tyrosine has been researched along with Lipid Metabolism, Inborn Error in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| FINCKE, ML | 1 |
| Aliverti, A; Carpanelli, E; Coda, A; Mattevi, A; Mattiroli, F; Pandini, V; Razeto, A | 1 |
| François, J | 1 |
| Acquaviva, C; Aydin, A; Benoist, JF; Callebaut, I; Elion, J; Guffon, N; Ogier de Baulny, H; Porquet, D; Touati, G | 1 |
| Dimmick, JE; Hardwick, DF | 1 |
1 review(s) available for tyrosine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Metabolic cirrhoses of infancy and early childhood.
Topics: Amino Acid Metabolism, Inborn Errors; Cystic Fibrosis; Cystinosis; Fructose Intolerance; Galactosemias; Genetics, Medical; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Mucopolysaccharidoses; Niemann-Pick Diseases; Polycystic Kidney Diseases; Tyrosine | 1976 |
4 other study(ies) available for tyrosine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Classification; Clinical Laboratory Techniques; Galactosemias; Genetics, Medical; Humans; Intellectual Disability; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Mass Screening; Phenylketonurias; Tyrosine | 1965 |
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 |
Metabolic disorders and corneal changes.
Topics: Amino Acid Metabolism, Inborn Errors; Amyloidosis; Cornea; Corneal Dystrophies, Hereditary; Dysautonomia, Familial; Fabry Disease; Glycogen Storage Disease; Humans; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidoses; Tyrosine | 1981 |
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patients.
Topics: Amino Acid Sequence; Amino Acid Substitution; Asparagine; Child; Child, Preschool; Female; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Methylmalonic Acid; Methylmalonyl-CoA Mutase; Molecular Sequence Data; Mutation, Missense; Tyrosine; White People | 2001 |