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Keyphrases
Acid Maltase Deficiency
100%
Molecular Pathology
100%
α-glucosidase
100%
Lysosomal Enzymes
44%
Late-onset
41%
Glycoprotein
27%
Infantile Onset
27%
Neutral alpha-glucosidase
20%
α-glucosidase Activity
17%
Post-translational
17%
Evolving Model
13%
Chromosomal Locus
13%
Molecular Biology
13%
Gene Replacement Therapy
13%
Morphological Changes
13%
Whole Cell
13%
Membrane Glycoproteins
13%
Unknown Function
13%
Cellular Pathology
13%
Lysosomal Acid Lipase
13%
Reduced Rate
13%
Mutant Cells
13%
Enzyme Replacement Therapy
13%
Microsomal Enzymes
13%
Cellular Alterations
13%
Lysosomal Storage Disease
13%
Processing Enzymes
13%
Membrane Assembly
13%
Dual Role
13%
Biochemical Properties
13%
Renal Tissue
13%
Acid alpha-glucosidase Deficiency
13%
Natural Saccharides
13%
Biosynthetic Labelling
13%
Glycoprotein Processing
13%
Free Translation
10%
Recombinant
10%
Vitrocell
10%
Glycoprotein Biosynthesis
6%
Biochemistry, Genetics and Molecular Biology
Maltase
100%
Deficiency
100%
Alpha-Glucosidase
94%
Enzyme
79%
Glycoprotein
37%
Glucosidase
19%
Anabolism
14%
Hydrolase
13%
Morphology
11%
Biochemistry
11%
Molecular Biology
11%
Whole Cell
11%
Membrane Glycoproteins
11%
Lysosomal Storage Disease
11%
Cell Mutant
11%
Carbohydrates
11%