Competition for a unique response element mediates retinoic acid inhibition of vitamin D3-stimulated transcription. (Q38353899)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8702813%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

title

Competition for a unique response element mediates retinoic acid inhibition of vitamin D3-stimulated transcription (English)

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17 October 2019

1 reference

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17 October 2019

X Cao

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17 October 2019

H J Zhu

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17 October 2019

L Zhang

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17 October 2019

X Feng

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17 October 2019

F P Ross

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17 October 2019

language of work or name

English

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publication date

1 August 1996

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Journal of Biological Chemistry

17 October 2019

published in

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17 October 2019

volume

271

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17 October 2019

issue

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17 October 2019

page(s)

20650-20654

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Integrins: versatility, modulation, and signaling in cell adhesion

17 October 2019

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Retinoid X receptor interacts with nuclear receptors in retinoic acid, thyroid hormone and vitamin D3 signalling

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Response element selectivity for heterodimerization of vitamin D receptors with retinoic acid and retinoid X receptors.

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Vitamin D3-thyroid hormone receptor heterodimer polarity directs ligand sensitivity of transactivation

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The orientation and spacing of core DNA-binding motifs dictate selective transcriptional responses to three nuclear receptors

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Multiplicity generates diversity in the retinoic acid signalling pathways

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Sequence elements in the human osteocalcin gene confer basal activation and inducible response to hormonal vitamin D3.

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Cooperativity in transactivation between retinoic acid receptor and TFIID requires an activity analogous to E1A

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Jun-Fos and receptors for vitamins A and D recognize a common response element in the human osteocalcin gene

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Inhibition of estrogen-responsive gene activation by the retinoid X receptor beta: evidence for multiple inhibitory pathways

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Retinoid X receptors stimulate and 9-cis retinoic acid inhibits 1,25-dihydroxyvitamin D3-activated expression of the rat osteocalcin gene

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