Keyphrases
Acid Maltase Deficiency
83%
Biochemical Properties
11%
Biosynthetic Labeling
13%
Cellular Alterations
11%
Cellular Pathology
11%
Chromosomal Locus
11%
Dual Role
11%
Enzyme Replacement Therapy
11%
Evolving Model
13%
Free Translation
11%
Gene Replacement Therapy
11%
Glucosidase
17%
Glycoprotein
35%
Glycoprotein Biosynthesis
5%
Infantile Onset
23%
Late-onset
35%
Lysosomal Acid Lipase
11%
Lysosomal Enzymes
37%
Lysosomal Storage Disease
11%
Membrane Assembly
11%
Membrane Glycoproteins
11%
Microsomal Enzymes
11%
Molecular Biology
11%
Molecular Pathology
83%
Morphological Changes
11%
Mutant Cells
11%
Neutral Endoglucanase
19%
Post-translational
14%
Processing Enzymes
11%
Recombinant
8%
Reduced Rate
11%
Renal Tissue
11%
Saccharides
11%
Unknown Function
11%
Whole Cell
11%
α-glucosidase
79%
α-glucosidase Activity
16%
Biochemistry, Genetics and Molecular Biology
Alpha-Glucosidase
100%
Anabolism
13%
Biochemistry
10%
Cell Mutant
10%
Enzyme
70%
Glucosidase
16%
Glycoprotein
33%
Hydrolase
11%
Lysosomal Storage Disease
10%
Maltase
83%
Membrane Glycoproteins
10%
Molecular Biology
10%
Morphology
10%
Saccharide
10%
Transmembrane Protein
10%
Whole Cell
10%
Neuroscience
Alpha Glucosidase
83%
Anabolism
14%
Carbohydrates
10%
Enzyme Replacement Therapy
10%
Glucan 1,4 Alpha Glucosidase
83%
Glucosidase
16%
Glycoprotein
35%
Hydrolase
12%
Lysosome Enzyme
33%
Microsome Enzyme
12%
Neuromuscular
10%
Transmembrane Protein
10%