A. R. Amiel, H. T. Johnston, K. Nedoncelle, J. F. Warner, S. Ferreira et al., Characterization of Morphological and Cellular Events Underlying Oral Regeneration in the Sea Anemone, Nematostella vectensis, International Journal of Molecular Sciences, vol.47, issue.12, pp.28449-28471, 2015.
DOI : 10.1016/j.zool.2014.06.005

A. M. Abdol, E. Röttinger, F. Jansson, and J. A. Kaandorp, A novel technique to combine and analyse spatial and temporal expression datasets: A case study with the sea anemone Nematostella vectensis to identify potential gene interactions, Developmental Biology, vol.428, issue.1, pp.204-214, 2017.
DOI : 10.1016/j.ydbio.2017.06.004

D. A. Baker, B. Mille-baker, S. M. Wainwright, D. Ish-horowicz, and N. J. Dibb, Mae mediates MAP kinase phosphorylation of Ets transcription factors in Drosophila, Nature, vol.411, issue.6835, pp.330-334, 2001.
DOI : 10.1038/35077122

S. Bertrand, A. Camasses, I. Somorjai, . Belgacem, . Mr et al., Amphioxus FGF signaling predicts the acquisition of vertebrate morphological traits, Proc. Natl. Acad. Sci. USA, pp.9160-9165, 2011.
DOI : 10.1007/s00427-008-0256-6

URL : https://hal.archives-ouvertes.fr/hal-00831149

S. Bertrand, T. Iwema, and H. Escriva, FGF Signaling Emerged Concomitantly with the Origin of Eumetazoans, Molecular Biology and Evolution, vol.31, issue.2, pp.310-318, 2014.
DOI : 10.1093/molbev/mst222

R. Burdine, . Chen, . Eb, . Kwok, . Sf et al., egl-17 encodes an invertebrate fibroblast growth factor family member required specifically for sex myoblast migration in Caenorhabditis elegans, Proc. Natl. Sci. USA 94, pp.2433-2437, 1997.
DOI : 10.1016/0092-8674(93)90688-M

T. Casci, J. Vinós, and M. Freeman, Sprouty, an Intracellular Inhibitor of Ras Signaling, Cell, vol.96, issue.5, pp.655-665, 1999.
DOI : 10.1016/S0092-8674(00)80576-0

Y. Chen, P. Chi, S. Rockowitz, P. J. Iaquinta, T. Shamu et al., ETS factors reprogram the androgen receptor cistrome and prime prostate tumorigenesis in response to PTEN loss, Nature Medicine, vol.9, issue.8, pp.1023-1029, 2013.
DOI : 10.1186/gb-2008-9-9-r137

D. Chourrout, F. Delsuc, P. Chourrout, R. B. Edvardsen, F. Rentzsch et al., Minimal ProtoHox cluster inferred from bilaterian and cnidarian Hox complements, Nature, vol.8, issue.7103, pp.684-687, 2006.
DOI : 10.1038/nature04863

URL : https://hal.archives-ouvertes.fr/halsde-00315426

J. A. Darling, A. R. Reitzel, P. M. Burton, M. E. Mazza, J. F. Ryan et al., Rising starlet: the starlet sea anemone,Nematostella vectensis, BioEssays, vol.214, issue.2, pp.211-221, 2005.
DOI : 10.1017/S0094837300005352

E. H. Davidson, J. P. Rast, P. Oliveri, A. Ransick, C. Calestani et al., A Provisional Regulatory Gene Network for Specification of Endomesoderm in the Sea Urchin Embryo, Developmental Biology, vol.246, issue.1, pp.162-190, 2002.
DOI : 10.1006/dbio.2002.0635

E. H. Davidson, J. P. Rast, P. Oliveri, A. Ransick, C. Calestani et al., A Genomic Regulatory Network for Development, Science, vol.295, issue.5560, pp.1669-1678, 2002.
DOI : 10.1126/science.1069883

S. P. Davies, H. Reddy, M. Caivano, and P. Cohen, Specificity and mechanism of action of some commonly used protein kinase inhibitors, Biochemical Journal, vol.351, issue.1, pp.95-1050264, 2000.
DOI : 10.1042/bj3510095

B. M. Degnan, S. M. Degnan, T. Naganuma, and D. E. Morse, multigene family is conserved throughout the Metazoa, Nucleic Acids Research, vol.21, issue.15, pp.3479-3484, 1993.
DOI : 10.1093/nar/21.15.3479

D. R. Desilva, E. A. Jones, M. F. Favata, B. D. Jaffee, R. L. Magolda et al., Inhibition of mitogen-activated protein kinase kinase blocks T cell proliferation but does not induce or prevent anergy, J. Immunol. Am. Assoc. Immnol, vol.160, pp.4175-4181, 1998.

K. Dorey and E. Amaya, FGF signalling: diverse roles during early vertebrate embryogenesis, Development, vol.137, issue.22, pp.3731-3742, 2010.
DOI : 10.1242/dev.037689

B. W. Draper, D. W. Stock, and C. B. Kimmel, to promote posterior mesodermal development, Development, vol.130, issue.19, pp.4639-4654, 2003.
DOI : 10.1242/dev.00671

L. Duloquin, G. Lhomond, and C. Gache, Localized VEGF signaling from ectoderm to mesenchyme cells controls morphogenesis of the sea urchin embryo skeleton, Development, vol.134, issue.12, pp.2293-2302, 2007.
DOI : 10.1242/dev.005108

M. Fernandez-serra, C. Consales, A. Livigni, and M. I. Arnone, Role of the ERK-mediated signaling pathway in mesenchyme formation and differentiation in the sea urchin embryo, Developmental Biology, vol.268, issue.2, pp.384-402, 2004.
DOI : 10.1016/j.ydbio.2003.12.029

J. H. Fritzenwanker, G. Genikhovich, Y. Kraus, and U. Technau, Early development and axis specification in the sea anemone Nematostella vectensis, Developmental Biology, vol.310, issue.2, pp.264-279, 2007.
DOI : 10.1016/j.ydbio.2007.07.029

J. H. Fritzenwanker, M. M. Saina, and U. U. Technau, Analysis of forkhead and snail expression reveals epithelial???mesenchymal transitions during embryonic and larval development of Nematostella vectensis, Developmental Biology, vol.275, issue.2, pp.389-402, 2004.
DOI : 10.1016/j.ydbio.2004.08.014

S. A. Green, R. P. Norris, M. Terasaki, and C. J. Lowe, FGF signaling induces mesoderm in the hemichordate Saccoglossus kowalevskii, Development, vol.140, issue.5, 2013.
DOI : 10.1242/dev.083790

A. Gutierrez-hartmann, D. L. Duval, and A. P. Bradford, ETS transcription factors in endocrine systems, Trends in Endocrinology & Metabolism, vol.18, issue.4, pp.150-158, 2007.
DOI : 10.1016/j.tem.2007.03.002

N. N. Hacohen, S. S. Kramer, D. D. Sutherland, Y. Y. Hiromi, and M. A. Krasnow, sprouty Encodes a Novel Antagonist of FGF Signaling that Patterns Apical Branching of the Drosophila Airways, Cell, vol.92, issue.2, pp.253-263, 1998.
DOI : 10.1016/S0092-8674(00)80919-8

C. Hand and K. R. Uhlinger, The Culture, Sexual and Asexual Reproduction, and Growth of the Sea Anemone Nematostella vectensis, The Biological Bulletin, vol.182, issue.2, pp.169-176, 1992.
DOI : 10.2307/1542110

B. G. Herrmann, S. Labeit, A. Poustka, T. R. King, and H. Lehrach, Cloning of the T gene required in mesoderm formation in the mouse, Nature, vol.343, issue.6259, pp.617-622, 1990.
DOI : 10.1038/343617a0

V. F. Hinman, A. Nguyen, and E. H. Davidson, Caught in the evolutionary act: Precise cis-regulatory basis of difference in the organization of gene networks of sea stars and sea urchins, Developmental Biology, vol.312, issue.2, pp.584-595, 2007.
DOI : 10.1016/j.ydbio.2007.09.006

P. Hollenhorst, RAS/ERK pathway transcriptional regulation through ETS/AP-1 binding sites, Small GTPases, vol.13, issue.3, pp.154-158, 2012.
DOI : 10.1101/gad.6.3.481

Y. Huang, J. A. Thoms, M. L. Tursky, K. Knezevic, D. Beck et al., MAPK/ERK2 phosphorylates ERG at serine 283 in leukemic cells and promotes stem cell signatures and cell proliferation, Leukemia, vol.279, issue.7, pp.1552-1561, 2016.
DOI : 10.4161/cc.7.5.5402

A. Ikmi, S. A. Mckinney, K. M. Delventhal, and M. C. Gibson, TALEN and CRISPR/Cas9-mediated genome editing in the early-branching metazoan Nematostella vectensis, Nature Communications, vol.14, issue.5486, 2014.
DOI : 10.1038/nmeth.2019

A. Kar and A. Gutierrez-hartmann, Molecular mechanisms of ETS transcription factor-mediated tumorigenesis, Critical Reviews in Biochemistry and Molecular Biology, vol.36, issue.6, pp.522-543, 2013.
DOI : 10.1016/j.leukres.2011.09.012

H. Kataoka, M. Hayashi, R. Nakagawa, Y. Tanaka, N. Izumi et al., Etv2/ER71 induces vascular mesoderm from Flk1+PDGFR?+ primitive mesoderm, Blood. Am. Soc. Hematol, vol.118, pp.6975-6986, 2011.

T. Kawahara, H. K. Shareef, A. K. Aljarah, H. Ide, Y. Li et al., ELK1 is up-regulated by androgen in bladder cancer cells and promotes tumor progression, Oncotarget, vol.6, issue.30, pp.29860-29876, 2015.
DOI : 10.18632/oncotarget.5007

T. Kiyota, A. Kato, and Y. Kato, Ets-1 Regulates Radial Glia Formation During Vertebrate Embryogenesis, Organogenesis, vol.7, issue.2, pp.93-101, 2007.
DOI : 10.1128/MCB.24.24.10954-10964.2004

B. Koh, M. M. Hufford, D. Pham, M. R. Olson, T. Wu et al., The ETS Family Transcription Factors Etv5 and PU.1 Function in Parallel To Promote Th9 Cell Development, The Journal of Immunology, vol.197, issue.6, pp.2465-2472, 2016.
DOI : 10.4049/jimmunol.1502383

S. Kramer, M. Okabe, N. Hacohen, M. A. Krasnow, and Y. Hiromi, Sprouty: a common antagonist of FGF and EGF signaling pathways in Drosophila, Development, vol.126, pp.2515-2525, 1999.

S. Kumburegama, N. Wijesena, R. Xu, and A. H. Wikramanayake, Strabismusmediated primary archenteron invagination is uncoupled from Wnt/?-catenindependent endoderm cell fate specification in Nematostella vectensis (Anthozoa, Cnidaria): implications for the evolution of gastrulation, EvoDevo, vol.2, issue.2, 2011.

S. Kumburegama, N. Wijesena, and R. Xu, Strabismus-mediated primary archenteron invagination is uncoupled from Wnt/?-catenin-dependent endoderm cell fate specification in Nematostella ?, EvoDevo, 2011.

A. Kusserow, K. Pang, C. Sturm, J. Lentfer, H. A. Schmidt et al., Unexpected complexity of the Wnt gene family in a sea anemone, Nature, vol.21, issue.7022, pp.156-160, 2005.
DOI : 10.1038/35056041

V. Laudet, C. Niel, M. Duterque-coquillaud, D. Leprince, and D. Stéhelin, Evolution of the ets Gene Family, Biochemical and Biophysical Research Communications, vol.190, issue.1, pp.8-14, 1993.
DOI : 10.1006/bbrc.1993.1002

V. Laudet, C. Hänni, D. Stéhelin, and M. Duterque-coquillaud, Molecular phylogeny of the ETS gene family, Oncogene, vol.18, issue.6, pp.1351-1359, 1999.
DOI : 10.1038/sj.onc.1202444

M. J. Layden, M. Boekhout, and M. Q. Martindale, Nematostella vectensis achaete-scute homolog NvashA regulates embryonic ectodermal neurogenesis and represents an ancient component of the metazoan neural specification pathway, Development, vol.139, issue.5, pp.1013-1022, 2012.
DOI : 10.1242/dev.073221

M. J. Layden, E. Röttinger, F. S. Wolenski, T. D. Gilmore, and M. Q. Martindale, Microinjection of mRNA or morpholinos for reverse genetic analysis in the starlet sea anemone, Nematostella vectensis, Nature Protocols, vol.74, issue.5, pp.924-934, 2013.
DOI : 10.1038/nprot.2013.044

M. J. Layden, F. Rentzsch, and E. Röttinger, as a model system to investigate development and regeneration, Wiley Interdisciplinary Reviews: Developmental Biology, vol.303, issue.4, pp.408-428, 2016.
DOI : 10.1016/j.ydbio.2006.11.022

M. J. Layden, H. Johnston, A. R. Amiel, J. Havrilak, B. Steinworth et al., MAPK signaling is necessary for neurogenesis in Nematostella vectensis, BMC Biology, vol.2, issue.1, pp.61-12915, 2016.
DOI : 10.1186/2041-9139-2-17

L. Leclère, M. Bause, C. Sinigaglia, J. Steger, and F. Rentzsch, Development of the aboral domain in Nematostella requires ?-catenin and the opposing activities of six3/6 and frizzled5, Development, vol.8, issue.143, pp.1766-1777, 2016.

P. N. Lee, K. Pang, D. Q. Matus, and M. Q. Martindale, A WNT of things to come: Evolution of Wnt signaling and polarity in cnidarians, Seminars in Cell & Developmental Biology, vol.17, issue.2, pp.157-167, 2006.
DOI : 10.1016/j.semcdb.2006.05.002

P. N. Lee, S. Kumburegama, H. Q. Marlow, M. Q. Martindale, and A. H. Wikramanayake, Asymmetric developmental potential along the animal???vegetal axis in the anthozoan cnidarian, Nematostella vectensis, is mediated by Dishevelled, Developmental Biology, vol.310, issue.1, pp.169-186, 2007.
DOI : 10.1016/j.ydbio.2007.05.040

W. Longabaugh and H. Bolouri, Understanding the Dynamic Behavior of Genetic Regulatory Networks by Functional Decomposition, Current Genomics, vol.7, issue.6, pp.333-341, 2006.
DOI : 10.2174/138920206778948718

C. R. Magie, M. Daly, and M. Q. Martindale, Gastrulation in the cnidarian Nematostella vectensis occurs via invagination not ingression, Developmental Biology, vol.305, issue.2, pp.483-497, 2007.
DOI : 10.1016/j.ydbio.2007.02.044

H. Marlow, D. Q. Matus, and M. Q. Martindale, Ectopic activation of the canonical wnt signaling pathway affects ectodermal patterning along the primary axis during larval development in the anthozoan Nematostella vectensis, Developmental Biology, vol.380, issue.2, pp.324-334, 2013.
DOI : 10.1016/j.ydbio.2013.05.022

M. Q. Martindale and A. Hejnol, A Developmental Perspective: Changes in the Position of the Blastopore during Bilaterian Evolution, Developmental Cell, vol.17, issue.2, pp.162-174, 2009.
DOI : 10.1016/j.devcel.2009.07.024

M. Q. Martindale, K. Pang, and J. R. Finnerty, Investigating the origins of triploblasty: `mesodermal' gene expression in a diploblastic animal, the sea anemone Nematostella vectensis (phylum, Cnidaria; class, Anthozoa), Development, vol.131, issue.10, pp.2463-2474, 2004.
DOI : 10.1242/dev.01119

D. Q. Matus, K. Pang, H. Marlow, C. W. Dunn, G. H. Thomsen et al., Molecular evidence for deep evolutionary roots of bilaterality in animal development, Proc. Natl. Acad. Sci. USA 103, pp.11195-11200, 2006.
DOI : 10.1002/dvdy.20483

D. Q. Matus, G. H. Thomsen, and M. Q. Martindale, Dorso/Ventral Genes Are Asymmetrically Expressed and Involved in Germ-Layer Demarcation during Cnidarian Gastrulation, Current Biology, vol.16, issue.5, pp.499-505, 2006.
DOI : 10.1016/j.cub.2006.01.052

D. Q. Matus, G. H. Thomsen, and M. Q. Martindale, FGF signaling in gastrulation and neural development in Nematostella vectensis, an anthozoan cnidarian, Development Genes and Evolution, vol.133, issue.2, pp.137-148, 2007.
DOI : 10.1101/SQB.1997.062.01.017

D. Q. Matus, C. R. Magie, K. Pang, M. Q. Martindale, and G. H. Thomsen, The Hedgehog gene family of the cnidarian, Nematostella vectensis, and implications for understanding metazoan Hedgehog pathway evolution, Developmental Biology, vol.313, issue.2, pp.501-518, 2008.
DOI : 10.1016/j.ydbio.2007.09.032

M. E. Mazza, K. Pang, M. Q. Martindale, and J. R. Finnerty, Genomic organization, gene structure, and developmental expression of three clustered otx genes in the sea anemone Nematostella vectensis, J. Exp. Zool, vol.308, pp.494-506, 2007.

P. Oliveri and E. Davidson, Gene regulatory network controlling embryonic specification in the sea urchin, Current Opinion in Genetics & Development, vol.14, issue.4, 2004.
DOI : 10.1016/j.gde.2004.06.004

M. Ormestad, M. Martindale, and E. Rottinger, A comparative gene expression database for invertebrates, EvoDevo, vol.2, issue.1, 2011.
DOI : 10.1016/j.ydbio.2007.05.040

S. Ota, N. Tonou-fujimori, and K. Yamasu, The roles of the FGF signal in zebrafish embryos analyzed using constitutive activation and dominant-negative suppression of different FGF receptors, Mechanisms of Development, vol.126, issue.1-2, pp.1-17, 2009.
DOI : 10.1016/j.mod.2008.10.008

C. Peng, W. Zeng, J. Su, Y. Kuang, Y. He et al., Cyclin-dependent kinase 2 (CDK2) is a key mediator for EGF-induced cell transformation mediated through the ELK4/c-Fos signaling pathway, Oncogene, vol.13, issue.9, pp.1170-1179, 2016.
DOI : 10.1038/nature07638

A. Pourtier-manzanedo, C. Vercamer, E. Van-belle, V. Mattot, F. Mouquet et al., Expression of an Ets-1 dominant-negative mutant perturbs normal and tumor angiogenesis in a mouse ear model, Oncogene, vol.22, issue.12, pp.1795-1806, 2003.
DOI : 10.1038/sj.onc.1206215

N. H. Putnam, M. Srivastava, U. Hellsten, B. Dirks, J. Chapman et al., Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization, Science, vol.196, issue.4295, pp.86-94, 2007.
DOI : 10.1126/science.860134

F. Rentzsch, R. Anton, M. Saina, M. Hammerschmidt, T. W. Holstein et al., Asymmetric expression of the BMP antagonists chordin and gremlin in the sea anemone Nematostella vectensis: Implications for the evolution of axial patterning, Developmental Biology, vol.296, issue.2, pp.375-387, 2006.
DOI : 10.1016/j.ydbio.2006.06.003

F. Rentzsch, J. H. Fritzenwanker, C. B. Scholz, and U. Technau, FGF signalling controls formation of the apical sensory organ in the cnidarian Nematostella vectensis, Development, vol.135, issue.10, pp.1761-1769, 2008.
DOI : 10.1242/dev.020784

F. Rizzo, M. Fernandez-serra, P. Squarzoni, A. Archimandritis, and M. I. Arnone, Identification and developmental expression of the ets gene family in the sea urchin (Strongylocentrotus purpuratus), Developmental Biology, vol.300, issue.1, pp.35-48, 2006.
DOI : 10.1016/j.ydbio.2006.08.012

F. Rizzo, J. A. Coffman, and M. I. Arnone, An Elk transcription factor is required for Runx-dependent survival signaling in the sea urchin embryo, Developmental Biology, vol.416, issue.1, pp.173-186, 2016.
DOI : 10.1016/j.ydbio.2016.05.026

E. Röttinger, L. Besnardeau, and T. Lepage, A Raf/MEK/ERK signaling pathway is required for development of the sea urchin embryo micromere lineage through phosphorylation of the transcription factor Ets, Development, vol.131, issue.5, pp.1075-1087, 2004.
DOI : 10.1242/dev.01000

E. Röttinger, A. Saudemont, V. Duboc, L. Besnardeau, D. Mcclay et al., FGF signals guide migration of mesenchymal cells, control skeletal morphogenesis and regulate gastrulation during sea urchin development, Development, vol.135, issue.2, pp.353-365, 2008.
DOI : 10.1242/dev.014282

E. Röttinger, P. Dahlin, and M. Q. Martindale, A Framework for the Establishment of a Cnidarian Gene Regulatory Network for ???Endomesoderm??? Specification: The Inputs of ??-Catenin/TCF Signaling, PLoS Genetics, vol.2, issue.12, 2012.
DOI : 10.1371/journal.pgen.1003164.s013

E. Röttinger, T. Q. Dubuc, A. R. Amiel, and M. Q. Martindale, Nodal signaling is required for mesodermal and ventral but not for dorsal fates in the indirect developing hemichordate, Ptychodera flava, Biology Open, vol.4, issue.7, 2015.
DOI : 10.1242/bio.011809

J. F. Ryan, P. M. Burton, M. E. Mazza, G. K. Kwong, J. C. Mullikin et al., The cnidarian-bilaterian ancestor possessed at least 56 homeoboxes: evidence from the starlet sea anemone, Nematostella vectensis, Genome Biol, vol.7, 2006.

J. F. Ryan, M. E. Mazza, K. Pang, D. Q. Matus, A. D. Baxevanis et al., Pre-Bilaterian Origins of the Hox Cluster and the Hox Code: Evidence from the Sea Anemone, Nematostella vectensis, PLoS ONE, vol.4, issue.1, 2007.
DOI : 10.1371/journal.pone.0000153.s013

S. Schulte-merker and J. C. Smith, Mesoderm formation in response to Brachyury requires FGF signalling, Current Biology, vol.5, issue.1, pp.62-67, 1995.
DOI : 10.1016/S0960-9822(95)00017-0

N. Selvaraj, V. Kedage, and P. C. Hollenhorst, Comparison of MAPK specificity across A.R. Amiel et al, Developmental Biology, vol.430, pp.346-361, 2015.

A. D. Sharrocks, The ETS-domain transcription factor family, The International Journal of Biochemistry & Cell Biology, vol.29, issue.12, pp.827-837, 2001.
DOI : 10.1016/S1357-2725(97)00086-1

C. Sinigaglia, H. Busengdal, L. Leclère, U. Technau, and F. Rentzsch, The Bilaterian Head Patterning Gene six3/6 Controls Aboral Domain Development in a Cnidarian, PLoS Biology, vol.296, issue.1, 2013.
DOI : 10.1371/journal.pbio.1001488.s010

C. Sinigaglia, H. Busengdal, A. Lerner, P. Oliveri, and F. Rentzsch, Molecular characterization of the apical organ of the anthozoan Nematostella vectensis, Developmental Biology, vol.398, issue.1, 2014.
DOI : 10.1016/j.ydbio.2014.11.019

M. Srivastava, C. Larroux, D. R. Lu, K. Mohanty, J. Chapman et al., Early evolution of the LIM homeobox gene family, BMC Biology, vol.8, issue.1, pp.1741-7007, 2010.
DOI : 10.1186/1741-7007-8-4

A. Stathopoulos, B. Tam, M. Ronshaugen, M. Frasch, and M. Levine, pyramus and thisbe: FGF genes that pattern the mesoderm of Drosophila embryos, Genes & Development, vol.18, issue.6, pp.687-699, 2004.
DOI : 10.1101/gad.1166404

U. Technau and C. B. Scholz, Origin and evolution of endoderm and mesoderm, Int. J. Dev. Biol, vol.47, pp.531-539, 2003.

U. Technau and R. E. Steele, Evolutionary crossroads in developmental biology: Cnidaria, Development, vol.138, issue.8, pp.1447-1458, 2011.
DOI : 10.1242/dev.048959

A. H. Wikramanayake, M. Hong, P. N. Lee, K. Pang, C. A. Byrum et al., An ancient role for nuclear ??-catenin in the evolution of axial polarity and germ layer segregation, Nature, vol.426, issue.6965, pp.446-450, 2003.
DOI : 10.1038/nature02113

H. Yasuo and C. Hudson, FGF8/17/18 functions together with FGF9/16/20 during formation of the notochord in Ciona embryos, Developmental Biology, vol.302, issue.1, pp.92-103, 2007.
DOI : 10.1016/j.ydbio.2006.08.075

Y. Yasuoka, M. Kobayashi, D. Kurokawa, K. Akasaka, H. Saiga et al., Evolutionary origins of blastoporal expression and organizer activity of the vertebrate gastrula organizer gene lhx1 and its ancient metazoan paralog lhx3, Development, vol.136, issue.12, 2005.
DOI : 10.1242/dev.028530