[HTML][HTML] Molecular mechanism of PPARα action and its impact on lipid metabolism, inflammation and fibrosis in non-alcoholic fatty liver disease
Peroxisome proliferator-activated receptor α (PPARα) is a ligand-activated transcription
factor belonging, together with PPARγ and PPARβ/δ, to the NR1C nuclear receptor …
factor belonging, together with PPARγ and PPARβ/δ, to the NR1C nuclear receptor …
Nuclear receptors linking metabolism, inflammation, and fibrosis in nonalcoholic fatty liver disease
T Puengel, H Liu, A Guillot, F Heymann… - International journal of …, 2022 - mdpi.com
Nonalcoholic fatty liver disease (NAFLD) and its progressive form nonalcoholic
steatohepatitis (NASH) comprise a spectrum of chronic liver diseases in the global …
steatohepatitis (NASH) comprise a spectrum of chronic liver diseases in the global …
PPARα gene expression correlates with severity and histological treatment response in patients with non-alcoholic steatohepatitis
S Francque, A Verrijken, S Caron, J Prawitt… - Journal of …, 2015 - Elsevier
Background & Aims Peroxisome proliferator-activated receptors (PPARs) have been
implicated in non-alcoholic steatohepatitis (NASH) pathogenesis, mainly based on animal …
implicated in non-alcoholic steatohepatitis (NASH) pathogenesis, mainly based on animal …
Nuclear receptors and nonalcoholic fatty liver disease
MC Cave, HB Clair, JE Hardesty, KC Falkner… - … et Biophysica Acta (BBA …, 2016 - Elsevier
Nuclear receptors are transcription factors which sense changing environmental or
hormonal signals and effect transcriptional changes to regulate core life functions including …
hormonal signals and effect transcriptional changes to regulate core life functions including …
[PDF][PDF] Hepatoprotective effects of the dual peroxisome proliferator‐activated receptor alpha/delta agonist, GFT505, in rodent models of nonalcoholic fatty liver disease …
Nonalcoholic fatty liver disease (NAFLD) covers a spectrum of liver damage ranging from
simple steatosis to nonalcoholic steatohepatitis (NASH), fibrosis, and cirrhosis. To date, no …
simple steatosis to nonalcoholic steatohepatitis (NASH), fibrosis, and cirrhosis. To date, no …
Treating NASH by targeting peroxisome proliferator-activated receptors
Abstract The pathophysiology of Non-Alcoholic Steatohepatitis (NASH) encompasses a
complex set of intra-and extrahepatic driving mechanisms, involving numerous metabolic …
complex set of intra-and extrahepatic driving mechanisms, involving numerous metabolic …
PPARs and metabolic disorders associated with challenged adipose tissue plasticity
Peroxisome proliferator-activated receptors (PPARs) are members of a family of nuclear
hormone receptors that exert their transcriptional control on genes harboring PPAR …
hormone receptors that exert their transcriptional control on genes harboring PPAR …
Roles of PPARs in NAFLD: potential therapeutic targets
Non-alcoholic fatty liver disease (NAFLD) is a liver pathology with increasing prevalence
due to the obesity epidemic. Hence, NAFLD represents a rising threat to public health …
due to the obesity epidemic. Hence, NAFLD represents a rising threat to public health …
[HTML][HTML] Transcriptional regulation of metabolic pathways via lipid-sensing nuclear receptors PPARs, FXR, and LXR in NASH
Abstract Non-Alcoholic Fatty Liver Disease (NAFLD) comprises a wide spectrum of liver
injuries from simple steatosis to steatohepatitis and cirrhosis. Non-Alcoholic Steatohepatitis …
injuries from simple steatosis to steatohepatitis and cirrhosis. Non-Alcoholic Steatohepatitis …
Genome-wide profiling of liver X receptor, retinoid X receptor, and peroxisome proliferator-activated receptor α in mouse liver reveals extensive sharing of binding …
M Boergesen, TÅ Pedersen, B Gross… - … and cellular biology, 2012 - Am Soc Microbiol
The liver X receptors (LXRs) are nuclear receptors that form permissive heterodimers with
retinoid X receptor (RXR) and are important regulators of lipid metabolism in the liver. We …
retinoid X receptor (RXR) and are important regulators of lipid metabolism in the liver. We …