K. L. Ayers, L. S. Lambeth, N. M. Davidson, A. H. Sinclair, A. Oshlack et al., Identification of candidate gonadal sex differentiation genes in the chicken embryo using RNA-seq, BMC Genomics, vol.16, p.704, 2015.

D. Bachiller, J. Klingensmith, C. Kemp, J. A. Belo, R. M. Anderson et al., The organizer factors Chordin and Noggin are required for mouse forebrain development, Nature, vol.403, pp.658-661, 2000.

I. Bar, S. Cummins, and A. Elizur, Transcriptome analysis reveals differentially expressed genes associated with germ cell and gonad, 2016.

, Table 22 Comparison of sex-specifically expressed genes in developing gonads of Xenopus and red-eared slider (Trachemys scripta), American alligator, and zebrafish development in the Southern bluefin tuna

, BMC Genomics, vol.17, p.217

A. Beverdam and P. Koopman, Expression profiling of purified mouse gonadal somatic cells during the critical time window of sex determination reveals novel candidate genes for human sexual dysgenesis syndromes, Hum Mol Genet, vol.15, pp.417-431, 2006.

H. Chen, J. S. Palmer, R. D. Thiagarajan, M. E. Dinger, E. Lesieur et al., Identification of novel markers of mouse fetal ovary development, PLoS One, vol.7, p.41683, 2012.

M. Czerwinski, A. Natarajan, L. Barske, L. L. Looger, and B. Capel, A timecourse analysis of systemic and gonadal effects of temperature on sexual development of the red-eared slider turtle Trachemys scripta elegans, Dev Biol, vol.420, pp.166-177, 2016.

W. Gong, L. Pan, Q. Lin, Y. Zhou, C. Xin et al., Transcriptome profiling of the developing postnatal mouse testis using next-generation sequencing, Sci China Life Sci, vol.56, pp.1-12, 2013.

J. T. Haselman, A. W. Olmstead, and S. J. Degitz, Global gene expression during early differentiation of Xenopus (Silurana) tropicalis gonad tissues, Gen Comp Endocrinol, vol.214, pp.103-113, 2015.

S. A. Jameson, A. Natarajan, J. Cool, T. Defalco, D. M. Maatouk et al., Temporal transcriptional profiling of somatic and germ cells reveals biased lineage priming of sexual fate in the fetal mouse gonad, PLoS Genet, vol.8, issue.3, p.1002575, 2012.

R. Lin, L. Wang, Y. Zhao, J. Gao, and Z. Chen, Gonad transcriptome of discus fish (Symphysodon haraldi) and discovery of sex-related genes, Aquac Res, vol.48, pp.5993-6000, 2017.

S. Nef, O. Schaad, N. R. Stallings, C. R. Cederroth, J. L. Pitetti et al., Gene expression during sex determination reveals a robust female genetic program at the onset of ovarian development, Dev Biol, vol.287, pp.361-377, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00016568

P. D. Nieuwkoop, J. Faber, A. North-holland, D. Ogunyemi, J. Xu et al., Differentially expressed genes in adipocytokine signaling pathway of adipose tissue in pregnancy, J Diabetes Mellitus, vol.3, pp.86-95, 1956.

W. N. Pappano, I. C. Scott, T. G. Clark, R. L. Eddy, T. B. Shows et al., Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes, Genomics, vol.52, pp.236-239, 1998.

R. P. Piprek, A. Pecio, J. Z. Kubiak, and J. M. Szymura, Differential effects of busulfan on gonadal development in five divergent anuran species, Reprod Toxicol, vol.34, issue.3, pp.393-401, 2012.
URL : https://hal.archives-ouvertes.fr/inserm-00696195

R. P. Piprek, M. Kloc, and J. Z. Kubiak, Early development of the gonads: origin and differentiation of the somatic cells of the genital ridges, Results Probl Cell Differ, vol.58, pp.1-22, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01334064

R. P. Piprek, M. Kloc, J. P. Tassan, and J. Z. Kubiak, Development of Xenopus laevis bipotential gonads into testis or ovary is driven by sex-specific cell-cell interactions, proliferation rate, cell migration and deposition of extracellular matrix, Dev Biol, vol.432, pp.298-310, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01659527

R. P. Piprek, M. Damulewicz, M. Kloc, and J. Z. Kubiak, Transcriptome analysis identifies genes involved in sex determination and development of Xenopus laevis gonads, Differentiation, vol.100, pp.46-56, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01739955

Y. Sasai, B. Lu, H. Steinbeisser, D. Geissert, L. K. Gont et al., Xenopus chordin: a novel dorsalizing factor activated by organizer-specific homeobox genes, Cell, vol.79, pp.779-790, 1994.

J. Scheider, F. Afonso-grunz, K. Hoffmeier, R. Horres, F. Groher et al., Gene expression of chicken gonads is sex-and side-specific, Sex Dev, vol.8, pp.178-191, 2014.

C. L. Small, J. E. Shima, M. Uzumcu, M. K. Skinner, and M. D. Griswold, Profiling gene expression during the differentiation and development of the murine embryonic gonad, Biol Reprod, vol.72, pp.492-501, 2005.

R. Sreenivasan, M. Cai, R. Bartfai, X. Wang, A. Christoffels et al., Transcriptomic analyses reveal novel genes with sexually dimorphic expression in the zebrafish gonad and brain, PLoS One, vol.3, p.1791, 2008.

L. X. Sun, J. Teng, Y. Zhao, N. Li, H. Wang et al., Gonad transcriptome analysis of high-temperature-treated females and hightemperature-induced sex-reversed neomales in nile tilapia, Int J Mol Sci, vol.19, issue.3, p.689, 2018.

A. Toker, The biology and biochemistry of diacylglycerol signalling, EMBO Rep, vol.6, issue.4, pp.310-314, 2005.

T. Tsukiyama, M. Matsuda-tsukiyama, M. Bohgaki, S. Terai, S. Tanaka et al., Ymer acts as a multifunctional regulator in nuclear factor-?B and Fas signaling pathways, Mol Med, vol.18, pp.587-597, 2012.

D. Xu, K. N. Shen, Z. Fan, W. Huang, F. You et al., The testis and ovary transcriptomes of the rock bream (Oplegnathus fasciatus): a bony fish with a unique neo Y chromosome, Genom Data, vol.7, pp.210-213, 2016.

R. Yatsu, S. Miyagawa, S. Kohno, B. B. Parrott, K. Yamaguchi et al., RNA-seq analysis of the gonadal transcriptome during Alligator mississippiensis temperature-dependent sex determination and differentiation, BMC Genomics, vol.17, p.77, 2016.

S. Yoshimoto, E. Okada, H. Umemoto, K. Tamura, Y. Uno et al., A W-linked DM-domain gene, DM-W, participates in primary ovary development in Xenopus laevis, Proc Natl Acad Sci U S A, vol.105, pp.2469-2474, 2008.

S. Yoshimoto, N. Ikeda, Y. Izutsu, T. Shiba, N. Takamatsu et al., Opposite roles of DMRT1 and its W-linked paralogue, DM-W, in sexual dimorphism of Xenopus laevis: implications of a ZZ/ZWtype sex-determining system, Development, vol.137, pp.2519-2526, 2010.

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