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Genistein reduces glycosaminoglycan levels in a mouse model of mucopolysaccharidosis type II

BACKGROUND AND PURPOSE: Mucopolysaccharidoses (MPS) are lysosomal storage disorders resulting from a deficit of specific lysosomal enzymes catalysing glycosaminoglycan (GAG) degradation. The typical pathology involves most of the organ systems, including the brain, in its severe forms. The soy isofl...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Friso, A, Tomanin, R, Salvalaio, M, Scarpa, M
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Blackwell Publishing Ltd 2010
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2839266/
https://ncbi.nlm.nih.gov/pubmed/20136838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1476-5381.2009.00565.x
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