Adamantyl-substituted retinoid-related molecules bind small heterodimer partner and modulate the Sin3A repressor.
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Involvement of corepressor complex subunit GPS2 in transcriptional pathways governing human bile acid biosynthesisLipid-sensors, enigmatic-orphan and orphan nuclear receptors as therapeutic targets in breast-cancerInsights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast CancerNuclear receptors and epigenetic regulation: opportunities for nutritional targeting and disease preventionNuclear receptors in bone physiology and diseasesStructural insights into gene repression by the orphan nuclear receptor SHPRole of nuclear receptor SHP in metabolism and cancer.Condensin complexes regulate mitotic progression and interphase chromatin structure in embryonic stem cells.Nuclear receptor SHP, a death receptor that targets mitochondria, induces apoptosis and inhibits tumor growth.Adamantyl-substituted retinoid-derived molecules that interact with the orphan nuclear receptor small heterodimer partner: effects of replacing the 1-adamantyl or hydroxyl group on inhibition of cancer cell growth, induction of cancer cell apoptosisThe lipophilic bullet hits the targets: medicinal chemistry of adamantane derivativesUpregulation of miR-150* and miR-630 induces apoptosis in pancreatic cancer cells by targeting IGF-1R.Characterization of the mitochondrial localization of the nuclear receptor SHP and regulation of its subcellular distribution by interaction with Bcl2 and HNF4α.Ligand-dependent regulation of the activity of the orphan nuclear receptor, small heterodimer partner (SHP), in the repression of bile acid biosynthetic CYP7A1 and CYP8B1 genes.Arginine methylation by PRMT5 at a naturally occurring mutation site is critical for liver metabolic regulation by small heterodimer partnerThe orphan nuclear receptor SHP is a positive regulator of osteoblastic bone formation.A pleiotropic role for the orphan nuclear receptor small heterodimer partner in lipid homeostasis and metabolic pathways.New Insights into Orphan Nuclear Receptor SHP in Liver CancerReversal by RARα agonist Am580 of c-Myc-induced imbalance in RARα/RARγ expression during MMTV-Myc tumorigenesis.Farnesoid X receptor deficiency in mice leads to increased intestinal epithelial cell proliferation and tumor developmentThe role of FXR in disorders of bile acid homeostasis.FXR agonists enhance the sensitivity of biliary tract cancer cells to cisplatin via SHP dependent inhibition of Bcl-xL expression.Functional specificities of Brm and Brg-1 Swi/Snf ATPases in the feedback regulation of hepatic bile acid biosynthesis.Minireview: role of orphan nuclear receptors in cancer and potential as drug targetsDecoding the role of the nuclear receptor SHP in regulating hepatic stellate cells and liver fibrogenesis.Epigenomic regulation of bile acid metabolism: emerging role of transcriptional cofactors.Nuclear receptor small heterodimer partner in apoptosis signaling and liver cancer.A Novel Small Molecule Activator of Nuclear Receptor SHP Inhibits HCC Cell Migration via Suppressing Ccl2.Nuclear receptor 4A (NR4A) family - orphans no more.NF-κB p65 recruited SHP regulates PDCD5-mediated apoptosis in cancer cells.Adamantyl arotinoids that inhibit IκB kinase α and IκB kinase β.Small heterodimer partner SHP mediates liver X receptor (LXR)-dependent suppression of inflammatory signaling by promoting LXR SUMOylation specifically in astrocytes.Adamantyl-substituted retinoid-related molecules induce apoptosis in human acute myelogenous leukemia cells.Maximal adamantyl-substituted retinoid-related molecule-induced apoptosis requires NF-κB noncanonical and canonical pathway activationSHP (small heterodimer partner) suppresses the transcriptional activity and nuclear localization of Hedgehog signalling protein Gli1.Highly twisted adamantyl arotinoids: synthesis, antiproliferative effects and RXR transactivation profiles.Catalyst-free multicomponent synthesis of novel adamantyl-containing tetrahydropyrimidine carboxylates.Adamantyl Retinoid-Related Molecules Induce Apoptosis in Pancreatic Cancer Cells by Inhibiting IGF-1R and Wnt/β-Catenin Pathways.An adamantyl-substituted retinoid-derived molecule that inhibits cancer cell growth and angiogenesis by inducing apoptosis and binds to small heterodimer partner nuclear receptor: effects of modifying its carboxylate group on apoptosis, proliferatioInsights into the binding mode and mechanism of action of some atypical retinoids as ligands of the small heterodimer partner (SHP).
P2860
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P2860
Adamantyl-substituted retinoid-related molecules bind small heterodimer partner and modulate the Sin3A repressor.
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Adamantyl-substituted retinoid ...... modulate the Sin3A repressor.
@ast
Adamantyl-substituted retinoid ...... modulate the Sin3A repressor.
@en
type
label
Adamantyl-substituted retinoid ...... modulate the Sin3A repressor.
@ast
Adamantyl-substituted retinoid ...... modulate the Sin3A repressor.
@en
prefLabel
Adamantyl-substituted retinoid ...... modulate the Sin3A repressor.
@ast
Adamantyl-substituted retinoid ...... modulate the Sin3A repressor.
@en
P2093
P2860
P1433
P1476
Adamantyl-substituted retinoid ...... d modulate the Sin3A repressor
@en
P2093
David D Moore
Lulu Farhana
Marcia I Dawson
P2860
P304
P356
10.1158/0008-5472.CAN-06-2164
P407
P577
2007-01-01T00:00:00Z