Browse Items (4 total)
- Tags: Moore David D
A nuclear-receptor-dependent phosphatidylcholine pathway with antidiabetic effects.
Tags: 2011, BILE acids, Busby Scott A, Department of Integrative Medical Sciences, Griffin Patrick R, Homeostasis, HYPOGLYCEMIC agents, Insulin Resistance, LABORATORY mice, LECITHIN, Lee Jae Man, Lee Yoon-Kwang, Mamrosh Jennifer L, Moore David D, Nature, NEOMED College of Medicine, Ortlund Eric A, Pathak Manish C, triglycerides
The orphan nuclear receptor small heterodimer partner is required for thiazolidinedione effects in leptin-deficient mice.
Tags: 2015, Animals, Bile Acids and Salts/metabolism, Cytoplasmic and Nuclear/biosynthesis/*genetics/metabolism, Department of Integrative Medical Sciences, Diabetes Mellitus/*drug therapy/genetics/metabolism, Gene Expression Regulation/drug effects, Glucose/metabolism, Hepatocytes/drug effects, Humans, Insulin Resistance/genetics, Insulin/*metabolism, Journal of biomedical science, Lee Yoon-Kwang, Leptin/deficiency/genetics, Lipid Metabolism/drug effects, Messenger/genetics, Mice, Moore David D, NEOMED College of Medicine, Obese, Park Young Joo, PPAR gamma/*biosynthesis/genetics, Receptors, RNA, Thiazolidinediones/*administration & dosage, Tseng Hsiu-Ting
Forkhead box transcription factor O1 inhibits cholesterol 7alpha-hydroxylase in human hepatocytes and in high fat diet-fed mice.
Tags: 2009, Adenoviridae/genetics, Animals, Bile Acids and Salts/biosynthesis, Biochimica et biophysica acta, Cell Line, Cell Nucleus/drug effects/metabolism, Chiang John Y L, Cholesterol 7-alpha-Hydroxylase/*antagonists & inhibitors/genetics/metabolism, Department of Integrative Medical Sciences, Dietary Fats/*administration & dosage/*pharmacology, Down-Regulation/drug effects, Enzymologic/drug effects, Feeding Behavior/*drug effects, Forkhead Box Protein O1, Forkhead Transcription Factors/genetics/*metabolism, Gene Expression Regulation, Gene Knockdown Techniques, Gene Transfer Techniques, Hepatocytes/drug effects/*enzymology, Humans, Inbred C57BL, Insulin Resistance, Insulin/metabolism, Lee Yoon-Kwang, Li Tiangang, Ma Huiyan, Male, Messenger/genetics/metabolism, Mice, Moore David D, NEOMED College of Medicine, Park Young Joo, RNA, RNA Interference/drug effects, Strom Stephen, Tumor
All-trans-retinoic acid ameliorates hepatic steatosis in mice by a novel transcriptional cascade.
Tags: 2014, Animals, Axe David, Basic Helix-Loop-Helix Transcription Factors/genetics, Blood Glucose/analysis, Chiang John Y L, Cook Aaron, Cytoplasmic and Nuclear/*physiology, Department of Integrative Medical Sciences, Department of Pharmaceutical Sciences, Fatty Liver/*drug therapy/metabolism, Gene Expression Regulation, Genetic, Hardwick James P, Hepatology (Baltimore, Md.), Inbred C57BL, Kim Chun-Ki, Kim Seong-Chul, Lee Mikang, Lee Yoon-Kwang, Li Tiangang, Lipid Metabolism, Liver/metabolism, Male, Mice, Moore David D, NEOMED College of Medicine, NEOMED College of Pharmacy, Non-alcoholic Fatty Liver Disease, PPAR gamma/*genetics, Receptors, Repressor Proteins/genetics, Retinoic Acid Receptor alpha, Retinoic Acid/physiology, Smallwood Nicole, Transcription, Tretinoin/pharmacology/*therapeutic use