The caudal limit of Otx2 expression positions the isthmic organizerBROCCOLL, V; BONCINEILL, E; WURST, W et al.Nature (London). 1999, Vol 401, Num 6749, pp 164-168, issn 0028-0836Article

The chick/quail transplantation model : Discovery of the isthmic organizer centerALVARADO-MALLART, Rosa-Magda.Brain research reviews. 2005, Vol 49, Num 2, pp 109-113, issn 0165-0173, 5 p.Conference Paper

Conserved interactions of a compact highly active enhancer/promoter upstream of the rhodopsin kinase (GRK1) geneYOUNG, Joyce E; KASPEREK, Eileen M; VOGT, Todd M et al.Genomics (San Diego, Calif.). 2007, Vol 90, Num 2, pp 236-248, issn 0888-7543, 13 p.Article

The TINS lecture understanding the roles of Otx1 and Otx2 in the control of brain morphogenesisACAMPORA, D; SIMEONE, A.Trends in neurosciences (Regular edition). 1999, Vol 22, Num 3, pp 116-122, issn 0166-2236Article

A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizerMILLET, S; CAMPBELL, K; EPSTEIN, D. J et al.Nature (London). 1999, Vol 401, Num 6749, pp 161-164, issn 0028-0836Article

INCREASED DOPAMINERGIC INNERVATION IN THE BRAIN OF CONDITIONAL MUTANT MICE OVEREXPRESSING OTX2: EFFECTS ON LOCOMOTOR BEHAVIOR AND SEIZURE SUSCEPTIBILITYTRIPATHI, P. P; DI GIOVANNANTONIO, L. G; SANGUINETTI, E et al.Neuroscience. 2014, Vol 261, pp 173-183, issn 0306-4522, 11 p.Article

Expression of the Otx2 homeobox gene in the developing mammalian brain : embryonic and adult expression in the pineal glandRATH, Martin F; MUNOZ, Estela; GANGULY, Surajit et al.Journal of neurochemistry. 2006, Vol 97, Num 2, pp 556-566, issn 0022-3042, 11 p.Article

Analyse de la fonction des gènes HNF3 beta, Lim1 et Otx2 dans l'endoderme viscéral antérieur de l'embryon de souris au cours de la gastrulation = Analysis of the function of HNF3β, Lim1 and Otx2 in the anterior visceral endoderm of the mouse embryo during gastrulationPerea Gomez, Aitana; Ang, Siew-Lan.2001, 100 p.Thesis

Gènes à homéoboîtes actifs dans le développement cérébral et conservés au cours de l'évolution = Conserved homeobox genes in the developing brainBONCINELLI, E; GULISANO, M; PANNESE, M et al.Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie. 1993, Vol 316, Num 9, pp 972-984, issn 0764-4469Article

Contribution à l'étude de la spécification du territoire mes/métencéphalique du tube neural aviaire = Specification of the mes/metencephalic territory of the avian neural tubeMillet, Sandrine; Alvarado, Rosa.1997, 153 p.Thesis

Polymorphisms in the Homeobox Gene OTX2 May Be a Risk Factor for Bipolar DisorderSABUNCIYAN, Sarven; YOLKEN, Robert; RAGAN, Christina M et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 8, pp 1083-1086, issn 1552-4841, 4 p.Article

OTX1 and OTX2 expression correlates with the clinicopathologic classification of medulloblastomasDE HAAS, Talitha; OUSSOREN, Esmeralda; PIETSCH, Torsten et al.Journal of neuropathology and experimental neurology. 2006, Vol 65, Num 2, pp 176-186, issn 0022-3069, 11 p.Article

Branchiootorenal Syndrome and Oculoauriculovertebral Spectrum Features Associated With Duplication of SIX1, SIX6, and OTX2 Resulting From a Complex Chromosomal RearrangementZHISHUO OU; MARTIN, Donna M; BEDOYAN, Jirair K et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 19, pp 2480-2489, issn 1552-4825, 10 p.Article

Formation de la frontière entre cerveaux moyen et postérieur : implication des gènes Otx2 et Gbx2 : Mécanismes moléculaires du développement précoce du système nerveux = Formation of the midbrain-hindbrain boundary : involvement of both Otx2 and Gbx2 genes : Molecular mechanisms of early development in nervous systemHIDALGO-SANCHEZ, Matias; MILLET, Sandrine; BLOCH-GALLEGO, Evelyne et al.Journal de la Société de biologie. 2000, Vol 194, Num 3-4, pp 113-118, issn 1295-0661Article

Etude de la fonction du gène Otx2 au cours du développement embryonnaire chez la souris = Analysis of the function of the mouse Otx2 gene during embryonic developmentRhinn, Muriel; Ang, Siew-Lan.1999, 157 p.Thesis

Hydrocephalus in the Otx2^+/- mutant mouseMAKIYAMA, Y; SHOJI, S; MIZUSAWA, H et al.Experimental neurology (Print). 1997, Vol 148, Num 1, pp 215-221, issn 0014-4886Article

Retinoic acid induces a tissue-specific deletion in the expression domain of Otx2CLOTMAN, F; VAN MAELE-FABRY, G; PICARD, J. J et al.Neurotoxicology and teratology. 1997, Vol 19, Num 3, pp 163-169, issn 0892-0362Conference Paper

Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomaliesNOLEN, Leisha D; AMOR, David; JAMIESON, Robyn V et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 16, pp 1711-1718, issn 1552-4825, 8 p.Article

Elucidating the phenomenon of HESC-derived RPE : Anatomy of cell genesis, expansion and retinal transplantationVUGLER, Anthony; CARR, Amanda-Jayne; DA CRUZ, Lyndon et al.Experimental neurology (Print). 2008, Vol 214, Num 2, pp 347-361, issn 0014-4886, 15 p.Article

TOXICITE SUR LE DEVELOPPEMENT DES INHIBITEURS DE LA DELTA-7 STEROL REDUCTASE CHEZ LE RAT : MODELE D'ETUDE POUR LE SYNDROME CONGENITAL HUMAIN : SLO/RSH = DEVELOPMENTAL TOXICITY OF THE Δ7-STEROL REDUCTASE INHIBITORS IN THE RAT : A MODEL FOR THE STUDY OF THE HUMAN CONGENITAL SYNDROME SLO/RSHKolf Clauw, Martine; Roux, Charles.1997, 160 p.Thesis