alanine has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 12 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Excerpt | Relevance | Reference |
---|---|---|
" In addition a dose-response effect of alanine was observed." | 1.27 | Alanine decreases the protein requirements of infants with inborn errors of amino acid metabolism. ( Algert, S; Kelts, DG; Nyhan, WL; Prodanos, C; Wolff, JA, 1985) |
"Orotic aciduria was present (max: 693 mg/day) and was related to NH4 levels." | 1.25 | [Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)]. ( Beaudry, MA; Collu, R; Dallairf, L; Ducharme, JR; Leboeuf, G; Letarte, J; Melancon, SB, 1975) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 6 (50.00) | 18.7374 |
1990's | 4 (33.33) | 18.2507 |
2000's | 2 (16.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Marini, JC | 1 |
Erez, A | 1 |
Castillo, L | 1 |
Lee, B | 1 |
Strautnieks, S | 1 |
Malcolm, S | 1 |
Maestri, NE | 1 |
Lord, C | 1 |
Glynn, M | 1 |
Bale, A | 1 |
Brusilow, SW | 1 |
Tuchman, M | 1 |
Yudkoff, M | 1 |
Wiltshire, EJ | 1 |
Poplawski, NK | 1 |
Harbord, MG | 1 |
Harrison, RJ | 1 |
Fletcher, JM | 1 |
Beaudry, MA | 1 |
Letarte, J | 1 |
Collu, R | 1 |
Leboeuf, G | 1 |
Ducharme, JR | 1 |
Melancon, SB | 1 |
Dallairf, L | 1 |
Oberholzer, VG | 2 |
Palmer, T | 1 |
Carpenter, KH | 1 |
Bonham, JR | 1 |
Clarke, A | 1 |
Batshaw, ML | 1 |
Naylor, EW | 1 |
Thomas, GH | 1 |
MacKenzie, AE | 1 |
MacLeod, HL | 1 |
Heick, HM | 1 |
Korneluk, RG | 1 |
Kay, JD | 1 |
Seakins, JW | 1 |
Hjelm, M | 1 |
Wolff, JA | 1 |
Kelts, DG | 1 |
Algert, S | 1 |
Prodanos, C | 1 |
Nyhan, WL | 1 |
12 other studies available for alanine and Deficiency Disease, Ornithine Carbamoyltransferase
Article | Year |
---|---|
Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.
Topics: Alanine; Ammonia; Animals; Arginine; Citrulline; Disease Models, Animal; Female; Glycine; Injections | 2007 |
Novel mutation affecting a splice site in exon 4 of the ornithine carbamoyl transferase gene.
Topics: Alanine; Amino Acid Sequence; Arginine; Base Sequence; DNA; DNA Primers; Exons; Female; Humans; Infa | 1993 |
The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.
Topics: Adult; Aged; Alanine; Amino Acid Metabolism, Inborn Errors; Female; Glutamine; Heterozygote; Humans; | 1998 |
Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
Topics: Adolescent; Adult; Alanine; Amino Acids; Ammonia; Asparagine; Carbon-Nitrogen Ligases; Child; Child, | 1999 |
Ornithine carbamoyltransferase deficiency presenting with chorea in a female.
Topics: Alanine; Chorea; Female; Glutamine; Humans; Infant; Ornithine Carbamoyltransferase Deficiency Diseas | 2000 |
[Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].
Topics: Alanine; Amino Acids; Ammonia; Child, Preschool; Dietary Proteins; Erythrocytes; Growth Disorders; H | 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 |
Rett's syndrome and ornithine carbamoyltransferase deficiency.
Topics: Alanine; Ammonia; Female; Humans; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Re | 1990 |
False positive alanine tolerance test results in heterozygote detection of urea cycle disorders.
Topics: Alanine; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthas | 1989 |
False positive results from the alanine loading test for ornithine carbamoyltransferase deficiency heterozygosity.
Topics: Adult; Alanine; Allopurinol; Ammonia; False Positive Reactions; Female; Genetic Carrier Screening; H | 1989 |
Effect of partial ornithine carbamoyltransferase deficiency on urea synthesis and related biochemical events.
Topics: Alanine; Ammonia; Child; Female; Humans; Kinetics; Male; Ornithine Carbamoyltransferase Deficiency D | 1987 |
Alanine decreases the protein requirements of infants with inborn errors of amino acid metabolism.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Weight; Dietary Proteins; Female; H | 1985 |