PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 10366427-0 1999 Role of vitamin D3 receptor in the synergistic differentiation of WEHI-3B leukemia cells by vitamin D3 and retinoic acid. Tretinoin 107-120 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 8-27 26504088-1 2015 The biological actions of 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) are mediated by the vitamin D receptor (VDR), whose expression in bone cells is regulated positively by 1,25(OH)2D3, retinoic acid, and parathyroid hormone through both intergenic and intronic enhancers. Tretinoin 182-195 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 85-103 26504088-1 2015 The biological actions of 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) are mediated by the vitamin D receptor (VDR), whose expression in bone cells is regulated positively by 1,25(OH)2D3, retinoic acid, and parathyroid hormone through both intergenic and intronic enhancers. Tretinoin 182-195 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 105-108 19474283-11 2009 CONCLUSIONS: These results suggested selective cooperation of RAR and VDR in the regulation of the nephrin gene, i.e. (1) ATRA induces nephrin gene expression via RAR independently of RXR and VDR and (2) 1,25(OH)(2)D(3) induces nephrin gene expression via selective cooperation of RAR and VDR, which is independent of RXR. Tretinoin 122-126 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 70-73 14666262-5 2003 The possibility that retinoic acid would induce the expression of the vitamin D receptor and synergize with vitamin D, a known inhibitor of HC11 cell growth, was also investigated. Tretinoin 21-34 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 70-88 28635660-0 2017 Diverse Regulation of Vitamin D Receptor Gene Expression by 1,25-Dihydroxyvitamin D and ATRA in Murine and Human Blood Cells at Early Stages of Their Differentiation. Tretinoin 88-92 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 22-40 10366427-4 1999 No VDR was detected in untreated WEHI-3B D- cells; however, RA and 1,25-(OH)2D3 when used as single agents caused a slight induction of the VDR and in combination produced a marked increase in the VDR. Tretinoin 60-62 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 140-143 10366427-4 1999 No VDR was detected in untreated WEHI-3B D- cells; however, RA and 1,25-(OH)2D3 when used as single agents caused a slight induction of the VDR and in combination produced a marked increase in the VDR. Tretinoin 60-62 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 140-143 10366427-9 1999 These findings suggest that (a) induction of VDR expression is a key component in the synergistic differentiation induced by 1,25-(OH)2D3 and RA and (b) RAR and not RXR must be activated for enhanced induction of the VDR and for the synergistic differentiation produced by RA and 1, 25-(OH)2D3. Tretinoin 142-144 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 45-48 10366427-9 1999 These findings suggest that (a) induction of VDR expression is a key component in the synergistic differentiation induced by 1,25-(OH)2D3 and RA and (b) RAR and not RXR must be activated for enhanced induction of the VDR and for the synergistic differentiation produced by RA and 1, 25-(OH)2D3. Tretinoin 153-155 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 45-48 10366427-9 1999 These findings suggest that (a) induction of VDR expression is a key component in the synergistic differentiation induced by 1,25-(OH)2D3 and RA and (b) RAR and not RXR must be activated for enhanced induction of the VDR and for the synergistic differentiation produced by RA and 1, 25-(OH)2D3. Tretinoin 153-155 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 217-220 8574944-1 1995 The effects of retinoic acid (RA), and calcitriol are mediated by specific nuclear receptors (RARs and VDR, respectively). Tretinoin 15-28 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 103-106 8574944-1 1995 The effects of retinoic acid (RA), and calcitriol are mediated by specific nuclear receptors (RARs and VDR, respectively). Tretinoin 30-32 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 103-106 8382933-6 1993 In contrast to the effects of RA on osteoblast-related gene regulation, RA was found to increase the quantity of estrogen receptor as well as of 1,25-dihydroxy vitamin D3 receptor (VDR) in BFO cells. Tretinoin 72-74 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 160-179 8203489-6 1994 Although RA increased VDR levels, RA did not potentiate the effect of 1,25(OH)2D on ALP activity. Tretinoin 9-11 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 22-25 8382933-6 1993 In contrast to the effects of RA on osteoblast-related gene regulation, RA was found to increase the quantity of estrogen receptor as well as of 1,25-dihydroxy vitamin D3 receptor (VDR) in BFO cells. Tretinoin 72-74 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 181-184 8382933-8 1993 These RA effects on ER and VDR seem to be specific, since glucocorticoid receptor quantities were not affected by RA treatment. Tretinoin 6-8 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 27-30 32866959-5 2021 In summary, we conclude that epidermal hyperproliferation of mouse skin in response to a topically administered vitamin D receptor antagonist/partial agonist (ZK159222) is induced via increased retinoic acid synthesis, retinoic acid levels and increased RARgamma-mediated pathways. Tretinoin 194-207 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 112-130 32866959-5 2021 In summary, we conclude that epidermal hyperproliferation of mouse skin in response to a topically administered vitamin D receptor antagonist/partial agonist (ZK159222) is induced via increased retinoic acid synthesis, retinoic acid levels and increased RARgamma-mediated pathways. Tretinoin 219-232 vitamin D (1,25-dihydroxyvitamin D3) receptor Mus musculus 112-130