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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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Main Authors: Tanimoto, K., Le, T., Zhu, L., Witkowska, H.E., Robinson, S., Hall, S., Hwang, P., DenBesten, P., Li, W.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2008
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3677966/
https://ncbi.nlm.nih.gov/pubmed/18434575
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