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A New Resorufin-Based Alpha-Glucosidase Assay for High Throughput Screening
Mutations in α-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...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2737366/ https://ncbi.nlm.nih.gov/pubmed/19371716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ab.2009.04.010 |
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