phenylalanine has been researched along with Lipid Metabolism, Inborn Error in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aliverti, A; Carpanelli, E; Coda, A; Mattevi, A; Mattiroli, F; Pandini, V; Razeto, A | 1 |
| Brady, RO | 2 |
| Menkes, JH | 1 |
| Carpenter, DG; Carter, CH | 1 |
1 review(s) available for phenylalanine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Inherited metabolic diseases and pathogenesis of mental retardation.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Carbohydrate Metabolism, Inborn Errors; Cytochrome Reductases; Deoxyglucose; Dihydrolipoamide Dehydrogenase; Energy Metabolism; Gangliosides; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Phenylalanine; Pyruvate Dehydrogenase Complex Deficiency Disease | 1978 |
4 other study(ies) available for phenylalanine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
The crucial step in ether phospholipid biosynthesis: structural basis of a noncanonical reaction associated with a peroxisomal disorder.
Topics: Alkyl and Aryl Transferases; Amino Acid Sequence; Amino Acid Substitution; Animals; Binding Sites; Catalysis; Chondrodysplasia Punctata, Rhizomelic; Conserved Sequence; Crystallography, X-Ray; Dictyostelium; Dimerization; Flavin-Adenine Dinucleotide; Histidine; Humans; Hydrogen Bonding; Lipid Metabolism, Inborn Errors; Models, Biological; Models, Chemical; Models, Molecular; Molecular Sequence Data; Molecular Structure; Peroxisomal Disorders; Phenylalanine; Phospholipid Ethers; Protein Binding; Protein Conformation; Protein Structure, Secondary; Protein Structure, Tertiary; Recombinant Proteins; Sequence Homology, Amino Acid; Spectrum Analysis, Raman; Substrate Specificity; Tyrosine | 2007 |
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Gangliosidoses; Glutathione; Glycine; Glycogen Storage Disease Type II; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nerve Tissue Proteins; Nervous System Diseases; Phenylalanine; Phenylketonurias | 1976 |
Lipid metabolism of brain tissue in culture.
Topics: Age Factors; Animals; Brain; Carbon Isotopes; Chromatography, Gas; Chromatography, Thin Layer; Culture Media; Culture Techniques; Demyelinating Diseases; Fatty Acids; Fatty Acids, Nonesterified; Gangliosides; Glycolipids; Humans; Lipid Metabolism, Inborn Errors; Lipids; Palmitic Acids; Phenylalanine; Phospholipids; Rats; Stearic Acids; Triglycerides | 1972 |
Inborn errors of metabolism associated with unusual odors.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Malabsorption Syndromes; Maple Syrup Urine Disease; Methionine; Odorants; Phenylalanine; Tryptophan; Valerates | 1970 |