The evolution of the vertebrate Dlx gene family.Stock D.W., Ellies D.L., Zhao Z., Ekker M., Ruddle F.H., Weiss K.M.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)StrainSwiss WebsterCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 93:10858-10863 (1996)Cited in73Mapped to15
A BMP-inducible gene, dlx5, regulates osteoblast differentiation and mesoderm induction.Miyama K., Yamada G., Yamamoto T.S., Takagi C., Miyado K., Sakai M., Ueno N., Shibuya H.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCDev. Biol. 208:123-133 (1999)Cited in1Mapped to4
Dlx genes encode DNA-binding proteins that are expressed in an overlapping and sequential pattern during basal ganglia differentiation.Liu J.K., Ghattas I., Liu S., Chen S., Rubenstein J.L.R.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1; 2 AND 3)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCDev. Dyn. 210:498-512 (1997)Cited in2Mapped to12
An early phase of embryonic Dlx5 expression defines the rostral boundary of the neural plate.Yang L., Zhang H., Hu G., Wang H., Abate-Shen C., Shen M.M.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1 AND 3)TissueEmbryonic headCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Neurosci. 18:8322-8330 (1998)Cited in1Mapped to5
Bone morphogenetic protein-2-induced alkaline phosphatase expression is stimulated by Dlx5 and repressed by Msx2.Kim Y.J., Lee M.H., Wozney J.M., Cho J.Y., Ryoo H.M.View abstractCited forFUNCTION, DNA-BINDING, INDUCTIONCategoriesFunction, ExpressionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 279:50773-50780 (2004)Cited in2Mapped to21
BMP-2 induces Osterix expression through up-regulation of Dlx5 and its phosphorylation by p38.Ulsamer A., Ortuno M.J., Ruiz S., Susperregui A.R., Osses N., Rosa J.L., Ventura F.View abstractCited forFUNCTION, PHOSPHORYLATION AT SER-34 AND SER-217, MUTAGENESIS OF SER-34 AND SER-217, SUBCELLULAR LOCATION, INDUCTIONCategoriesFunction, PTM / Processing, Expression, Phenotypes & Variants, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 283:3816-3826 (2008)Cited in1Mapped to10
Calmodulin-dependent kinase II regulates Dlx5 during osteoblast differentiation.Seo J.H., Jin Y.H., Jeong H.M., Kim Y.J., Jeong H.G., Yeo C.Y., Lee K.Y.View abstractCited forPHOSPHORYLATIONCategoriesPTM / ProcessingSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochem. Biophys. Res. Commun. 384:100-104 (2009)Cited in1Mapped to4
Dlx5 Is a cell autonomous regulator of chondrocyte hypertrophy in mice and functionally substitutes for Dlx6 during endochondral ossification.Zhu H., Bendall A.J.View abstractCited forFUNCTION, TISSUE SPECIFICITY, DEVELOPMENTAL STAGECategoriesFunction, ExpressionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCPLoS ONE 4:E8097-E8097 (2009)Cited in1Mapped to10
Mash1 regulates neurogenesis in the ventral telencephalon.Casarosa S., Fode C., Guillemot F.View abstractCategoriesExpressionSourceMGI: 101926PubMedEurope PMCDevelopment 126:525-534 (1999)Mapped to47
Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse.Crackower M.A., Motoyama J., Tsui L.C.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 101926PubMedEurope PMCDev Biol 201:78-89 (1998)Mapped to33
Bapx1: an evolutionary conserved homologue of the Drosophila bagpipe homeobox gene is expressed in splanchnic mesoderm and the embryonic skeleton.Tribioli C., Frasch M., Lufkin T.View abstractCategoriesSequencesSourceMGI: 101926PubMedEurope PMCMech. Dev. 65:145-162 (1997)Cited in2Mapped to32
Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons.Anderson S.A., Qiu M., Bulfone A., Eisenstat D.D., Meneses J., Pedersen R., Rubenstein J.L.View abstractCategoriesExpressionSourceMGI: 101926PubMedEurope PMCNeuron 19:27-37 (1997)Mapped to61
Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches.Qiu M., Bulfone A., Ghattas I., Meneses J.J., Christensen L., Sharpe P.T., Presley R., Pedersen R.A., Rubenstein J.L.View abstractCategoriesSequences, ExpressionSourceMGI: 101926PubMedEurope PMCDev Biol 185:165-184 (1997)Mapped to17
Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism.Zhang H., Hu G., Wang H., Sciavolino P., Iler N., Shen M.M., Abate-Shen C.View abstractCategoriesInteractionSourceMGI: 101926PubMedEurope PMCMol Cell Biol 17:2920-2932 (1997)Mapped to15
Expression of murine Lhx5 suggests a role in specifying the forebrain.Sheng H.Z., Bertuzzi S., Chiang C., Shawlot W., Taira M., Dawid I., Westphal H.View abstractCategoriesSequences, ExpressionSourceMGI: 101926PubMedEurope PMCDev Dyn 208:266-277 (1997)Mapped to21
Dlx5 and Dlx6: an evolutionary conserved pair of murine homeobox genes expressed in the embryonic skeleton.Chen X., Li X., Wang W., Lufkin T.CategoriesSequencesSourceMGI: 101926PubMedEurope PMCAnn N Y Acad Sci 785:38-47 (1996)Mapped to8
Cloning and characterization of two members of the vertebrate Dlx gene family.Simeone A., Acampora D., Pannese M., D'Esposito M., Stornaiuolo A., Gulisano M., Mallamaci A., Kastury K., Druck T.[...], Boncinelli E.View abstractCategoriesSequencesSourceMGI: 101926PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 91:2250-2254 (1994)Cited in41Mapped to14
Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain.Qiu M., Bulfone A., Martinez S., Meneses J.J., Shimamura K., Pedersen R.A., Rubenstein J.L.View abstractCategoriesSequencesSourceMGI: 101926PubMedEurope PMCGenes Dev 9:2523-2538 (1995)Mapped to28
Identification of signaling pathways that specify a subset of migrating enteric neural crest cells at the wavefront in mouse embryos.Zhou B., Feng C., Sun S., Chen X., Zhuansun D., Wang D., Yu X., Meng X., Xiao J.[...], Feng J.View abstractSourceMGI: 101926PubMedEurope PMCDev Cell 59:1689-1706.e8 (2024)Mapped to99+
Loss of Neogenin alters branchial arch development and leads to craniofacial skeletal defects.Quilez S., Dumontier E., Baim C., Kam J., Cloutier J.F.View abstractSourceMGI: 101926PubMedEurope PMCFront Cell Dev Biol 12:1256465-1256465 (2024)Mapped to99+
Hedgehog activation promotes osteogenic fates of growth plate resting zone chondrocytes through transient clonal competency.Orikasa S., Matsushita Y., Manabe H., Fogge M., Lee Z., Mizuhashi K., Sakagami N., Ono W., Ono N.View abstractSourceMGI: 101926PubMedEurope PMCJCI Insight 9:e165619-e165619 (2024)Mapped to15
DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons.Cheffer A., Garcia-Miralles M., Maier E., Akol I., Franz H., Srinivasan V.S.V., Vogel T.View abstractSourceMGI: 101926PubMedEurope PMCCereb Cortex 33:10272-10285 (2023)Mapped to99+
The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4.Luzzio A., Edie S., Palmer K., Caddle L.B., Urban R., Goodwin L.O., Welsh I.C., Reinholdt L.G., Bergstrom D.E.[...], Murray S.A.View abstractSourceMGI: 101926PubMedEurope PMCMamm Genome 34:453-463 (2023)Mapped to29
Dysfunction of programmed embryo senescence is linked to genetic developmental defects.de Lope C., Garcia-Lucena R., Magarinos M., Leon Y., Casa-Rodriguez N., Contreras N., Escudero-Iriarte C., Varela-Nieto I., Maire P., Palmero I.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 101926PubMedEurope PMCDevelopment 150:dev200903-dev200903 (2023)Mapped to62
Molecular profiling of the vestibular lamina highlights a key role for Hedgehog signalling.Qiu T., Huteckova B., Seppala M., Cobourne M.T., Chen Z., Hovorakova M., Buchtova M., Tucker A.S.View abstractCategoriesFunctionSourceMGI: 101926PubMedEurope PMCDevelopment 150:dev201464-dev201464 (2023)Mapped to99+