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Type _____ familial dyslipidemia is due to either:- absent or defective LDL receptors - defective Apo B-100
Peroxisomal beta-oxidation of VLCFAs lead to the formation of _____ and H2O2
In extrahepatic tissues, acetoacetate is activated to _____ via the enzyme thiophorase (ketone body metabolism)
Sphingomyelin is converted to _____ via the enzyme sphingomyelinase
Type _____ familial dyslipidemia is due to a defective Apo E allele
Apoprotein _____ is an activator of the enzyme LCAT (lecithin cholesterol acyltransferase)
The IDL expresses only apolipoprotein _____ and E on its surface
Dehydroepiandrosterone (DHEA) may be converted to _____ via the enzyme 3-hydroxysteroid dehydrogenase
Cholesterol synthesis:Cyclization of _____ to give rise to the parent steroid, lanosterol
_____ -carbon steroids have estrogenic activity
Lipid Classification and Chemistry
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Fatty Acid Oxidation
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Ketone Body Metabolism
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Fatty Acid Synthesis
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Metabolism of Triacylglycerols
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Phospholipid Metabolism
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Cholesterol Metabolism and Biosynthesis
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Bile Acids and Bile Salts
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Lipoprotein Metabolism and Transport
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Dyslipidemias and Atherosclerosis
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Prostaglandins and Eicosanoids
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Fatty Liver and Lipotropic Factors
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