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Despite the absence of correlation of the examined VDR (show CYP27B1 Proteins) polymorphisms with colorectal cancer in the combined analysis, ApaI and BsmI loci are statistically significantly associated with colorectal cancer in the elderly and female patients, respectively
An association of the three genetic VDR (show CYP27B1 Proteins) variants.
vitamin D and VDR (show CYP27B1 Proteins) have roles in carcinogenesis [review]
VDR (show CYP27B1 Proteins) and MEGALIN (show LRP2 Proteins) gene variations can alter age-related cognitive trajectories differentially between men and women among AFrican American urban adults, specifically in global mental status and domains of verbal fluency, visual/working memory, and executive function.
VDR (show CYP27B1 Proteins) is important for the maintenance of physiological level of Axin1 (show AXIN1 Proteins)
Vitamin D receptor has a role in skeletal muscle integrity/function maintenance
VDR (show CYP27B1 Proteins) polymorphism, FOK1, associated with greater vitamin D3-dependent growth inhibition of plasmablastic lymphoma and myeloma cells
Allelic variations in CYP2R1 (show CYP2R1 Proteins) and GC affect vitamin D levels, but variant alleles on VDR (show CYP27B1 Proteins) and DHCR7 (show DHCR7 Proteins) were not correlated with vitamin D deficiency.
We also report that VDR (show CYP27B1 Proteins) gene polymorphisms may be a risk for the development of vitiligo (show MITF Proteins) in an Egyptian population.
VDR (show CYP27B1 Proteins) receptor genes polymorphism was found in patients, diagnosed with dermatomyositis or systemic lupus erythematosus.
Reduced Vitamin D receptor is associated with melanoma.
Expression of TauT is differentially regulated by Vitamin D(3) and retinoic acid via formation of VDR and RXR complexes in the nuclei in a cell type-dependent manner.
The expression of TNF-alpha (show TNF Proteins) and VDR in post-angioplasty coronary artery neointimal lesions of hypercholesterolemic swine, was examined.
Vitamin D receptor activation, and inducible nitric oxide synthase (NOS2 (show NOS2 Proteins)), were strongly induced during Cooperia oncophora reinfection. Several canonical pathways associated with NOS2 (show NOS2 Proteins) were impacted.
Two novel SNPs identified in coding region of VDR are associated with growth traits.
The data support the hypothesis that Vdr (show CYP27B1 Proteins) in mature adipocytes alters the metabolic response to high-fat diets and exerts anti-proliferative effects on the mammary epithelium.
The data demonstrate that deficiency in the vitamin D signaling via VDR (show CYP27B1 Proteins) knockout enhances the pathological phenotype in this experimental cardiomyopathy and suggest an important role for vitamin D in modulating disease severity in common cardiovascular disorders.
Absence of VDR (show CYP27B1 Proteins) or presence of an unliganded VDR (show CYP27B1 Proteins) does not affect the profile and function of ex vivo generated bone marrow-derived dendritic cells.
JNK1 (show MAPK8 Proteins) physically and functionally interacted with VDR (show CYP27B1 Proteins) and positively regulated VDR (show CYP27B1 Proteins) expression at transcriptional and translational levels, which influenced calcitriol-mediated inhibition of cancer cell proliferation.
Vitamin D receptor activation reduces dissecting abdominal aortic aneurysm formation induced by Ang-II (show AGT Proteins) in apoE (show APOE Proteins)(-/-) mice
VDR (show CYP27B1 Proteins) may function as a selective suppressor/de-repressor of gene expression in the absence of 1,25-dihydroxyvitamin D3.
In the presence of normocalcemia, absence of VDR (show CYP27B1 Proteins) or its ligand-activated transcription of genes has no direct regulatory effect on murine glucose homeostasis or gene expression in islets of Langerhans.
The Vdr (show CYP27B1 Proteins)-/- mouse model displays sex- and site-specific differences in skeletal structures with long-term feeding of a rescue diet.
The endothelial cell VDR (show CYP27B1 Proteins) plays a tonic inhibitory role in regulating glucose disposal and could prove to be a factor in controlling glucose homeostasis in the intact organism.
This gene encodes the nuclear hormone receptor for vitamin D3. This receptor also functions as a receptor for the secondary bile acid lithocholic acid. The receptor belongs to the family of trans-acting transcriptional regulatory factors and shows sequence similarity to the steroid and thyroid hormone receptors. Downstream targets of this nuclear hormone receptor are principally involved in mineral metabolism though the receptor regulates a variety of other metabolic pathways, such as those involved in the immune response and cancer. Mutations in this gene are associated with type II vitamin D-resistant rickets. A single nucleotide polymorphism in the initiation codon results in an alternate translation start site three codons downstream. Alternative splicing results in multiple transcript variants encoding different proteins.
vitamin D3 receptor
, 1,25-dihydroxyvitamin D3 receptor
, nuclear receptor subfamily 1 group I member 1
, vitamin D nuclear receptor variant 1
, vitamin D (1,25-dihydroxyvitamin D3) receptor
, vitamin D receptor
, vitamin D (1,25- dihydroxyvitamin D3) receptor