Ball, G. F.; University of Maryland, College Park, MD, United States
Balthazart, Jacques ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Département des sciences biomédicales et précliniques
Language :
English
Title :
Neuroendocrine Regulation of Reproductive Behavior in Birds
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Bibliography
Absil P., Baillien M., Ball G.F., Panzica G., Balthazart J. The control of preoptic aromatase activity by afferent inputs in Japanese quail. Brain Res. Rev. 2001, 37:38-58.
Absil P., Riters L.V., Balthazart J. Preoptic aromatase cells project to the mesencephalic central gray in the male Japanese quail (Coturnix japonica). Horm. Behav. 2001, 40:369-383.
Absil P., Braquenier J.B., Balthazart J., Ball G.F. Effects of lesions of nucleus taeniae on appetitive and consummatory aspects of male sexual behavior in Japanese quail. Brain Behav. Evol. 2002, 60:13-35.
Adkins E.K. Functional castration of the female Japanese quail. Physiol. Behav. 1973, 10:619-621.
Adkins E.K. Effects of diverse androgens on the sexual behavior and morphology of castrated male quail. Horm. Behav. 1977, 8:201-207.
Adkins E.K., Adler N.T. Hormonal control of behavior in the Japanese quail. J. Comp. Physiol. Psychol. 1972, 81:27-36.
Adkins E.K., Boop J.J., Koutnik D.L., Morris J.B., Pnieswski E.E. Further evidence that androgen aromatization is essential for the activation of copulation in male quail. Physiol. Behav. 1980, 24:441-446.
Adkins E.K., Nock B.L. Behavioral responses to sex steroids of gonadectomized and sexually regressed quail. J. Endocrinol. 1976, 68:49-55.
Adkins E.K., Nock B.L. The effects of the antiestrogen CI-628 on sexual behavior activated by androgen and estrogen in quail. Horm. Behav. 1976, 7:417-429.
Adkins E.K., Pniewski E.E. Control of reproductive behavior by sex steroids in male quail. J. Comp. Physiol. Psychol. 1978, 92:1169-1178.
Adkins-Regan E. Effect of sex steroids on the reproductive behavior of castrated male ring doves (Streptopelia sp.). Physiol. Behav. 1981, 26:561-565.
Adkins-Regan E. Hormones and Animal Social Behavior 2005, Princeton University Press, Princeton, NJ.
Albert K.A., Helmer-Matyjek E., Nairn A.A., Müller T.H., Haycock J.W., Greene L.A., Goldstein M., Greengard P. Calcium/phospholipid-dependent protein kinase (protein kinase C) phosphorylates and activates tyrosine hydroxylase. Proc. Natl. Acad. Sci. U.S.A. 1984, 81:7713-7717.
Allee W.C., Collias N. The influence of estradiol on the social organization of flocks of hens. Endocrinology 1940, 27:87-94.
Alward B.A., Balthazart J., Ball G.F. Differential effects of global versus local testosterone on singing behavior and its underlying neural substrate. Proc. Natl. Acad. Sci. U.S.A. 2013, 110:19573-19578.
Alward B.A., Parker S.E., Balthazart J., Ball G.F. Anatomical specificity of testosterone in the regulation of song and the associated neuroplasticity in canaries. Abst. Soc. Neurosci. 2015, poster CC9/539.509.
Ames M.M., Lerner P., Lovenberg W. Tyrosine hydroxylase: activation by protein phosphorylation and end product inhibition. J. Biol. Chem. 1978, 253:27-31.
Arbogast L.A. Estrogen genomic and membrane actions at an intersection. Trends Endocrinol. Metab. 2008, 19:1-2.
Armstrong E.A. Coursthip and Display among Birds 1947, Lindsay Drumond, London.
Arnold A.P. The effects of castration on song development in zebra finches (Poephila guttata). J. Exp. Zool. 1975, 191:261-278.
Arnold A.P. The passerine bird song system as a model in neuroendocrine research. J. Exp. Zool. 1990, 4(Suppl.):22-30.
Azcoitia I., Sierra A., Veiga S., Honda S., Harada N., Garcia-Segura L.M. Brain aromatase is neuroprotective. J. Neurobiol. 2001, 47:318-329.
Bakker J., Baum M.J. Neuroendocrine regulation of GnRH release in induced ovulators. Front. Neuroendocrinol. 2000, 21:220-262.
Ball G.F. The neural integration of environmental information by seasonally breeding birds. Am. Zool. 1993, 33:185-199.
Ball G.F., Balthazart J. Neuroendocrine mechanisms regulating reproductive cycles and reproductive behavior in birds. Hormones, Brain and Behavior 2002, 649-798. Academic Press, San Diego, CA. D.W. Pfaff, A.P. Arnold, A.M. Etgen, S.E. Fahrbach, R.T. Rubin (Eds.).
Ball G.F., Balthazart J. Hormonal regulation of brain circuits mediating male sexual behavior in birds. Physiol. Behav. 2004, 83:329-346.
Ball G.F., Balthazart J. How useful is the appetitive and consummatory distinction for our understanding of the neuroendocrine control of sexual behavior?. Horm. Behav. 2008, 53(2):307-311.
Ball G.F., Balthazart J. Japanese quail as a model system for studying the neuroendocrine control of reproductive and social behaviors. ILAR J. 2010, 51:310-325.
Ball G.F., Bentley G.E. Neuroendocrine mechanisms mediating the photoperiodic and social regulation of seasonal reproduction in birds. Reproduction in Context: Social and Environmental Influences on Reproductive Physiology and Behavior 2000, 129-158. MIT Press, Cambridge. K. Wallen, J.E. Schneider (Eds.).
Ball G.F., Ketterson E.D. Sex differences in the response to environmental cues regulating seasonal reproduction in birds. Phil. Trans. R. Soc. Lond. B Biol. Sci. 2008, 363:231-246.
Ball G.F., Riters L.V., Balthazart J. Neuroendocrinology of song behavior and avian brain plasticity: multiple sites of action of sex steroid hormones. Front. Neuroendocrinol. 2002, 23:137-178.
Ball G.F., Tlemçani O., Balthazart J. Induction of the Zenk protein after sexual interactions in male Japanese quail. Neuroreport 1997, 8:2965-2970.
Ball G.F., Wingfield J.C. Changes in plasma levels of luteinizing hormone and sex steroid hormones in relation to multiple-broodedness and nest-site density in male starlings. Physiol. Zool. 1987, 60:191-199.
Balthazart J. Hormonal correlates of behavior. Avian Biology 1983, vol. VII:221-365. Academic Press, New York.
Balthazart J. Steroid metabolism and the activation of social behavior. Advances in Comparative and Environmental Physiology 1989, vol. 3:105-159. Springer Verlag, Berlin.
Balthazart J., Absil P. Identification of catecholaminergic inputs to and outputs from aromatase-containing brain areas of the Japanese quail by tract tracing combined with tyrosine hydroxylase immunocytochemistry. J. Comp. Neurol. 1997, 382:401-428.
Balthazart J., Absil P., Gérard M., Appeltants D., Ball G.F. Appetitive and consummatory male sexual behavior in Japanese quail are differentially regulated by subregions of the preoptic medial nucleus. J. Neurosci. 1998, 18:6512-6527.
Balthazart J., Baillien M., Ball G.F. Rapid and reversible inhibition of brain aromatase activity. J. Neuroendocrinol. 2001, 13:61-71.
Balthazart J., Stamatakis A., Bacola S., Absil P., Dermon C.R. Effects of lesions of the medial preoptic nucleus on the testosterone-induced metabolic changes in specific brain areas in male quail. Neuroscience 2001, 108:447-466.
Balthazart J., Baillien M., Ball G.F. Rapid control of brain aromatase activity by glutamatergic inputs. Endocrinology 2006, 147:359-366.
Balthazart J., Baillien M., Charlier T.D., Ball G.F. Calcium-dependent phosphorylation processes control brain aromatase in quail. Eur. J. Neurosci. 2003, 17:1591-1606.
Balthazart J., Baillien M., Cornil C.A., Ball G.F. Preoptic aromatase modulates male sexual behavior: slow and fast mechanisms of action. Physiol. Behav. 2004, 83:247-270.
Balthazart J., Ball G.F. New insights into the regulation and function of brain estrogen synthase (aromatase). TINS 1998, 21:243-249.
Balthazart J., Ball G.F. Is brain estradiol a hormone or a neurotransmitter?. Trends Neurosci. 2006, 29:241-249.
Balthazart J., Ball G.F. Topography in the preoptic region: differential regulation of appetitive and consummatory male sexual behaviors. Front. Neuroendocrinol. 2007, 28:161-178.
Balthazart J., Castagna C., Ball G.F. Aromatase inhibition blocks the activation and sexual differentiation of appetitive male sexual behavior in Japanese quail. Behav. Neurosci. 1997, 111:381-397.
Balthazart J., Charlier T.D., Barker J.M., Yamamura T., Ball G.F. Sex steroid-induced neuroplasticity and behavioral activation in birds. Eur. J. Neurosci. 2010, 32:2116-2132.
Balthazart J., Cornil C.A., Charlier T.D., Taziaux M., Ball G.F. Estradiol, a key endocrine signal in the sexual differentiation and activation of reproductive behavior in quail. J. Exp. Zool. Pt. A Ecol. Genet. Physiol. 2009, 311:323-345.
Balthazart J., Delville Y., Sulon Y., Hendrick J.C. Plasma levels of luteinizing hormone and of five steroids in photostimulated, castrated and testosterone-treated male and female Japanese quail (Coturnix coturnix japonica). Gen. Endocrinol. (Life Sci. Adv.) 1987, 5:31-36.
Balthazart J., Deviche P. Effect of exogenous hormones on the reproductive behaviour of adult male domestic ducks. I. Behavioural effects of intramuscular injections. Behav. Proc. 1977, 2:129-146.
Balthazart J., Dupiereux V., Aste N., Viglietti-Panzica C., Barrese M., Panzica G.C. Afferent and efferent connections of the sexually dimorphic medial preoptic nucleus of the male quail revealed by in vitro transport of DiI. Cell Tissue Res. 1994, 276:455-475.
Balthazart J., Evrard L., Surlemont C. Effects of the non-steroidal aromatase inhibitor, R76713 on testosterone-induced sexual behavior in the Japanese quail (Coturnix coturnix japonica). Horm. Behav. 1990, 24:510-531.
Balthazart J., Foidart A., Hendrick J.C. The induction by testosterone of aromatase activity in the preoptic area and activation of copulatory behavior. Physiol. Behav. 1990, 47:83-94.
Balthazart J., Foidart A. Brain aromatase and the control of male sexual behavior. J. Steroid Biochem. Mol. Biol. 1993, 44:521-540.
Balthazart J., Foidart A., Surlemont C., Vockel A., Harada N. Distribution of aromatase in the brain of the Japanese quail, ring dove, and zebra finch: an immunocytochemical study. J. Comp. Neurol. 1990, 301:276-288.
Balthazart J., Gahr M., Surlemont C. Distribution of estrogen receptors in the brain of the Japanese quail: an immunocytochemical study. Brain Res. 1989, 501:205-214.
Balthazart J., Hendrick J.C. Annual variation in reproductive behavior, testosterone, and plasma FSH levels in the Rouen duck, Anas platyrhynchos. Gen. Comp. Endocrinol. 1976, 28:171-183.
Balthazart J., Hirschberg D. Testosterone metabolism and sexual behavior in the chick. Horm. Behav. 1979, 12:253-263.
Balthazart J., Malacarne G., Deviche P. Stimulatory effects of 5b-dihydrotestosterone on the sexual behavior in the domestic chick. Horm. Behav. 1981, 15:246-258.
Balthazart J., Reid J., Absil P., Foidart A., Ball G.F. Appetitive as well as consummatory aspects of male sexual behavior in quail are activated by androgens and estrogens. Behav. Neurosci. 1995, 109:485-501.
Balthazart J., Schoffeniels E. Pheromones are involved in the control of sexual behaviour in birds. Naturwissenschaften 1979, 66:55-56.
Balthazart J., Schumacher M., Ottinger M.A. Sexual differences in the Japanese quail: behavior, morphology, and intracellular metabolism of testosterone. Gen. Comp. Endocrinol. 1983, 51:191-207.
Balthazart J., Surlemont C. Androgen and estrogen action in the preoptic area and activation of copulatory behavior in quail. Physiol. Behav. 1990, 48:599-609.
Balthazart J., Surlemont C. Copulatory behavior is controlled by the sexually dimorphic nucleus of the quail POA. Brain Res. Bull. 1990, 25:7-14.
Balthazart J., Surlemont C., Harada N. Aromatase as a cellular marker of testosterone action in the preoptic area. Physiol. Behav. 1992, 51:395-409.
Balthazart J., Taziaux M. The underestimated role of olfaction in avian reproduction?. Behav. Brain Res. 2009, 200:248-259.
Balthazart J., Tlemçani O., Harada N. Localization of testosterone-sensitive and sexually dimorphic aromatase-immunoreactive cells in the quail preoptic area. J. Chem. Neuroanat. 1996, 11:147-171.
Balthazart J., Verheyen G., Schumacher M., Decuypere E. Changes in progesterone metabolism in the chicken hypothalamus during induced egg laying stop and molting. Gen. Comp. Endocrinol. 1988, 72:282-295.
Barfield R.J. Activation of copulatory behavior by androgen implanted into the preoptic area of the male fowl. Horm. Behav. 1969, 1:37-52.
Barfield R.J. Activation of sexual and aggressive behavior by androgen implantation into the male ring dove brain. Endocrinology 1971, 89:1470-1476.
Barfield R.J., Rubin B.S., Glaser J.H., Davis P.G. Sites of action of ovarian hormones in the regulation of oestrous responsiveness in rats. Hormones and Behaviour in Higher Vertebrates 1983, 2-17. Springer-Verlag, Berlin. J. Balthazart, E. Pröve, R. Gilles (Eds.).
Barker J.M., Ball G.F., Balthazart J. Anatomically discrete sex differences and enhancement by testosterone of cell proliferation in the telencephalic ventricle zone of the adult canary brain. J. Chem. Neuroanat. 2014, 55:1-8.
Barnett D.K., Bunnell T.M., Millar R.P., Abbott D.H. Gonadotropin-releasing hormone II stimulates female sexual behavior in marmoset monkeys. Endocrinology 2006, 147:615-623.
Baum M.J., Everitt B.J. Increased expression of c-fos in the medial preoptic area after mating in male rats: role of afferent inputs from the medial amygdala and midbrain central tegmental field. Neuroscience 1992, 50:627-646.
Beach F.A. Hormones and Behavior 1948, Paul B. Hoeber, Inc., New York.
Beach F.A. Sexual attractivity, proceptivity, and receptivity in female mammals. Horm. Behav. 1976, 7:105-138.
Beach F.A., Inman N.G. Effects of castration and androgen replacement on mating in male quail. Proc. Natl. Acad. Sci. U.S.A. 1965, 54:1426-1431.
Beletsky L.D., Orians G.H., Wingfield J.C. Relationship of steroid hormones and polygyny to territorial status, breeding experience, and reproductive success in male red-winged blackbirds. Auk 1989, 106:107-117.
Belle M.D., Sharp P.J., Lea R.W. Aromatase inhibition abolishes courtship behaviours in the ring dove (Streptopelia risoria) and reduces androgen and progesterone receptors in the hypothalamus and anterior pituitary gland. Mol. Cell. Biochem. 2005, 276:193-204.
Belle M.D.C., Lea R.W. Androgen receptor immunolocalization in brains of courting and brooding male and female ring doves (Streptopelia risoria). Gen. Comp. Endocrinol. 2001, 124:173-187.
Bentley G.E., Jensen J.P., Kaur G.J., Wacker D.W., Tsutsui K., Wingfield J.C. Rapid inhibition of female sexual behavior by gonadotropin-inhibitory hormone (GnIH). Horm. Behav. 2006, 49:550-555.
Bernard D.J., Abuav-Nussbaum R., Horton T.H., Turek F.W. Photoperiodic effects on gonadotropin-releasing hormone (GnRH) content and the GnRH-immunoreactive neuronal system of male Siberian hamsters. Biol. Reprod. 1999, 60:272-276.
Berthold A.A. Transplantation der Hoden. Arch. für Anat. Physiol. Wiss. Med. 1849, 16:42-46.
Birkhead T.R., Moller A.P. Sperm Competition in Birds 1992, Academic Press, San Diego, CA.
Breazile J.E., Kuenzel W.J. Systema nervosum centrale. Handbook of Avian Anatomy: Nomina Anatomicum Avium. Nuttall Ornithological Club 1993, 493-554. Mass, Cambridge. J.J. Baumel, A.S. King, J.E. Breazile, H.E. Evans, J.C. Vanden Berge (Eds.).
Brenowitz E., Margoliash D., Nordeen K.W. The neurobiology of birdsong. J. Neurobiol. 1997, 33:495-709.
Brenowitz E.A., Larson T.A. Neurogenesis in the adult avian song-control system. Cold Spring Harb. Perspect. Biol. 2015, 7:a019000.
Brockway B.F. Hormonal and experiential factors influencing the nestbox oriented behaviour of budgerigars (Melopsittacus undulatus). Behaviour 1969, 35:1-26.
Brown S.D., Johnson F., Bottjer S.W. Neurogenesis in adult canary telencephalon is independent of gonadal hormone levels. J. Neurosci. 1993, 13:2024-2032.
Buntin J.D. Role of prolactin in avian incubation behavior and care of young: is there a causal relationship?. Ann. N.Y. Acad. Sci. 1986, 474:252-267.
Buntin J.D. Neural and hormonal control of parental behavior in birds. Adv. Study Behav. 1996, 1996:161-213.
Buntin J.D., El Halawani M.E., Ottinger M.A., Fan Y., Fivizzani A.J. An analysis of sex and breeding stage differences in prolactin binding activity in brain and hypothalamic GnRH concentration in Wilson's phalarope, a sex role-reversed species. Gen. Comp. Endocrinol. 1998, 109:119-132.
de Bournonville C., Ball G.F., Cornil C.A., Balthazart J. Non-ovarian aromatization regulates sexual motivation and receptivity in female quail. Abst. Soc. Neurosci. 2015, poster P23/246.203.
de Bournonville C., Dickens M.J., Ball G.F., Balthazart J., Cornil C.A. Dynamic changes in brain aromatase activity following sexual interactions in males: where, when and why?. Psychoneuroendocrinology 2013, 38:789-799.
Carere C., Ball G.F., Balthazart J. Sex differences in projections from preoptic area aromatase cells to the periaqueductal gray in Japanese quail. J. Comp. Neurol. 2007, 500:894-907.
Caro S.P., Balthazart J. Pheromones in birds: myth or reality?. J. Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 2010, 196:751-766.
Caro S.P., Balthazart J., Bonadonna F. The perfume of reproduction in birds: chemosignaling in avian social life. Horm. Behav. 2015, 68:25-42.
Charlier T.D., Ball G.F., Balthazart J. Inhibition of steroid receptor coactivator-1 blocks estrogen and androgen action on male sex behavior and associated brain plasticity. J. Neurosci. 2005, 25:906-913.
Charlier T.D., Ball G.F., Balthazart J. Sexual behavior activates the expression of the immediate early genes c-fos and Zenk (egr-1) in catecholaminergic neurons of male Japanese quail. Neuroscience 2005, 131:13-30.
Charlier T.D., Harada N., Balthazart J., Cornil C.A. Human and quail aromatase activity is rapidly and reversibly inhibited by phosphorylating conditions. Endocrinology 2011, 152:4199-4210.
Charlier T.D., Newman A.E., Heimovics S.A., Po K.W., Saldanha C.J., Soma K.K. Rapid effects of aggressive interactions on aromatase activity and oestradiol in discrete brain regions of wild male white-crowned sparrows. J. Neuroendocrinol. 2011, 23:742-753.
Cheng M.-F., Zuo M. Proposed pathways for vocal self-stimulation: met-enkephalinergic projections linking the midbrain vocal nucleus, auditory-responsive thalamic regions and neurosecretory hypothalamus. J. Neurobiol. 1994, 25:361-379.
Cheng M.F. Effect of estrogen on behavior of ovariectomized ring doves (Streptopelia risoria). J. Comp. Physiol. Psychol. 1973, 83:234-239.
Cheng M.F. Effect of ovariectomy on the reproductive behavior of female ring doves (Streptopelia risoria). J. Comp. Physiol. Psychol. 1973, 83:221-233.
Cheng M.F. Role of gonadotrophin releasing hormones in the reproductive behaviour of female ring doves (Streptopelia risoria). J. Endocrinol. 1977, 74:37-45.
Cheng M.F. Progress and prospects in ring dove research: a personal view. Adv. Study Anim. Behav. 1979, 9:97-129.
Cheng M.F. Female cooing promotes ovarian development in ring doves. Physiol. Behav. 1986, 37:371-374.
Cheng M.F. For whom does the female dove coo? A case for the role of vocal self-stimulation. Anim. Behav. 1992, 43:1035-1044.
Cheng M.F. Vocal self stimulation: from the ring dove story to emotion-based vocal communication. Adv. Study Behav. 2003, 33:309-353.
Cheng M.F. The role of vocal self-stimulation in female responses to males: implications for state-reading. Horm. Behav. 2008, 53:1-10.
Cheng M.F., Balthazart J. The role of nest-building activity in the gonadotrophin secretions and the reproductive successes of ring doves (Streptopelia risoria). J. Comp. Physiol. Psychol. 1982, 96:303-324.
Cheng M.F., Desiderio C., Havens M., Johnson A. Behavioral stimulation of ovarian growth. Horm. Behav. 1988, 22:388-401.
Cheng M.F., Durand S.E. Song and the limbic brain: a new function for the bird's own song. Ann. N.Y. Acad. Sci. 2004, 1016:611-627.
Cheng M.F., Follett B.K. Plasma luteinizing hormone during the breeding cycle of the female ring dove. Horm. Behav. 1976, 7:199-205.
Cheng M.F., Lehrman D. Gonadal hormone specificity in the sexual behavior of ring doves. Psychoneuroendocrinology 1975, 1:95-102.
Cheng M.F., Peng J.P., Johnson P. Hypothalamic neurons preferentially respond to female nest coo stimulation: demonstration of direct acoustic stimulation of luteinizing hormone release. J. Neurosci. 1998, 18:5477-5489.
Cheng M.F., Silver R. Estrogen-progesterone regulation of nest-building and incubation behavior in ovariectomized ring doves (Streptopelia risoria). J. Comp. Physiol. Psychol. 1975, 88:256-263.
Clayton D.F., London S.E. Advancing avian behavioral neuroendocrinology through genomics. Front. Neuroendocrinol. 2014, 35:58-71.
Clutton-Brock T.H. The Evolution of Parental Care 1991, Princeton Univ. Press, Princeton NJ.
Cohen J., Cheng M.F. Role of vocalization in the reproductive cycle of ring doves (Streptopelia risoria): effects of hypoglossal nerve section on the reproductive behavior and physiology of the female. Horm. Behav. 1979, 13:113-127.
Collias N.E., Collias E.C. Nest Building and Bird Behavior 1984, Princeton Univ. Press, Princeton NJ.
Coolen L.M., Peters H.J.P.W., Veening J.G. Distribution of Fos immunoreactivity following mating versus anogenital investigation in the male rat brain. Neuroscience 1997, 77:1151-1161.
Cornil C.A., Ball G.F., Balthazart J. Functional significance of the rapid regulation of brain estrogen action: where do the estrogens come from?. Brain Res. 2006, 1126:2-26.
Cornil C.A., Ball G.F., Balthazart J. Rapid control of male typical behaviors by brain-derived estrogens. Front. Neuroendocrinol. 2012, 33:425-446.
Cornil C.A., Ball G.F., Balthazart J. The dual action of estrogen hypothesis. Trends Neurosci. 2015, 38:408-416.
Cornil C.A., Dalla C., Papadopoulou-Daifoti Z., Baillien M., Balthazart J. Estradiol rapidly activates male sexual behavior and affects brain monoamine levels in the quail brain. Behav. Brain Res. 2006, 166:110-123.
Cornil C.A., Dalla C., Papadopoulu-Daifoti Z., Baillien M., Dejace C., Ball G.F., Balthazart J. Rapid decreases in preoptic aromatase activity and brain monoamine concentrations after engaging in male sexual behavior. Endocrinology 2005, 146:3809-3820.
Cornil C.A., Leung C.H., Pletcher E.R., Naranjo K.C., Blauman S.J., Saldanha C.J. Acute and specific modulation of presynaptic aromatization in the vertebrate brain. Endocrinology 2012, 153:2562-2567.
Cornil C.A., Taziaux M., Baillien M., Ball G.F., Balthazart J. Rapid effects of aromatase inhibition on male reproductive behaviors in Japanese quail. Horm. Behav. 2006, 49:45-67.
Cozzi B., Stankov B., Viglietti-Panzica C., Capsoni S., Aste N., Lucini V., Fraschini F., Panzica G. Distribution and characterization of melatonin receptors in the brain of the Japanese quail, Coturnix japonica. Neurosci. Lett. 1993, 150:149-152.
Cross E., Roselli C.E. 17beta-estradiol rapidly facilitates chemoinvestigation and mounting in castrated male rats. Am. J. Physiol. Regul. Integr. Comp. Physiol. 1999, 276:R1346-R1350.
Crossin G.T., Dawson A., Phillips R.A., Trathan P.N., Gorman K.B., Adlard S., Williams T.D. Seasonal patterns of prolactin and corticosterone secretion in an Antarctic seabird that moults during reproduction. Gen. Comp. Endocrinol. 2012, 175:74-81.
Daubner S.C., Lauriano C., Haycock J.W., Fitzpatrick P.F. Site-directed mutagenesis of serine 40 of rat tyrosine hydroxylase. J. Biol. Chem. 1992, 267:12639-12646.
Davies N.B. Dunnock Behaviour and Social Evolution 1992, Oxford University Press, Oxford, UK.
Davis D.E., Domm L.V. The Influence of Hormones on the Sexual Behavior of the Fowl Essays in Biology 1943, 171-181. University of California, Berkeley.
Davis J.E., Guinan J.A. Parental behavior correlates to baseline corticosterone of mates and offspring in nesting eastern bluebirds (Sialia sialis). Gen. Comp. Endocrinol. 2014, 201:1-7.
Dawson A., Goldsmith A.R. Prolactin and gonadotrophin secretion in wild starlings (Sturnus vulgaris) during the annual cycle and in relation to nesting, incubation, and rearing young. Gen. Comp. Endocrinol. 1982, 48:213-221.
Dawson A., King V.M., Bentley G.E., Ball G.F. Photoperiodic control of seasonality in birds. J. Biol. Rhythms 2001, 16:365-380.
Dawson A., Sharp P.J. Photorefractoriness in birds-photoperiodic and non-photoperiodic control. Gen. Comp. Endocrinol. 2007, 153:378-384.
Delville Y., Balthazart J. Hormonal control of female sexual behavior in the Japanese quail. Horm. Behav. 1987, 21:288-309.
Delville Y., Sulon J., Balthazart J. Diurnal variations of sexual receptivity in the female Japanese quail. Horm. Behav. 1986, 20:13-33.
Dermon C.R., Stamatakis A., Tlemçani O., Balthazart J. Performance of appetitive or consummatory components of male sexual behavior is mediated by different brain areas: a 2-deoxyglucose autoradiographic study. Neuroscience 1999, 94:1261-1277.
Dewing P., Boulware M.I., Sinchak K., Christensen A., Mermelstein P.G., Micevych P. Membrane estrogen receptor-alpha interactions with metabotropic glutamate receptor 1a modulate female sexual receptivity in rats. J. Neurosci. 2007, 27:9294-9300.
Dickens M.J., Cornil C.A., Balthazart J. Acute stress differentially affects aromatase activity in specific brain nuclei of adult male and female quail. Endocrinology 2011, 152:4242-4251.
Dickens M.J., de Bournonville C., Balthazart J., Cornil C.A. Relationships between rapid changes in local aromatase activity and estradiol concentrations in male and female quail brain. Horm. Behav. 2014, 65:154-164.
Dominguez J.M., Gil M., Hull E.M. Preoptic glutamate facilitates male sexual behavior. J. Neurosci. 2006, 26:1699-1703.
Domjan M., Hall S. Determinants of social proximity in Japanese quail (Coturnix coturnix japonica): male behavior. J. Comp. Psychol. 1986, 100:59-67.
Domjan M., Hall S. Sexual dimorphism in the social proximity behavior of Japanese quail (Coturnix coturnix japonica). J. Comp. Psychol. 1986, 100:68-71.
Domjan M., Mahometa M.J., Mills A.D. Relative contributions of the male and the female to sexual behavior and reproductive success in the Japanese quail (Coturnix japonica). J. Comp. Psychol. 2003, 117:391-399.
Domjan M., Nash S. Stimulus control of social behaviour in male Japanese quail. Anim. Behav. 1988, 36:1006-1015.
Domm L.V., Davis D.E., Blivaiss B.B. Observations on the sexual behavior of hormonally treated brown leghorn fowl. Anat. Rec. 1942, 84:481-482.
Drent R. Incubation Avian Biology 1975, vol. 5:333-420. Academic Press, New York.
Drnevich J., Replogle K.L., Lovell P., Hahn T.P., Johnson F., Mast T.G., Nordeen E., Nordeen K., Strand C., London S.E., Mukai M., Wingfield J.C., Arnold A.P., Ball G.F., Brenowitz E.A., Wade J., Mello C.V., Clayton D.F. Impact of experience-dependent and -independent factors on gene expression in songbird brain. Proc. Natl. Acad. Sci. U.S.A. 2012, 109(Suppl. 2):17245-17252.
Dudley C.A., Moss R.L. Facilitation of sexual receptivity in the female rat by C-terminal fragments of LHRH. Physiol. Behav. 1991, 50:1205-1208.
Dufty A.M., Goldsmith A.R., Wingfield J.C. Prolactin secretion in a brood parasite, the brown-headed cowbird, Molothrus ater. J. Zool. Lond. 1986, 212:669-675.
Dufty A.M., Wingfield J.C. Endocrine changes in breeding brown-headed cowbirds and their implications for the evolution of brood parasitism. Behavioural Rhythms 1986, 93-108. Privat IEC, Toulouse. Y. Quéinnec, N. Delvolvé (Eds.).
Duncan K.A., Saldanha C.J. Neuroinflammation induces glial aromatase expression in the uninjured songbird brain. J. Neuroinflammation 2011, 8:81.
Durand S.E., Tepper J.M., Cheng M.F. The shell region of the nucleus ovoidalis: a subdivision of the avian auditory thalamus. J. Comp. Neurol. 1992, 323:495-518.
Eens M. Understanding the complex song of the European starling: an integrated ethological approach. Adv. Study Anim. Behav. 1997, 26:355-434.
El Halawani M.E., Mauro L.J., Phillips R.E., Youngren O.M. Neuroendocrine control of prolactin and incubation behavior in gallinaceous birds. Progress in Comparative Endocrinology 1990, 678-684. Wiley-Liss, Inc., New York. A. Epple, M.H. Stetson (Eds.).
El Halawani M.E., Silsby J.L., Behnke E.J., Fehrer S.C. Hormonal induction of incubation behavior in ovariectomized female turkeys (Meleagris gallopavo). Biol. Reprod. 1986, 35:59-67.
Erickson C.J., Hutchison J.B. Induction of nest-material collecting in male Barbary doves by intracerebral androgen. J. Reprod. Fert. 1977, 50:9-16.
Erpino M.J. Hormonal control of coursthip behaviour in the pigeon (Columba livia). Anim. Behav. 1969, 17:401-405.
Etienne A., Fischer H. Untersuchung über das Verhalten kastrierter Stockenten (Anas platyrhynchos L.) und dessen beeinflussung durch Testosteron. Z. Tierpsychol. 1964, 21:348-358.
Farner D.S. Generation and regulation of annual cycles in migratory passerine birds. Am. Zool. 1986, 26:493-501.
Feder H.H., Storey A., Goodwin D., Reboulleau C., Silver R. Testosterone and "5alpha-dihydrotestosterone' levels in peripheral plasma of male and female ring doves (Streptopelia risoria) during the reproductive cycle. Biol. Reprod. 1977, 16:666-677.
Fee M.S., Scharff C. The songbird as a model for the generation and learning of complex sequential behaviors. ILAR J. 2010, 51:362-377.
Fivizzani A.J., Oring L.W. Plasma steroid hormones in relation to behavioral sex role reversal in the spotted sandpiper, Actitis macularia. Biol. Reprod. 1986, 35:1195-1201.
Foidart A., Harada N., Balthazart J. Effects of steroidal and non steroidal aromatase inhibitors on sexual behavior and aromatase-immunoreactive cells and fibers in the quail brain. Brain Res. 1994, 657:105-123.
Foidart A., Lakaye B., Grisar T., Ball G.F., Balthazart J. Estrogen receptor-beta in quail: cloning, tissue expression and neuroanatomical distribution. J. Neurobiol. 1999, 40:327-342.
Foidart A., Meddle S.L., Balthazart J. Mating-induced Fos and aromatase are not colocalized in the preoptic area. Neuroreport 1999, 10:907-912.
Foidart A., Reid J., Absil P., Yoshimura N., Harada N., Balthazart J. Critical re-examination of the distribution of aromatase-immunoreactive cells in the quail forebrain using antibodies raised against human placental aromatase and against the recombinant quail, mouse or human enzyme. J. Chem. Neuroanat. 1995, 8:267-282.
Foster R.G., Follett B.K., Lythgoe J.N. Rhodopsin-like sensitivity of extra-retinal photoreceptors mediating the photoperiodic response in quail. Nature 1985, 313:50-52.
Friedman M.B. Interactions between visual and vocal courtship stimuli in the neuroendocrine response of female doves. J. Comp. Physiol. Psychol. 1977, 91:1408-1416.
Fusani L., Gahr M., Hutchison J.B. Aromatase inhibition reduces specifically one display of the ring dove courtship behavior. Gen. Comp. Endocrinol. 2001, 122:23-30.
Gahr M., Güttinger H.-R., Kroodsma D.E. Estrogen receptors in the avian brain: survey reveals general distribution and forebrain areas unique to songbirds. J. Comp. Neurol. 1993, 327:112-122.
Garcia-Fernandez J.M., Cernuda-Cernuda R., Davies W.I., Rodgers J., Turton M., Peirson S.N., Follett B.K., Halford S., Hughes S., Hankins M.W., Foster R.G. The hypothalamic photoreceptors regulating seasonal reproduction in birds: a prime role for VA opsin. Front. Neuroendocrinol. 2015, 37:13-28.
Garcia-Segura L.M., Veiga S., Sierra A., Melcangi R.C., Azcoitia I. Aromatase: a neuroprotective enzyme. Prog. Neurobiol. 2003, 71:31-41.
Garcia-Segura L.M., Wozniak A., Azcoitia I., Rodriguez J.R., Hutchison R.E., Hutchison J.B. Aromatase expression by astrocytes after brain injury: implications for local estrogen formation in brain repair. Neuroscience 1999, 89:567-578.
Gerlach N.M., Ketterson E.D. Experimental elevation of testosterone lowers fitness in female dark-eyed juncos. Horm. Behav. 2013, 63:782-790.
Gibson M.J., Cheng M.F. Neural mediation of estrogen-dependent courtship behavior in female ring doves. J. Comp. Physiol. Psychol. 1979, 93:855-867.
Goldman S.A., Nottebohm F. Neuronal production, migration, and differentiation in a vocal control nucleus of the adult female canary brain. Proc. Natl. Acad. Sci. U.S.A. 1983, 80:2390-2394.
Goldsmith A.R. Prolactin in avian reproductive cycles. Hormones and Behaviour in Higher Vertebrates 1983, 375-387. Springer-Verlag, Berlin. J. Balthazart, E. Pröve, R. Gilles (Eds.).
Goodale H.D. Castration in relation to secondary sexual characters in brown leghorns. Am. Nat. 1913, 47:159-169.
Goodman R.L., Jansen H.T., Billings H.J., Coolen L.M., Lehman M.N. Neural systems mediating seasonal breeding in the ewe. J. Neuroendocrinol. 2010, 22:674-681.
Goodson J.L., Kingsbury M.A. What's in a name? Considerations of homologies and nomenclature for vertebrate social behavior networks. Horm. Behav. 2013, 64:103-112.
Gorman M.L. The endocrine basis of pair-formation behaviour in the male eider Somateria mollissima. IBIS 1974, 116:451-465.
Gould E. How widespread is adult neurogenesis in mammals?. Nat. Rev. Neurosci. 2007, 8:481-488.
Gould E., Reeves A.J., Graziano M.S.A., Gross C.G. Neurogenesis in the neocortex of adult primates. Science 1999, 286:548-552.
Gratto-Trevor C.L., Oring L.W., Fivizzani A.J., El Halawani M.E., Cooke F. The role or prolactin in parental care in a monogamous and a polyandrous shorebird. Auk 1990, 107:718-729.
Guhl A.M. Heterosexual dominance and mating behaviour in chickens. Behaviour 1949, 2.
Güntürkün O., Karten H.J. An immunocytochemical analysis of the lateral geniculate complex in the pigeon (Columba livia). J. Comp. Neurol. 1991, 314:721-749.
Güntürkün O., Miceli O., Watanabe M. Anatomy of the avian thalamofugal pathway. Vision, Brain and Behavior in Birds 1993, 115-135. MIT Press, Cambridge, Mass. H.P. Zeigler, H.J. Bischof (Eds.).
Guyomarc'h C., Guyomarc'h J.C. La stimulation du développement sexuel des femelles de caille japonaise, Coturnix coturnix japonica, par des chants de mâles: mise en évidence de période privilégiées dans le nycthémère. C.R. Acad. Sci. Paris Sér. III 1982, 295:37-40.
Guyomarc'h C., Guyomarc'h J.C., Garnier D.H. Influence de la perception de vocalisations de mâles sur la reproduction chez les femelles de Coturnix coturnix japonica. Biol. Behav. 1981, 6:167-182.
Haesler S., Rochefort C., Georgi B., Licznerski P., Osten P., Scharff C. Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. PLoS Biol. 2007, 5:e321.
Hagelin J.C. Odors and chemical signaling. Reproductive Biology and Phylogeny of Birds, Part B 2007, 75-119. Science Publishers, Enfield (NH) Jersey, Plymouth. B.G.M. Jamieson (Ed.).
Hagelin J.C., Jones I.L., Rasmussen L.E. A tangerine-scented social odour in a monogamous seabird. Proc. R. Soc. Lond. Biol. 2003, 270:1323-1329.
Hahn T.P., Boswell T., Wingfield J.C., Ball G.F. Temporal flexibility in avian reproduction. Current Ornithology 1997, 39-80. Plenum Press, New York. V.J. Nolan (Ed.).
Hahn T.P., MacDougall-Shackleton S.A. Adaptive specialization, conditional plasticity and phylogenetic history in the reproductive cue response systems of birds. Phil. Trans. R. Soc. Lond. Ser. B Biol. Sci. 2008, 363:267-286.
Harding C.F., Sheridan K., Walters M.J. Hormonal specificity and activation of sexual behavior in male zebra finches. Horm. Behav. 1983, 17:111-133.
Hau M. Timing of breeding in variable environments: tropical birds as model systems. Horm. Behav. 2001, 40:281-290.
Hau M., Stoddard S.T., Soma K.K. Territorial aggression and hormones during the non-breeding season in a tropical bird. Horm. Behav. 2004, 45:40-49.
Hegner R.E., Wingfield J.C. Effects of experimental manipulation of testosterone levels on parental investment and breeding success in male house sparrows. Auk 1987, 104:462-469.
Hiatt E.S., Goldsmith A.R., Farner D.S. Plasma levels of prolactin and gonadotropins during the reproductive cycle of white-crowned sparrows (Zonotrichia leucophrys). Auk 1987, 104:208-217.
Hinde R.A. The nest building behavior of domesticated canaries. Proc. Zool. Soc. Lond. 1958, 131:1-48.
Hinde R.A. Interaction of internal and external factors in integration of canary reproduction. Sex and Behavior 1965, 381-415. John Wiley & Sons, Inc., New York. F.A. Beach (Ed.).
Hinde R.A., Steel E. The influence of daylength and male vocalizations on the estrogen-dependent behavior of female canaries and budgerigars, with discussion of data from other species. Adv. Study Anim. Behav. 1978, 8:39-73.
Hinde R.A., Steel E.A. Integration of reproductive behaviour in female canaries. Symp. Soc. Exp. Biol. 1966, 20:401-426.
Hirschenhauser K., Winkler H., Oliveira R.F. Comparative analysis of male androgen responsiveness to social environment in birds: the effects of mating system and paternal incubation. Horm. Behav. 2003, 43:508-519.
Hochberg Z., Bick T., Pelman R., Brandes J.M., Barzilai D. The dual effect of calcium on aromatization by cultured human trophoblast. J. Steroid Biochem. 1986, 24:1217-1219.
Höhn E.O. Seasonal changes in the mallard's penis and their hormonal control. Proc. R. Soc. Lond. Biol. 1960, 134:547-555.
Holstege G., Kerstens L., Moes M.C., Vanderhorst V.G. Evidence for a periaqueductal gray-nucleus retroambiguus-spinal cord pathway in the rat. Neuroscience 1997, 80:587-598.
Horn G. Memory, Imprinting, and the Brain 1985, Clarendon Press, Oxford.
Hull E.M., Wood R.I., McKenna K.E. The neurobiology of male sexual behavior. Knobil and Neill's Physiology of Reproduction 2005, 1729-1824. Academic Press, San Diego, New York. third ed. J.D. Neill (Ed.).
Hutchison J.B. Effects of hypothalamic implants of gonadal steroids on courtship behaviour in Barbary doves (Streptopelia risoria). J. Endocrinol. 1971, 50:97-113.
Hutchison J.B., Steimer T.H. Formation of behaviorally effective 17beta-estradiol in the dove brain: steroid control of preoptic aromatase. Endocrinology 1986, 118:2180-2187.
Hutchison R.E. Hormonal differentiation of sexual behavior in Japanese quail. Horm. Behav. 1978, 11:363-387.
Jacob J., Balthazart J., Schoffeniels E. Sex differences in the chemical composition of uropygial gland waxes in domestic ducks. Biochem. Syst. Ecol. 1979, 7:149-153.
Joëls M. Steroid hormones and excitability in the mammalian brain. Front. Neuroendocrinol. 1997, 18:2-48.
Johnson A.L., Van Tienhoven A. Plasma concentrations of six steroids and LH during the ovulatory cycle of the hen. Biol. Reprod. 1980, 23:386-393.
Kauffman A.S., Rissman E.F. A critical role for the evolutionarily conserved gonadotropin-releasing hormone II: mediation of energy status and female sexual behavior. Endocrinology 2004, 145:3639-3646.
Kelly M.J., Ronnekleiv O.K. Rapid membrane effects of estrogen in the central nervous system. Hormones, Brain and Behavior 2002, 361-380. Academic press, San Diego. D.W. Pfaff, A.P. Arnold, A.M. Etgen, S.E. Fahrbach, R.T. Rubin (Eds.).
Kingsbury M.A., Kelly A.M., Schrock S.E., Goodson J.L. Mammal-like organization of the avian midbrain central gray and a reappraisal of the intercollicular nucleus. PLoS One 2011, 6:e20720.
Kirn J., O'Loughlin B., Kasparian S., Nottebohm F. Cell death and neuronal recruitment in the high vocal center of adult male canaries are temporally related to changes in song. Proc. Natl. Acad. Sci. U.S.A. 1994, 91:7844-7848.
Klatt J.D., Goodson J.L. Sex-specific activity and function of hypothalamic nonapeptide neurons during nest-building in zebra finches. Horm. Behav. 2013, 64:818-824.
Komisaruk B.R. Effects of local brain implants of progesterone on reproductive behavior in ring doves. J. Comp. Physiol. Psychol. 1967, 64:219-224.
Konkle A.T., Balthazart J. Sex differences in the rapid control of aromatase activity in the quail preoptic area. J. Neuroendocrinol. 2011, 23:424-434.
Korenbrot C.C., Schomberg D.W., Erickson C.J. Radioimmunoassay of plasma estradiol during the breeding cycle of ring doves (Streptopelia risoria). Endocrinology 1974, 94:1126-1132.
Kosonsiriluk S., Chaiworakul V., Thayananuphat A., Mauro L.J., El Halawani M.E. GABAergic neurotransmission in the premammillary nucleus of the Turkey hypothalamus regulates reproductive seasonality and the onset of photorefractoriness. Neuroendocrinology 2015, 10.1159/000442206.
Kosonsiriluk S., Mauro L.J., Chaiworakul V., Chaiseha Y., El Halawani M.E. Photoreceptive oscillators within neurons of the premammillary nucleus (PMM) and seasonal reproduction in temperate zone birds. Gen. Comp. Endocrinol. 2013, 190:149-155.
Kriegsfeld L.J., Nelson R.J. Photoperiod affects the gonadotropin-releasing hormone neuronal system of male prairie voles (Microtus ochrogaster). Neuroendocrinology 1999, 69:238-244.
Kroodsma D.E. Reproductive development in a female song bird: differential stimulation by quality of male song. Science 1976, 192:574-575.
Küppers E., Ivanova T., Karolczak M., Beyer C. Estrogen: a multifunctional messenger to nigrostriatal dopaminergic neurons. J. Neurocytol. 2000, 29:375-385.
Lea R.W. Prolactin and avian incubation: a comparison between Galliformes and Columbiformes. Sitta 1987, 1:117-141.
Lea R.W., Clark J.A., Tsutsui K. Changes in central steroid receptor expression, steroid synthesis, and dopaminergic activity related to the reproductive cycle of the ring dove. Microsc. Res. Tech. 2001, 55:12-26.
Leboucher G., Béguin N., Lacroix A., Kreutzer M. Progesterone inhibits female courtship behavior in domestic canaries (Serinus canaria). Horm. Behav. 2000, 38:123-129.
Leboucher G., Béguin N., Mauget R., Kreutzer M. Effects of fadrozole on sexual displays and reproductive activity in the female canary. Physiol. Behav. 1998, 65:233-240.
Leboucher G., Kreutzer M., Dittami J. Copulation-solicitation displays in female canaries (Serinus canaria): are oestradiol implants necessary?. Ethology 1994, 97:190-197.
Lehman M.N., Ladha Z., Coolen L.M., Hileman S.M., Connors J.M., Goodman R.L. Neuronal plasticity and seasonal reproduction in sheep. Eur. J. Neurosci. 2010, 32:2152-2164.
Lehrman D.S. The reproductive behavior of ring doves. Sci. Am. 1963, 11:433-438.
Lehrman D.S. Interaction between internal and external environments in the regulation of the reproductive cycle of the ring dove. Sex and Behavior 1965, 355-380. John Wiley & Sons, Inc., New York. F.A. Beach (Ed.).
Lisk R.D. Neural localization for androgen activation of copulatory behavior in the male rat. Endocrinology 1967, 80:754-761.
Lofts B., Murton R.K., Westwood N.J. Gonadal cycles and the evolution of breeding seasons in British Columbidae. J. Zool. 1966, 150:249-272.
Lorenz K. The comparative method in studying innate behavior patterns. Symp. Soc. Exp. Biol. 1950, 4:221-268.
Lynn S.E. Endocrine and neuroendocrine regulation of fathering behavior in birds. Horm. Behav. 2015.
MacDougall-Shackleton S.A., Stevenson T.J., Watts H.E., Pereyra M.E., Hahn T.P. The evolution of photoperiod response systems and seasonal GnRH plasticity in birds. Integr. Comp. Biol. 2009, 49:580-589.
Maney D.L., Richardson R.D., Wingfield J.C. Central administration of chicken gonadotropin-releasing hormone-II enhances courtship behavior in a female sparrow. Horm. Behav. 1997, 32:11-18.
Martinez-Vargas M.C. Nest building in the ring dove (Streptopelia risoria): hormonal and social factors. Behaviour 1974, 50:123-151.
Martinez-Vargas M.C., Erickson C.J. Social and hormonal determinants of nest building in the ring dove (Streptopelia risoria). Behaviour 1973, 45:12-37.
Martinez-Vargas M.C., Stumpf W.E., Sar M. Estrogen localization in the dove brain. Phylogenetic considerations and implications for nomenclature. Anatomical Neuroendocrinology 1975, 166-175. Karger, Basel. W.E. Stumpf, L.D. Grant (Eds.).
McEwen B.S. Steroid hormone actions on the brain: when is the genome involved?. Horm. Behav. 1994, 28:396-405.
McEwen B.S. Invited review: estrogens effects on the brain: multiple sites and molecular mechanisms. J. Appl. Physiol. 2001, 91:2785-2801.
McGlothlin J.W., Jawor J.M., Ketterson E.D. Natural variation in a testosterone-mediated trade-off between mating effort and parental effort. Am. Nat. 2007, 170:864-875.
McKinney F. The behaviour of ducks the behaviour of domestic animals. Baillière 1969, 593-626. Tindall & Cassell, London. E.S.E. Hafez (Ed.).
Meddle S.L., Foidart A., Wingfield J.C., Ramenofsky M., Balthazart J. Effects of sexual interactions with a male on Fos-like immunoreactivity in the female quail brain. J. Neuroendocrinol. 1999, 11:771-784.
Meddle S.L., King V.M., Follett B.K., Wingfield J.C., Ramenofsky M., Foidart A., Balthazart J. Copulation activates Fos-like immunoreactivity in the male quail forebrain. Behav. Brain Res. 1997, 85:143-159.
Meisel R.L., Sachs B.D. The physiology of male sexual behavior. The Physiology of Reproduction 1994, vol. 2:3-105. Raven Press, New York.
Meitzen J., Mermelstein P.G. Estrogen receptors stimulate brain region specific metabotropic glutamate receptors to rapidly initiate signal transduction pathways. J. Chem. Neuroanat. 2011, 42:236-241.
Mello C.V., Vicario D.S., Clayton D.F. Song presentation induces gene expression in the songbird forebrain. Proc. Natl. Acad. Sci. U.S.A. 1992, 89:6818-6822.
Micevych P., Christensen A. Membrane-initiated estradiol actions mediate structural plasticity and reproduction. Front. Neuroendocrinol. 2012, 33:331-341.
Moore M. Hormonal response of free-living male white-crowned sparrows to experimental manipulation of female sexual behavior. Horm. Behav. 1982, 16:323-329.
Moore M.C. Effect of female displays on the endocrine physiology and behaviour of male white-crowned sparrows, Zonotrichia leucophrys. J. Zool. Lond. 1983, 199:137-148.
Moore M.C., Kranz R. Evidence for androgen independence of male mounting behavior in white-crowned sparrows (Zonotrichia leucophrys gambelii). Horm. Behav. 1983, 17:414-423.
Morel G., Bourlière F. Recherches écologiques sur les Quelea quelea (L.) de la basse vallée du Sénégal. II. La reproduction. Alauda 1956, 24:97-122.
Moss R.L., Dudley C.A. Neuropeptides and the Social Aspects of Female Reproductive Behavior in the Rat Molecular and Cellular Basis of Social Behavior in Vertebrates 1989, 209-237. Springer Verlag, Berlin. J. Balthazart (Ed.).
Moss R.L., Dudley C.A. Differential effects of a luteinizing-hormone-releasing hormone (LHRH) antagonist analogue on lordosis behavior induced by LHRH and the LHRH fragment Ac-LHRH5-10. Neuroendocrinology 1990, 52:138-142.
Moss R.L., Gu Q., Wong M. Estrogen: nontranscriptional signaling pathway. Rec. Prog. Horm. Res. 1997, 52:33-69.
Murphy A.Z., Hoffman G.E. Distribution of gonadal steroid receptor-containing neurons in the preoptic-periaqueductal gray-brainstem pathway: a potential circuit for the initiation of male sexual behavior. J. Comp. Neurol. 2001, 438:191-212.
Murton R.K., Westwood N.J. Integration of gonadotrophin and steroid secretion, spermatogenesis and behaviour in the reproductive cycle of male pigeon. Neural and Endocrine Aspects of Behaviour in Birds 1975, 51-89. Elsevier, Amsterdam. P. Wright, P.G. Caryl, D.M. Vowles (Eds.).
Naftolin F., Horvath T.L., Jakab R.L., Leranth C., Harada N., Balthazart J. Aromatase immunoreactivity in axon terminals of the vertebrate brain - an immunocytochemical study on quail, rat, monkey and human tissues. Neuroendocrinology 1996, 63:149-155.
Nagle L., Kreutzer M.L., Vallet E.M. Obtaining copulation solicitation displays in female canaries without estradiol implants. Experientia 1993, 49:1022-1023.
Nakane Y., Ikegami K., Ono H., Yamamoto N., Yoshida S., Hirunagi K., Ebihara S., Kubo Y., Yoshimura T. A mammalian neural tissue opsin (Opsin 5) is a deep brain photoreceptor in birds. Proc. Natl. Acad. Sci. U.S.A. 2010, 107:15264-15268.
Nelson R.J. An Introduction to Behavioral Endocrinology 2005, Sinauer Associates, Inc., Sunderland, Massachussets.
Nicholls T.J., Golsmith A.R., Dawson A. Photorefractoriness in birds and comparison with mammals. Physiol. Rev. 1988, 68:133-176.
Niessen N.A., Balthazart J., Ball G.F., Charlier T.D. c-fos down-regulation inhibits testosterone-dependent male sexual behavior and the associated learning. Eur. J. Neurosci. 2013, 38:3325-3337.
Noble G.K., Wurm M. The effect of hormones on the breeding behavior of the laughing gulls. Anat. Rec. 1940, 78(Suppl.):50-51.
Noble G.K., Wurm M. The effect of testosterone propionate on the black-crowned night heron. Endocrinology 1940, 26:837-850.
Noble R. The effects of estrogen and progesterone on copulation in female quail (Coturnix coturnix japonica) housed in continuous dark. Horm. Behav. 1972, 3:199-204.
Nottebohm F. A brain for all seasons: cyclical anatomical changes in song-control nuclei of the canary brain. Science 1981, 214:1368-1370.
Nottebohm F. From bird song to neurogenesis. Sci. Am. 1989, 260:74-79.
Numan M., Insel T.R. The Neurobiology of Parental Behavior 2003, Springer Verlag, New York.
Numan M., Sheehan T.P. Neuroanatomical circuitry for mammalian maternal behavior. Ann. N.Y. Acad. Sci. 1997, 807:101-125.
O'Connell M.E., Reboulleau C., Feder H.H., Silver R. Social interactions and androgen levels in birds. I. Female characteristics associated with increased plasma androgen levels in the male ring dove (Streptopelia risoria). Gen. Comp. Endocrinol. 1981, 44:454-463.
O'Loghlen A.L., Beecher M.D. Sexual preferences for mate song types in female song sparrows. Anim. Behav. 1997, 53:835-841.
Oksche A., Farner D.S., Serventy D.L., Wolff F., Nicholls C.A. The hypothalamo-hypophysial neurosecretory system of the zebra finch (Taeniopygia castanotis). Z. Zellforsch. 1963, 58:846-914.
Oliver J., Baylé J.D. Brain photoreceptors for the photo-induced testicular response in birds. Experientia 1982, 38:1021-1029.
Onagbesan O.M., Podie M.J. Calcium-dependent stimulation of estrogen secretion by FSH from theca cells of the domestic hen (Gallus domesticus). Gen. Comp. Endocrinol. 1989, 75:177-186.
Oring L.W., Fivizzani A.J., El Halawani M.E. Changes in plasma prolactin associated with laying and hatch in the spotted sandpiper. Auk 1986, 103:820-822.
Oring L.W., Fivizzani A.J., El Halawani M.E., Goldsmith A.R. Seasonal changes in prolactin and luteinizing hormone in the polyandrous spotted sandpiper, Actitis macularia. Gen. Comp. Endocrinol. 1986, 62:394-403.
Oring L.W., Fivizzani A.J., El Halawani M.E. Testosterone-induced inhibition of incubation in the spotted sandpiper (Actitis mecularia). Horm. Behav. 1989, 23:412-423.
Palkovits M. Isolated removal of hypothalamic or other brain nuclei of the rat. Brain Res. 1973, 59:449-450.
Panzica G.C., Viglietti-Panzica C., Balthazart J. The sexually dimorphic medial preoptic nucleus of quail: a key brain area mediating steroid action on male sexual behavior. Front. Neuroendocrinol. 1996, 17:51-125.
Panzica G.C., Viglietti-Panzica C., Calcagni M., Anselmetti G.C., Schumacher M., Balthazart J. Sexual differentiation and hormonal control of the sexually dimorphic preoptic medial nucleus in quail. Brain Res. 1987, 416:59-68.
Panzica G.C., Viglietti-Panzica C., Sanchez F., Sante P., Balthazart J. Effects of testosterone on a selected neuronal population within the preoptic sexually dimorphic nucleus of the Japanese quail. J. Comp. Neurol. 1991, 303:443-456.
Pedersen H.C. Effects of exogenous prolactin on parental behaviour in free-living female willow ptarmigan Lagopus l. lagopus. Anim. Behav. 1989, 38:926-934.
Perrins C.M. The timing of birds' breeding season. IBIS 1970, 112:242-255.
Peterson R.S., Saldanha C.J., Schlinger B.A. Rapid upregulation of aromatase mRNA and protein following neural injury in the zebra finch (Taeniopygia guttata). J. Neuroendocrinol. 2001, 13:317-323.
Peterson R.S., Yarram L., Schlinger B.A., Saldanha C.J. Aromatase is pre-synaptic and sexually dimorphic in the adult zebra finch brain. Proc. Biol. Sci. 2005, 272:2089-2096.
Pfaff D., Keiner M. Atlas of estradiol-concentrating cells in the central nervous system of the female rat. J. Comp. Neurol. 1973, 151:121-158.
Pfaff D.W. Estrogen and Brain Function 1980, Springer-Verlag, New York.
Pfaus J.G., Smith W.J., Coopersmith C.B. Appetitive and consummatory sexual behaviors of female rats in bilevel chambers - I. A correlational and factor analysis and the effects of ovarian hormones. Horm. Behav. 1999, 35:224-240.
Phillips R.E., McKinney F. The role of testosterone in the displays of some ducks. Anim. Behav. 1962, 10:244-246.
Pinxten R., De Ridder E., Balthazart J., Eens M. Context-dependent effects of castration and testosterone treatment on song in male European starlings. Horm. Behav. 2002, 42:307-318.
Pleim E.T., Brown T.J., MacLusky N.J., Etgen A.M., Barfield R.J. Dilute estradiol implants and progestin receptor induction in the ventromedial nucleus of the hypothalamus: correlation with receptive behavior in female rats. Endocrinology 1989, 124:1807-1812.
Prior N.H., Yap K.N., Soma K.K. Acute and chronic effects of an aromatase inhibitor on pair-maintenance behavior of water-restricted zebra finch pairs. Gen. Comp. Endocrinol. 2014, 196:62-71.
Pröve E. Der Einfluss von Kastration und Testosteronsubstitution auf das Verhalten manlicher Zebrafinken. J. Ornithol. 1974, 115:338-347.
Ramirez V.D., Zheng J.B., Siddique K.M. Membrane receptors for estrogen, progesterone, and testosterone in the rat brain: fantasy or reality. Cell. Mol. Neurobiol. 1996, 16:175-198.
Rathinam T., Kuenzel W.J. Attenuation of gonadal response to photostimulation following ablation of neurons in the lateral septal organ of chicks. Brain Res. Bull. 2005, 64:455-461.
Reiner A.D., Perkel J., Bruce L., Butler A., Csillag A., Kuenzel W., Medina L., Paxinos G., Shimizu T., Striedter G., Wild M., Ball G.F., Durand S., Güntürkün O., Lee D.W., Mello C.V., White S.A., Hough G., Kubikova L., Smulders T.V., Wada K., Dugas-Ford J., Husband S., Yamamoto K., Yu J.,C.,S., Jarvis E.D. Revised nomenclature for avian telencephalon and some related brainstem nuclei. J. Comp. Neurol. 2004, 473:377-414.
Reisbick S., Rosenblatt J.S., Mayer A.D. Decline of maternal behavior in the virgin and lactating rat. J. Comp. Physiol. Psychol. 1975, 89:722-732.
Remage-Healey L., Maidment N.T., Schlinger B.A. Forebrain steroid levels fluctuate rapidly during social interactions. Nat. Neurosci. 2008, 11:1327-1334.
Replogle K., Arnold A.P., Ball G.F., Band M., et al. The Songbird Neurogenomics (SoNG) initiative: community-based tools and strategies for study of brain gene function and evolution. BMC Genomics 2008.
Rissman E.F., Clendenon A.L., Krohmer R.W. Role of androgens in the regulation of sexual behavior in the female musk shrew. Neuroendocrinology 1990, 51:468-473.
Rissman E.F., Harada N., Roselli C.E. Effect of vorozole, an aromatase enzyme inhibitor, on sexual behavior, aromatase activity and neural immunoreactivity. J. Neuroendocrinol. 1996, 8:199-210.
Riters L.V., Ball G.F. Lesions to the medial preoptic area affect singing in the male European starling (Sturnus vulgaris). Horm. Behav. 1999, 36:276-286.
Riters L.V., Eens M., Pinxten R., Duffy D.L., Balthazart J., Ball G.F. Seasonal changes in courtship song and the medial preoptic area in male European starlings (Sturnus vulgaris). Horm. Behav. 2000, 38:250-261.
Rodriguez-Sierra J.F., Blake C.A. Catechol oestyrogens: their contraceptive effects and possible involvement in some reproductive processes of the rat. Hormones and Behaviour in Higher Vertebrates 1983, 40-55. Springer-Verlag, Berlin. J. Balthazart, E. Pröve, R. Gilles (Eds.).
Rohmann K.N., Schlinger B.A., Saldanha C.J. Subcellular compartmentalization of aromatase is sexually dimorphic in the adult zebra finch brain. Dev. Neurobiol. 2007, 67:1-9.
Roselli C.E. Synergistic induction of aromatase activity in the rat brain by estradiol and 5alpha-dihydrotestosterone. Neuroendocrinology 1991, 53:79-84.
Roselli C.E. Subcellular localization and kinetic properties of aromatase activity in rat brain. J. Steroid Biochem. Mol. Biol. 1995, 52:469-477.
Roselli C.E., Horton L.E., Resko J.A. Time-course and steroid specificity of aromatase induction in rat hypothalamus-preoptic area. Biol. Reprod. 1987, 37:628-633.
Roselli C.E., Resko J.A. Androgens regulate brain aromatase activity in adult male rats through a receptor mechanism. Endocrinology 1984, 114:2183-2189.
de Roux N., Genin E., Carel J.C., Matsuda F., Chaussain J.L., Milgrom E. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc. Natl. Acad. Sci. U.S.A. 2003, 100:10972-10976.
Sachs B.D. Photoperiodic control of reproductive behavior and physiology of the male Japanese quail (Coturnix coturnix japonica). Horm. Behav. 1969, 1:7-24.
Sachs B.D. The appetitive-consummatory distinction: is this 100-year-old baby worth saving? Reply to Ball and Balthazart. Horm. Behav. 2008, 53:315-318.
Saldanha C.J., Burstein S.R., Duncan K.A. Induced synthesis of oestrogens by glia in the songbird brain. J. Neuroendocrinol. 2013, 25:1032-1038.
Saldanha C.J., Peterson R.S., Yarram L., Schlinger B.A. The synaptocrine hypothesis: a novel mechanism of estrogen delivery. Horm. Behav. 2003, 44:74.
Saldanha C.J., Rohmann K.N., Coomaralingam L., Wynne R.D. Estrogen provision by reactive glia decreases apoptosis in the zebra finch (Taeniopygia guttata). J. Neurobiol. 2005, 64:192-201.
Saldanha C.J., Silverman A.J., Silver R. Direct innervation of GnRH neurons by encephalic photoreceptors in birds. J. Biol. Rhythms 2001, 16:39-49.
Schlinger B.A. Sex steroids and their actions on the birdsong system. J. Neurobiol. 1997, 33:619-631.
Schlinger B.A., Amur-Umarjee S., Shen P., Campagnoni A.T., Arnold A.P. Neuronal and non-neuronal aromatase in primary cultures of developing zebra finch telencephalon. J. Neurosci. 1994, 14:7541-7552.
Schlinger B.A., Arnold A.P. Brain is the major site of estrogen synthesis in a male songbird. Proc. Natl. Acad. Sci. U.S.A. 1991, 88:4191-4194.
Schlinger B.A., Arnold A.P. Circulating estrogens in a male songbird originate in the brain. Proc. Natl. Acad. Sci. U.S.A. 1992, 89:7650-7653.
Schlinger B.A., Brenowitz E.A. Neural and hormonal control of birdsong. Hormones, Brain and Behavior 2002, 799-839. Academic Press, San Diego. D.W. Pfaff, A.P. Arnold, A.M. Etgen, S.E. Fahrbach, R.T. Rubin (Eds.).
Schlinger B.A., Callard G.V. Localization of aromatase in synaptosomal and microsomal subfractions of quail (Coturnix coturnix japonica) brain. Neuroendocrinology 1989, 49:434-441.
Schmidt K.L., Pradhan D.S., Shah A.H., Charlier T.D., Chin E.H., Soma K.K. Neurosteroids, immunosteroids, and the Balkanization of endocrinology. Gen. Comp. Endocrinol. 2008, 157:266-274.
Schulz S.B., Haesler S., Scharff C., Rochefort C. Knockdown of FoxP2 alters spine density in Area X of the zebra finch. Genes Brain Behav. 2010, 9:732-740.
Schumacher M. Rapid membrane effects of steroid hormones: an emerging concept in neuroendocrinology. Trends Neurosci. 1990, 13:359-362.
Schumacher M., Balthazart J. Testosterone-induced brain aromatase is sexually dimorphic. Brain Res. 1986, 370:285-293.
Scott B.B., Lois C. Generation of tissue-specific transgenic birds with lentiviral vectors. Proc. Natl. Acad. Sci. U.S.A. 2005, 102:16443-16447.
Scott B.B., Lois C. Generation of transgenic birds with replication-deficient lentiviruses. Nat. Protoc. 2006, 1:1406-1411.
Searcy W.A. Measuring responses of female birds to male song. Animal Communication 1992, 175-189. Plenum Press, New York. P.K. McGregor (Ed.).
Searcy W.A., Capp M.S. Estradiol dosage and the solicitation display assay in red-winged blackbirds. Condor 1997, 99:826-828.
Searcy W.A., Marler P. A test for responsiveness to song structure and programming in female sparrows. Science 1981, 213:926-928.
Segovia S., Guillamón A. Sexual dimorphism in the vomeronasal pathway and sex differences in reproductive behaviors. Brain Res. Rev. 1993, 18:51-74.
Seiwert C.M., Adkins-Regan E. The foam production system of the male Japanese quail: characterization of structure and function. Brain Behav. Evol. 1998, 52:61-80.
Seredynski A.L., Balthazart J., Ball G.F., Cornil C.A. Estrogen receptor beta activation rapidly modulates male sexual motivation through the transactivation of metabotropic glutamate receptor 1a. J. Neurosci. 2015, 35:13110-13123.
Seredynski A.L., Balthazart J., Christophe V.J., Ball G.F., Cornil C.A. Neuroestrogens rapidly regulate sexual motivation but not performance. J. Neurosci. 2013, 33:164-174.
Sharp P.J., Li Q.S., Georgiou G., Lea R.W. Expression of fos-like immunoreactivity in the hypothalamus of the ring dove (Streptopelia risoria) at the onset of incubation. J. Neuroendocrinol. 1996, 8:291-298.
Shodono M., Nakamura T., Tanabe Y., Wakabayashi K. Simultaneous determinations of oestradiol-17 beta, progesterone and luteinizing hormone in the plasma during the ovulatory cycle of the hen. Acta Endocrinol. (Copenh.) 1975, 78:565-573.
Silver R. The parental behavior of ring doves. Am. Sci. 1978, 66:209-215.
Silver R. Prolactin and parenting in the pigeon family. J. Exp. Zool. 1984, 232:617-625.
Silver R., Andrews H., Ball G.F. Parental care in an ecological perspective: a quantitative analysis of avian subfamilies. Am. Zool. 1985, 25:823-840.
Silver R., Ball G.F. Brain, hormone and behavior interactions in avian reproduction: status and prospectus. Condor 1989, 91:966-978.
Silver R., Ramos C. Vasoactive intestinal polypeptide in avian reproduction. Comp. Physiol 1990, vol. 8:191-204. Karger, Basel. J. Balthazart (Ed.).
Silver R., Reboulleau C., Lehrman D.S., Feder H.H. Radioimmunoassay of plasma progesterone during the reproductive cycle of male and female ring doves (Streptopelia risoria). Endocrinology 1974, 94:1547-1554.
Silver R., Witkovsky P., Horvath P., Alones V., Barnstable C.J., Lehman M.N. Coexpression of opsin- and VIP-like immunoreactivity in CSF-contacting neurons of the avian brain. Cell Tissue Res. 1988, 253:189-198.
Silverin B. Reproductive organs and breeding behaviour of the male pied flycatcher Ficedula hypoleuca (Pallas). Ornis Scand. 1975, 6:15-26.
Silverin B. Circannual rhythms in gonads and endocrine organs of the great tit Parus major in south-west Sweden. Ornis Scand. 1978, 9:207-213.
Silverin B. Effects of long-acting testosterone treatment of free-living pied flycatchers, Ficedula hypoleuca, during the breeding period. Anim. Behav. 1980, 28:906-912.
Silverin B. Endocrine aspects of avian mating systems. Proc. XIX Int. Ornit. Congress 1988, 2:1676-1684.
Silverin B., Baillien M., Foidart A., Balthazart J. Distribution of aromatase activity in the brain and peripheral tissues of passerine and nonpasserine avian species. Gen. Comp. Endocrinol. 2000, 117:34-53.
Silverin B., Goldsmith A.R. Plasma prolactin concentrations in breeding pied flycatchers (Ficedula hypoleuca) with an experimentally prolonged brooding period. Horm. Behav. 1990, 24:104-113.
Simonneaux V., Ansel L., Revel F.G., Klosen P., Pevet P., Mikkelsen J.D. Kisspeptin and the seasonal control of reproduction in hamsters. Peptides 2009, 30:146-153.
Slawski B.A., Buntin J.D. Preoptic area lesions disrupt prolactin-induced parental feeding behavior in ring doves. Horm. Behav. 1995, 29:248-266.
Smiley K.O., Adkins-Regan E. Relationship between prolactin, reproductive experience, and parental care in a biparental songbird, the zebra finch (Taeniopygia guttata). Gen. Comp. Endocrinol. 2015.
Smith J.T., Clay C.M., Caraty A., Clarke I.J. KiSS-1 messenger ribonucleic acid expression in the hypothalamus of the ewe is regulated by sex steroids and season. Endocrinology 2007, 148:1150-1157.
Södersten P. Steinach and Young, discoverers of the effects of estrogen on male sexual behavior and the "male brain'(1,2). eNeuro 2015, 2.
Södersten P. A historical and personal perspective on the aromatization revolution: steinach confirmed. Brain Aromatase, Estrogens and Behavior 2012, 281-314. Oxford University Press, New York. J. Balthazart, G.F. Ball (Eds.).
Soma K.K., Sullivan K., Wingfield J. Combined aromatase inhibitor and antiandrogen treatment decreases territorial aggression in a wild songbird during the nonbreeding season. Gen. Comp. Endocrinol. 1999, 115:442-453.
Soma K.K., Sullivan K.A., Tramontin A.D., Saldanha C.J., Schlinger B.A., Wingfield J.C. Acute and chronic effects of an aromatase inhibitor on territorial aggression in breeding and nonbreeding male song sparrows. J. Comp. Physiol. [A] 2000, 186:759-769.
Soma K.K., Tramontin A.D., Wingfield J.C. Oestrogen regulates male aggression in the non-breeding season. Proc. Biol. Sci. 2000, 267:1089-1096.
Soma K.K., Wingfield J.C. Endocrinology of aggression in the nonbreeding season. Proceedings of the 22th International Ornithological Congress. Birdlife South Africa, Johannesburg 1999, 1606-1620. N. Adams, R. Slotow (Eds.).
Soma K.K., Wingfield J.C. Dehydroepiandrosterone in songbird plasma: seasonal regulation and relationship to territorial aggression. Gen. Comp. Endocrinol. 2001, 123:144-155.
Soma K.K., Wissman A.M., Brenowitz E.A., Wingfield J.C. Dehydroepiandrosterone (DHEA) increases territorial song and the size of an associated brain region in a male songbird. Horm. Behav. 2002, 41:203-212.
Steimer T. Aromatase activity in rat brain synaptosomes. Is an enzyme associated with the neuronal cell membrane involved in mediating non-genomic effects of androgens?. Eur. J. Neurosci. 1988, (Suppl.), 9.
Steimer T., Hutchison J.B. Androgen increases formation of behaviourally effective oestrogen in dove brain. Nature 1981, 292:345-347.
Steimer T., Hutchison J.B. Micromethods for the in vitro study of steroid metabolism in the brain using radiolabelled tracers. Neuroendocrine Research Methods 1991, vol. 2:875-919. Harwood Academic Publishers, Chur, Switzerland.
Steinach E. Sex and Life 1940, Viking Press, New York.
Stevenson T.J., Ball G.F. Disruption of neuropsin mRNA expression via RNA interference facilitates the photoinduced increase in thyrotropin-stimulating subunit beta in birds. Eur. J. Neurosci. 2012, 36:2859-2865.
Stevenson T.J., Bernard D.J., McCarthy M.M., Ball G.F. Photoperiod-dependent regulation of gonadotropin-releasing hormone 1 messenger ribonucleic acid levels in the songbird brain. Gen. Comp. Endocrinol. 2013, 190:81-87.
Taziaux M., Cornil C.A., Balthazart J. Aromatase inhibition blocks the expression of sexually-motivated cloacal gland movements in male quail. Behav. Process. 2004, 67:461-469.
Taziaux M., Cornil C.A., Dejace C., Arckens L., Ball G.F., Balthazart J. Neuroanatomical specificity in the expression of the immediate early gene c-fos following expression of appetitive and consummatory male sexual behaviour in Japanese quail. Eur. J. Neurosci. 2006, 23:1869-1887.
Taziaux M., Keller M., Bakker J., Balthazart J. Sexual behavior activity tracks rapid changes in brain estrogen concentrations. J. Neurosci. 2007, 27:6563-6572.
Taziaux M., Keller M., Ball G.F., Balthazart J. Site-specific effects of anosmia and cloacal gland anesthesia on Fos expression induced in male quail brain by sexual behavior. Behav. Brain Res. 2008, 194:52-65.
Temple S.A. Plasma testosterone titers during the annual reproductive cycle of starlings (Sturnus vulgaris). Gen. Comp. Endocrinol. 1974, 22:470-479.
Thayananuphat A., Youngren O.M., Kang S.W., Bakken T., Kosonsiriluk S., Chaiseha Y., El Halawani M.E. Dopamine and mesotocin neurotransmission during the transition from incubation to brooding in the turkey. Horm. Behav. 2011, 60:327-335.
Thompson R.R., Goodson J.L., Ruscio M.G., Adkins-Regan E. Role of the archistriatal nucleus taeniae in the sexual behavior of male Japanese quail (Coturnix japonica): a comparison of function with the medial nucleus of the amygdala in mammals. Brain Behav. Evol. 1998, 51:215-229.
Timberlake W., Silva K.M. Appetitive behavior in ethology, psychology, and behavior systems. Behavioral Design 1995, vol. 11:211-253. Plenum Press, New York. N.S. Thompson (Ed.).
Tinbergen N. The Study of Instinct 1951, Clarendon Press, Oxford.
Tlemçani O., Ball G.F., D'Hondt E., Vandesande F., Sharp P.J., Balthazart J. Fos induction in the Japanese quail brain after expression of appetitive and consummatory aspects of male sexual behavior. Brain Res. Bull. 2000, 52:249-262.
Tomaszycki M.L., Banerjee S.B., Adkins-Regan E. The role of sex steroids in courtship, pairing and pairing behaviors in the socially monogamous zebra finch. Horm. Behav. 2006, 50:141-147.
Tramontin A.D., Brenowitz E.A. Seasonal plasticity in the adult brain. TINS 2000, 23:251-258.
Tsutsui K., Ubuka T., Bentley G.E., Kriegsfeld L.J. Gonadotropin-inhibitory hormone (GnIH): discovery, progress and prospect. Gen. Comp. Endocrinol. 2012, 177:305-314.
Tsutsui K., Ubuka T., Son Y.L., Bentley G.E., Kriegsfeld L.J. Contribution of GnIH research to the progress of reproductive neuroendocrinology. Front. Endocrinol. (Lausanne) 2015, 6:179.
Ubuka T., Haraguchi S., Tobari Y., Narihiro M., Ishikawa K., Hayashi T., Harada N., Tsutsui K. Hypothalamic inhibition of socio-sexual behaviour by increasing neuroestrogen synthesis. Nat. Commun. 2014, 5:3061.
Ubuka T., Tsutsui K. Gonadotropin-inhibitory hormone inhibits aggressive behavior of male quail by increasing neuroestrogen synthesis in the brain beyond its optimum concentration. Gen. Comp. Endocrinol. 2014, 205:49-54.
Ubuka T., Tsutsui K. Review: neuroestrogen regulation of socio-sexual behavior of males. Front. Neurosci. 2014, 8:323.
Unger E.K., Burke K.J., Yang C.F., Bender K.J., Fuller P.M., Shah N.M. Medial amygdalar aromatase neurons regulate aggression in both sexes. Cell Rep. 2015, 10(4):453-462.
Veney S.L., Rissman E.F. Steroid implants in the medial preoptic area or ventromedial nucleus of the hypothalamus activate female sexual behaviour in the musk shrew. J. Neuroendocrinol. 2000, 12:1124-1132.
Viglietti-Panzica C., Panzica G.C., Fiori M.G., Calcagni M., Anselmetti G.C., Balthazart J. A sexually dimorphic nucleus in the quail preoptic area. Neurosci. Lett. 1986, 64:129-134.
Villavicencio C.P., Apfelbeck B., Goymann W. Parental care, loss of paternity and circulating levels of testosterone and corticosterone in a socially monogamous song bird. Front. Zool. 2014, 11:11.
Vleck C.M. Hormonal control of incubation behavior. Avian Incubation 2002, 54-62. Oxford Univ. Press, Oxford. D.C. Deeming (Ed.).
Vockel A., Pröve E., Balthazart J. Sex- and age-related differences in the activity of testosterone-metabolizing enzymes in microdissected nuclei of the zebra finch brain. Brain Res. 1990, 511:291-302.
Voigt C., Ball G.F., Balthazart J. Sex differences in the expression of sex steroid receptor mRNA in the quail brain. J. Neuroendocrinol. 2009, 21:1045-1062.
Wada K., Howard J.T., McConnell P., Whitney O., Lints T., Rivas M.V., Horita H., Patterson M.A., White S.A., Scharff C., Haesler S., Zhao S., Sakaguchi H., Hagiwara M., Shiraki T., Hirozane-Kishikawa T., Skene P., Hayashizaki Y., Carninci P., Jarvis E.D. A molecular neuroethological approach for identifying and characterizing a cascade of behaviorally regulated genes. Proc. Natl. Acad. Sci. U.S.A. 2006, 103:15212-15217.
Watson J.T., Adkins-Regan E. Activation of sexual behavior by implantation of testosterone propionate and estradiol benzoate into the preoptic area of the male Japanese quail (Coturnix japonica). Horm. Behav. 1989, 23:251-268.
Watson J.T., Adkins-Regan E. Neuroanatomical localization of sex steroid-concentrating cells in the Japanese quail (Coturnix japonica): autoradiography with [3H]-testosterone, [3H]-estradiol, and [3H]-dihydrotestosterone. Neuroendocrinology 1989, 49:51-64.
Watson J.T., Adkins-Regan E. Testosterone implanted in the preoptic area of male Japanese quail must be aromatized to activate copulation. Horm. Behav. 1989, 23:432-447.
White S.J. Effects of stimuli emanating from the nest on the reproductive cycle in the ring dove. I. Pre-laying behavior. Anim. Behav. 1975, 23:854-868.
White S.J. Effects of stimuli emanating from the nest on the reproductive cycle in the ring dove. II. Building during the pre-laying period. Anim. Behav. 1975, 23.
Whitney O., Pfenning A.R., Howard J.T., Blatti C.A., Liu F., Ward J.M., Wang R., Audet J.N., Kellis M., Mukherjee S., Sinha S., Hartemink A.J., West A.E., Jarvis E.D. Core and region-enriched networks of behaviorally regulated genes and the singing genome. Science 2014, 346:1256780.
Wiedenheft B., Sternberg S.H., Doudna J.A. RNA-guided genetic silencing systems in bacteria and archaea. Nature 2012, 482:331-338.
Wild J.M. Birdsong: anatomical foundations and central mechanisms of sensorimotor integration. Neuroscience of Birdsong 2008, 136-151. Cambridge University Press, New York, NY. H.P. Ziegler, P. Marler (Eds.).
Wild J.M., Balthazart J. Neural pathways mediating control of reproductive behavior in male Japanese quail. J. Comp. Neurol. 2013, 521:2067-2087.
Wild J.M., Botelho J.F. Involvement of the avian song system in reproductive behaviour. Biol. Lett. 2015, 11. 20150773.
Williams T.D. Physiological Adaptations for Breeding in Birds 2012, Princeton University Press, Princeton NJ.
Wingfield J.C. Hormone-behavior interactions and mating systems in male and female birds. Th Edifferences between the Sexes 1994, 303-330. Cambridge University Press, Cambridge UK. R.V. Short, E. Balaban (Eds.).
Wingfield J.C. Communicative behaviors, hormone-behavior interactions and reproduction in vertebrates. Physiology of Reproduction 2006, 1995-2040. Academic Press, Elsevier, San Diego. third ed. J.D. Neil (Ed.).
Wingfield J.C. Coping with change: a framework for environmental signals and how neuroendocrine pathways might respond. Front. Neuroendocrinol. 2015, 37:89-96.
Wingfield J.C., Farner D.S. Control of seasonal reproduction in temperate-zone birds. Prog. Reprod. Biol. 1980, 5:62-101.
Wingfield J.C., Farner D.S. Endocrinology of reproduction in wild species. Avian Biology 1993, vol. 9:163-327. Academic Press, New York.
Wingfield J.C., Goldsmith A.R. Plasma levels of prolactin and gonadal steroids in relation to multiple-brooding and renesting in free-living populations of the song sparrow, Melospiza melodia. Horm. Behav. 1990, 24:89-103.
Wingfield J.C., Hegner R.E., Dufty A.M., Ball G.F. The "challenge hypothesis': theoretical implications for patterns of testosterone secretion, mating systems and breedings strategies. Am. Nat. 1990, 136:829-846.
Wingfield J.C., Jacobs J., Hillgarth N. Ecological constraints and the evolution of hormone-behavior interrelationships. Ann. N.Y. Acad. Sci. 1997, 807:22-41.
Wingfield J.C., Moore M.C. Hormonal, social, and environmental factors in the reproductive biology of free-living male birds. Psychobiology of Reproductive Behavior: An Evolutionary Perspective 1987, 148-175. Prentice-Hall, Englewood Cliffs NJ. D. Crews (Ed.).
Wingfield J.C., Silverin B. Ecophysiological studies of hormone-behavior relations in birds. Hormones, Brain and Behavior 2002, 587-647. Academic Press, San Diego, CA. D.W. Pfaff, A.P. Arnold, A.M. Etgen, S.E. Fahrbach, R.T. Rubin (Eds.).
Wingfield J.C., Soma K.K. Spring and autumn territoriality in song sparrows: same behavior, different mechanisms?. Integr. Comp. Biol. 2002, 42:11-20.
Wingfield J.C., Soma K.K., Wikelski M., Meddle S.L., Hau M. Life cycles, behavioural traits and endocrine mechanisms. Avian Endocrinology 2002, 1-17. Narosa Publishing House, New Delhi. A. Dawson, C.M. Chaturvedi (Eds.).
Wingfield J.C., Whaling C.S., Marler P. Communication in vertebrate aggression and reproduction: the role of hormones. The Physiology of Reproduction 1994, 303-341. Raven Press, New York. second ed. E. Knobil, J.D. Neill (Eds.).
Wood-Gush D.G.M., Gilbert A.B. The control of the nesting behaviour of the domestic hen. II. The role of the ovary. Anim. Behav. 1964, 12:451-453.
Wood-Gush D.G.M., Gilbert A.B. The nesting behaviour of hens with ovarian transplants. Anim. Behav. 1970, 18:52-54.
Wood-Gush D.G.M., Gilbert A.B. Some hormones involved in the nesting behaviour of hens. Anim. Behav. 1973, 21:98-103.
Wynne R.D., Coomaralingam L., Rohmann K.N., Saldanha C.J. Locally Synthesized Estradiol via Glial Aromatization Decreases Neural Injury in the Zebra Finch 2004, SBN 04 Lisbonne.
Wynne R.D., Saldanha C.J. Glial aromatization decreases neural injury in the zebra finch (Taeniopygia guttata): influence on apoptosis. J. Neuroendocrinol. 2004, 16:676-683.
Wynne R.D., Walters B.J., Bailey D.J., Saldanha C.J. Inhibition of injury-induced glial aromatase reveals a wave of secondary degeneration in the songbird brain. Glia 2008, 56:97-105.
Xie J., Kuenzel W.J., Sharp P.J., Jurkevich A. Appetitive and consummatory sexual and agonistic behaviour elicits FOS expression in aromatase and vasotocin neurones within the preoptic area and bed nucleus of the stria terminalis of male domestic chickens. J. Neuroendocrinol. 2011, 23:232-243.
Young K.A., Ball G.F., Nelson R.J. Photoperiod-induced testicular apoptosis in European starlings (Sturnus vulgaris). Biol. Reprod. 2001, 64:706-713.
Zeier H., Karten H.J. The archistriatum of the pigeon: organization of afferent and efferent connections. Brain Res. 1971, 31:313-326.
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