lysine has been researched along with Alpha-Aminoadipic Semialdehyde Deficiency Disease in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (37.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Guo, W; Guo, Y; Jian, Y; Wang, M; Wang, X; Wu, J; Yang, C | 1 |
| Ban, Z; Chang, Y; Gan, Q; Guo, W; Guo, Y; Jing, Y; Qian, W; Tang, R; Wang, F; Wang, G; Wang, M; Wang, X; Wu, S; Yang, C; Zhang, F; Zhang, Q; Zhao, L; Zhou, J | 1 |
| García-Villoria, J; Girós, M; Ribes, A; Ruiz, A; Torres, MA; Tort, F; Ugarteburu, O | 1 |
| Duvall Wannmacher, CM; Ferreira, GC; Leipnitz, G; Schuck, PF; Seminotti, B; Tonin, AM; Viegas, CM; Wajner, M; Zanatta, A | 1 |
| DONATH, A; RICHTERICH, R; ROSSI, E; SPAHR, A | 1 |
| WOODY, NC | 1 |
| FREYCON, F; FREYCON, MT | 1 |
| Biery, BJ; Cox, RP; Geisbrecht, BV; Geraghty, MT; Goodman, BK; Gould, SJ; Morrell, JC; Sacksteder, KA | 1 |
8 other study(ies) available for lysine and Alpha-Aminoadipic Semialdehyde Deficiency Disease
| Article | Year |
|---|---|
The Metabolite Saccharopine Impairs Neuronal Development by Inhibiting the Neurotrophic Function of Glucose-6-Phosphate Isomerase.
Topics: Animals; Female; Glucose-6-Phosphate Isomerase; Hyperlysinemias; Lysine; Male; Mice; Saccharopine Dehydrogenases | 2022 |
The lysine catabolite saccharopine impairs development by disrupting mitochondrial homeostasis.
Topics: Animals; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Homeostasis; Hyperlysinemias; Lysine; Mice; Mitochondria, Liver; Mutation; Saccharopine Dehydrogenases | 2019 |
Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient.
Topics: Child; Diet; Epilepsies, Myoclonic; Female; Homozygote; Humans; Hyperlysinemias; Lactic Acid; Lysine; Mitochondrial Diseases; Mitochondrial Proteins; Mutation; Nervous System Malformations; Phosphotransferases (Alcohol Group Acceptor); Pipecolic Acids; Pyridoxal Phosphate; RNA, Messenger; Vitamin B Complex | 2016 |
Inhibition of creatine kinase activity by lysine in rat cerebral cortex.
Topics: Analysis of Variance; Animals; Cerebral Cortex; Creatine Kinase; Disease Models, Animal; Electron Transport; Energy Metabolism; Glutathione; Hyperlysinemias; Isoenzymes; Lysine; Rats; Rats, Wistar; Sodium-Potassium-Exchanging ATPase | 2009 |
CONGENITAL LYSINE INTOLERANCE WITH PERIODIC AMMONIA INTOXICATION.
Topics: Ammonia; Biopsy; Blood Chemical Analysis; Dietary Proteins; Genetics, Medical; Humans; Hyperlysinemias; Infant; Liver; Liver Function Tests; Lysine; Metabolic Diseases; Periodicity; Proteins; Toxicology | 1964 |
HYPERLYSINEMIA.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Alcohols; Aminobutyrates; Anemia; Arginine; Asthenia; Blood Chemical Analysis; Child; Chromatography; Genetics, Medical; Growth; Humans; Hyperlysinemias; Infant; Lysine; Maple Syrup Urine Disease; Muscular Diseases; Ornithine; Seizures; Urine | 1964 |
[HYPERLYSINEMIA].
Topics: Amino Acid Metabolism, Inborn Errors; Biochemical Phenomena; Blood; Humans; Hyperlysinemias; Lysine | 1965 |
Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia.
Topics: Amino Acid Sequence; Base Sequence; Chromosomes, Human, Pair 7; Cloning, Molecular; Consanguinity; DNA Mutational Analysis; Exons; Female; Gene Expression Profiling; Genes, Recessive; Homozygote; Humans; Hyperlysinemias; In Situ Hybridization, Fluorescence; Lysine; Male; Molecular Sequence Data; Multienzyme Complexes; Mutation; Physical Chromosome Mapping; RNA Splice Sites; RNA, Messenger; Saccharopine Dehydrogenases; Sequence Alignment; Sequence Deletion | 2000 |