All natural DR3-type vitamin D response elements show a similar functionality in vitro.
about
A novel SNP in a vitamin D response element of the CYP24A1 promoter reduces protein binding, transactivation, and gene expressionRegulation of the human cyclin C gene via multiple vitamin D3-responsive regions in its promoterRegulation of multiple insulin-like growth factor binding protein genes by 1alpha,25-dihydroxyvitamin D3.Regulation of the human p21(waf1/cip1) gene promoter via multiple binding sites for p53 and the vitamin D3 receptor.Environmental risk factors for multiple sclerosis: a review with a focus on molecular mechanismsStructural considerations of vitamin D signalingStructural basis of VDR-DNA interactions on direct repeat response elementsThe human hyaluronan synthase 2 gene is a primary retinoic acid and epidermal growth factor responding geneThe yin and yang of vitamin D receptor (VDR) signaling in neoplastic progression: operational networks and tissue-specific growth controlA novel bile acid-activated vitamin D receptor signaling in human hepatocytes.Vitamin D binding protein and monocyte response to 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D: analysis by mathematical modeling.The coupling of epidermal growth factor receptor down regulation by 1alpha,25-dihydroxyvitamin D3 to the hormone-induced cell cycle arrest at the G1-S checkpoint in ovarian cancer cells.The paracrine feedback loop between vitamin D₃ (1,25(OH)₂D₃) and PTHrP in prehypertrophic chondrocytesPatterns of genome-wide VDR locations.Tight junction CLDN2 gene is a direct target of the vitamin D receptor.1α,25(OH)(2)-Vitamin D3 increases dysferlin expression in vitro and in a human clinical trial.1,25-Dihydroxyvitamin D3 suppresses telomerase expression and human cancer growth through microRNA-498.Genome-wide approaches for identification of nuclear receptor target genes.Peroxisome proliferation-activated receptor δ agonist GW0742 interacts weakly with multiple nuclear receptors, including the vitamin D receptor.Bipartite pattern discovery by entropy minimization-based multiple local alignment.Discovery of the first irreversible small molecule inhibitors of the interaction between the vitamin D receptor and coactivatorsActivation of vitamin D receptor (VDR)- and peroxisome proliferator-activated receptor (PPAR)-signaling pathways through 1,25(OH)(2)D(3) in melanoma cell lines and other skin-derived cell linesIdentification of genetic variants affecting vitamin D receptor binding and associations with autoimmune disease.Novel VDR antagonists based on the GW0742 scaffold.The claudin-16 channel gene is transcriptionally inhibited by 1,25-dihydroxyvitamin D.
P2860
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P2860
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@en
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@nl
type
label
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@en
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@nl
prefLabel
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@en
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@nl
P2860
P1433
P1476
All natural DR3-type vitamin D response elements show a similar functionality in vitro.
@en
P2860
P304
P356
10.1042/0264-6021:3520301
P407
P478
P577
2000-12-01T00:00:00Z