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DLX5 encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. Additionally we are shipping Distal-Less Homeobox 5 Antibodies (96) and Distal-Less Homeobox 5 Kits (14) and many more products for this protein.
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Retinoic acid treatment leads to a progressive loss of Dlx5 and Dlx6 expression in the first pharyngeal arch.
These data indicate that certain missense mutations diminish the ability of the Dlx5 homeodomain to recognize and bind target DNAs, and they likely destabilize the formation of functional complexes.
In cells grown on titanium support, DLX5 and RUNX1 (show RUNX1 Proteins) were respectively upregulated (+3.12-fold) and downregulated (-2.14-fold)
Absent expression of the osteoblast-specific maternally imprinted genes, DLX5 and DLX6, causes split hand/split foot malformation type I.
Heterozygous DLX5 nonsense mutation c.G115T(p.E39X) associated with isolated split-hand/foot malformation with reduced penetrance and variable expressivity in two unrelated Polish families.
A novel heterozygous mutation in exon 3 of DLX5 found in the family members with SHFM1 (show SHFM1 Proteins) phenotype.
Genome sequencing of the deletion breakpoints showed that the DLX5 and DLX6 genes are disomic but the putative DYNC1I1 (show DYNC1I1 Proteins) exon 15 and 17 enhancers are deleted.
The duplicated region harbors only DLX5 and DLX6, which are known for their role in SHFM1 (show SHFM1 Proteins).
The strongest evidence for altered methylation patterns in shiftworkers was observed for DLX5 gene.
Cyclic tensile stress may induce differentiation of periodontal ligament stem cells towards mineralized tissue cells by promoting Dlx5 mRNA expression and decreasing Msx2 expression.
Two patients that have in common a p63-Dlx5/Dlx6 pathway dysregulation.
Imprinting analysis shows that DLX5 is maternally expressed in some organs and tissues but not imprinted in others.
High DLX5 expression is associated with T-cell lymphomagenesis.
Both transient and stable expression of Necdin (show NDN Proteins) induced osteoblast-specific markers in an osteogenic cell line through formation of a complex with distal-less Homeobox 5 (Dlx5) and Runx2 (show RUNX2 Proteins) promoter activation.
DLX5 and DLX6 reciprocally inhibit BMP/H2-mediated H1 enhancer regulation in mandible embryonic development.
We found that in Dlx5;6 DKO limbs, the AER expresses lower levels of Wnt5a (show WNT5A Proteins), shows scattered beta-catenin (show CTNNB1 Proteins) responsive cells and altered basolateral and planar cell polarity (PCP (show BMP1 Proteins)).
Dlx5 and Dlx6 expression determines uterine architecture and adenogenesis and is needed for implantation
The results presented here indicate that loss of Dlx5 causes a down-modulation of miR (show MLXIP Proteins)-9 and of miR (show MLXIP Proteins)-200-class, which results in the over-expression of the Foxg1 (show FOXG1 Proteins) protein.
Lck (show LCK Proteins)-Dlx5 mice develop T-ALLs that consistently acquire overexpression of Myc (show MYC Proteins) and activation of Akt (show AKT1 Proteins).
Study demonstrated a novel role of miR (show MLXIP Proteins)-124 and Dlx5 in regulating the differentiation of mesenchymal stem cells toward the myogenic lineage, that is, miR (show MLXIP Proteins)-124 inhibits myogenic differentiation partially through targeting Dlx5 expression.
Mash1 (show ASCL1 Proteins) is required for the expression of GAD67 (show GAD1 Proteins) and Dlx5 in taste bud cells.
Dlx5 and Mef2 (show MEF2C Proteins) directly bound to the runx2 (show RUNX2 Proteins) enhancer, and the binding sites were required for the osteoblast-specific expression
Data indicate that retinoic acid (RA) induces the expression patterns of genes normally expressed in the posterior tooth-forming region, such as pitx2 (show PITX2 Proteins) and dlx2b.
This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.
distal-less homeobox 5
, homeobox Dlx5
, homeobox protein DLX-2
, homeobox protein DLL-3
, putative transcription factor DLL3
, distal-less homeo box 5
, homeobox protein DLX-5
, split hand/foot malformation type 1 with sensorineural hearing loss
, homeobox protein DLX-3
, distal-less homeobox protein 5
, distal-less homeobox gene 5
, distal-less homeobox protein 2b
, homeobox protein Dlx2b