Page last updated: 2024-11-08

serine and Alcaptonuria

serine has been researched along with Alcaptonuria 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.

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 Alcaptonuria

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