Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
about
The role of peroxisome proliferator-activated receptors in carcinogenesis and chemopreventionPleiotropic Actions of Peroxisome Proliferator-Activated Receptors (PPARs) in Dysregulated Metabolic Homeostasis, Inflammation and Cancer: Current Evidence and Future PerspectivesReview of the Structural and Dynamic Mechanisms of PPARγ Partial AgonismAdvancing Biological Understanding and Therapeutics Discovery with Small-Molecule ProbesThe inflammatory response in sepsisNuclear receptors in bone physiology and diseasesSomething old, something new and something very old: drugs for treating type 2 diabetesTargeting xenobiotic receptors PXR and CAR for metabolic diseasesModulation of the transcriptional activity of peroxisome proliferator-activated receptor gamma by protein-protein interactions and post-translational modificationsPPAR-γ as a therapeutic target in cardiovascular disease: evidence and uncertaintyPartial agonist, telmisartan, maintains PPARγ serine 112 phosphorylation, and does not affect osteoblast differentiation and bone massMultidomain integration in the structure of the HNF-4α nuclear receptor complexGQ-16, a Novel Peroxisome Proliferator-activated Receptor (PPAR ) Ligand, Promotes Insulin Sensitization without Weight GainMedium Chain Fatty Acids Are Selective Peroxisome Proliferator Activated Receptor (PPAR) γ Activators and Pan-PPAR Partial AgonistsResveratrol modulates the inflammatory response via an estrogen receptor-signal integration networkA natural-product switch for a dynamic protein interfaceIdentification of PPARgamma partial agonists of natural origin (II): in silico prediction in natural extracts with known antidiabetic activityCHARMM Force Field Parameterization of Peroxisome Proliferator-Activated Receptor γ LigandsProtein Footprinting Comes of Age: Mass Spectrometry for Biophysical Structure Assessment.Integrating mass spectrometry of intact protein complexes into structural proteomicsPeptide-column interactions and their influence on back exchange rates in hydrogen/deuterium exchange-MS.MicroRNA-27a promotes podocyte injury via PPARγ-mediated β-catenin activation in diabetic nephropathy.A photocleavable masked nuclear-receptor ligand enables temporal control of C. elegans development.Leptin revisited: its mechanism of action and potential for treating diabetes.Artemisia scoparia enhances adipocyte development and endocrine function in vitro and enhances insulin action in vivoRepression of phosphoinositide-dependent protein kinase 1 expression by ciglitazone via Egr-1 represents a new approach for inhibition of lung cancer cell growthRole of the adipose PPARγ-adiponectin axis in susceptibility to stress and depression/anxiety-related behaviors.Adipose tissue NAD+ biology in obesity and insulin resistance: From mechanism to therapyDiscovery of Novel Insulin Sensitizers: Promising Approaches and Targets.Diosgenin relieves goiter via the inhibition of thyrocyte proliferation in a mouse model of Graves' disease.Betulinic acid is a PPARγ antagonist that improves glucose uptake, promotes osteogenesis and inhibits adipogenesis.Role of the SIK2-p35-PJA2 complex in pancreatic β-cell functional compensation.CNX-013-B2, a unique pan tissue acting rexinoid, modulates several nuclear receptors and controls multiple risk factors of the metabolic syndrome without risk of hypertriglyceridemia, hepatomegaly and body weight gain in animal models.High-fat and obesogenic diets: current and future strategies to fight obesity and diabetes.A novel non-agonist peroxisome proliferator-activated receptor γ (PPARγ) ligand UHC1 blocks PPARγ phosphorylation by cyclin-dependent kinase 5 (CDK5) and improves insulin sensitivityThe peroxisome-proliferator activated receptor-γ agonist pioglitazone modulates aberrant T cell responses in systemic lupus erythematosus.Thiazolidinediones and the promise of insulin sensitization in type 2 diabetes.The serine/threonine phosphatase PPM1B (PP2Cβ) selectively modulates PPARγ activity.Noncanonical mechanisms to regulate nuclear receptor signaling.Retinaldehyde dehydrogenase 1 deficiency inhibits PPARγ-mediated bone loss and marrow adiposity.
P2860
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P2860
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@ast
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@en
type
label
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@ast
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@en
prefLabel
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@ast
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@en
P2093
P2860
P50
P356
P1433
P1476
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
@en
P2093
Bruce M Spiegelman
Dana S Kuruvilla
David P Marciano
Dina Laznik
Dušica Vidović
Jang Hyun Choi
John B Bruning
Michael D Cameron
Michael J Chalmers
Naresh Kumar
P2860
P2888
P304
P356
10.1038/NATURE10383
P407
P577
2011-09-04T00:00:00Z
P5875
P6179
1004606531