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Glucosylceramidase
(Glucocerebrosidase)
Summary
Description:
A glycosidase that hydrolyzes a glucosylceramide to yield free ceramide plus glucose. Deficiency of this enzyme leads to abnormally high concentrations of glucosylceramide in the brain in GAUCHER DISEASE. EC 3.2.1.45.
Also Known As:
Glucocerebrosidase; Acid beta-Glucosidase; Glucosylceramide beta-Glucosidase; Glucocerebroside beta-Glucosidase; Glucosyl Ceramidase Show All >>
Networked: 1049
relevant articles (23 outcomes,
70 trials/studies)
for this Bio-Agent
Key Diseases for which Glucosylceramidase is
Relevant
-
Gaucher Disease (Gaucher's Disease)
:
20 outcomes 52 studies in 902 results
-
Neurologic Manifestations (Neurological Manifestations)
:
2 outcomes in 9 results
-
Lysosomal Storage Diseases (Lysosomal Storage Disease)
:
1 outcome 1 study in 61 results
-
Thrombocytopenia (Thrombopenia)
:
1 outcome in 6 results
-
Splenomegaly
:
1 outcome in 3 results
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Drugs Related to Glucosylceramidase
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Mannose (D-Mannose)
-
imiglucerase (Cerezyme)
-
alglucerase (Ceredase)
-
Lysergic Acid Diethylamide (LSD)
-
Glucosylceramidase (Glucocerebrosidase)
-
Complementary DNA (cDNA)
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Glucose (Dextrose)
-
Synucleins
-
DNA (Deoxyribonucleic Acid)
-
conduritol epoxide
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Therapies Related to Glucosylceramidase
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Enzyme Replacement Therapy
-
Enzyme Therapy
-
Intravenous Infusions
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Complementary Therapies (Alternative Medicine)
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Therapeutics
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