scispace - formally typeset
C

Carlos Encinas Dominguez

Researcher at University of Arizona

Publications -  9
Citations -  2086

Carlos Encinas Dominguez is an academic researcher from University of Arizona. The author has contributed to research in topics: Calcitriol receptor & Retinoid X receptor. The author has an hindex of 6, co-authored 9 publications receiving 2000 citations.

Papers
More filters
Journal ArticleDOI

The nuclear vitamin D receptor: biological and molecular regulatory properties revealed.

TL;DR: The scope of this review will be limited to highlighting the actions of 1,25(OH)2D3 mediated by nuclear VDR and discussing new developments in the structure/function analysis of the receptor, including the phenotype of VDR knockout mice and the biochemical classification of patients with point mutations in the receptor.
Journal ArticleDOI

Functionally relevant polymorphisms in the human nuclear vitamin D receptor gene.

TL;DR: Functional relevance for both the F/f and L/S common polymorphisms in hVDR is demonstrated, and novel evidence for a third genetic variable impacting receptor potency is provided.
Journal ArticleDOI

Liganded VDR induces CYP3A4 in small intestinal and colon cancer cells via DR3 and ER6 vitamin D responsive elements

TL;DR: Data suggest that 1,25D(3)-dependent, VDR-mediated induction of CYP3A4 may constitute a chemoprotective mechanism for detoxification of enteric xenobiotics and carcinogens.
Journal ArticleDOI

Cloning of a Functional Vitamin D Receptor from the Lamprey (Petromyzon marinus), an Ancient Vertebrate Lacking a Calcified Skeleton and Teeth

TL;DR: It is proposed that, in this evolutionarily ancient vertebrate, VDR may function in part, like pregnane X receptors and constitutive androstane receptors, to induce P450 enzymes for xenobiotic detoxification.
Journal ArticleDOI

Molecular and functional comparison of 1,25-dihydroxyvitamin D(3) and the novel vitamin D receptor ligand, lithocholic acid, in activating transcription of cytochrome P450 3A4.

TL;DR: It is proposed that VDR is a bifunctional regulator, with the 1,25(OH)2D3‐liganded conformation facilitating high affinity endocrine actions, and the LCA‐liganding configuration mediating local, lower affinity cellular detoxification by upregulation of CYP3A4 in the colon.