aspartic acid has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 6 studies
Aspartic Acid: One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
aspartic acid : An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
L-aspartic acid : The L-enantiomer of aspartic acid.
Ornithine Carbamoyltransferase Deficiency Disease: An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 4 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Matsuura, T | 2 |
| Hoshide, R | 2 |
| Kiwaki, K | 1 |
| Komaki, S | 1 |
| Koike, E | 1 |
| Endo, F | 1 |
| Oyanagi, K | 1 |
| Suzuki, Y | 1 |
| Kato, I | 1 |
| Ishikawa, K | 1 |
| Nelson, J | 1 |
| Qureshi, IA | 1 |
| Vasudevan, S | 1 |
| Sarma, DS | 1 |
| Nishiyori, A | 1 |
| Yoshino, M | 1 |
| Tananari, Y | 1 |
| Mastuda, I | 1 |
| Mori, M | 1 |
| Kato, H | 1 |
| Snyderman, SE | 1 |
| Sansaricq, C | 1 |
| Phansalkar, SV | 1 |
| Schacht, RC | 1 |
| Norton, PM | 1 |
| Oberholzer, VG | 1 |
| Palmer, T | 1 |
| Inoue, Y | 1 |
| Ohkura, T | 1 |
| Matsumoto, I | 1 |
| Rudewicz, PJ | 1 |
6 other studies available for aspartic acid and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Four newly identified ornithine transcarbamylase (OTC) mutations (D126G, R129H, I172M and W332X) in Japanese male patients with early-onset OTC deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Base Sequence; DNA Mutational Analysi | 1994 |
The effects of various inhibitors on the regulation of orotic acid excretion in sparse-fur mutant mice (spf/Y) deficient in ornithine transcarbamylase.
Topics: Adenine; Animals; Antimetabolites; Aspartic Acid; Creatinine; Cycloheximide; Injections, Intraperito | 1993 |
Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male.
Topics: Age of Onset; Amino Acid Substitution; Ammonia; Animals; Aspartic Acid; COS Cells; DNA; DNA Mutation | 1998 |
The therapy of hyperammonemia due to ornithine transcarbamylase defiency in a male neonate.
Topics: Amino Acids; Amino Acids, Essential; Ammonia; Arginine; Aspartic Acid; Deficiency Diseases; Exchange | 1975 |
Increased excretion of N-carbamoyl compounds in patients with urea cycle defects.
Topics: Alanine; Argininosuccinate Synthase; Argininosuccinic Aciduria; Aspartic Acid; Carbamates; Child; Ch | 1976 |
Fast atom bombardment tandem mass spectrometric analysis of N-carbamoylamino acids.
Topics: Amino Acids; Aspartic Acid; beta-Alanine; Carbamates; Humans; Ornithine Carbamoyltransferase Deficie | 1991 |