UTP-Hexose-1-Phosphate Uridylyltransferase
"UTP-Hexose-1-Phosphate Uridylyltransferase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An enzyme that catalyzes the synthesis of UDPgalactose from UTP and galactose-1-phosphate. It is present in low levels in fetal and infant liver, but increases with age, thereby enabling galactosemic infants who survive to develop the capacity to metabolize galactose. EC 2.7.7.10.
| Descriptor ID |
D005694
|
| MeSH Number(s) |
D08.811.913.696.445.900
|
| Concept/Terms |
UTP-Hexose-1-Phosphate Uridylyltransferase- UTP-Hexose-1-Phosphate Uridylyltransferase
- UTP Hexose 1 Phosphate Uridylyltransferase
- Uridylyltransferase, UTP-Hexose-1-Phosphate
- UDP Galactose Pyrophosphorylase
- Galactose Pyrophosphorylase, UDP
- Pyrophosphorylase, UDP Galactose
- Galactose-1-Phosphate Uridyltransferase
- Galactose 1 Phosphate Uridyltransferase
- Uridyltransferase, Galactose-1-Phosphate
- Galactosephosphate Uridylyltransferase
- Uridylyltransferase, Galactosephosphate
|
Below are MeSH descriptors whose meaning is more general than "UTP-Hexose-1-Phosphate Uridylyltransferase".
Below are MeSH descriptors whose meaning is more specific than "UTP-Hexose-1-Phosphate Uridylyltransferase".
This graph shows the total number of publications written about "UTP-Hexose-1-Phosphate Uridylyltransferase" by people in this website by year, and whether "UTP-Hexose-1-Phosphate Uridylyltransferase" was a major or minor topic of these publications.
Below are the most recent publications written about "UTP-Hexose-1-Phosphate Uridylyltransferase" by people in Profiles.
-
Effect of genotype on galactose-1-phosphate in classic galactosemia patients. Mol Genet Metab. 2018 11; 125(3):258-265.
-
Biochemical changes and clinical outcomes in 34 patients with classic galactosemia. J Inherit Metab Dis. 2018 03; 41(2):197-208.
-
Gestational dating by metabolic profile at birth: a California cohort study. Am J Obstet Gynecol. 2016 Apr; 214(4):511.e1-511.e13.
-
Modifiers of ovarian function in girls and women with classic galactosemia. J Clin Endocrinol Metab. 2013 Jul; 98(7):E1257-65.
-
Cryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemia. J Inherit Metab Dis. 2013 Nov; 36(6):1049-61.
-
N- and O-linked glycosylation of total plasma glycoproteins in galactosemia. Mol Genet Metab. 2012 Aug; 106(4):442-54.
-
L-Ascorbate biosynthesis in higher plants: the role of VTC2. Trends Plant Sci. 2008 Nov; 13(11):567-73.
-
Galactose-1-phosphate uridyl transferase (GALT) genotype and phenotype, galactose consumption, and the risk of borderline and invasive ovarian cancer (United States). Cancer Causes Control. 2002 Mar; 13(2):113-20.
-
Stable isotope dilution analysis of galactitol in amniotic fluid: an accurate approach to the prenatal diagnosis of galactosemia. Pediatr Res. 1984 Aug; 18(8):714-8.
-
Curious neurologic sequelae in galactosemia. Pediatrics. 1984 Mar; 73(3):309-12.