Page last updated: 2024-11-08

alanine and Deficiency Disease, Ornithine Carbamoyltransferase

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.

Research Excerpts

ExcerptRelevanceReference
" In addition a dose-response effect of alanine was observed."1.27Alanine 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)

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19906 (50.00)18.7374
1990's4 (33.33)18.2507
2000's2 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Marini, JC1
Erez, A1
Castillo, L1
Lee, B1
Strautnieks, S1
Malcolm, S1
Maestri, NE1
Lord, C1
Glynn, M1
Bale, A1
Brusilow, SW1
Tuchman, M1
Yudkoff, M1
Wiltshire, EJ1
Poplawski, NK1
Harbord, MG1
Harrison, RJ1
Fletcher, JM1
Beaudry, MA1
Letarte, J1
Collu, R1
Leboeuf, G1
Ducharme, JR1
Melancon, SB1
Dallairf, L1
Oberholzer, VG2
Palmer, T1
Carpenter, KH1
Bonham, JR1
Clarke, A1
Batshaw, ML1
Naylor, EW1
Thomas, GH1
MacKenzie, AE1
MacLeod, HL1
Heick, HM1
Korneluk, RG1
Kay, JD1
Seakins, JW1
Hjelm, M1
Wolff, JA1
Kelts, DG1
Algert, S1
Prodanos, C1
Nyhan, WL1

Other Studies

12 other studies available for alanine and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.
    American journal of physiology. Endocrinology and metabolism, 2007, Volume: 293, Issue:6

    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.
    Human molecular genetics, 1993, Volume: 2, Issue:11

    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.
    Medicine, 1998, Volume: 77, Issue:6

    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.
    Molecular genetics and metabolism, 1999, Volume: 66, Issue:1

    Topics: Adolescent; Adult; Alanine; Amino Acids; Ammonia; Asparagine; Carbon-Nitrogen Ligases; Child; Child,

1999
Ornithine carbamoyltransferase deficiency presenting with chorea in a female.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:8

    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)].
    Diabete & metabolisme, 1975, Volume: 1

    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.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Apr-01, Volume: 68, Issue:1

    Topics: Alanine; Argininosuccinate Synthase; Argininosuccinic Aciduria; Aspartic Acid; Carbamates; Child; Ch

1976
Rett's syndrome and ornithine carbamoyltransferase deficiency.
    Journal of inherited metabolic disease, 1990, Volume: 13, Issue:3

    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.
    The Journal of pediatrics, 1989, Volume: 115, Issue:4

    Topics: Alanine; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthas

1989
False positive results from the alanine loading test for ornithine carbamoyltransferase deficiency heterozygosity.
    The Journal of pediatrics, 1989, Volume: 115, Issue:4

    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.
    Clinical science (London, England : 1979), 1987, Volume: 72, Issue:2

    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.
    Journal of neurogenetics, 1985, Volume: 2, Issue:1

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Weight; Dietary Proteins; Female; H

1985