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The local regulation of vitamin D in sinonasal tissue during chronic rhinosinusitis may be independent of serum 25(OH)D levels. Vitamin D may be dysregulated at multiple levels, with decreased transcription of the metabolic gene CYP27B1 (show CYP27B1 ELISA Kits) and increased transcription of the catabolic gene CYP24A1.
High CYP24A1 expression is associated with Lung Adenocarcinoma.
More recent evidence has identified loss of function mutations in CYP24A1 in association with hypercalcemia, hypercalciuria and nephrolithiasis in humans. [review]
Uremic serum increased the intracellular expression of IL-6 (show IL6 ELISA Kits), IFN-gamma (show IFNG ELISA Kits), TLR7 (show TLR7 ELISA Kits), TLR9 (show TLR9 ELISA Kits), VDR (show CYP27B1 ELISA Kits), CYP27b1 (show CYP27B1 ELISA Kits) and CYP24a1
Biallelic mutations in CYP24A1 or SLC34A1 were associated with infantile idiopathic hypercalcemia with vitamin D hypersensitivity
CYP24A1 association with the susceptibility of esophageal squamous cell carcinoma in a Northern Chinese population.
CYP24A1 was expressed in a >2-fold higher fraction of spermatozoa from normal than infertile men.
Our results indicate that CYP24A1, central in the degradation of the physiologically active 1,25[OH]2D, is important in the association of lower levels of 25[OH]D and increased risk of SLE.
Findings offer direct evidence that Cyp24a1 functions as an oncogene (show RAB1A ELISA Kits) in PTC (show F9 ELISA Kits), where its overexpression activates multiple signaling cascades to promote malignant progression.
The aim of the present study was to investigate the mRNA expression levels of the CYP24A1 and CYP27B1 (show CYP27B1 ELISA Kits) genes in malignant and normal breast tissues. The results demonstrated that the mRNA expression of CYP27B1 (show CYP27B1 ELISA Kits) was downregulated in the tumor tissues, compared with the adjacent normal tissues (P<0.01), whereas the mRNA expression of CYP24A1 was significantly upregulated in the tumor tissues (P<0.01).
CYP24A1 activity is not essential for intramembranous bone formation.
results link CYP24 activity to the pathophysiology of FGF23 (show FGF23 ELISA Kits)-dependent renal phosphate wasting states and implicate pharmacologic CYP24 inhibition as a therapeutic adjunct for their treatment.
Gsalpha is required in proximal tubules for suppressing renal vitamin D 24-hydroxylase mRNA levels and for maintaining normal serum 1,25(OH)2D.
Data suggest that control of CYP24A1 increase during diabetes has a beneficial effect on senescence induction and caspase-3 (show CASP3 ELISA Kits) increased expression.
the mechanism through which 1,25(OH)(2)D(3) induces the CYP24A1 enzyme
The expression of vitamin D 24-hydroxylase gene was directly regulated by serum calcium rather than 25-hydroxyvitamin D 1 alpha-hydroxylase.
Results show that Inhibition of 24-OHase activity modulates serum calcitriol PK in normal C3H/HeJ mice.
Cyp24a1 deficiency delays fracture repair and strongly suggest that vitamin D metabolites hydroxylated at position 24, such as 24,25(OH)2D3, play an important role in the mechanisms leading to normal fracture hea (show TTC7A ELISA Kits)
1,25(OH)2D is the preferred substrate for CYP24 in murine kidney mitochondria.
findings demonstrate that regulation of both the 25-hydroxyvitamin D-1 alpha-hydroxylase and 25-hydroxyvitamin D-24-hydroxylase genes by phosphorus is disordered in hypophosphatemic mice at the level of renal mRNA expression
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein initiates the degradation of 1,25-dihydroxyvitamin D3, the physiologically active form of vitamin D3, by hydroxylation of the side chain. In regulating the level of vitamin D3, this enzyme plays a role in calcium homeostasis and the vitamin D endocrine system. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
1,25-@dihydroxyvitamin D3 24-hydroxylase
, 1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial
, cytochrome P450 24A1
, cytochrome P450, subfamily XXIV (vitamin D 24-hydroxylase)
, cytochrome P450-CC24
, exo-mitochondrial protein
, vitamin D 24-hydroxylase
, vitamin D(3) 24-hydroxylase
, 25-hydroxyvitamin D-24-hydroxylase
, cytochrome P450, 24
, cytochrome P450, 24a1
, 25-hydroxyvitamin D3 24-hydroxylase
, Cytochrom P450 (25-hydroxyvitamin D24-hydroxylase)
, cytochrome P450, subfamily 24
, 25-hydroxyvitamin D3-24-hydroxylase