Kiindulópont Radioaktív kivétel acid alpha glucosidase borda Koksz Társadalom kutatások
Inhibitors of α‐amylase and α‐glucosidase: Potential linkage for whole cereal foods on prevention of hyperglycemia - Gong - 2020 - Food Science & Nutrition - Wiley Online Library
Acid alpha-glucosidase - Wikipedia
Detection of Active Mammalian GH31 α-Glucosidases in Health and Disease Using In-Class, Broad-Spectrum Activity-Based Probes | ACS Central Science
Endolysosomal N-glycan processing is critical to attain the most active form of the enzyme acid alpha-glucosidase - ScienceDirect
Antibodies against recombinant human alpha-glucosidase do not seem to affect clinical outcome in childhood onset Pompe disease | Orphanet Journal of Rare Diseases | Full Text
Acid alpha-glucosidase or acid maltase, is an enzyme that helps to break down glycogen in the lysosome. 3d illustration Stock Photo - Alamy
The Pharmacological Chaperone AT2220 Increases the Specific Activity and Lysosomal Delivery of Mutant Acid Alpha-Glucosidase, and Promotes Glycogen Reduction in a Transgenic Mouse Model of Pompe Disease | PLOS ONE
Consensus treatment recommendations for lateonset Pompe disease
Acid alpha-glucosidase or acid maltase, is an enzyme that helps to break down glycogen in the lysosome. 3d illustration Stock Photo - Alamy
Rescue of Advanced Pompe Disease in Mice with Hepatic Expression of Secretable Acid α-Glucosidase - ScienceDirect
Acid Alpha-glucosidase Molecular Structure Isolated on Black Stock Illustration - Illustration of hydrogen, oxygen: 177440257
Structure of human lysosomal acid α-glucosidase–a guide for the treatment of Pompe disease | Nature Communications
Inhibitory effects of pu-erh tea on alpha glucosidase and alpha amylase: a systemic review | Nutrition & Diabetes
Mechanism of action of alpha-glucosidase inhibitors. | Download Scientific Diagram
Figure 2, Hydrolytic reactions of the red and blue dyes - Probe Reports from the NIH Molecular Libraries Program - NCBI Bookshelf
Glycoengineered Acid α-Glucosidase With Improved Efficacy at Correcting the Metabolic Aberrations and Motor Function Deficits in a Mouse Model of Pompe Disease: Molecular Therapy
Schematic drawing of consequences of α-glucosidase deficiency and ERT... | Download Scientific Diagram
Pompe's Disease and the Effects of Alpha-Glucosidase Deficiency
Gene therapy with secreted acid alpha-glucosidase rescues Pompe disease in a novel mouse model with early-onset spinal cord and respiratory defects - eBioMedicine