Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Additionally we are shipping DLX3 Antibodies (56) and DLX3 Proteins (6) and many more products for this protein.
Showing 1 out of 2 products:
genetic analysis revealed a novel de novo missense mutation c.533A>G (p.Q178R) in the conserved homeodomain of the DLX3 gene. This DLX3 mutation is the sixth causative mutation for TDO to be identified so far.
ER-alpha (show ESR1 ELISA Kits) regulates the osteoblast differentiation through modulation of Dlx3 expression and/or interaction with Dlx3.
Results suggest that Dlx3 is a novel target of PKA, and that PKA mediates BMP signaling during osteoblast differentiation, at least in part, by phosphorylating Dlx3 and modulating its stability and function.
rs2278163 SNP of DLX3 might be associated with dental caries susceptibility in Japanese children. T and C alleles of rs2278163 SNP may potentially be involved in caries susceptibility and caries protection respectively.
In conclusion, results of our study suggest that the NOTCH (show NOTCH1 ELISA Kits)-signaling pathway, which is activated during the osteogenic differentiation of DFCs.
DLX3 orchestrates the expression of multiple regulators of trophoblast differentiation and that expression of these regulatory genes is abnormal in fetal growth restriction.
DLX3 stimulates osteogenic differentiation via BMP2 (show BMP2 ELISA Kits) dependent pathway.
Increased DLX3 expression in idiopathic fetal growth restricion (FGR (show FGR ELISA Kits)) may contribute to trophoblast dysfunction observed in FGR (show FGR ELISA Kits).
DLX3 acts upstream of syncytin, 3beta-hydroxysteroid dehydrogenase, and the human gonadotropin beta-subunit (show POLG ELISA Kits) to play a regulatory role in villous cytotrophoblast differentiation.
DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes
study demonstrates the co-expression of DLX3, PPARG (show PPARG ELISA Kits) and SP1 (show SP1 ELISA Kits) in trophoblast binucleated cell (BNC)nuclei; this suggests a possible role of these transcription factors through BNC specific genes at the time of pre-placental differentiation
DLX3 has a central role in controlling IFNT gene expression by associating with ETS2 on the IFNT promoter.
our data show that DLX3 promotes the expression of the EMP (show MAEA ELISA Kits) genes Amelx (show AMELX ELISA Kits), Enam (show ENAM ELISA Kits), Klk4 (show KLK4 ELISA Kits), and Odam (show ODAM ELISA Kits) in amelogenesis.
The DLX3 regulates transcription factors crucial for bone formation and DLX3 attenuates bone mass accrual to support bone homeostasis by osteogenic gene pathway regulation.
We show that the deletion of Dlx3 in epidermis and isthums/infundibulum area leads to hair shaft differentiation but not hair growth.
we provide a novel insight that BMP-2 (show BMP2 ELISA Kits)-induced Dlx3 expression is regulated by p38 (show CRK ELISA Kits)/Smad5 (show SMAD5 ELISA Kits) signaling pathway in osteoblasts.
used a conditional knockout approach to analyze the effects of neural crest deletion of Dlx3 on craniofacial bones development
regulation of Dlx3 by HR affects the IRS (show IARS ELISA Kits) keratin expression, thus modulating the formation of IRS (show IARS ELISA Kits) of hair follicle.
The transcription factor Dlx3 is essential in dentin formation by directly regulating a crucial matrix protein.
Dlx3 ablation in epidermis is linked to altered epidermal differentiation, barrier development, and IL-17 (show IL17A ELISA Kits)-associated skin inflammation.
Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.
distal-less homeobox 3
, distal-less homeo box 3
, DLX3 homeodomain containing protein
, homeobox protein DLX-3
, DII C