- PMC 4520262. PMID 25345088.
Media related to
Glucocerebroside at
Wikimedia Commons Glucocerebrosides at the U.S.
National Library of
Medicine Medical...
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either glucose or galactose; the two
major types are
therefore called glucocerebrosides (a.k.a. glucosylceramides) and
galactocerebrosides (a.k.a. galactosylceramides)...
- or
Gaucher disease (/ɡoʊˈʃeɪ/) (GD) is a
genetic disorder in
which glucocerebroside (a sphingolipid, also
known as glucosylceramide) ac****ulates in cells...
- a
lysosomal storage disease characterized by an ac****ulation of
glucocerebrosides in
macrophages that
infiltrate many
vital organs.
Mutations in the...
- Galactocerebrosides: a type of
cerebroseide with
galactose as the
saccharide moiety Glucocerebrosides: a type of
cerebroside with
glucose as the
saccharide moiety; often...
- synthase) is a
glucosyltransferase enzyme involved in the
production of
glucocerebrosides (also
called glucosylceramides). It is
responsible for the
first step...
-
Glycolipids Fabry's
disease Krabbe disease Metachromatic leukodystrophy Glucocerebrosides Gaucher's
disease Lipid storage disorder Lynn, D. Joanne, Newton,...
-
Juvenile hexosaminidase A
deficiency Chronic hexosaminidase A
deficiency Glucocerebroside Gaucher disease Type I Type II Type III
Sphingomyelinase Lysosomal...
-
treatment of
Gaucher disease Type 1. It is a
hydrolytic lysosomal glucocerebroside-specific enzyme,
which is a
recombinant form of glucocerebrosidase...
-
Klenk did
research on phospholipids, glycolipids, cerebrosides,
glucocerebrosides, sphingosines, sphingolipids, glycosphingolipids, gangliosides, plasmalogens...
