description.references Dal Bosco A., Rebollar P.G., Boiti C., Zerani M., Castellini C. 2011. Ovulation induction in rabbit does: current knowledge and perspectives. Anim. Reprod. Sci., 129: 106-117. https://doi.org/10.1016/j.anireprosci.2011.11.007 es_ES
dc.description.references Dal Bosco A., Cardinali R., Brechia G., Rebollar P.G., Fatnassi M., Millán P., Mattioli S., Castellini C. 2014. Induction of ovulation in rabbits by adding Lecirelin to the seminal dose: In vitro and in vivo effects of different excipients. Anim. Reprod. Sci., 150: 44-49. https://doi.org/10.1016/j.anireprosci.2014.08.009 es_ES
dc.description.references Dissen G.A., Romero, C., Hirshfield A.N., Ojeda S.R. 2001. Nerve growth factor is required for early follicular development in the mammalian ovary. Endocrinol., 142: 2078-2086. https://doi.org/10.1210/endo.142.5.8126 es_ES
dc.description.references Dissen G.A., Garcia-Rudaz C., Paredes A., Mayer C., Mayerhofer A., Ojeda S.R. 2009. Excessive ovarian production of nerve growth factor facilitates development of cystic ovarian morphology in mice and is a feature of polycystic ovarian syndrome in humans. Endocrinol., 150: 2906-2914. https://doi.org/10.1210/en.2008-1575 es_ES
dc.description.references Djakiew D. 1992. Role of nerve growth factor-like protein in the paracrine regulation of prostate growth. J. Androl., 13: 476-487. https://doi.org/10.1002/j.1939-4640.1992.tb00341.x es_ES
dc.description.references Dongliang Lv., Mengjie Z., Jie N., Weidong L., Yijie R., Dawei Z., Jianhong H. 2023. NGF regulates Sertoli cells growth and prevents LPS-induced junction protein damage via PI3K/AKT/NFkB signaling. Theriogenol., 195: 138-148. https://doi.org/10.1016/j.theriogenology.2022.10.017 es_ES
dc.description.references Fernández-Carmona J., Pascual J.J., Cervera C. 2000. The use of fat in rabbit diets. World Rabbit Science, 8: 29-59. es_ES
dc.description.references Fernández-Pacheco C., Millán P., Rodríguez M., Formoso-Rafferty N., Velasco B., Rebollar P.G. 2021a. Pituitary and ovarian hormones: is their plasma concentration affected by litter size in primiparous lactating rabbit does? World Rabbit Science, 29: 162-168. https://doi.org/10.4995/wrs.2021.15122 es_ES
dc.description.references Fernández-Pacheco C., Millán P., Rodríguez M., Formoso-Rafferty N., Sánchez-Rodríguez A., Lorenzo P.L., Arias-Álvarez M., García-García R.M., Rebollar, P.G. 2021b. Influence of different regimes of moderate maternal feed restriction during pregnancy of primiparous rabbit does on long-term metabolic energy homeostasis, productive performance and welfare. Animals, 11: 2736. https://doi.org/10.3390%2Fani11092736 es_ES
dc.description.references Flood M.R., Gage T.L., Bunch T.D. 1993. Effect of various growth-promoting factors on preimplantation bovine embryo development in vitro. Theriogenol., 39: 823-833. https://doi.org/10.1016/0093-691X(93)90421-Z es_ES
dc.description.references García-García R.M., Arias-Álvarez M., Rebollar P.G., Revuelta L., Lorenzo P.L. 2009. Influence of different reproductive rhythms on serum estradiol and testosterone levels, features of follicular population and atresia rate, and oocyte maturation in controlled suckling rabbits. Anim. Reprod. Sci., 114: 423-433. https://doi.org/10.1016/j.anireprosci.2008.10.007 es_ES
dc.description.references García-García R.M., Sakr O., Velasco B., Aguado F., Lorenzo P.L., Rebollar P.G. 2010. La duración del suministro de propilenglicol a conejas primíparas afecta al peso y viabilidad de sus camadas. Bol. Cunic., 163: 39-46. es_ES
dc.description.references García-García R.M., Masdeu M., Sánchez-Rodríguez A., Millán P., Arias-Álvarez M., Sakr O.G., Rebollar P.G. 2018a. β-nerve growth factor identification in male rabbit genital tract and seminal plasma and its role in ovulation induction in rabbit does. It. J. Anim. Sci., 17: 442-453. https://doi.org/10.1080/1828051X.2017.1382315 es_ES
dc.description.references García-García R.M., Arias-Álvarez M, Sánchez Rodríguez A., Rebollar P.G., Lorenzo P.L. 2018b. NGF system is differentially expressed in the ovary, oviduct and uterus of rabbit does although independent of serum hormonal levels. Reprod. Dom. Anim., 53. Suppl 2: 88. es_ES
dc.description.references García-García R.M., Arias-Álvarez M., Sánchez-Rodríguez A., Lorenzo P.L., Rebollar P.G. 2020. Role of nerve growth factor in the reproductive physiology of female rabbits: a review. Theriogenol., 150: 321-328 https://doi.org/10.1016/j.theriogenology.2020.01.070 es_ES
dc.description.references García-García R.M., Arias-Álvarez M., Millán P., Rodríguez M., Sánchez-Rodríguez A., Lorenzo P.L., Rebollar P.G. 2021a. Gestation Food Restriction and Refeeding Compensate Maternal Energy Status and Alleviate Metabolic Consequences in Juvenile Offspring in a Rabbit Model. Nutrients, 13: 310. https://doi.org/10.3390/nu13020310 es_ES
dc.description.references García-García R.M., Arias-Álvarez M., Rodríguez M., Sánchez-Rodríguez A., Formoso-Rafferty N., Lorenzo P.L., Rebollar P.G. 2021b. Effects of feed restriction during pregnancy on maternal reproductive outcome, foetal hepatic IGF gene expression and offspring performance in the rabbit. Animal, 15: 100382. https://doi.org/10.1016/j.animal.2021.100382 es_ES
dc.description.references Gurr M.I., Harwood J.L., Frayn K.N. 2002. Lipid biochemistry: an introduction. 5th ed. Oxford, UK: Blackwell Science Ltd. https://doi.org/10.1002/9780470774366 es_ES
dc.description.references Harper G.P., Thoenen H. 1980. The distribution of nerve growth factor in the male sex organs of mammals. J. Neurochem., 34: 893-903. https://doi.org/10.1111/j.1471-4159.1980.tb09663.x es_ES
dc.description.references Hughes J., Kwong W.Y., Li D., Salter A.M., Lea R.G., Sinclair K.D. 2010. Effects of omega-3 and -6 polyunsaturated fatty acids on ovine follicular-cell steroidogenesis, embryo development and molecular markers of fatty acid metabolism. Reproduction, 141: 105-112. https://doi.org/10.1530/REP-10-0337 es_ES
dc.description.references Jin W., Tanaka A., Watanabe G., Matsuda H., Taya, K. 2010. Effect of NGF on the motility and acrosome reaction of golden hamster spermatozoa in vitro. J. Reprod.. Develop., 56: 437-443. https://doi.org/10.1262/jrd.09-219n es_ES
dc.description.references Katz D.M., Erb M., Lillis R., Neet K. 1990. Trophic regulation of nodose ganglion cell development: evidence for an expanded role of nerve growth factor during embryogenesis in the rat. Experimental Neurology, 110: 1-10. https://doi.org/10.1016/0014-4886(90)90046-U es_ES
dc.description.references Kershaw-Young C.M., Druart X., Vaughan J., Maxwell W.M.C. 2012. β-Nerve growth factor is a major component of alpaca seminal plasma and induces ovulation in female alpacas. Reprod., Fert. Develop., 24: 1093-1097. https://doi.org/10.1071/rd12039 es_ES
dc.description.references Kouba M., Benatmane F., Blochet J.E., Mourot J. 2008. Effect of a linseed diet on lipid oxidation, fatty acid composition of muscle, perirenal fat, and raw and cooked rabbit meat. Meat Sci., 80: 829-834. https://doi.org/10.1016/j.meatsci.2008.03.029 es_ES
dc.description.references Kumar S., Sharma V.K., Singh S., Hariprasad G.R., Mal G., Srinivasan A., Yadav S. 2013. Proteomic identification of camel seminal plasma: purification of β-nerve growth factor. Anim. Reprod. Sci., 136: 289-295. https://doi.org/10.1016/j.anireprosci.2012.11.001 es_ES
dc.description.references Lebas F., Theau-Clment M., Remy B., Drion P.J., Beckers F. 1996. Production of anti-PMSG antibodies and its relation to the productivity of rabbit does. World Rabbit Science, 4: 57-62. https://doi.org/10.4995/wrs.1996.271 es_ES
dc.description.references Levanti M.B., Germanà A., Abbate F., Montalbano G., Vega J.A., Germanà G. 2005. TrkA and p75NTR in the ovary of adult cow and pig. J. Anat., 207: 93-96. https://doi.org/10.1111/j.1469-7580.2005.00423.x es_ES
dc.description.references Li C., Zhou X. 2013. The potential roles of neurotrophins in male reproduction. Reproduction, 145: R89-R95. https://doi.org/10.1530/REP-12-0466 es_ES
dc.description.references Li C., Watanabe G., Weng Q., Jin W., Furuta C., Suzuki A.K., Kawaguchi M., Taya, K. 2005. Expression of nerve growth factor (NGF), and its receptors TrkA and p75 in the reproductive organs of the adult male rats. Zoological Sci., 22: 933-937. https://doi.org/10.2108/zsj.22.933 es_ES
dc.description.references Lin D.S., Anderson G.J., Connor W.E. 1991. High levels of the (n-6) fatty acid 4, 7, 10, 13, 16-docosapentaenoate in the retinas of rabbits are reduced by feeding dietary fish oil from birth to adult life. J. Nutr. 121: 1924-1931. https://doi.org/10.1093/jn/121.12.1924 es_ES
dc.description.references Linher-Melville K., Li J. 2013. The roles of glial cell line-derived neurotrophic factor, brain-derived neurotrophic factor and nerve growth factor during the final stage of folliculogenesis: a focus on oocyte maturation. Reproduction, 145: R43-R54. https://doi.org/10.1530/rep-12-0219 es_ES
dc.description.references López-Tello J., Arias-Álvarez M., Jiménez-Martínez M.A., Barbero-Fernández A., García R.M., Rodríguez M., Lorenzo P.L., Torres-Rovira L., Astiz S., González-Bulnes A. 2016. The effects of sildenafil citrate and haemodynamics in a rabbit model of intaruterine growth restriction. Reprod. Fertil. Dev., 29: 1239-1248. https://doi.org/10.1071/RD15330 es_ES
dc.description.references López-Tello J., Arias-Álvarez M., Jimenez-Martinez M.A., Garcia-Garcia R.M., Rodríguez, M., González P.L.L., Bermejo-Poza R., González-Bulnes A., Rebollar, P.G. 2017. Competition for materno-fetal resource partitioning in a rabbit model of undernourished pregnancy. PLoS ONE, 12: e0169194. https://doi.org/10.1371/journal.pone.0169194 es_ES
dc.description.references Lorenzo P.L., García-García R.M., Árias-Álvarez M., Rebollar P.G. 2014. Reproductive and nutritional management on ovarian response and embryo quality on rabbit does. Reprod. Domes. Anim., 49: 49-55. https://doi.org/10.1111/rda.12367 es_ES
dc.description.references Manal A.F., Tony M.A., Ezzo O.H. 2010. Feed restriction of pregnant nulliparous rabbit does: Consequences on reproductive per-formance and maternal behaviour. Anim. Reprod. Sci. 2010, 120: 179-186. https://doi.org/10.1016/j.anireprosci.2010.03.010 es_ES
dc.description.references Maranesi M., Zerani M., Leonardi L., Pistilli A., Arruda-Alencar J., Stabile A.M., Rende M., Castellini C., Petrucci L., Parillo F., Moura A., Boiti C. 2015. Gene expression and localization of NGF and its cognate receptors NTRK 1 and NGFR in the sex organs of male rabbits. Reprod. Domest. Anim., 50: 918-925. https://doi.org/10.1111/rda.12609 es_ES
dc.description.references Maranesi M., Parillo F., Leonardi L., Rebollar P.G., Alonso B., Petrucci L., Gobetti A., Boiti C., Arrua-alencar J., Moura A., Zerani M. 2016. Expression of nerve growth factor and its receptors in the uterus of rabbits: functional involvement in prostaglandin synthesis. Domes. Anim. Endocrinol., 56: 20-28. https://doi.org/10.1016/j.domaniend.2016.02.001 es_ES
dc.description.references Maranesi M., Petrucci L., Leonardi L., Piro F., Rebollar P.G., Millán P., Cocci P., Vullo C., Parillo F., Moura A., González-Mariscal G., Boiti C., Zerani M. 2018. New insights on a NGF-mediated pathway to induce ovulation in rabbits (Oryctolagus cuniculus). Biol. Reprod., 98: 634-643. https://doi.org/10.1093/biolre/ioy041 es_ES
dc.description.references Marei W.F., Wathes D.C., Fouladi-Nashta, A.A. 2009. The effect of linolenic acid on bovine oocyte maturation and development. Biol. Reprod., 81: 1064-1072. https://doi.org/10.1095/biolreprod.109.076851 es_ES
dc.description.references Maruccio L., Castaldo L., D’Angelo L., Gatta C., Lucini C., Cotea C., Solcan C., Nechita E.L. 2016. Neurotrophins and specific receptors in the oviduct tracts of Japanese quail (Coturnix coturnix japonica). Ann. Anat., 207: 38-46. https://doi.org/10.1016/j.aanat.2016.04.033 es_ES
dc.description.references Masdeu M., García-García R.M., Millán P., Revuelta L., Sakr O.G., Blanco P.G., Cortegano D., Lorenzo P.L., Rebollar, P.G. 2012. 188 effect of rabbit seminal plasma in ovulating response. Reprod., Fert. Develop., 25: 243-243. https://doi.org/10.1071/RDv25n1Ab188 es_ES
dc.description.references Masdeu M., García-García R.M., Cardinali R., Millán P., Arias-Álvarez M., Castellini C., Lorenzo P.L., Rebollar, P.G. 2015. Induction of ovulation in rabbit does using purified nerve growth factor and camel seminal plasma. In: 41st Annual Conference of the IETS, 10-13 January 2015, Versalles France. p. 1. http://www.iets.org/2015/ es_ES
dc.description.references Mayerhofer A., Dissen G.A., Parrot J.A., Hill D.F., Mayerhofer D., Garfield R.E., Ojeda S.R. 1996. Involvement of nerve growth factor in the ovulatory cascade: trkA receptor activation inhibits gap junctional communication between thecal cells. Endocrinol., 137: 5662-5670. https://doi.org/10.1210/endo.137.12.8940397 es_ES
dc.description.references Minuti A., Bani P., Piccioli-Cappelli O., Uboldi O., Bacciu N., Trevisi E. 2015. Metabolic and biochemical changes in plasma of the periparturient rabbit does with different litter size. Animals, 9: 614-621. https://doi.org/10.1017/s1751731114002675 es_ES
dc.description.references Miralles F., Philippe P., Czernichow P., Scharfmann R. 1998. Expression of nerve growth factor and its high-affinity receptor Trk-A in the rat pancreas during embryonic and fetal life. J. Endocrinol., 156: 431-439. https://doi.org/10.1210/endo.137.12.8940397 es_ES
dc.description.references Moret B. 1980. Comportement d’oestrus chez la lapine. Cuniculture, 33: 159-161. es_ES
dc.description.references Mourvaki E., Cardinali R., Dal Bosco A., Corazzi L., Castellini C. 2010. Effects of flaxseed dietary supplementation on sperm quality and on lipid composition of sperm subfractions and prostatic granules in rabbit. Theriogenol., 73: 629-637. https://doi.org/10.1016/j.theriogenology.2009.10.019 es_ES
dc.description.references Nafeaa A., Ahmed S.A.E., Fat Hallah S. 2011. Effect of feed restriction during pregnancy on performance and productivity of New Zealand white rabbit does. Vet. Med. Int., 2011: 839737. https://doi.org/10.4061/2011/839737 es_ES
dc.description.references Nico B., Mangieri D., Benagiano V., Crivellato E., Ribatti D. 2008. Nerve growth factor as an angiogenic factor. Microvascular Res., 75: 135-141. https://doi.org/10.1016/j.mvr.2007.07.004 es_ES
dc.description.references Otten U., Ehrhard P., Peck R. 1989. Nerve growth factor induces growth and differentiation of human B lymphocytes. Proc. Nat. Acad. Sci., 86: 10059-10063. https://doi.org/10.1073%2Fpnas.86.24.10059 es_ES
dc.description.references Papp B.A., Somfai T., Tartaglione M., Varga E., Gardon J.C. 2005. The effect of nerve growth factor on nuclear progression of porcine oocytes during in vitro maturation and embryo development. Acta Vet. Hung., 53: 91-101. https://doi.org/10.1556/avet.53.2005.1.9 es_ES
dc.description.references Palumbo M.A., Giuffrida E., Gulino F.A., Leonardi E., Cantarella G., Bernardini R. 2013. Nerve growth factor (NGF) levels in follicular fluid of infertile patients undergoing to in vitro fertilization (IVF) cycle. Gynaecol. Endocrinol., 29: 1002-1004. https://doi.org/10.3109/09513590.2013.829450 es_ES
dc.description.references Partridge G.G., Daniels Y., Fordyce R.A. 1986. The effects of energy intake during pregnancy in doe rabbits on pup birth weight, milk output and maternal body composition change in the ensuing lactation. J. Agric. Sci., 107: 697-708. https://doi.org/10.1017/S0021859600069859 es_ES
dc.description.references Pascual J.J., Cervera C., Fernández-Carmona J. 2002. A feeding program for young rabbit does based on lucerne diets. World Rabbit Sci., 10: 7-13. https://doi.org/10.4995/wrs.2002.471 es_ES
dc.description.references Pascual J.J., Savietto D., Cervera C., Baselga M. 2013. Resources allocation in reproductive rabbit does: a review of feeding and genetic strategies for suitable performance. World Rabbit Sci., 21: 123-144. https://doi.org/10.4995/wrs.2013.1236 es_ES
dc.description.references Pei Y. 2010. Effect of nerve growth factor (NGF) on the development of preimplantation rabbit embryos in vitro. Vet. Res. Comm., 34: 11-18. https://doi.org/10.1007/s11259-009-9325-1 es_ES
dc.description.references Peiretti P.G., Meineri G. 2010. Effects of diets with increasing levels of golden flaxseed on carcass characteristics, meat quality and lipid traits of growing rabbits. It. J. Anim. Sci., 9(e70): 372-377. https://doi.org/10.4081/ijas.2010.e70 es_ES
dc.description.references Quintela L.A., Peña A.I., Vega M.D., Gullón J., Prieto C., Barrio M., Becerra J.J., Herradón P.G. 2009. Reproductive performance of rabbit does artificially inseminated via intravaginal administration of [des-Gly 10, d-Ala6]-LHRH ethylamide as ovulation inductor. Reprod. Domest. Anim., 44: 829-833. https://doi.org/10.1111/j.1439-0531.2008.01095.x es_ES
dc.description.references Quiroga A.C., García-García R.M., Arias-Álvarez M., Gimeno-Martos S., Lorenzo P.L., Rebollar P.G. 2022. Ovulation induction in rabbit does using microencapsulated rrbetaNGF. World Rabbit Sci., 30: 244. https://doi.org//10.4995/wrs.2022.17799 es_ES
dc.description.references Ramírez V.D., Soufi W.L. 1994. Neuroendocrine control of the rabbit ovarian cycle. In: Knobil, E, Neill, JD (eds) The Physiology of Reproduction, 2nd ed. New York Raven Press: 585-611. es_ES
dc.description.references Ratto M.H., Silva M.E., Huanca W., Huanca T., Adams G.P. 2013. Induction of superovulation in South American camelids. Anim. Reprod. Sci., 136: 164-169. https://doi.org/10.1016/j.anireprosci.2012.10.006 es_ES
dc.description.references Rebollar P.G., Alvariño M.R., Illera J.C., Silván G. 1997. Effect of gonadoreline and naloxone on induction of ovulation and plasma LH in rabbit. J. Physiol. Biochem, 53: 205-210. PMID:9291531. es_ES
dc.description.references Rebollar P.G., Espinosa A., Lorenzo P.L., Carabaño R. 2004. Transitory disturbances in growing lactating rabbits after transient doe-litter separation. Reprod. Nutr. Dev., 44: 437-447. https://doi.org/10.1051/rnd:2004050 es_ES
dc.description.references Rebollar P.G., Milanés A., Pereda N., Millán P., Cano P., Esquifino A.I., Villarroel M., Silván G., Lorenzo P.L. 2006a. Oestrus synchronisation of rabbit does at early post-partum by doelitter separation or eCG injection, reproductive parameters and endocrine profiles. Anim. Reprod. Sci., 93, 218-230. https://doi.org/10.1016/j.anireprosci.2005.06.032 es_ES
dc.description.references Rebollar P.G., Pereda N., Villarroel M., Millán P., Lorenzo P.L. 2006b. Oestrus synchronization of rabbit does at early post-partum by dam-litter separation or eCG injection: effect on kit mortality and growth. Livest. Sci., 103: 13-22. https://doi.org/10.1016%2Fj.livsci.2005.12.008 es_ES
dc.description.references Rebollar P.G., Pérez-Cabal M.A., Pereda N., Lorenzo P.L., Arias-Álvarez M., García-Rebollar P. 2009. Effects of parity order and reproductive management on the efficiency of rabbit productive systems. Livest. Sci., 121: 227-233. https://doi.org/10.1016/j.livsci.2008.06.018 es_ES
dc.description.references Rebollar P.G., Pereda N., Schwarz B., Millán P., Lorenzo P.L., Nicodemus N. 2011. Effect of feed restriction or feeding high-fibre diet during the rearing period on body composition, serum parameters and productive performance of rabbit does. Anim. Feed Sc. Technol., 163: 67-76. https://doi.org/10.1016/j.anifeedsci.2010.10.005 es_ES
dc.description.references Rebollar P.G., Dal Bosco A., Millán P., Cardinali R., Brecchia G, Sylla L., Lorenzo P.L., Castellini C. 2012. Ovulating induction methods in rabbit does: the pituitary and ovarian responses. Theriogenology, 77: 292-298. https://doi.org/10.1016/j.theriogenology.2011.07.041 es_ES
dc.description.references Rebollar P.G., García-García R.M., Arias-Álvarez M., Millán P., Rey A.I., Rodríguez M., Formoso-Rafferty N., De la Riva S., Masdeu M., Lorenzo P.L. 2014. Reproductive long-term effects, endocrine response and fatty acid profile of rabbit does fed diets supplemented with n-3 fatty acids. Anim. Reprod. Sci., 146: 202-209. https://doi.org/10.1016/j.anireprosci.2014.02.021 es_ES
dc.description.references Ren L., Medan M.S., Weng Q., Jin W., Li C., Watanabe G., Taya K. 2005. Immunolocalization of nerve growth factor (NGF) and its receptors (TrkA and p75LNGFR) in the reproductive organs of Shiba goats. J. Reprod. Develop., 51: 399-404. https://doi.org/10.1262/jrd.16082 es_ES
dc.description.references Rodríguez M., García-García R.M., Arias-Álvarez M., Formoso-Rafferty N., Millán P., López-Tello J., Lorenzo P.L., González-Bulnes A., Rebollar P.G. 2017a. A diet supplemented with n-3 polyunsaturated fatty acids influences the metabolic and endocrine response of rabbit does and their offspring. J. Anim. Sci., 95: 2690-2700. https://doi.org/10.2527/jas.2017.1429 es_ES
dc.description.references Rodríguez M., Carro M.D., Valiente V., Formoso-Rafferty N., Rebollar P.G. 2017b. Effects of dietary fish oil supplementation on performance, meat quality and cecal fermentation of growing rabbits. J. Anim. Sci., 95: 3620-3630. https://doi.org/10.2527/jas.2017.1690 es_ES
dc.description.references Rodríguez M., García-García R.M., Arias-Álvarez M., Millán P., Febrel N., Formoso-Rafferty N., López-Tello J., Lorenzo P.L., Rebollar P.G. 2018. Improvements in the conception rate, milk composition and embryo quality of rabbit does after dietary enrichment with n-3 polyunsaturated fatty acids. Animal 12: 2080-2088. https://doi.org/10.1017/s1751731117003706 es_ES
dc.description.references Rommers J.M., Kemp B., Meijerhof R., Noordhuizen J.P. 2001. The effect of litter size before weaning on subsequent body development, feed intake, and reproductive performance of young rabbit does. J. Anim. Sci., 79: 1973-1982. https://doi.org/10.2527/2001.7981973x es_ES
dc.description.references Rosell J.M., De la Fuente L.F. 2009. Culling and mortality in breeding rabbits. Prev. Vet. Med., 88: 120-127. https://doi.org/10.1016/j.prevetmed.2008.08.003 es_ES
dc.description.references Sakr O.G., García-García R.M., Arias-Álvarez M., Millán P., Lorenzo P.L., Rebollar P.G. 2010. Body reserves and ovarian performance in primiparous lactating rabbit does submitted to early weaning as a strategy to decrease energy deficit. Anim. Reprod. Sci., 121: 294-300. https://doi.org/10.1016/j.anireprosci.2010.06.008 es_ES
dc.description.references Sánchez-Almanzar V., Sánchez-Rodríguez A., Velasco B., Arias-Álvarez M., Millán P., Cediel R., Lorenzo P.L., García-García R.M., Rebollar P.G. 2019. Efecto del factor de crecimiento nervioso recombinante de conejo (rrbNGF) en la dosis seminal sobre la respuesta hipofisaria y reproductiva en conejas nulíparas. Asociación Interprofesional para el Desarrollo Agrario AIDA. XVIII Jornadas sobre Producción Animal 358-360. es_ES
dc.description.references Sánchez-Rodríguez A., Arias-Álvarez M., Rebollar P.G., Bautista J.M., Lorenzo P.L., García-García, R.M. 2018. Gene expression and immunolocalization of low-affinity neurotrophin receptor (p75) in rabbit male reproductive tract during sexual maturation. Reprod. Dom. Anim. 53 (Suppl2): 62-65. https://doi.org/10.1111/rda.13257 es_ES
dc.description.references Sánchez-Rodríguez A., Arias-Álvarez M., Timón P., Bautista J.M., Rebollar P.G., Lorenzo P.L., García-García M.R. 2019a. Characterization of beta Nerve growth Factor-TRkA system in male reproductive tract of rabbit and the relationship between beta-NGF and testosterone levels with seminal quality during sexual maturation. Theriogenology, 126: 206-213. https://doi.org/10.1016/j.theriogenology.2018.12.013 es_ES
dc.description.references Sánchez-Rodríguez A., Abad P., Arias-Álvarez M., Rebollar P.G., Bautista J.M., Lorenzo P.L., García-García M.R. 2019b. Recombinant rabbit beta nerve growth factor production and its biological effects on sperm and ovulation in rabbits. Plos One, 14: e0219780. https://doi.org/10.1371/journal.pone.0219780 es_ES
dc.description.references Sánchez-Rodríguez A., Arias-Álvarez M., Millán P., Lorenzo P.L., García-García R.M., Rebollar P.G. 2020. Physiological effects on rabbit sperm and reproductive response to recombinant rabbit beta nerve growth factor administered by intravaginal route in rabbit does. Theriogenology, 157: 327-334. https://doi.org/10.1016/j.theriogenology.2020.08.003 es_ES
dc.description.references Saeednia S., Bahadoran H., Amidi F., Asadi M.H., Naji M., Fallahi P., Nejad N.A. 2015. Nerve growth factor in human semen: Effect of nerve growth factor on the normozoospermic men during cryopreservation process. Iran J. Basic Med. Sci., 18: 292-299. PMID: 25945243; PMCID: PMC4414996. es_ES
dc.description.references Shi T.Y., Chen G., Huang X., Yuan Y., Wu X., Wu B., Li Z., Shun F., Chen H., Shi, H. 2012. Effects of reactive oxygen species from activated leucocytes on human sperm motility, viability and morphology. Andrologia, 44: 696-703. https://doi.org/10.1111/j.1439-0272.2011.01252.x es_ES
dc.description.references Silva M.E., Smulders J.P., Guerra M., Valderrama X.P., Letelier C., Adams G.P., Ratto M.H. 2011. Cetrorelix suppresses the preovulatory LH surge and ovulation induced by ovulation-inducing factor (OIF) present in llama seminal plasma. Reprod. Biol. Endocrinol., 9: 74. https://doi.org/10.1186/1477-7827-9-74 es_ES
dc.description.references Silva M., Ulloa-Leal C., Valderrama X.P., Bogle O.A., Adams G.P., Ratto M.H. 2017. Nerve growth factor from seminal plasma origin (spβ-NGF) increases CL vascularization and level of mRNA expression of steroidogenic enzymes during the early stage of corpus luteum development in llamas. Theriogenol., 103: 69-75. https://doi.org/10.1016/j.theriogenology.2017.07.041 es_ES
dc.description.references Skrivanová E., Worgan H.J., Pinloche E., Maroubeck M., Newbold C.J., McEwan N.R. 2010. Changes in the bacterial population of the caecum and stomach of the rabbit in response to addition of dietary caprylic acid. Vet. Microbiol., 144: 334-339. https://doi.org/10.1016/j.vetmic.2010.01.013 es_ES
dc.description.references Song E.J., Yoo Y.S. 2011. Nerve growth factor-induced neurite outgrowth is potentiated by stabilization of TrkA receptors. BMB Reports, 44: 182-186. https://doi.org/10.5483/bmbrep.2011.44.3.182 es_ES
dc.description.references Stradaioli G., Verini-Sulpizi A., Monaci M., Canali C., Boiti C. 1997. Effect of different doses of PMSG on ovarian response and in vitro embryo development in rabbits. World Rabbit Sci., 5: 143-148. https://doi.org/10.4995/wrs.1997.334 es_ES
dc.description.references Streiter S., Fisch B., Sabbah B., Ao A., Abir R. 2016. The importance of neuronal growth factors in the ovary. Mol. Hum. Reprod. 22: 3-17. https://doi.org/10.1093/molehr/gav057 es_ES
dc.description.references Theau-Clément M., Poujardieu B., Bellereaud J. 1990. Influence des traitements lumineux, modes de reproduction et états physiologiques sur la productivité de lapines multipares. In Proc.: 5émes Jour. Rech. Cunicole, Paris, Comm, 7. es_ES
dc.description.references Turrini P., Gaetano C., Antonelli A., Capogrossi M.C., Aloe L. 2002. Nerve growth factor induces angiogenic activity in a mouse model of hindlimb ischemia. Neurosci. Lett., 323: 109-112. https://doi.org/10.1016/s0304-3940(02)00090-3 es_ES
dc.description.references Ubilla E., Rebollar P.G. 1995. Influence of the post-partum day on plasma estradiol-17beta levels, sexual behaviour and conception rate in artificially inseminated lactating does. Anim. Reprod. Sci., 38: 337-344. https://doi.org/10.1016/0378-4320(94)01366-T es_ES
dc.description.references Ubilla E., Alvariño J.M.R., Esquifino A., Agrasal C. 1992. Effect of induction of parturition by administration of a prostaglandin Fα analogue in rabbits: possible modification of prolactin, LH and FSH secretion patterns. Anim. Reprod. Sci., 27: 13-20. https://doi.org/10.1016/0378-4320(92)90066-M es_ES
dc.description.references Velasco B., Rebollar P.G., Marco M., Costa R., García-Rebollar P. 2009. Cambios en la productividad anual de una explotación comercial por la extensificación del ritmo reproductivo. Bol. Cunic., 161: 26-30. es_ES
dc.description.references Viudes-de-Castro M.P., Lavara R., Marco-Jiménez F., Cortell C., Vicente J.S. 2007. Ovulation induced by mucosa vaginal absorption of buserelin and triptorelin in rabbit. Theriogenology, 68: 1031-1036. https://doi.org/10.1016/j.theriogenology.2007.08.004 es_ES
dc.description.references Wang D.H., Ren J., Zhou C.J., Han Z., Wang L., Liang C.G. 2018. Supplementation with CTGF, SDF1, NGF, and HGF promotes ovine in vitro oocyte maturation and early embryo development. Dom. Anim. Endocrinol., 65: 38-48. https://doi.org/10.1016/j.domaniend.2018.05.003 es_ES
dc.description.references Wathes D.C., Abayasekara D.R.E., Aitken R.J. 2007. Polyunsaturated fatty acids in male and female reproduction. Biol. Reprod., 77: 190-201. https://doi.org/10.1095/biolreprod.107.060558 es_ES
dc.description.references Weng Q., Shi Z., Tukada J., Watanabe G., Taya K. 2009. Immunodetection of NGF, trkA, p75 and inhibin α-subunit in interstitial cells of golden hamsters treated with hCG. J.Reprod. Develop., 55: 622-628. https://doi.org/10.1262/jrd.20208 es_ES
dc.description.references Wheeler E.F., Bothwell M. 1992. Spatiotemporal patterns of expression of NGF and the low-affinity NGF receptor in rat embryos suggest functional roles in tissue morphogenesis and myogenesis. J. Neurosci., 12: 930-945. https://doi.org/10.1523%2FJNEUROSCI.12-03-00930.1992 es_ES
dc.description.references Wilson J.L., Chen W., Dissen G.A., Ojeda S.R., Cowley M.A., Garcia-Rudaz C., Enriori P.J. 2014. Excess of nerve growth factor in the ovary causes a polycystic ovary-like syndrome in mice, which closely resembles both reproductive and metabolic aspects of the human syndrome. Endocrinology, 155: 4494-4506. https://doi.org/10.1210/en.2014-1368 es_ES
dc.description.references Xiccato G. 1996. Nutrition of lactating does. In Proc.: 6th World Rabbit Congress, 9-12 July 1996 , Toulouse, France. Pp29-47. es_ES
dc.description.references Xiccato G., Bernardini M., Castellini C., Dalle Zote A., Queaque P.I., Trocino A. 1999. Effect of postweaning feeding on the performance and energy balance of female rabbits at different physiological states. J. Anim. Sci., 77: 416-426. https://doi.org/10.2527/1999.772416x es_ES
dc.description.references Xiccato G., Trocino A., Sartori A., Queaque P.I. 2004. Effect of parity order and litter weaning age on the performance and body energy balance of rabbit does. Livest. Prod. Sci., 85: 239-251. https://doi.org/10.1016/S0301-6226(03)00125-8 es_ES
dc.description.references Xiccato G., Trocino A., Boiti C., Brecchia G. 2005. Reproductive rhythm and litter weaning age as they affect rabbit doe performance and body energy balance. Anim. Sci., 81: 289-296. https://doi.org/10.1079/ASC50270289 es_ES
dc.description.references Zerani M., Boiti C., Zampini D., Brecchia G., Dall’Aglio C., Ceccarelli P., Gobbetti A. 2004. Ob receptor in rabbit ovary and leptin in vitro regulation of corpora lutea. J. Endocrinol., 183: 279-288. https://doi.org/10.1677/joe.1.05507 es_ES
dc.description.references Zerani M., Boiti C., Dall’Aglio C., Pascucci L., Maranesi M., Brecchia G., Marionetti C., Guelfi G., Zampini D., Gobbetti A. 2005. Leptin receptor expression and in vitro leptin actions on prostaglandin release and nitric oxide synthase activity in the rabbit oviduct. J. Endocrinol. 185: 319-325. https://doi.org/10.1677/joe.1.05983 es_ES
dc.description.references Zhai Y., Yao G., Rao F., Wang Y., Song X., Sun F. 2018. Excessive nerve growth factor impairs bidirectional communication between the oocyte and cumulus cells resulting in reduced oocyte competence. Reprod. Biol. Endocrinol., 16: 28. https://doi.org/10.1186/s12958-018-0349-7 es_ES


Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem