What substrate accumulates in the lysosomes of a patient with Tay-Sachs disease? _____
What do fungal plasma membranes contain that others lack?_____
The main component of VLDL is _____ (60%)
Carnitine acyltransferase-1 (CPT-1) is regulated via negative feedback by _____
Which lysosomal storage disease is characterized by a cherry red spot on the macula and no hepatosplenomegaly? _____
What salivary enzyme begins the initial digestion of fats? _____
Primary carnitine deficiency is characterized by muscle weakness and hypotonia, which is provoked by prolonged _____ (especially if fasting)
Thromboxane A2 (TXA2) is synthesized by the platelet enzyme _____
What substrate accumulates in the lysosomes of a patient with Fabry disease? _____
PGI2, PGE1, PGE2, PGF2-alpha, and thromboxane A2 are synthesized from arachidonic acid by _____.
Fatty acid oxidation (beta-oxidation)
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Fatty acid synthesis
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Ketone body metabolism
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Cholesterol synthesis and regulation
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Lipoprotein metabolism
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Phospholipid metabolism
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Eicosanoid synthesis and function
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Steroid hormone synthesis
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Adipose tissue metabolism
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Brown vs. white adipose tissue
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Disorders of lipid metabolism
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Integration with carbohydrate metabolism
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