Detalhe da pesquisa
1.
Genetic deletion of the circadian clock transcription factor BMAL1 and chronic alcohol consumption differentially alter hepatic glycogen in mice.
Am J Physiol Gastrointest Liver Physiol
; 314(3): G431-G447, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29191941
2.
Chronic ethanol consumption disrupts diurnal rhythms of hepatic glycogen metabolism in mice.
Am J Physiol Gastrointest Liver Physiol
; 308(11): G964-74, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25857999
3.
Involvement of the mitochondrial permeability transition pore in chronic ethanol-mediated liver injury in mice.
Am J Physiol Gastrointest Liver Physiol
; 306(4): G265-77, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24356880
4.
Chronic ethanol consumption enhances sensitivity to Ca(2+)-mediated opening of the mitochondrial permeability transition pore and increases cyclophilin D in liver.
Am J Physiol Gastrointest Liver Physiol
; 299(4): G954-66, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20651005
5.
Alcohol and Liver Clock Disruption Increase Small Droplet Macrosteatosis, Alter Lipid Metabolism and Clock Gene mRNA Rhythms, and Remodel the Triglyceride Lipidome in Mouse Liver.
Front Physiol
; 11: 1048, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33013449
6.
Genetic Deletion of Syndecan-4 Alters Body Composition, Metabolic Phenotypes, and the Function of Metabolic Tissues in Female Mice Fed A High-Fat Diet.
Nutrients
; 11(11)2019 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31752080
7.
Chronic exposure to a high-fat diet induces hepatic steatosis, impairs nitric oxide bioavailability, and modifies the mitochondrial proteome in mice.
Antioxid Redox Signal
; 15(2): 447-59, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20919931