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Displaying 20 of 34 results for "DLX5"
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  1. Crystal structure of a distal-less homeobox protein 5 (Dlx5) from Homo sapiens at 1.85 A resolution PDB

    ID: PDB:4RDU

    Description: Homeobox protein DLX-5

  2. Expression data from Lck-Dlx5 lymphoma BioProject

    ID: PRJNA326700

    Keywords: Transcriptome or Gene expression

    Access Type: download

  3. Expression data from Lck-Dlx5 lymphoma OmicsDI

    ID: E-GEOD-83685

    Date Released: 07-03-2016

    Description: Lck-Dlx5 induces T-cell lymphoma but the mechanism is unknown. We used microarrays to detail the global programme of gene expression un...

  4. Identification of downstream transcriptional targets of Dlx5 during early mouse inner ear (otocyst/otic vesicle) development ArrayExpress

    ID: E-GEOD-22381

    Description: essed in discrete regions of the otic vesicle and Dlx5 is one of those that is expressed highly in the presumptive dorsal vestibular region. Mice lacking Dlx5 have vestibular defects. Specifically, they fail to f...

  5. Identification of downstream transcriptional targets of Dlx5 during early mouse inner ear (otocyst/otic vesicle) development BioProject

    ID: PRJNA127635

    Keywords: Transcriptome or Gene expression

    Access Type: download

  6. Identification of downstream transcriptional targets of Dlx5 during early mouse inner ear (otocyst/otic vesicle) development OmicsDI

    ID: E-GEOD-22381

    Date Released: 07-12-2011

    Description: essed in discrete regions of the otic vesicle and Dlx5 is one of those that is expressed highly in the presumptive dorsal vestibular region. Mice lacking Dlx5 have vestibular defects. Specifically, they fail to f...

  7. Expression data from Lck-Dlx5 lymphoma ArrayExpress

    ID: E-GEOD-83685

    Description: Lck-Dlx5 induces T-cell lymphoma but the mechanism is unknown. We used microarrays to detail the global programme of gene expression un...

  8. ociated fibroblasts by CAGE sequencing identified DLX5 and RUNX2 long variant as novel regulators involved in periodontitis.... BioProject

    ID: PRJNA322829

    Keywords: Transcriptome or Gene expression

    Access Type: download

  9. ociated fibroblasts by CAGE sequencing identified DLX5 and RUNX2 long variant as novel regulators involved in periodontitis... BioProject

    ID: PRJNA323558

    Access Type: download

  10. The genome wide transcriptional profiling of periodontitis-associated fibroblasts identified DLX5 and RUNX2 as central regulatory elements [RNA-seq] BioProject

    ID: PRJNA323570

    Keywords: Transcriptome or Gene expression

    Access Type: download

  11. Mus musculus strain:B6D2F1N : Mus musculus strain:B6D2F1N Transcriptome or Gene expression BioProject

    ID: PRJNA299798

    Keywords: transcriptome

    Access Type: download

    dataset.description: We first show that Dlx5/6 expression begins in Müllerian ducts epithelia and persists then in the uterine luminal and glandular epithelia throughout ...
  12. Profiling data on the developing olfactory/GnRH system reveal cellular and molecular pathways potentially relevant for the Kallmann syndrome ArrayExpress

    ID: E-GEOD-52800

    Description: es. We also profiled the OE from embryos null for Dlx5, a homeogene essential for olfactory development, that causes a KS-like phenotype when deleted. We also applied analysis of conserved co-expression to integrate the obtained data with information on KS disease genes. The prevalent categories of genes differentially expressed during development are neuronal differentiation, extracellular remodelling and cell adhesion. From the analysis of Dlx5 mutant tissues we identify about 120 genes with a prevalence of intermediate filaments, cell signalling, epithelial and neuronal differentiation. Filtering for true OE expression and for the presence of Dlx5 binding sites, yielded twenty genes, of the following categories: 1) transmembrane adhesion/receptor molecules, 2) axon-glia interaction molecules, 3) synaptic proteins, 4) scaffold/adapter for signalling molecules. To functionally analyze these genes in vivo, we used three zebrafish fluorescent reporter zebrafish strains, in which we monitored early phases of olfactory/GnR...

  13. Transcription profiling of mouse branchial arches from Dlx2-/-, Dlx1/2 -/- or Dlx5/6 -/- ArrayExpress

    ID: E-GEOD-4774

    Description: The Dlx homeobox genes have central roles in controlling patterning and differentiation of the brain and craniofacial primordia. In the bra...

  14. The solution structure of the homeobox domain of human Homeobox protein DLX-5 PDB

    ID: PDB:2DJN

    Description: Homeobox protein DLX-5

  15. Profiling data on the developing olfactory/GnRH system reveal cellular and molecular pathways potentially relevant for the Kallmann syndrome. OmicsDI

    ID: E-GEOD-52800

    Date Released: 02-18-2014

    Description: es. We also profiled the OE from embryos null for Dlx5, a homeogene essential for olfactory development, that causes a KS-like phenotype when deleted. We also applied analysis of conserved co-expression to integrate the obtained data with information on KS disease genes. The prevalent categories of genes differentially expressed during development are neuronal differentiation, extracellular remodelling and cell adhesion. From the analysis of Dlx5 mutant tissues we identify about 120 genes with a prevalence of intermediate filaments, cell signalling, epithelial and neuronal differentiation. Filtering for true OE expression and for the presence of Dlx5 binding sites, yielded twenty genes, of the following categories: 1) transmembrane adhesion/receptor molecules, 2) axon-glia interaction molecules, 3) synaptic proteins, 4) scaffold/adapter for signalling molecules. To functionally analyze these genes in vivo, we used three zebrafish fluorescent reporter zebrafish strains, in which we monitored early phases of olfactory/GnR...

  16. Transcription profiling of mouse branchial arches from Dlx2-/-, Dlx1/2 -/- or Dlx5/6 -/- OmicsDI

    ID: E-GEOD-4774

    Date Released: 06-10-2011

    Description: The Dlx homeobox genes have central roles in controlling patterning and differentiation of the brain and craniofacial primordia. In the bra...

  17. Profiling data on the developing olfactory/GnRH system reveal cellular and molecular pathways potentially relevant for the Kallmann syndrome. BioProject

    ID: PRJNA230053

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: es. We also profiled the OE from embryos null for Dlx5, a homeogene essential for olfactory development, that causes a KS-like phenotype when deleted. We also applied analysis of conserved co-expression to integrate the obtained data with information on KS disease genes. The prevalent categories of genes differentially expressed during development are neuronal differentiation, extracellular remodelling and cell adhesion. From the analysis of Dlx5 mutant tissues we identify about 120 genes with a prevalence of intermediate filaments, cell signalling, epithelial and neuronal differentiation. Filtering for true OE expression and for the presence of Dlx5 binding sites, yielded twenty genes, of the following categories: 1) transmembrane adhesion/receptor molecules, 2) axon-glia interaction molecules, 3) synaptic proteins, 4) scaffold/adapter for signalling molecules. To functionally analyze these genes in vivo, we used three zebrafish fluorescent reporter zebrafish strains, in which we monitored early phases of olfactory/GnR...
  18. DLX5_RAT UniProt:Swiss-Prot

    ID: P50575

    Description: Homeobox protein DLX-5 Homeobox Phosphoserine; by MAPK14; in vitro Phosphoserine; by MAPK14; ...

  19. Highly efficient in vivo delivery of functional RNAs using new versatile MS2-chimeric retrovirus-like particles BioProject

    ID: PRJNA277806

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: g MS2-retrovirus chimeras. We delivered RUNX2- or DLX5-mRNA into primary human bone-marrow mesenchymal-stem-cells. We used microarrays to detail the global programme of gene expression confirming the effects of pro-osteogenic genes transduced by MS2 chimeric lentiviral particles. Overall design: Immature bone marrow mesenchymal stem cells were transduced with viral particles containing either MS2RLP-
  20. Genome-wide profiling of p63 binding sites identifies genes and regulatory elements for p63-related disorders ArrayExpress

    ID: E-GEOD-17611

    Description: ent to control expression of the distally located DLX5/DLX6 genes essential for limb development. Our data demonstrate that target genes and regulatory elements detected in this study can serve as powerful tools to identify causative mutations of unresolved ectodermal disorders. ChIP-seq profiles of p63 in primary human keratinocytes established from two different normal individuals....


Displaying 20 of 34 results for "DLX5"