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Pituitary gland development and disease: from stem cell to hormone productionOtx2 and Oct4 drive early enhancer activation during embryonic stem cell transition from naive pluripotency.Characterization of dsRed2-positive cells in the doublecortin-dsRed2 transgenic adult rat retina.HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES CellsCRISPR/Cas9-based generation of knockdown mice by intronic insertion of artificial microRNA using longer single-stranded DNATranscriptional Reactivation of OTX2, RX1 and SIX3 during Reprogramming Contributes to the Generation of RPE Cells from Human iPSCs.Deletion of OTX2 in neural ectoderm delays anterior pituitary developmentNovel mutations in PAX6, OTX2 and NDP in anophthalmia, microphthalmia and coloboma.Suboptimization of developmental enhancersNeurotransmitter signaling pathways required for normal development in Xenopus laevis embryos: a pharmacological survey screenOTX2 impedes self-renewal of porcine iPS cells through downregulation of NANOG expressionMicroarray discovery of new OGT substrates: the medulloblastoma oncogene OTX2 is O-GlcNAcylated.Genetic regulation of vertebrate eye development.Can the 'neuron theory' be complemented by a universal mechanism for generic neuronal differentiation.OTX2 Activity at Distal Regulatory Elements Shapes the Chromatin Landscape of Group 3 Medulloblastoma.OTX2 exhibits cell-context-dependent effects on cellular and molecular properties of human embryonic neural precursors and medulloblastoma cells.OTX2 expression contributes to proliferation and progression in Myc-amplified medulloblastoma.PCDHB14- and GABRB1-like nervous system developmental genes are altered during early neuronal differentiation of NCCIT cells treated with ethanol.Zebrafish Lbh-like Is Required for Otx2-mediated Photoreceptor Differentiation.Combinatorial regulation of a Blimp1 (Prdm1) enhancer in the mouse retina.Genome-Wide Target Analyses of Otx2 Homeoprotein in Postnatal CortexOTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.Panel-based whole exome sequencing identifies novel mutations in microphthalmia and anophthalmia patients showing complex Mendelian inheritance patterns.Landscape of Pleiotropic Proteins Causing Human Disease: Structural and System Biology Insights.The origins of the circumventricular organs.Prdm13 is required for Ebf3+ amacrine cell formation in the retina.Characterization of a novel OTX2-driven stem cell program in Group 3 and Group 4 medulloblastoma.Developmental pathway genes and neural plasticity underlying emotional learning and stress-related disorders.OTX2 Defines a Subgroup of Atypical Teratoid Rhabdoid Tumors With Close Relationship to Choroid Plexus Tumors.Transcriptome variations among human embryonic stem cell lines are associated with their differentiation propensity.Comprehensive interactome of Otx2 in the adult mouse neural retina.Midbrain-hindbrain involvement in septo-optic dysplasia.Agnathia-otocephaly complex and asymmetric velopharyngeal insufficiency due to an in-frame duplication in OTX2.An Evolutionarily Conserved Network Mediates Development of the zona limitans intrathalamica, a Sonic Hedgehog-Secreting Caudal Forebrain Signaling Center.Otx2 promotes granule cell precursor proliferation and Shh-dependent medulloblastoma maintenance in vivoNew insights into the phenotypic spectrum of 14q22q23 deletions: a case report and literature review
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
The homeobox gene Otx2 in development and disease.
@en
type
label
The homeobox gene Otx2 in development and disease.
@en
prefLabel
The homeobox gene Otx2 in development and disease.
@en
P1476
The homeobox gene Otx2 in development and disease
@en
P2093
Francis Beby
P356
10.1016/J.EXER.2013.03.007
P577
2013-03-21T00:00:00Z