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Immunological cell type characterization and Th1–Th17 cytokine production in a mouse model of Gaucher disease
Gaucher disease is a lysosomal storage disease resulting from insufficient enzyme acid β-glucosidase (glucocerebrosidase, GCase, EC 4.2.1.25) activity and the resultant accumulation of glucosylceramide. Macrophage (Mφ) lineage cells are thought to be the major disease effectors because of their secr...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3382074/ https://ncbi.nlm.nih.gov/pubmed/22595426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2012.04.020 |
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