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Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Additionally we are shipping DLX4 Proteins (6) and DLX4 Kits (1) and many more products for this protein.
Showing 10 out of 117 products:
Human Monoclonal DLX4 Primary Antibody for WB - ABIN393260
Jugessur, Shi, Gjessing, Lie, Wilcox, Weinberg, Christensen, Boyles, Daack-Hirsch, Nguyen, Christiansen, Lidral, Murray: Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. in PLoS ONE 2010
Show all 5 references for ABIN393260
Human Polyclonal DLX4 Primary Antibody for ELISA, WB - ABIN1534050
Nakamura, Stock, Wydner, Bollekens, Takeshita, Nagai, Chiba, Kitamura, Freeland, Zhao, Minowada, Lawrence, Weiss, Ruddle: Genomic analysis of a new mammalian distal-less gene: Dlx7. in Genomics 1997
Show all 2 references for ABIN1534050
Mouse (Murine) Polyclonal DLX4 Primary Antibody for WB - ABIN610693
Drees, Friederich, Fradelizi, Louvard, Beckerle, Golsteyn: Characterization of the interaction between zyxin and members of the Ena/vasodilator-stimulated phosphoprotein family of proteins. in The Journal of biological chemistry 2000
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Cow (Bovine) Polyclonal DLX4 Primary Antibody for WB - ABIN2780384
Awwad, Do, Stevenson, Fu, Lo-Coco, Costello, Campbell, Berg: Overexpression of BP1, a homeobox gene, is associated with resistance to all-trans retinoic acid in acute promyelocytic leukemia cells. in Annals of hematology 2008
Human Polyclonal DLX4 Primary Antibody for WB - ABIN2779826
Kelly, Jerome-Majewska, Papaioannou: The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis. in Human molecular genetics 2004
study indicated that DLX4 hypermethylation was a frequent event and acted as an independent prognostic biomarker in de novo myelodysplastic syndrome patients
Our study reveals that BP1 overexpression serves as an independent risk factor in de novo AML (show RUNX1 Antibodies) patients.
Collectively, our findings indicate that DLX4 exerts opposing effects on the megakaryocytic and erythroid lineages in part by inducing IL-1beta (show IL1B Antibodies) and NF-kappaB (show NFKB1 Antibodies) signaling.
DLX4 induces CD44 (show CD44 Antibodies) by stimulating IL-1beta (show IL1B Antibodies)-mediated NF-kappaB (show NFKB1 Antibodies) activity, thereby promoting peritoneal metastasis of ovarian cancer
This first finding of a DLX4 mutation in a family with Cleft lip and/or palate establishes DLX4 as a potential cause of human clefts
DLX4 promotes ovarian tumor angiogenesis in part by stimulating iNOS (show NOS2 Antibodies) expression.
Aberrant DNA methylation (show HELLS Antibodies) of the DLX4 and SIM1 (show SIM1 Antibodies) genes may be a novel progression marker for uterine cervical low-grade squamous intraepithelial lesions.
indicate that gains of DLX4 and ERBB2 (show ERBB2 Antibodies) occur in South African breast cancer patients irrespectively of their race and factors known to influence prognosis
a DLX4 overexpression vector lacking the 3'UTR (show UTS2R Antibodies) was shown to abolish miR (show MLXIP Antibodies)-122-induced inhibition of proliferation in the HCC (show FAM126A Antibodies) cell line Hep3B.
DLX4 can functionally replace c-MYC (show MYC Antibodies).
Genomic structure and functional control of the Dlx3 (show DLX3 Antibodies)-7 bigene cluster
nuclear import of Dlx4 is compromised by specific residues that flank the nuclear localization signal
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. The DLX proteins are postulated to play a role in forebrain and craniofacial development. Three transcript variants have been described for this gene, however, the full length nature of one variant has not been described. Studies of the two splice variants revealed that one encoded isoform functions as a repressor of the beta-globin gene while the other isoform lacks that function.
distal-less homeobox 4
, beta protein 1
, distal-less homeo box 7
, distal-less homeo box 9
, homeobox protein DLX-4
, homeobox protein DLX-7
, homeobox protein DLX-8
, DII D