Abetalipoproteinemia is an _____ inherited malabsorption disorder that is caused by a mutation in the microsomal triglyceride transfer protein
_____ is a PUFA containing 6 double bonds
Dehydroepiandrosterone (DHEA) may be converted to _____ via the enzyme 3-hydroxysteroid dehydrogenase
In the cytosol, _____ may be converted to acetyl-CoA via the enzyme ATP citrate lyase (fatty acid synthesis)
Each cycle of β-oxidation produces _____ molecule of FADH2 and one molecule of NADH
17-hydroxyprogesterone may be converted to _____ via the enzyme 17,20-lyase
In preparation for β-oxidation, fatty acids are converted to _____ via the enzyme fatty acyl-CoA synthetase
_____ deficiency is characterized by the accumulation of 8 to 10-carbon acyl carnitines in the blood
The chylomicron remnant expresses only apolipoprotein _____ and E on its surface
The phospholipid _____ is also known as phosphatidylethanolamine.
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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