lysine has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, YN; Jiang, MY; Li, XZ; Lin, YT; Liu, L; Mei, HF; Peng, MZ; Shao, YX; Sheng, HY; Su, L; Yin, X | 1 |
| Guan, KL; Huang, W; Lei, Q; Lin, Y; Xiong, Y; Yao, J; Yu, W; Zhao, S | 1 |
| Harada, E; Hirose, S; Ichikawa, K; Kumashiro, R; Kuno, T; Kuriya, N; Kuromaru, R; Nishiyori, A; Tokunaga, Y; Watanabe, Y; Yoshino, M | 1 |
| DeBree, PK; Grift, J; Van Bree-Blom, EJ; Van Gennip, AH; Wadman, SK | 1 |
| Donati, MA; Filippi, L; Resti, M; Zammarchi, E | 1 |
| Shih, VE | 1 |
| Bachmann, C; Cejka, J; Gronemeyer, WH; Krieger, I | 1 |
7 other study(ies) available for lysine and Deficiency Disease, Ornithine Carbamoyltransferase
| Article | Year |
|---|---|
Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency.
Topics: Adolescent; Adult; Ammonia; Arginine; Child; Child, Preschool; China; Creatine; Female; Humans; Hyperammonemia; Lysine; Male; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Urea; Young Adult | 2020 |
Lysine 88 acetylation negatively regulates ornithine carbamoyltransferase activity in response to nutrient signals.
Topics: Acetylation; Carbamyl Phosphate; Cell Line; Humans; Infant, Newborn; Kinetics; Lysine; Mutation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Signal Transduction | 2009 |
Late-onset ornithine transcarbamylase deficiency in male patients: prognostic factors and characteristics of plasma amino acid profile.
Topics: Adolescent; Adult; Age of Onset; Amino Acids; Ammonia; Child; Glutamine; Humans; Liver; Lysine; Male; Middle Aged; Ornithine Carbamoyltransferase Deficiency Disease; Prognosis; Regression Analysis | 2006 |
Urinary purines and pyrimidines in patients with hyperammonemia of various origins.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Preschool; Female; Humans; Infant, Newborn; Lysine; Male; Ornithine Carbamoyltransferase Deficiency Disease; Purines; Pyrimidines; Reye Syndrome | 1980 |
Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiency.
Topics: Absorption; Ammonia; Arginine; Child, Preschool; Citrulline; Diagnosis, Differential; Dietary Proteins; Female; Glutamine; Hepatitis; Humans; Infant; Lysine; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Urea | 1996 |
Congenital hyperammonemic syndromes.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthase (Ammonia); Citrulline; Diagnosis, Differential; Humans; Hyperargininemia; Infant, Newborn; Infant, Newborn, Diseases; Lysine; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Syndrome; Urea | 1976 |
Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase (OTC) deficiency.
Topics: Acid-Base Imbalance; Amino Acid Metabolism, Inborn Errors; Ammonia; Blood Urea Nitrogen; Dietary Proteins; Female; Glutamates; Humans; Infant, Newborn; Lysine; Ornithine Carbamoyltransferase Deficiency Disease; Propionates; Urine | 1976 |