BIOMAT Database Logo BIOMAT Database Logo

Beta-D-galactosidase in human urine: deficiency in generalized gangliosidosis. 1969

G H Thomas

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D008052 Lipid Metabolism, Inborn Errors Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable. Lipid Metabolism, Inborn Error
D008297 Male Males
D003124 Colorimetry Any technique by which an unknown color is evaluated in terms of standard colors. The technique may be visual, photoelectric, or indirect by means of spectrophotometry. It is used in chemistry and physics. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
D005260 Female Females
D005696 Galactosidases A family of galactoside hydrolases that hydrolyze compounds with an O-galactosyl linkage. EC 3.2.1.-. Galactosidase
D005732 Gangliosides A subclass of ACIDIC GLYCOSPHINGOLIPIDS. They contain one or more sialic acid (N-ACETYLNEURAMINIC ACID) residues. Using the Svennerholm system of abbrevations, gangliosides are designated G for ganglioside, plus subscript M, D, or T for mono-, di-, or trisialo, respectively, the subscript letter being followed by a subscript arabic numeral to indicated sequence of migration in thin-layer chromatograms. (From Oxford Dictionary of Biochemistry and Molecular Biology, 1997) Ganglioside,Sialoglycosphingolipids
D006026 Glycoside Hydrolases Any member of the class of enzymes that catalyze the cleavage of the glycosidic linkage of glycosides and the addition of water to the resulting molecules. Endoglycosidase,Exoglycosidase,Glycohydrolase,Glycosidase,Glycosidases,Glycoside Hydrolase,Endoglycosidases,Exoglycosidases,Glycohydrolases,Hydrolase, Glycoside,Hydrolases, Glycoside
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

G H Thomas
Generalized gangliosidosis: beta-galactosidase deficiency.
May 1968, Science (New York, N.Y.),
G H Thomas
beta-D-galactosidase activities in juvenile GM1-gangliosidosis.
October 1978, Acta neurologica Scandinavica,
G H Thomas
[Deficiency of GM1 ganglioside beta-galactosidase--GM1 gangliosidosis].
April 1988, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme,
G H Thomas
Beta-galactosidase deficiency in GM1 gangliosidosis of Friesian calves.
July 1973, Research in veterinary science,
G H Thomas
[beta-Galactosidosis (acid beta-galactosidase deficiency: GM1 gangliosidosis, Morquio B disease)].
January 1998, Ryoikibetsu shokogun shirizu,
G H Thomas
Generalized gangliosidosis: acid beta-galactosidase deficiency with early onset, rapid mental deterioration and minimal bone dysplasia.
October 1976, Journal of neurology,
G H Thomas
Leukocyte beta-galactosidase activity in the diagnosis of generalized GM 1 gangliosidosis.
March 1972, Pediatrics,
G H Thomas
Neuronal GM1 gangliosidosis in a Siamese cat with beta-galactosidase deficiency.
November 1971, Science (New York, N.Y.),
G H Thomas
Neuronal-visceral GM1 gangliosidosis in a dog with beta-galactosidase deficiency.
October 1976, Science (New York, N.Y.),
G H Thomas
Neurovisceral and skeletal GM1-gangliosidosis in dogs with beta-galactosidase deficiency.
August 1985, Science (New York, N.Y.),
Copied contents to your clipboard!