Page last updated: 2024-11-08

serine and Ornithine Carbamoyltransferase Deficiency Disease

serine has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 1 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Qureshi, I1
Rouleau, T1
Letarte, J1
Ouellet, R1

Other Studies

1 other study available for serine and Ornithine Carbamoyltransferase Deficiency Disease

ArticleYear
Significance of transported glycine in the conjugation of sodium benzoate in spf mutant mice with ornithine transcarbamylase deficiency.
    Biochemistry international, 1986, Volume: 12, Issue:6

    Topics: Animals; Benzoates; Benzoic Acid; Carbon Radioisotopes; Glycine; Kinetics; Liver; Mice; Mice, Mutant

1986