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Differential distribution of heparan sulfate glycoforms and elevated expression of heparan sulfate biosynthetic enzyme genes in the brain of mucopolysaccharidosis IIIB mice
The primary pathology in mucopolysaccharidosis (MPS) IIIB is lysosomal storage of heparan sulfate (HS) glycosaminoglycans, leading to complex neuropathology and dysfunction, for which the detailed mechanisms remain unclear. Using antibodies that recognize specific HS glycoforms, we demonstrate diffe...
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Main Authors: | , , , , , , , |
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Formáid: | Artigo |
Teanga: | Inglês |
Foilsithe: |
Springer US
2011
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Ábhair: | |
Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3070083/ https://ncbi.nlm.nih.gov/pubmed/21225451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11011-010-9230-x |
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