Lipid trafficking defects in Niemann-Pick type C disease
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Descrição
Niemann–Pick type C disease: cellular pathology and
Lipid-mediated motor-adaptor sequestration impairs axonal lysosome
Patient with Niemann-Pick disease type C: over 20 years' follow-up
PDF) Niemann–Pick C1 Is a Late Endosome-Resident Protein That
Unbiased yeast screens identify cellular pathways affected in
Elevation of plasma lysosphingomyelin-509 and urinary bile acid
Lipid trafficking defects in Niemann-Pick type C disease
Critical role for glycosphingolipids in Niemann-Pick disease type
The pathogenesis of Niemann–Pick type C disease: a role for
Abnormal accumulation and recycling of glycoproteins visualized in
Inhibition of Histone Deacetylases 1, 2, and 3 Enhances Clearance
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