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Enzyme replacement therapy on hypophosphatasia mouse model

Hypophosphatasia (HPP) is an inborn error of metabolism caused by deficiency of the tissue-nonspecific alkaline phosphatase (TNSALP), resulting in a defect of bone mineralization. Natural substrates for this ectoenzyme accumulate extracellulary including inorganic pyrophosphate (PPi), an inhibitor o...

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Detalhes bibliográficos
Main Authors: Oikawa, Hirotaka, Tomatsu, Shunji, Haupt, Bisong, Montaño, Adriana M., Shimada, Tsutomu, Sly, William S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4020913/
https://ncbi.nlm.nih.gov/pubmed/23978959
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-013-9646-7
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