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Cell Metabolism, ISSN 1550-4131, 05/2012, Volume 15, Issue 5, pp. 665 - 674
Nonalcoholic fatty liver disease (NAFLD) is associated with increased cardiovascular and liver-related mortality. NAFLD is characterized by both triglyceride... 
RAT-LIVER | RISK-FACTORS | MACROPHAGE APOPTOSIS | PROTEIN-KINASE | ENDOCRINOLOGY & METABOLISM | HMG-COA REDUCTASE | STEATOHEPATITIS | 3-HYDROXY-3-METHYLGLUTARYL COENZYME | PREVALENCE | MICRORNA EXPRESSION | MODULATION | CELL BIOLOGY | Sirtuin 1 - metabolism | Up-Regulation | Cholesterol - blood | Humans | Middle Aged | Sterol Esterase - metabolism | Male | MicroRNAs - metabolism | Desmosterol - metabolism | Cardiovascular Diseases - genetics | Cholesterol - genetics | Sirtuin 1 - genetics | Case-Control Studies | Phosphorylation - genetics | Hydroxymethylglutaryl CoA Reductases - metabolism | Adenylate Kinase - metabolism | Non-alcoholic Fatty Liver Disease | Sterol O-Acyltransferase - metabolism | Adult | Female | Lipid Metabolism - genetics | Sterol Regulatory Element Binding Protein 2 - genetics | Sterol Regulatory Element Binding Protein 2 - metabolism | Fatty Liver - genetics | Receptors, LDL - genetics | Gene Expression | Fatty Liver - metabolism | Cardiovascular Diseases - metabolism | Fatty Liver - blood | Liver - metabolism | Receptors, LDL - metabolism | Cholesterol - metabolism | Cholesterol, LDL - genetics | Phenotype | Sterol Esterase - genetics | Desmosterol - blood | Cholesterol, LDL - metabolism | MicroRNAs - genetics | Sterol O-Acyltransferase - genetics | Adenylate Kinase - genetics | Hydroxymethylglutaryl CoA Reductases - genetics | Enzymes | Liver diseases | Low density lipoproteins | Genes | Esters | Triglycerides | Cholesterol | MicroRNA | Fatty liver | Blood cholesterol | Physiological aspects | Hydrolases | Blood lipids | Health aspects | Statins | Index Medicus | atherosclerosis | Nonalcoholic steatohepatitis | cholesterol | Nonalcoholic fatty liver disease | fatty liver | lipogenesis | hypercholesterolemia | HMG CoA reductase
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by Peden, John F and Hopewell, Jemma C and Saleheen, Danish and Chambers, John C and Hager, Jorg and Soranzo, Nicole and Collins, Rory and Danesh, John and Elliott, Paul and Farrall, Martin and Stirrups, Kathy and Zhang, Weihua and Hamsten, Anders and Parish, Sarah and Lathrop, Mark and Watkins, Hugh and Clarke, Robert and Deloukas, Panos and Kooner, Jaspal S and Goel, Anuj and Ongen, Halit and Strawbridge, Rona J and Heath, Simon and Mälarstig, Anders and Helgadottir, Anna and Öhrvik, John and Murtaza, Muhammed and Potter, Simon and Hunt, Sarah E and Delepine, Marc and Jalilzadeh, Shapour and Axelsson, Tomas and Syvanen, Ann-Christine and Gwilliam, Rhian and Bumpstead, Suzannah and Gray, Emma and Edkins, Sarah and Folkersen, Lasse and Kyriakou, Theodosios and Franco-Cereceda, Anders and Gabrielsen, Anders and Seedorf, Udo and Eriksson, Per and Offer, Alison and Bowman, Louise and Sleight, Peter and Armitage, Jane and Peto, Richard and Abecasis, Goncalo and Ahmed, Nabeel and Caulfield, Mark and Donnelly, Peter and Froguel, Philippe and Kooner, Angad S and McCarthy, Mark I and Samani, Nilesh J and Scott, James and Sehmi, Joban and Silveira, Angela and Hellénius, Mai-Lus and van't Hooft, Ferdinand M and Olsson, Gunnar and Rust, Stephan and Assman, Gerd and Barlera, Simona and Tognoni, Gianni and Franzosi, Maria Grazia and Linksted, Pamela and Green, Fiona R and Rasheed, Asif and Zaidi, Moazzam and Shah, Nabi and Samuel, Maria and Mallick, Nadeem H and Azhar, Muhammad and Zaman, Khan S and Samad, Abdus and Ishaq, Mohammad and Gardezi, Ali R and Fazal-ur-Rehman, Memon and Frossard, Philippe M and Spector, Tim and Peltonen, Leena and Nieminen, Markku S and Sinisalo, Juha and Salomaa, Veikko and Ripatti, Samuli and Bennett, Derrick and Leander, Karin and Gigante, Bruna and de Faire, Ulf and Pietri, Silvia and Gori, Francesca and Marchioli, Roberto and Sivapalaratnam, Suthesh and Kastelein, John J. P and Trip, Mieke D and Theodoraki, Eirini V and Dedoussis, George V and Engert, Jamie C and ... and Coronary Artery Dis C4D Genetics C and MuTHER Consortium and Coronary Artery Disease (C4D) Genetics Consortium and The Coronary Artery Disease (C4D) Genetics Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 4, pp. 339 - 344
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Science, ISSN 0036-8075, 7/2011, Volume 333, Issue 6039, pp. 233 - 238
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