Publications by authors named "J Towne"

CYP24A1 is a multifunctional, P450 mitochondrial enzyme that catabolizes the vitamin D hormone (calcitriol, 1,25(OH)2D3), its precursor (calcifediol, 25(OH)D3), and numerous vitamin D metabolites. In the kidney, Cyp24a1 is induced by 1,25(OH)2D3 and fibroblast growth factor 23 (FGF23) and potently suppressed by PTH to control the circulating levels of 1,25(OH)2D3. Cyp24a1 is controlled by a pair of promoter proximal (PRO) vitamin D response elements (VDREs) that are aided by distal, downstream (DS) enhancers.

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CYP24A1 is a multifunctional, P450 mitochondrial 24-hydroxylase enzyme that is responsible for catabolism of the most active vitamin D hormone (calcitriol, 1,25(OH)D), its precursor (calcifediol, 25(OH)D), and numerous other vitamin D metabolites at the 23- and 24-carbon positions. In the kidney, is induced by 1,25(OH)D, induced by FGF23, and potently suppressed by PTH to tightly control the circulating blood levels of 1,25(OH)D. This gene is believed to be under the control of a pair of classic promoter proximal (PRO) vitamin D response elements (VDREs) that are aided by distal, downstream (DS) containing enhancers that we identified more recently.

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The interleukin (IL)-23 pathway is a pathogenic driver in psoriasis, psoriatic arthritis, and inflammatory bowel disease. Currently, no oral therapeutics selectively target this pathway. JNJ-77242113 is a peptide targeting the IL-23 receptor with high affinity (K: 7.

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Article Synopsis
  • Long noncoding RNAs (lncRNAs) play a significant but not fully understood role in the regulation of inflammation, particularly in inflammatory bowel disease (IBD).
  • Researchers used RNA-sequencing data from IBD patients to identify gene modules where lncRNAs are coexpressed with protein-coding genes, some of which correlate with disease severity and immune responses.
  • The study highlighted a specific lncRNA, IRF1-AS1, linked to a response in inflammatory cytokines and identified other lncRNAs that could affect inflammation in response to stimuli, suggesting new pathways for IBD treatment.
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