GAN : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 4

Ganglioside Galactosyltransferase - 새창 Catalyzes the final step in the galactocerebroside biosynthesis pathway.
Synonyms : Ganglioside GM1 Synthase, UDP Galactose-Ceramide Galactosyltransferase, UDP Galactose-GM2 Galactosyltransferase, UDP-Galactose-GM2 Ganglioside Beta-1-3-Galactosyltransferase, UDPGal-GM2 Beta1-3-Galactosyltransferase, GM1 Synthase, Ganglioside
Gangliosides - 새창 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)
Synonyms :
Gangliosidoses - 새창 A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
Synonyms : Ganglioside Storage Diseases, Ganglioside Storage Disorders, Gangliosidosis, Ganglioside Storage Disease, Ganglioside Storage Disorder, Storage Disease, Ganglioside, Storage Diseases, Ganglioside, Storage Disorder, Ganglioside, Storage Disorders, Ganglioside
Gangliosidoses, GM2 - 새창 A group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASE system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS.
Synonyms : GM2 Gangliosidosis, Gangliosidoses GM2, GM2 Gangliosidose, GM2 Gangliosidoses, GM2, Gangliosidoses, Gangliosidose, GM2, Gangliosidosis, GM2
Gangliosidosis, GM1 - 새창 An autosomal recessive neurodegenerative disorder caused by the absence or deficiency of BETA-GALACTOSIDASE. It is characterized by intralysosomal accumulation of G(M1) GANGLIOSIDE and oligosaccharides, primarily in neurons of the central nervous system. The infantile form is characterized by MUSCLE HYPOTONIA, poor psychomotor development, HIRSUTISM, hepatosplenomegaly, and facial abnormalities. The juvenile form features HYPERACUSIS; SEIZURES; and psychomotor retardation. The adult form features progressive DEMENTIA; ATAXIA; and MUSCLE SPASTICITY. (From Menkes, Textbook of Child Neurology, 5th ed, pp96-7)
Synonyms : Beta-Galactosidase-1 Deficiency Disease, GM1 Gangliosidosis, Gangliosidosis G(M1), Gangliosidosis GM1, Gangliosidosis GM1, Adult, Gangliosidosis GM1, Infantile, Gangliosidosis GM1, Juvenile, Gangliosidosis GM1, Type 1, Gangliosidosis GM1, Type 2