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serine and Alkaptonuria

serine has been researched along with Alkaptonuria in 2 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.

Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.

Research Excerpts

ExcerptRelevanceReference
"Alkaptonuria is a rare metabolic disorder resulting from loss of homogentisate 1,2 dioxygenase (HGO) activity."1.29The molecular basis of alkaptonuria. ( Beltrán-Valero de Bernabé, D; Fernández-Cañón, JM; Fernández-Ruiz, E; Granadino, B; Peñalva, MA; Renedo, M; Rodríguez de Córdoba, S, 1996)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fernández-Cañón, JM1
Granadino, B1
Beltrán-Valero de Bernabé, D1
Renedo, M1
Fernández-Ruiz, E1
Peñalva, MA1
Rodríguez de Córdoba, S1
Ramos, SM1
Hernández, M1
Roces, A1
Larruga, JM1
González, P1
González, AM1
Pinto, FM1
Cabrera, VM1

Other Studies

2 other studies available for serine and Alkaptonuria

ArticleYear
The molecular basis of alkaptonuria.
    Nature genetics, 1996, Volume: 14, Issue:1

    Topics: Alkaptonuria; Amino Acid Sequence; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 3; Cl

1996
Molecular diagnosis of alkaptonuria mutation by analysis of homogentisate 1,2 dioxygenase mRNA from urine and blood.
    American journal of medical genetics, 1998, Jun-30, Volume: 78, Issue:2

    Topics: Alkaptonuria; Amino Acid Substitution; Dioxygenases; Female; Homogentisate 1,2-Dioxygenase; Humans;

1998