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Peroxisomal Metabolism
S. J. Gould
School of Medicine
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Chapter in Book/Report/Conference proceeding
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Keyphrases
Bile Acids
20%
Branched-chain Fatty Acids
20%
Cell-to-cell
20%
Cellular Tissue
20%
Chondrodysplasia Punctata
20%
Common Themes
20%
Composition Function
20%
D-bifunctional Protein Deficiency
20%
Enzyme-catalyzed
20%
Ether Lipids
20%
Ether-linked Lipid
20%
Eukaryotic Cells
20%
Fatty Acid Oxidation
60%
Fatty Acids
60%
Inactivating mutation
20%
Lipid Synthesis
20%
Long-chain Polyunsaturated Fatty Acids (LC-PUFA)
20%
Mammalian Cells
20%
Medium Chain Length
20%
Membranous Organelles
20%
Metabolic Function
20%
Metabolic Processes
20%
Methyl
20%
Neurological Disorders
20%
Oleate
20%
Oxidation Mechanism
40%
Palmitate
20%
Peroxisomal
60%
Peroxisomal Disorders
20%
Peroxisomal Enzymes
20%
Peroxisomal Metabolism
100%
Peroxisome
100%
Peroxisome Biogenesis
20%
Refsum Disease
20%
Single Membrane
20%
X-linked Adrenoleukodystrophy (X-ALD)
20%
Zellweger Syndrome
20%
Biochemistry, Genetics and Molecular Biology
Adrenoleukodystrophy
16%
Beta Oxidation
50%
Bile Acid
16%
Biogenesis
16%
Deficiency
16%
Enzyme
16%
Enzyme Catalysis
16%
Ether Lipid
33%
Lipogenesis
16%
Metabolic Pathway
100%
Mitochondrion
16%
Palmitic Acid
16%
Peroxisome
100%
Very Long Chain Fatty Acid
16%