| scholarly article | Q13442814 |
| P50 | author | Steffen Scholpp | Q37829813 |
| Michael Brand | Q50583632 | ||
| Cecilia B. Moens | Q55692076 | ||
| Timothy Erickson | Q59110153 | ||
| P2093 | author name string | Andrew Jan Waskiewicz | |
| P2860 | cites work | Structure of a HoxB1-Pbx1 heterodimer bound to DNA: role of the hexapeptide and a fourth homeodomain helix in complex formation | Q22008845 |
| The transcription factor Engrailed-2 guides retinal axons | Q24293543 | ||
| Pbx3 deficiency results in central hypoventilation | Q24670007 | ||
| Proteomics of early zebrafish embryos | Q25255768 | ||
| Structure of a DNA-bound Ultrabithorax-Extradenticle homeodomain complex | Q27617465 | ||
| Structure of HoxA9 and Pbx1 bound to DNA: Hox hexapeptide and DNA recognition anterior to posterior | Q27641842 | ||
| Compartments and their boundaries in vertebrate brain development | Q28256915 | ||
| Segmentation in the chick embryo hindbrain is defined by cell lineage restrictions | Q28280395 | ||
| Pbx proteins display hexapeptide-dependent cooperative DNA binding with a subset of Hox proteins | Q28300459 | ||
| Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs | Q28508521 | ||
| Requirement for Pbx1 in skeletal patterning and programming chondrocyte proliferation and differentiation | Q28512034 | ||
| Pbx1 is essential for adrenal development and urogenital differentiation | Q28513226 | ||
| The pancreatic islet factor STF-1 binds cooperatively with Pbx to a regulatory element in the somatostatin promoter: importance of the FPWMK motif and of the homeodomain | Q28574370 | ||
| PDX:PBX complexes are required for normal proliferation of pancreatic cells during development | Q28578151 | ||
| Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression | Q28585137 | ||
| The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain | Q28586297 | ||
| The Hox cofactor and proto-oncogene Pbx1 is required for maintenance of definitive hematopoiesis in the fetal liver | Q28586454 | ||
| Pbx1 inactivation disrupts pancreas development and in Ipf1-deficient mice promotes diabetes mellitus | Q28588048 | ||
| Ephrin-As and neural activity are required for eye-specific patterning during retinogeniculate mapping | Q28768597 | ||
| The hexapeptide LFPWMR in Hoxb-8 is required for cooperative DNA binding with Pbx1 and Pbx2 proteins | Q33889933 | ||
| Neural plate patterning: upstream and downstream of the isthmic organizer | Q34185965 | ||
| Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum | Q34323246 | ||
| Zebrafish Lmx1b.1 and Lmx1b.2 are required for maintenance of the isthmic organizer | Q34337070 | ||
| Rostral optic tectum acquires caudal characteristics following ectopic engrailed expression | Q34396938 | ||
| Hox cofactors in vertebrate development | Q34499501 | ||
| Polarity and laminar formation of the optic tectum in relation to retinal projection | Q35685279 | ||
| An extradenticle-induced conformational change in a HOX protein overcomes an inhibitory function of the conserved hexapeptide motif | Q35850266 | ||
| Engrailed and Hox homeodomain proteins contain a related Pbx interaction motif that recognizes a common structure present in Pbx. | Q35900314 | ||
| Divide et Impera--the midbrain-hindbrain boundary and its organizer | Q35947525 | ||
| Hox gene products modulate the DNA binding activity of Pbx1 and Pbx2 | Q36683631 | ||
| Engrailed cooperates with extradenticle and homothorax to repress target genes in Drosophila | Q37215807 | ||
| Morpholino-induced knockdown of zebrafish engrailed genes eng2 and eng3 reveals redundant and unique functions in midbrain--hindbrain boundary development | Q38298389 | ||
| FGF3 and FGF8 mediate a rhombomere 4 signaling activity in the zebrafish hindbrain. | Q38364037 | ||
| Pbx-1 Hox heterodimers bind DNA on inseparable half-sites that permit intrinsic DNA binding specificity of the Hox partner at nucleotides 3' to a TAAT motif. | Q39716685 | ||
| Paralog group 1 hox genes regulate rhombomere 5/6 expression of vhnf1, a repressor of rostral hindbrain fates, in a meis-dependent manner | Q40500223 | ||
| The EphA4 receptor tyrosine kinase is necessary for the guidance of nasal retinal ganglion cell axons in vitro | Q40841430 | ||
| Molecular mechanism of polyhomeotic activation by Engrailed | Q41029200 | ||
| The roles of engrailed | Q41064626 | ||
| Extra specificity from extradenticle: the partnership between HOX and PBX/EXD homeodomain proteins | Q41078307 | ||
| The Eph family in retinal axon guidance | Q41353205 | ||
| Isthmus-to-midbrain transformation in the absence of midbrain-hindbrain organizer activity. | Q42453883 | ||
| A short region of its homeodomain is necessary for engrailed nuclear export and secretion | Q42814221 | ||
| Pbx marks genes for activation by MyoD indicating a role for a homeodomain protein in establishing myogenic potential | Q42828894 | ||
| Differential expression of Eph receptors and ephrins correlates with the formation of topographic projections in primary and secondary visual circuits of the embryonic chick forebrain. | Q43633060 | ||
| Otx2andGbx2are required for refinement and not induction of mid-hindbrain gene expression | Q43826745 | ||
| Mutations in the Drosophila gene extradenticle affect the way specific homeo domain proteins regulate segmental identity | Q44066543 | ||
| Retroviral misexpression of engrailed genes in the chick optic tectum perturbs the topographic targeting of retinal axons | Q44790745 | ||
| The zebrafish buttonhead-like factor Bts1 is an early regulator ofpax2.1expression during mid-hindbrain development | Q44902326 | ||
| vhnf1 integrates global RA patterning and local FGF signals to direct posterior hindbrain development in zebrafish. | Q45040929 | ||
| The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum. | Q45944197 | ||
| Midbrain development induced by FGF8 in the chick embryo. | Q46013905 | ||
| extradenticle raises the DNA binding specificity of homeotic selector gene products | Q46446845 | ||
| Nuclear translocation of extradenticle requires homothorax, which encodes an extradenticle-related homeodomain protein | Q47072708 | ||
| Integrity of the midbrain region is required to maintain the diencephalic–mesencephalic boundary in zebrafishno isthmus/pax2.1mutants | Q47073181 | ||
| lazarus is a novel pbx gene that globally mediates hox gene function in zebrafish | Q47073219 | ||
| Engrailed and Fgf8 act synergistically to maintain the boundary between diencephalon and mesencephalon | Q47073461 | ||
| Eliminating zebrafish pbx proteins reveals a hindbrain ground state. | Q47073477 | ||
| Positioning of the midbrain-hindbrain boundary organizer through global posteriorization of the neuroectoderm mediated by Wnt8 signaling | Q47073539 | ||
| 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 | ||
| Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain | Q47073829 | ||
| Prep1.1 has essential genetic functions in hindbrain development and cranial neural crest cell differentiation | Q47074133 | ||
| Homeodomain to hexapeptide or PBC-interaction-domain distance: size apparently matters. | Q47430717 | ||
| Zebrafish hox genes: expression in the hindbrain region of wild-type and mutants of the segmentation gene, valentino | Q48041265 | ||
| FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. | Q48282491 | ||
| A role for iro1 and iro7 in the establishment of an anteroposterior compartment of the ectoderm adjacent to the midbrain-hindbrain boundary. | Q48307151 | ||
| The midbrain-hindbrain phenotype of Wnt-1-/Wnt-1- mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum | Q48480210 | ||
| Establishment of hindbrain segmental identity requires signaling by FGF3 and FGF8. | Q48546899 | ||
| Establishment of rostrocaudal polarity in tectal primordium: engrailed expression and subsequent tectal polarity | Q48615069 | ||
| The zebrafish spiel-ohne-grenzen (spg) gene encodes the POU domain protein Pou2 related to mammalian Oct4 and is essential for formation of the midbrain and hindbrain, and for pre-gastrula morphogenesis | Q48680174 | ||
| Lineage restriction maintains a stable organizer cell population at the zebrafish midbrain-hindbrain boundary | Q48852939 | ||
| EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region | Q49141522 | ||
| Requirements for transcriptional repression and activation by Engrailed in Drosophila embryos | Q52110663 | ||
| Engrailed defines the position of dorsal di-mesencephalic boundary by repressing diencephalic fate. | Q52173701 | ||
| Segmental expression of Hoxb-1 is controlled by a highly conserved autoregulatory loop dependent upon exd/pbx | Q52537224 | ||
| Über Entwickelungsgeschichte der Thiere. Beobachtung und Reflexion .. | Q56656641 | ||
| A Role for Gradient en Expression in Positional Specification on the Optic Tectum | Q63987363 | ||
| Pluripotentiality of the 2-day-old avian germinative neuroepithelium | Q68759905 | ||
| Specific residues in the Pbx homeodomain differentially modulate the DNA-binding activity of Hox and Engrailed proteins | Q73124224 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 504-517 | |
| P577 | publication date | 2006-08-10 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | Pbx proteins cooperate with Engrailed to pattern the midbrain-hindbrain and diencephalic-mesencephalic boundaries | |
| P478 | volume | 301 |
| Q43173533 | A trans-Regulatory Code for the Forebrain Expression of Six3.2 in the Medaka Fish |
| Q28593623 | An essential role for heat shock transcription factor binding protein 1 (HSBP1) during early embryonic development |
| Q40955969 | Control of brain patterning by Engrailed paracrine transfer: a new function of the Pbx interaction domain. |
| Q30521484 | Formation of the spinal network in zebrafish determined by domain-specific pax genes. |
| Q42775785 | FoxH1 negatively modulates flk1 gene expression and vascular formation in zebrafish |
| Q30451387 | Graded levels of Pax2a and Pax8 regulate cell differentiation during sensory placode formation |
| Q100385901 | H2O2 and Engrailed 2 paracrine activity synergize to shape the zebrafish optic tectum |
| Q50696862 | HOXA13 directly regulates EphA6 and EphA7 expression in the genital tubercle vascular endothelia |
| Q34128072 | Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system. |
| Q47131806 | Mis-expression of grainyhead-like transcription factors in zebrafish leads to defects in enveloping layer (EVL) integrity, cellular morphogenesis and axial extension. |
| Q38073140 | Novel mechanisms that pattern and shape the midbrain-hindbrain boundary |
| Q33290989 | Pbx homeodomain proteins pattern both the zebrafish retina and tectum. |
| Q51847771 | Pbx-dependent regulation oflbxgene expression in developing zebrafish embryos |
| Q47074113 | Pbx1 is essential for growth of zebrafish swim bladder |
| Q28585025 | Pbx3 is required for normal locomotion and dorsal horn development |
| Q89864872 | Pbx4 limits heart size and fosters arch artery formation by partitioning second heart field progenitors and restricting proliferation |
| Q52602912 | Segmentation of the zebrafish axial skeleton relies on notochord sheath cells and not on the segmentation clock. |
| Q37596069 | TALE factors poise promoters for activation by Hox proteins |
| Q55514652 | TALE factors use two distinct functional modes to control an essential zebrafish gene expression program. |
| Q26825693 | TALE transcription factors during early development of the vertebrate brain and eye |
| Q48985796 | TALE-class homeodomain transcription factors, homothorax and extradenticle, control dendritic and axonal targeting of olfactory projection neurons in the Drosophila brain |
| Q43177966 | The Hox cofactors Meis1 and Pbx act upstream of gata1 to regulate primitive hematopoiesis. |
| Q36125301 | The atypical homeoprotein Pbx1a participates in the axonal pathfinding of mesencephalic dopaminergic neurons |
| Q28607311 | The origin and evolution of chordate nervous systems |
| Q27021998 | The role of homeobox genes in retinal development and disease |
| Q49114792 | Zebrafish Tshz3b negatively regulates Hox function in the developing hindbrain. |
| Q42590691 | Zebrafish zic2a patterns the forebrain through modulation of Hedgehog-activated gene expression |
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