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Reduced Amelogenin-MMP20 Interactions in Amelogenesis Imperfecta

Amelogenin with a proline 41 to threonine mutation (P41T) is hydrolyzed at a lower rate by matrix metalloproteinase 20 (MMP20), resulting in an inherited tooth enamel defect, amelogenesis imperfecta (AI). The aim of this study was to elucidate the effect of P41T on the interactions between amelogeni...

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Detalhes bibliográficos
Main Authors: Tanimoto, K., Le, T., Zhu, L., Witkowska, H.E., Robinson, S., Hall, S., Hwang, P., DenBesten, P., Li, W.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3677966/
https://ncbi.nlm.nih.gov/pubmed/18434575
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