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Keyword [LCAT]
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1. The Clinical Research On The Relationship Between Serum LCAT,HDL2,HDL3 And TCM Syndromes In Chronic Glomerulonephritis
2. The Regulation Of Tea Polysaccharides On Blood Lipids And Its Mechanism In Hyperlipidemic Rats
3. Study On The Association Of LCAT Gene Polymorphisms With The Susceptibility Of Coronary Artery Diease
4. The Study Of Association Between LCAT Gene Polymorphism And The Phenomenon Of Familial Aggregation Of Cerebral Hemorrhage And Lipid
5. Regulative Effect Of Extract Of Lindley Eupatorium Herb On Blood Lipids And Mechanism In Experimental Hyperlipidemia Models
6. Establishment And Mechanism Research Of Atherosclerosis In Guinea Pig Model
7. Lcat Activity Effects On Lipid And Lipoprotein Metabolism In Mice
8. Rape Pollen Supercritical Carbon Dioxide Extract On Lipid Metabolism In Hyperlipidemic Rats
9. Experimental And Clinical Research On EA Fenglong Point With Hyperlipidemia
10. EA Fenglong Intervention Hyperlipidemia Experimental And Clinical Study
11. Relationship Between The Levels Of LCAT And Cetp And The Distribution Of Plasma Hdl Subclasses In Patients With Coronary Heart Disease
12. Relationship Between The Distribution Of HDL Subclasses And Lcat, CETP Levels In Patients With Type2Diabetes
13. Simvastatin Promotes The Expression Of Genes Associated With Reverse Cholesterol Transport In ApoE-knockout Mice Fed High-fat Diet
14. Hepatocyte-specific Knockout Of PP2Acα Ameliorated Hepatic Osteodystrophy Through LCAT Signal
15. Association Between LCAT Gene Rs3729639 Polymorphisms With Non-Alcoholic Fatty Liver Diseasein Chinese Han Population
16. Effect Of Huanglian Wendan Decoction On LCAT And EL In Patients With Type 2 Diabetes Complicated With Lipid Metabolism Disorder
17. Molecular mechanisms of a dominant form of type III hyperlipoproteinemia and the biogenesis of apolipoprotein E-containing high density lipoprotein
18. The molecular pathology of lecithin:cholesterol acyltransferase deficienc
19. CHOLESTERYL ESTER METABOLISM IN RABBITS: EFFECT OF CHOLESTEROL FEEDING AND CLOFIBRATE TREATMEN
20. Novel Homozygous Mutation Causing Familial Lecithin Cholesterol Acyltransferase Deficiency With Renal Damage:A Case Report And Literature Review
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