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A Phenotypic Compound Screening Assay for Lysosomal Storage Diseases
The lysosome is a vital cellular organelle that primarily functions as a recycling center for breaking down unwanted macromolecules through a series of hydrolases. Functional deficiencies in lysosomal proteins due to genetic mutations have been found in over 50 lysosomal storage diseases that exhibi...
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| Опубликовано в: : | J Biomol Screen |
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| Главные авторы: | , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2013
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4818652/ https://ncbi.nlm.nih.gov/pubmed/23983233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1087057113501197 |
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