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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...

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Detalhes bibliográficos
Main Authors: Friso, A, Tomanin, R, Salvalaio, M, Scarpa, M
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Ltd 2010
Assuntos:
Acesso em linha: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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