Ontology highlight
ABSTRACT:
SUBMITTER: Motabar O
PROVIDER: S-EPMC2737366 | biostudies-literature | 2009 Jul
REPOSITORIES: biostudies-literature
Motabar Omid O Shi Zhen-Dan ZD Goldin Ehud E Liu Ke K Southall Noel N Sidransky Ellen E Austin Christopher P CP Griffiths Gary L GL Zheng Wei W
Analytical biochemistry 20090414 1
Mutations in alpha-glucosidase cause accumulation of glycogen in lysosomes, resulting in Pompe disease, a lysosomal storage disorder. Small molecule chaperones that bind to enzyme proteins and correct the misfolding and mistrafficking of mutant proteins have emerged as a new therapeutic approach for the lysosomal storage disorders. In addition, alpha-glucosidase is a therapeutic target for type II diabetes, and alpha-glucosidase inhibitors have been used in the clinic as alternative treatments f ...[more]