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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 (106) and Distal-Less Homeobox 5 Proteins (7) and many more products for this protein.
Showing 10 out of 15 products:
These results indicate activation of DLX5 and RUNX2 (show RUNX2 ELISA Kits) via its distal promoter represents a unique feature of GFs, and is important for ECM (show MMRN1 ELISA Kits) regulation. Down-regulation of these transcription factors in PAFs could be associated with their property to degrade collagen, which may impact on the process of periodontitis.
these findings indicate that, in MSCs, DLX5 is a master regulator of osteogenesis. Furthermore, tanshinone IIA may be valuable for stem cell-based therapies of certain bone diseases.
As a result of disturbed imprinting, the upregulated DLX5 affects trophoblast proliferation in preeclampsia.
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 ELISA Kits) 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 ELISA Kits) phenotype.
Genome sequencing of the deletion breakpoints showed that the DLX5 and DLX6 genes are disomic but the putative DYNC1I1 (show DYNC1I1 ELISA Kits) 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 ELISA Kits).
FGF10 (show FGF10 ELISA Kits) pathway is downregulated in Dlx5(-/-) mice, and activation of FGF10 (show FGF10 ELISA Kits) signaling rescues cranial neural crest cell proliferation and myogenic differentiation.
High DLX5 expression is associated with T-cell lymphomagenesis.
Both transient and stable expression of Necdin (show NDN ELISA Kits) induced osteoblast-specific markers in an osteogenic cell line through formation of a complex with distal-less Homeobox 5 (Dlx5) and Runx2 (show RUNX2 ELISA Kits) 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 ELISA Kits), shows scattered beta-catenin (show CTNNB1 ELISA Kits) responsive cells and altered basolateral and planar cell polarity (PCP (show BMP1 ELISA Kits)).
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-9 and of miR-200-class, which results in the over-expression of the Foxg1 protein.
Lck (show LCK ELISA Kits)-Dlx5 mice develop T-ALLs that consistently acquire overexpression of Myc (show MYC ELISA Kits) and activation of Akt (show AKT1 ELISA Kits).
Study demonstrated a novel role of miR (show MLXIP ELISA Kits)-124 and Dlx5 in regulating the differentiation of mesenchymal stem cells toward the myogenic lineage, that is, miR (show MLXIP ELISA Kits)-124 inhibits myogenic differentiation partially through targeting Dlx5 expression.
Mash1 (show ASCL1 ELISA Kits) is required for the expression of GAD67 (show GAD1 ELISA Kits) and Dlx5 in taste bud cells.
Retinoic acid treatment leads to a progressive loss of Dlx5 and Dlx6 expression in the first pharyngeal arch.
Imprinting analysis shows that DLX5 is maternally expressed in some organs and tissues but not imprinted in others.
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 ELISA Kits) 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 homeo box 5
, homeobox protein DLX-5
, split hand/foot malformation type 1 with sensorineural hearing loss
, homeobox protein DLX-3
, homeobox protein DLL-3
, putative transcription factor DLL3
, distal-less homeobox 5
, distal-less homeobox protein 5
, distal-less homeobox gene 5
, distal-less homeobox protein 2b
, homeobox protein Dlx2b