S. Ohno, Evolution by Gene Duplication, 1970.
DOI : 10.1007/978-3-642-86659-3

P. Dehal and J. Boore, Two Rounds of Whole Genome Duplication in the Ancestral Vertebrate, PLoS Biology, vol.18, issue.10, p.314, 2005.
DOI : 10.1371/journal.pbio.0030314.st001

V. Ravi and B. Venkatesh, Rapidly evolving fish genomes and teleost diversity, Current Opinion in Genetics & Development, vol.18, issue.6, pp.544-550, 2008.
DOI : 10.1016/j.gde.2008.11.001

D. Steinke, S. Hoegg, H. Brinkmann, and A. Meyer, Three rounds (1R/2R/3R) of genome duplications and the evolution of the glycolytic pathway in vertebrates, BMC Biology, vol.4, issue.1, p.16, 2006.
DOI : 10.1186/1741-7007-4-16

A. Amores, A. Force, Y. Yan, L. Joly, and C. Amemiya, Zebrafish hox Clusters and Vertebrate Genome Evolution, Science, vol.282, issue.5394, pp.1711-1714, 1998.
DOI : 10.1126/science.282.5394.1711

E. Simpson and S. Davis, Minireview: aromatase and the regulation of estrogen biosynthesis--some new perspectives, Endocrinology, vol.142, pp.4589-4594, 2001.

I. Lange, A. Hartel, and H. Meyer, Evolution of oestrogen functions in vertebrates, The Journal of Steroid Biochemistry and Molecular Biology, vol.83, issue.1-5, pp.219-226, 2002.
DOI : 10.1016/S0960-0760(02)00225-X

E. Simpson, Aromatase: biologic relevance of tissue-specific expression, Semin Reprod Med, vol.22, pp.11-23, 2004.

E. Lephart, A review of brain aromatase cytochrome P450, Brain Research Reviews, vol.22, issue.1, pp.1-26, 1996.
DOI : 10.1016/0165-0173(96)00002-1

R. Brinton, Estrogen-induced plasticity from cells to circuits: predictions for cognitive function, Trends in Pharmacological Sciences, vol.30, issue.4, pp.212-222, 2009.
DOI : 10.1016/j.tips.2008.12.006

C. Saldanha, K. Duncan, and B. Walters, Neuroprotective actions of brain aromatase, Frontiers in Neuroendocrinology, vol.30, issue.2, pp.106-118, 2009.
DOI : 10.1016/j.yfrne.2009.04.016

N. Harada and S. Honda, Analysis of spatiotemporal regulation of aromatase in the brain using transgenic mice, The Journal of Steroid Biochemistry and Molecular Biology, vol.95, issue.1-5, pp.49-55, 2005.
DOI : 10.1016/j.jsbmb.2005.04.003

A. Tchoudakova and G. Callard, Identification of Multiple CYP19 Genes Encoding Different Cytochrome P450 Aromatase Isozymes in Brain and Ovary, Endocrinology, vol.139, issue.4, pp.2179-2189, 1998.
DOI : 10.1210/en.139.4.2179

A. Gonzalez and F. Piferrer, Characterization of aromatase activity in the sea bass: effects of temperature and different catalytic properties of brain and ovarian homogenates and microsomes, Journal of Experimental Zoology, vol.88, issue.5, pp.500-510, 2002.
DOI : 10.1002/jez.90005

F. Piferrer and M. Blazquez, Aromatase distribution and regulation in fish, Fish Physiology and Biochemistry, vol.58, issue.2-3, pp.215-226, 2005.
DOI : 10.1007/s10695-006-0027-0

N. Diotel, L. Page, Y. Mouriec, K. Tong, S. Pellegrini et al., Aromatase in the brain of teleost fish: Expression, regulation and putative functions, Frontiers in Neuroendocrinology, vol.31, issue.2, pp.172-192, 2010.
DOI : 10.1016/j.yfrne.2010.01.003
URL : https://hal.archives-ouvertes.fr/hal-00472008

M. Pasmanik and G. Callard, Aromatase and 5??-reductase in the teleost brain, spinal cord, and pituitary gland, General and Comparative Endocrinology, vol.60, issue.2, pp.244-251, 1985.
DOI : 10.1016/0016-6480(85)90320-X

P. Forlano, D. Deitcher, D. Myers, and A. Bass, Anatomical distribution and cellular basis for high levels of aromatase activity in the brain of teleost fish: aromatase enzyme and mRNA expression identify glia as source, J Neurosci, vol.21, pp.8943-8955, 2001.

A. Menuet, I. Anglade, L. Guevel, R. Pellegrini, E. Pakdel et al., Distribution of aromatase mRNA and protein in the brain and pituitary of female rainbow trout: Comparison with estrogen receptor ?, The Journal of Comparative Neurology, vol.140, issue.2, pp.180-193, 2003.
DOI : 10.1002/cne.10726
URL : https://hal.archives-ouvertes.fr/hal-00295588

A. Menuet, E. Pellegrini, F. Brion, M. Gueguen, and I. Anglade, Expression and estrogen-dependent regulation of the zebrafish brain aromatase gene, The Journal of Comparative Neurology, vol.102, issue.4, pp.304-320, 2005.
DOI : 10.1002/cne.20497
URL : https://hal.archives-ouvertes.fr/hal-00294769

P. Strobl-mazzulla, A. Nunez, E. Pellegrini, M. Gueguen, and O. Kah, Progenitor Radial Cells and Neurogenesis in Pejerrey Fish Forebrain, Brain, Behavior and Evolution, vol.76, issue.1, pp.20-31, 2010.
DOI : 10.1159/000316022
URL : https://hal.archives-ouvertes.fr/hal-00592393

A. Kriegstein and A. Alvarez-buylla, The Glial Nature of Embryonic and Adult Neural Stem Cells, Annual Review of Neuroscience, vol.32, issue.1, pp.149-184, 2009.
DOI : 10.1146/annurev.neuro.051508.135600

C. Lam, M. März, and U. Strahle, gfap and nestin reporter lines reveal characteristics of neural progenitors in the adult zebrafish brain, Developmental Dynamics, vol.488, issue.suppl 1, pp.475-486, 2009.
DOI : 10.1002/dvdy.21853

M. Mä-rz, P. Chapouton, N. Diotel, C. Vaillant, and B. Hesl, Heterogeneity in progenitor cell subtypes in the ventricular zone of the zebrafish adult telencephalon, Glia, vol.58, pp.870-888, 2010.

E. Pellegrini, K. Mouriec, I. Anglade, A. Menuet, L. Page et al., Identification of aromatase-positive radial glial cells as progenitor cells in the ventricular layer of the forebrain in zebrafish, The Journal of Comparative Neurology, vol.1334, issue.1, pp.150-167, 2007.
DOI : 10.1002/cne.21222
URL : https://hal.archives-ouvertes.fr/hal-00096389

I. Rothenaigner, M. Krecsmarik, J. Hayes, B. Bahn, and A. Lepier, Clonal analysis by distinct viral vectors identifies bona fide neural stem cells in the adult zebrafish telencephalon and characterizes their division properties and fate, Development, vol.138, issue.8, pp.1459-1469, 2011.
DOI : 10.1242/dev.058156
URL : https://hal.archives-ouvertes.fr/hal-00585364

K. Mouriec, M. Gueguen, C. Manuel, F. Percevault, and M. Thieulant, Androgens Upregulate cyp19a1b (Aromatase B) Gene Expression in the Brain of Zebrafish (Danio rerio) Through Estrogen Receptors1, Biology of Reproduction, vol.80, issue.5, pp.889-896, 2009.
DOI : 10.1095/biolreprod.108.073643
URL : https://hal.archives-ouvertes.fr/hal-00383313

K. Okubo, A. Takeuchi, R. Chaube, B. Paul-prasanth, and S. Kanda, Sex Differences in Aromatase Gene Expression in the Medaka Brain, Journal of Neuroendocrinology, vol.82, issue.5, pp.412-423, 2011.
DOI : 10.1111/j.1365-2826.2011.02120.x

L. Page, Y. Scholze, M. Kah, O. Pakdel, and F. , Assessment of Xenoestrogens Using Three Distinct Estrogen Receptors and the Zebrafish Brain Aromatase Gene in a Highly Responsive Glial Cell System, Environmental Health Perspectives, vol.114, issue.5, pp.752-758, 2006.
DOI : 10.1289/ehp.8141
URL : https://hal.archives-ouvertes.fr/hal-00068400

Y. Kazeto and J. Trant, Molecular biology of channel catfish brain cytochrome P450 aromatase (CYP19A2): cloning, preovulatory induction of gene expression, hormonal gene regulation and analysis of promoter region, Journal of Molecular Endocrinology, vol.35, issue.3, pp.571-583, 2005.
DOI : 10.1677/jme.1.01805

S. Jeng, J. Pasquier, W. Yueh, G. Chen, and Y. Lee, Differential regulation of the expression of cytochrome P450 aromatase, estrogen and androgen receptor subtypes in the brain???pituitary???ovarian axis of the Japanese eel (Anguilla japonica) reveals steroid dependent and independent mechanisms, General and Comparative Endocrinology, vol.175, issue.1, pp.163-172, 2012.
DOI : 10.1016/j.ygcen.2011.11.005

S. Ijiri, Y. Kazeto, P. Lokman, S. Adachi, and K. Yamauchi, Characterization of a cDNA Encoding P-450 aromatase (CYP19) from Japanese eel ovary and its expression in ovarian follicles during induced ovarian development, General and Comparative Endocrinology, vol.130, issue.2, pp.193-203, 2003.
DOI : 10.1016/S0016-6480(02)00589-0

I. Tzchori, G. Degani, A. Hurvitz, and B. Moav, Cloning and developmental expression of the cytochrome P450 aromatase gene (CYP19) in the European eel (Anguilla anguilla), General and Comparative Endocrinology, vol.138, issue.3, pp.271-280, 2004.
DOI : 10.1016/j.ygcen.2004.06.007

C. Henkel, E. Burgerhout, D. De-wijze, R. Dirks, and Y. Minegishi, Primitive Duplicate Hox Clusters in the European Eel's Genome, PLoS ONE, vol.6, issue.4, p.32231, 2012.
DOI : 10.1371/journal.pone.0032231.s008

B. Guo, X. Gan, and S. He, Hox genes of the Japanese eel Anguilla japonica and Hox cluster evolution in teleosts, J Exp Zool B Mol Dev Evol, vol.314, pp.135-147, 2010.

K. Yamamoto and K. Yamauchi, Sexual maturation of Japanese eel and production of eel larvae in the aquarium, Nature, vol.40, issue.5472, pp.220-222, 1974.
DOI : 10.1038/251220a0

S. Jeng, S. Dufour, and C. Chang, Differential expression of neural and gonadal aromatase enzymatic activities in relation to gonadal development in Japanese eel,Anguilla japonica, Journal of Experimental Zoology Part A: Comparative Experimental Biology, vol.88, issue.9, pp.802-812, 2005.
DOI : 10.1002/jez.a.194
URL : https://hal.archives-ouvertes.fr/hal-00096626

S. Dufour, E. Burzawa-gérard, L. Belle, N. Sbaihi, M. Vidal et al., Reproductive Endocrinology of the European Eel, Anguilla anguilla, In: Eel Biology, pp.373-383, 2003.
DOI : 10.1007/978-4-431-65907-5_25

A. Servili, L. Page, Y. Leprince, J. Caraty, A. Escobar et al., Organization of Two Independent Kisspeptin Systems Derived from Evolutionary-Ancient Kiss Genes in the Brain of Zebrafish, Endocrinology, vol.152, issue.4, pp.1527-1540, 2011.
DOI : 10.1210/en.2010-0948
URL : https://hal.archives-ouvertes.fr/hal-00586856

T. Mukuda and M. Ando, Brain atlas of the Japanese eel: Comparison to other fishes. Mem Fac Integrated Arts and Sci, pp.1-25, 2003.

S. Dufour, L. Belle, N. Baloche, S. Fontaine, and Y. , Positive feedback control by the gonads on gonadotropin (GTH) and gonadoliberin (GnRH) levels in experimentally matured female silver eels,Anguilla anguilla, Fish Physiology and Biochemistry, vol.159, issue.1-6, pp.157-162, 1989.
DOI : 10.1007/BF00004702

S. Jeng, W. Yueh, G. Chen, Y. Lee, and S. Dufour, Differential expression and regulation of gonadotropins and their receptors in the Japanese eel, Anguilla japonica, General and Comparative Endocrinology, vol.154, issue.1-3, pp.161-173, 2007.
DOI : 10.1016/j.ygcen.2007.05.026
URL : https://hal.archives-ouvertes.fr/hal-00179963

M. Pasmanik and G. Callard, )*, Endocrinology, vol.122, issue.4, pp.1349-1356, 1988.
DOI : 10.1210/endo-122-4-1349

E. Kallivretaki, R. Eggen, S. Neuhauss, O. Kah, and H. Segner, The zebrafish, brain-specific, aromatasecyp19a2 is neither expressed nor distributed in a sexually dimorphic manner during sexual differentiation, Developmental Dynamics, vol.211, issue.11, pp.3155-3166, 2007.
DOI : 10.1002/dvdy.21344

S. Tong, K. Mouriec, M. Kuo, E. Pellegrini, and M. Gueguen, (aromatase B) transgenic zebrafish line that expresses GFP in radial glial cells, genesis, vol.1, issue.2, pp.67-73, 2009.
DOI : 10.1002/dvg.20459
URL : https://hal.archives-ouvertes.fr/hal-00450594

R. Timmers, J. Lambert, J. Peute, H. Vullings, and P. Van-oordt, Localization of aromatase in the brain of the male African catfish,Clarias gariepinus (Burchell), by microdissection and biochemical identification, The Journal of Comparative Neurology, vol.61, issue.3, pp.368-377, 1987.
DOI : 10.1002/cne.902580305

N. Diotel, D. Rego, J. Anglade, I. Vaillant, C. Pellegrini et al., Activity and expression of steroidogenic enzymes in the brain of adult zebrafish, European Journal of Neuroscience, vol.170, issue.1, pp.45-56, 2011.
DOI : 10.1111/j.1460-9568.2011.07731.x
URL : https://hal.archives-ouvertes.fr/hal-00616835

K. Mouriec, E. Pellegrini, I. Anglade, A. Menuet, and F. Adrio, Synthesis of estrogens in progenitor cells of adult fish brain: Evolutive novelty or exaggeration of a more general mechanism implicating estrogens in neurogenesis?, Brain Research Bulletin, vol.75, issue.2-4, pp.274-280, 2008.
DOI : 10.1016/j.brainresbull.2007.10.030
URL : https://hal.archives-ouvertes.fr/hal-00266593

M. Vosges, L. Page, Y. Chung, B. Combarnous, Y. Porcher et al., 17??-Ethinylestradiol disrupts the ontogeny of the forebrain GnRH system and the expression of brain aromatase during early development of zebrafish, Aquatic Toxicology, vol.99, issue.4, pp.479-491, 2010.
DOI : 10.1016/j.aquatox.2010.06.009
URL : https://hal.archives-ouvertes.fr/hal-00592402

K. Marsh, L. Creutz, M. Hawkins, and J. Godwin, Aromatase immunoreactivity in the bluehead wrasse brain, Thalassoma bifasciatum: Immunolocalization and co-regionalization with arginine vasotocin and tyrosine hydroxylase, Brain Research, vol.1126, issue.1, pp.91-101, 2006.
DOI : 10.1016/j.brainres.2006.09.017

K. Mouriec, J. Lareyre, S. Tong, L. Page, Y. Vaillant et al., ) by estrogen receptors during zebrafish development, Developmental Dynamics, vol.43, issue.10, pp.2641-2651, 2009.
DOI : 10.1002/dvdy.22069

J. Balthazart, P. Absil, A. Foidart, M. Houbart, and N. Harada, Distribution of aromatase-immunoreactive cells in the forebrain of zebra finches (Taeniopygia guttata): Implications for the neural action of steroids and nuclear definition in the avian hypothalamus, Journal of Neurobiology, vol.99, issue.2, pp.129-148, 1996.
DOI : 10.1002/(SICI)1097-4695(199610)31:2<129::AID-NEU1>3.0.CO;2-D

P. Forlano, B. Schlinger, and A. Bass, Brain aromatase: New lessons from non-mammalian model systems, Frontiers in Neuroendocrinology, vol.27, issue.3, pp.247-274, 2006.
DOI : 10.1016/j.yfrne.2006.05.002

C. Saldanha, M. Tuerk, Y. Kim, A. Fernandes, and A. Arnold, Distribution and regulation of telencephalic aromatase expression in the zebra finch revealed with a specific antibody, The Journal of Comparative Neurology, vol.95, issue.4, pp.619-630, 2000.
DOI : 10.1002/1096-9861(20000807)423:4<619::AID-CNE7>3.0.CO;2-U

C. Saldanha, B. Walters, and G. Fraley, Neurons that co-localize aromatase- and kisspeptin-like immunoreactivity may regulate the HPG axis of the Mallard drake (Anas platyrhynchos), General and Comparative Endocrinology, vol.166, issue.3, pp.606-613, 2010.
DOI : 10.1016/j.ygcen.2010.01.007

I. Azcoitia, A. Sierra, S. Veiga, and L. Garcia-segura, Aromatase Expression by Reactive Astroglia Is Neuroprotective, Annals of the New York Academy of Sciences, vol.388, issue.1, pp.298-305, 2003.
DOI : 10.1196/annals.1286.028

L. Garcia-segura, A. Wozniak, I. Azcoitia, J. Rodriguez, and R. Hutchison, Aromatase expression by astrocytes after brain injury: implications for local estrogen formation in brain repair, Neuroscience, vol.89, issue.2, pp.567-578, 1999.
DOI : 10.1016/S0306-4522(98)00340-6

R. Peterson, D. Lee, G. Fernando, and B. Schlinger, Radial glia express aromatase in the injured zebra finch brain, The Journal of Comparative Neurology, vol.12, issue.2, pp.261-269, 2004.
DOI : 10.1002/cne.20157

M. Bentivoglio and P. Mazzarello, The history of radial glia, Brain Research Bulletin, vol.49, issue.5, pp.305-315, 1999.
DOI : 10.1016/S0361-9230(99)00065-9

M. Gotz and W. Huttner, The cell biology of neurogenesis, Nature Reviews Molecular Cell Biology, vol.16, issue.10, pp.777-788, 2005.
DOI : 10.1523/JNEUROSCI.0778-05.2005

D. Hansen, J. Lui, P. Parker, and A. Kriegstein, Neurogenic radial glia in the outer subventricular zone of human neocortex, Nature, vol.133, issue.7288, pp.554-561, 2010.
DOI : 10.1038/nature08845

L. Pinto and M. Gotz, Radial glial cell heterogeneity???The source of diverse progeny in the CNS, Progress in Neurobiology, vol.83, issue.1, pp.2-23, 2007.
DOI : 10.1016/j.pneurobio.2007.02.010

P. Rakic, Neuronal migration and contact guidance in the primate telencephalon, Postgrad Med J, vol.54, issue.1, pp.25-40, 1978.

T. Anthony and N. Heintz, Genetic lineage tracing defines distinct neurogenic and gliogenic stages of ventral telencephalic radial glial development, Neural Development, vol.3, issue.1, p.30, 2008.
DOI : 10.1186/1749-8104-3-30

T. Anthony, H. Mason, T. Gridley, G. Fishell, and N. Heintz, Brain lipid-binding protein is a direct target of Notch signaling in radial glial cells, Genes & Development, vol.19, issue.9, pp.1028-1033, 2005.
DOI : 10.1101/gad.1302105

N. Diotel, C. Vaillant, M. Gueguen, S. Mironov, and I. Anglade, Cxcr4 and Cxcl12 expression in radial glial cells of the brain of adult zebrafish, The Journal of Comparative Neurology, vol.159, issue.Suppl 1, pp.4855-4876, 2010.
DOI : 10.1002/cne.22492
URL : https://hal.archives-ouvertes.fr/inserm-00590787

G. Callard, J. Specker, J. Knapp, R. Nishioka, and H. Bern, Aromatase is concentrated in the proximal pars distalis of tilapia pituitary, General and Comparative Endocrinology, vol.71, issue.1, pp.70-79, 1988.
DOI : 10.1016/0016-6480(88)90296-1

M. Olivereau, P. Dubourg, P. Chambolle, and J. Olivereau, Effects of estradiol and mammalian LHRH on the ultrastructure of the pars distalis of the eel, Cell and Tissue Research, vol.40, issue.2, pp.425-437, 1986.
DOI : 10.1007/BF00215905

M. Yamashita, Z. Qian, T. Sano, E. Horvath, and K. Kovacs, Immunohistochemical study on so-called follicular cells and folliculostellate cells in the human adenohypophysis, Pathology International, vol.298, issue.5, pp.244-247, 2005.
DOI : 10.1006/bbrc.1997.6704

M. Acosta, V. Filippa, and M. F. , Folliculostellate cells in pituitary pars distalis of male viscacha: immunohistochemical, morphometric and ultrastructural study, European Journal of Histochemistry, vol.54, issue.1, p.1, 2010.
DOI : 10.4081/ejh.2010.e1

I. Rothenaigner, M. Krecsmarik, J. Hayes, B. Bahn, and A. Lepier, Clonal analysis by distinct viral vectors identifies bona fide neural stem cells in the adult zebrafish telencephalon and characterizes their division properties and fate, Development, vol.138, issue.8, 2011.
DOI : 10.1242/dev.058156
URL : https://hal.archives-ouvertes.fr/hal-00585364

C. Lam, M. Marz, and U. Strahle, gfap and nestin reporter lines reveal characteristics of neural progenitors in the adult zebrafish brain, Developmental Dynamics, vol.488, issue.suppl 1, pp.475-486, 2009.
DOI : 10.1002/dvdy.21853

P. Ekström, C. Johnsson, and L. Ohlin, Ventricular proliferation zones in the brain of an adult teleost fish and their relation to neuromeres and migration (secondary matrix) zones, Journal of Comparative Neurology, vol.370, issue.18, pp.92-110, 2001.
DOI : 10.1002/cne.1056

G. Zupanc, Neurogenesis, cell death and regeneration in the adult gymnotiform brain, J Exp Biol, vol.202, pp.1435-1446, 1999.

N. Diotel, D. Rego, J. Anglade, I. Vaillant, C. Pellegrini et al., The Brain of Teleost Fish, a Source, and a Target of Sexual Steroids, Frontiers in Neuroscience, vol.5, p.137, 2011.
DOI : 10.3389/fnins.2011.00137
URL : https://hal.archives-ouvertes.fr/hal-00877403

L. Page, Y. Diotel, N. Vaillant, C. Pellegrini, E. Anglade et al., Aromatase, brain sexualization and plasticity: the fish paradigm, European Journal of Neuroscience, vol.1334, issue.Suppl 2, pp.2105-2115, 2010.
DOI : 10.1111/j.1460-9568.2010.07519.x
URL : https://hal.archives-ouvertes.fr/hal-00586266

C. Barha and L. Galea, Influence of different estrogens on neuroplasticity and cognition in the hippocampus, Biochimica et Biophysica Acta (BBA) - General Subjects, vol.1800, issue.10, pp.1056-1067, 2010.
DOI : 10.1016/j.bbagen.2010.01.006

O. Brock, M. Keller, A. Veyrac, Q. Douhard, and J. Bakker, Short term treatment with estradiol decreases the rate of newly generated cells in the subventricular zone and main olfactory bulb of adult female mice, Neuroscience, vol.166, issue.2, pp.368-376, 2010.
DOI : 10.1016/j.neuroscience.2009.12.050
URL : https://hal.archives-ouvertes.fr/hal-01129527

M. Burek, K. Nordeen, and E. Nordeen, Estrogen promotes neuron addition to an avian song-control nucleus by regulating post-mitotic events, Developmental Brain Research, vol.85, issue.2, pp.220-224, 1995.
DOI : 10.1016/0165-3806(94)00215-L

L. Galea, Gonadal hormone modulation of neurogenesis in the dentate gyrus of adult male and female rodents, Brain Research Reviews, vol.57, issue.2, pp.332-341, 2008.
DOI : 10.1016/j.brainresrev.2007.05.008

V. Martinez-cerdeno, S. Noctor, and A. Kriegstein, Estradiol stimulates progenitor cell division in the ventricular and subventricular zones of the embryonic neocortex, European Journal of Neuroscience, vol.129, issue.12, pp.3475-3488, 2006.
DOI : 10.1111/j.1460-9568.2006.05239.x

C. Mazzucco, S. Lieblich, B. Bingham, M. Williamson, and V. Viau, Both estrogen receptor ?? and estrogen receptor ?? agonists enhance cell proliferation in the dentate gyrus of adult female rats, Neuroscience, vol.141, issue.4, pp.1793-1800, 2006.
DOI : 10.1016/j.neuroscience.2006.05.032

S. Suzuki, L. Gerhold, M. Bottner, S. Rau, D. Cruz et al., Estradiol enhances neurogenesis following ischemic stroke through estrogen receptors ?? and ??, The Journal of Comparative Neurology, vol.11, issue.6, pp.1064-1075, 2007.
DOI : 10.1002/cne.21240

A. Veyrac and J. Bakker, Postnatal and adult exposure to estradiol differentially influences adult neurogenesis in the main and accessory olfactory bulb of female mice, The FASEB Journal, vol.25, issue.3, pp.1048-1057, 2011.
DOI : 10.1096/fj.10-172635

N. Diotel, C. Vaillant, C. Gabbero, A. Fostier, and M. Gueguen, Effects of estradiol in adult neurogenesis and brain repair in zebrafish, Hormones and Behavior, vol.63, issue.2, 2012.
DOI : 10.1016/j.yhbeh.2012.04.003
URL : https://hal.archives-ouvertes.fr/inserm-00831715

A. Amores, T. Suzuki, Y. Yan, J. Pomeroy, and A. Singer, Developmental Roles of Pufferfish Hox Clusters and Genome Evolution in Ray-Fin Fish, Genome Research, vol.14, issue.1, pp.1-10, 2004.
DOI : 10.1101/gr.1717804

A. Force, W. Cresko, F. Pickett, S. Proulx, and C. Amemiya, The Origin of Subfunctions and Modular Gene Regulation, Genetics, vol.170, issue.1, pp.433-446, 2005.
DOI : 10.1534/genetics.104.027607

A. Force, M. Lynch, F. Pickett, A. Amores, and Y. Yan, Preservation of duplicate genes by complementary, degenerative mutations, Genetics, vol.151, pp.1531-1545, 1999.

W. Cresko, Y. Yan, D. Baltrus, A. Amores, and A. Singer, in stickleback and zebrafish, Developmental Dynamics, vol.34, issue.3, pp.480-489, 2003.
DOI : 10.1002/dvdy.10424