Microarray expression analysis and identification of serum biomarkers for Niemann–Pick disease, type C1

Niemann–Pick disease type C (NPC) is a lysosomal storage disorder characterized by liver disease and progressive neurodegeneration. Deficiency of either NPC1 or NPC2 leads to the accumulation of cholesterol and glycosphingolipids in late endosomes and early lysosomes. In order to identify pathologic...

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Bibliografiset tiedot
Päätekijät: Cluzeau, Celine V.M., Watkins-Chow, Dawn E., Fu, Rao, Borate, Bhavesh, Yanjanin, Nicole, Dail, Michelle K., Davidson, Cristin D., Walkley, Steven U., Ory, Daniel S., Wassif, Christopher A., Pavan, William J., Porter, Forbes D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2012
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Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3406758/
https://ncbi.nlm.nih.gov/pubmed/22619379
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds193
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