scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1032007276 |
P356 | DOI | 10.1186/1749-8104-4-12 |
P932 | PMC publication ID | 2674439 |
P698 | PubMed publication ID | 19341460 |
P5875 | ResearchGate publication ID | 24253051 |
P50 | author | Michael Brand | Q50583632 |
P2093 | author name string | Muriel Rhinn | |
Klaus Lun | |||
Michaela Geffarth | |||
Reiner Ahrendt | |||
P2860 | cites work | A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo | Q24564561 |
Cell determination boundaries as organizing regions for secondary embryonic fields | Q28274615 | ||
The caudal limit of Otx2 gene expression as a marker of the midbrain/hindbrain boundary: a study using in situ hybridisation and chick/quail homotopic grafts | Q28302345 | ||
Regionalisation of anterior neuroectoderm and its competence in responding to forebrain and midbrain inducing activities depend on mutual antagonism between OTX2 and GBX2 | Q28586025 | ||
Effective targeted gene 'knockdown' in zebrafish | Q29547445 | ||
Expression of a zebrafish caudal homeobox gene correlates with the establishment of posterior cell lineages at gastrulation | Q30986355 | ||
Positioning the isthmic organizer where Otx2 and Gbx2meet. | Q33927269 | ||
Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer | Q34076850 | ||
The midbrain--hindbrain boundary organizer. | Q34141435 | ||
Neural plate patterning: upstream and downstream of the isthmic organizer | Q34185965 | ||
Early anterior/posterior patterning of the midbrain and cerebellum | Q34345487 | ||
Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development | Q34362663 | ||
Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function | Q34434576 | ||
Divide et Impera--the midbrain-hindbrain boundary and its organizer | Q35947525 | ||
A zebrafish engrailed-like homeobox sequence expressed during embryogenesis | Q36415998 | ||
Expression of wnt10a in the central nervous system of developing zebrafish. | Q36764933 | ||
Expression pattern of two otx genes suggests a role in specifying anterior body structures in zebrafish. | Q36797827 | ||
Developmental regulation of zebrafish MyoD in wild-type, no tail and spadetail embryos | Q38287447 | ||
The Sp1-related transcription factors sp5 and sp5-like act downstream of Wnt/beta-catenin signaling in mesoderm and neuroectoderm patterning. | Q38514669 | ||
Wnt1 and wnt10b function redundantly at the zebrafish midbrain-hindbrain boundary | Q38521067 | ||
Zebrafish wnt8 encodes two wnt8 proteins on a bicistronic transcript and is required for mesoderm and neurectoderm patterning. | Q38523908 | ||
Direct regulation of the Xenopus engrailed-2 promoter by the Wnt signaling pathway, and a molecular screen for Wnt-responsive genes, confirm a role for Wnt signaling during neural patterning in Xenopus. | Q38527333 | ||
Zebrafishwnt8andwnt8bshare a common activity but are involved in distinct developmental pathways | Q38531729 | ||
cdx4 mutants fail to specify blood progenitors and can be rescued by multiple hox genes | Q40633690 | ||
Spiel-ohne-grenzen/pou2 mediates regional competence to respond to Fgf8 during zebrafish early neural development. | Q40657976 | ||
Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo | Q40672250 | ||
Early anteroposterior division of the presumptive neurectoderm in Xenopus | Q40702301 | ||
The caudal limit of Otx2 expression positions the isthmic organizer | Q40928475 | ||
Order and coherence in the fate map of the zebrafish nervous system | Q40976641 | ||
Visceral endoderm-restricted translation of Otx1 mediates recovery of Otx2 requirements for specification of anterior neural plate and normal gastrulation. | Q40995595 | ||
Sequential roles for Otx2 in visceral endoderm and neuroectoderm for forebrain and midbrain induction and specification. | Q41046046 | ||
Engrailed, Wnt and Pax genes regulate midbrain--hindbrain development | Q41064646 | ||
Early mesencephalon/metencephalon patterning and development of the cerebellum | Q41724283 | ||
Regional cell movement and tissue patterning in the zebrafish embryo revealed by fate mapping with caged fluorescein | Q41743027 | ||
Expression of the zebrafish paired box gene pax[zf-b] during early neurogenesis | Q41818633 | ||
Ace/Fgf8 is required for forebrain commissure formation and patterning of the telencephalon. | Q42488388 | ||
Wnt8 is required in lateral mesendodermal precursors for neural posteriorization in vivo. | Q43744674 | ||
Otx2 and Gbx2 are required for refinement and not induction of mid-hindbrain gene expression. | Q43826745 | ||
gbx2 Homeobox gene is required for the maintenance of the isthmic region in the zebrafish embryonic brain. | Q44632595 | ||
Interaction of Wnt and caudal-related genes in zebrafish posterior body formation | Q45263246 | ||
Midbrain development induced by FGF8 in the chick embryo. | Q46013905 | ||
Specification of the hindbrain fate in the zebrafish. | Q46101694 | ||
Specification of the Zebrafish Nervous System by Nonaxial Signals | Q46905446 | ||
Regulatory gene expression boundaries demarcate sites of neuronal differentiation in the embryonic zebrafish forebrain | Q47073096 | ||
Engrailed and Fgf8 act synergistically to maintain the boundary between diencephalon and mesencephalon | Q47073461 | ||
Positioning of the midbrain-hindbrain boundary organizer through global posteriorization of the neuroectoderm mediated by Wnt8 signaling | Q47073539 | ||
Differential expression of two zebrafish emx homeoprotein mRNAs in the developing brain | Q47073636 | ||
Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis | Q47073664 | ||
A series of no isthmus (noi) alleles of the zebrafish pax2.1 gene reveals multiple signaling events in development of the midbrain-hindbrain boundary | Q47073721 | ||
Analysis of Wnt8 for neural posteriorizing factor by identifying Frizzled 8c and Frizzled 9 as functional receptors for Wnt8. | Q47073727 | ||
valentino: a zebrafish gene required for normal hindbrain segmentation. | Q47073916 | ||
Expression of two zebrafish homologues of the murine Six3 gene demarcates the initial eye primordia | Q48037954 | ||
Zebrafish hox genes: expression in the hindbrain region of wild-type and mutants of the segmentation gene, valentino. | Q48041265 | ||
Ectopic expression of Hoxa-1 in the zebrafish alters the fate of the mandibular arch neural crest and phenocopies a retinoic acid-induced phenotype | Q48065965 | ||
Sequence and expression pattern of the Stra7 (Gbx-2) homeobox-containing gene induced by retinoic acid in P19 embryonal carcinoma cells | Q48068766 | ||
A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer | Q48110711 | ||
Cell autonomous and non-cell autonomous functions of Otx2 in patterning the rostral brain. | Q48118664 | ||
Regeneration of isthmic tissue is the result of a specific and direct interaction between rhombomere 1 and midbrain. | Q48130782 | ||
Coordinate embryonic expression of three zebrafish engrailed genes | Q48146193 | ||
Fgf8 and Gbx2 induction concomitant with Otx2 repression is correlated with midbrain-hindbrain fate of caudal prosencephalon | Q48182728 | ||
Cloning, expression and relationship of zebrafish gbx1 and gbx2 genes to Fgf signaling | Q48203653 | ||
Isolation and expression of the homeobox gene Gbx1 during mouse development | Q48208107 | ||
Sustained interactive Wnt and FGF signaling is required to maintain isthmic identity | Q48229313 | ||
Gbx2 interacts with Otx2 and patterns the anterior-posterior axis during gastrulation in Xenopus | Q48685519 | ||
Induction of a mesencephalic phenotype in the 2-day-old chick prosencephalon is preceded by the early expression of the homeobox gene en. | Q48717668 | ||
Neuroepithelial co-expression of Gbx2 and Otx2 precedes Fgf8 expression in the isthmic organizer | Q48964505 | ||
EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region | Q49141522 | ||
Cloning and embryonic expression analysis of the mouse Gbx1 gene. | Q52104313 | ||
Interaction between Otx2 and Gbx2 defines the organizing center for the optic tectum. | Q52170383 | ||
Forebrain and midbrain regions are deleted in Otx2−/− mutants due to a defective anterior neuroectoderm specification during gastrulation | Q54602798 | ||
A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain | Q70910667 | ||
Xenopus embryos regulate the nuclear localization of XMyoD | Q72718764 | ||
Expression of Otx homeodomain proteins induces cell aggregation in developing zebrafish embryos | Q73959518 | ||
P921 | main subject | Danio rerio | Q169444 |
Gastrulation brain homeobox 1 | Q29825330 | ||
Wingless-type MMTV integration site family, member 8a | Q29830803 | ||
P304 | page(s) | 12 | |
P577 | publication date | 2009-04-02 | |
P1433 | published in | Neural Development | Q15761981 |
P1476 | title | Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal | |
P478 | volume | 4 |
Q37892502 | Brain regionalization: of signaling centers and boundaries |
Q41979847 | Cerebellar development in the absence of Gbx function in zebrafish |
Q47866746 | Comprehensive analysis of target genes in zebrafish embryos reveals gbx2 involvement in neurogenesis |
Q38004616 | Development and evolution of cerebellar neural circuits |
Q37838909 | Development of the cerebellum and cerebellar neural circuits |
Q27334410 | Dynamic association with donor cell filopodia and lipid-modification are essential features of Wnt8a during patterning of the zebrafish neuroectoderm |
Q28587839 | Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2 |
Q34167636 | Evolutionarily conserved function of Gbx2 in anterior hindbrain development |
Q39282682 | Evolutionary mechanisms that generate morphology and neural-circuit diversity of the cerebellum. |
Q48270370 | Identification and expression analysis of the zebrafish homologs of the ceramide synthase gene family |
Q37783809 | Making senses development of vertebrate cranial placodes |
Q41222022 | Midbrain-Hindbrain Boundary Morphogenesis: At the Intersection of Wnt and Fgf Signaling |
Q27026327 | Neural crest induction at the neural plate border in vertebrates |
Q27022400 | Neurogenesis in zebrafish - from embryo to adult |
Q50504353 | Patterning, morphogenesis, and neurogenesis of zebrafish cranial sensory placodes. |
Q37958896 | Specification and regionalisation of the neural plate border. |
Q21129150 | The evolutionary and genetic origins of consciousness in the Cambrian Period over 500 million years ago |
Q29347277 | The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cord |
Q38025839 | The peripheral sensory nervous system in the vertebrate head: a gene regulatory perspective |
Q95831978 | The ubiquitin-conjugating enzyme UBE2K determines neurogenic potential through histone H3 in human embryonic stem cells |
Q33952203 | Toxicological assessment of trace β-diketone antibiotic mixtures on zebrafish (Danio rerio) by proteomic analysis |
Q91537063 | Wnt signaling regulates neural plate patterning in distinct temporal phases with dynamic transcriptional outputs |
Q39930689 | vox homeobox gene: a novel regulator of midbrain-hindbrain boundary development in medaka fish? |
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