نتایج جستجو برای: raralpha

تعداد نتایج: 280  

Journal: :The EMBO journal 2006
Maurizio Giannì Edoardo Parrella Ivan Raska Emilie Gaillard Elisa Agnese Nigro Claudine Gaudon Enrico Garattini Cécile Rochette-Egly

Nuclear retinoic acid (RA) receptors (RARs) activate gene expression through dynamic interactions with coregulators in coordination with the ligand and phosphorylation processes. Here we show that during RA-dependent activation of the RARalpha isotype, the p160 coactivator pCIP/ACTR/AIB-1/RAC-3/TRAM-1/SRC-3 is phosphorylated by p38MAPK. SRC-3 phosphorylation has been correlated to an initial fa...

Journal: :Blood 2004
Sylvie Côté Suzan McNamara Daria Brambilla Andrea Bianchini Giovanni Rizzo Sonia Victoria del Rincón Francesco Grignani Clara Nervi Wilson H Miller

Nuclear receptors are ligand-modulated transcription factors regulated by interactions with corepressors and coactivators, whose functions are not fully understood. Acute promyelocytic leukemia (APL) is characterized by a translocation, t(15;17), that produces a PML/RARalpha fusion oncoprotein, whose abnormal transcriptional function is successfully targeted by pharmacologic levels of all-trans...

Journal: :Molecular pharmacology 2007
Michael Schupp Joshua C Curtin Roy J Kim Andrew N Billin Mitchell A Lazar

Nuclear receptors (NRs) are transcription factors whose activity is regulated by the binding of small lipophilic ligands, including hormones, vitamins, and metabolites. Pharmacological NR ligands serve as important therapeutic agents; for example, all-trans retinoic acid, an activating ligand for retinoic acid receptor alpha (RARalpha), is used to treat leukemia. Another RARalpha ligand, (E)-S,...

Journal: :The Biochemical journal 1998
M R Song S K Lee Y W Seo H S Choi J W Lee M O Lee

Control of oestradiol-responsive gene regulation by oestrogen receptors (ERs) may involve complex cross-talk with retinoic acid receptors (RARs) and retinoid X receptors (RXRs). Recently, we have shown that ERalpha directly interacts with RARalpha and RXRalpha through their ligand binding domains (LBDs). In the present work, we extend these results by showing that ERbeta binds similarly to RARa...

Journal: :Molecular and cellular endocrinology 2007
Zdenek Dvorák Radim Vrzal Jitka Ulrichová Dana Macejová Slavomíra Ondková Július Brtko

Cellular signaling by glucocorticoid receptor and aryl hydrocarbon receptor is restricted by microtubules interfering agents (MIAs). This leads to down-regulation of drug metabolizing enzymes and drug interactions. Here we investigated the effects of all-trans-retinoic acid (ATRA) and MIAs, i.e. colchicine, nocodazole and taxol on the regulation of retinoic acid receptor (RAR) genes in primary ...

Journal: :PLoS ONE 2007
Giulia Somenzi Giusy Sala Stefano Rossetti MingQiang Ren Riccardo Ghidoni Nicoletta Sacchi

BACKGROUND Retinoic acid (RA), the bioactive derivative of Vitamin A, by epigenetically controlling transcription through the RA-receptors (RARs), exerts a potent antiproliferative effect on human cells. However, a number of studies show that RA can also promote cell survival and growth. In the course of one of our studies we observed that disruption of RA-receptor alpha, RARalpha, abrogates th...

Journal: :Circulation research 2001
C Gaetano A Catalano B Illi A Felici S Minucci R Palumbo F Facchiano A Mangoni S Mancarella J Mühlhauser M C Capogrossi

The effect of retinoic acid (RA) on endothelial cells is still controversial and was examined in the present study. In bovine aortic endothelial cells (BAECs), all-trans RA (ATRA) and 9-cis RA (9CRA), but not 13-cis RA (13CRA), induced fibroblast growth factor-2 (FGF-2) production and exhibited a biphasic dose-dependent effect to enhance BAEC proliferation and differentiation into tubular struc...

Journal: :The Biochemical journal 1999
J S Koo A M Jetten P Belloni J H Yoon Y D Kim P Nettesheim

To investigate which retinoid receptors are critical in the regulation by all-trans-retinoic acid (RA) of the mucin genes MUC2, MUC5AC and MUC5B in cultured normal human tracheobronchial epithelial (NHTBE) cells, we used pan-RAR-, pan-RXR- and RAR- isotype (alpha, beta and gamma)-selective agonists and RARalpha- and RARgamma-selective antagonists (RAR is RA receptor and RXR is retinoid X recept...

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