Enamelin Is Critical for Ameloblast Integrity and Enamel Ultrastructure Formation

Mutations in the human enamelin gene cause autosomal dominant hypoplastic amelogenesis imperfecta in which the affected enamel is thin or absent. Study of enamelin knockout NLS-lacZ knockin mice revealed that mineralization along the distal membrane of ameloblast is deficient, resulting in no true e...

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Detalhes bibliográficos
Main Authors: Hu, Jan C.-C., Hu, Yuanyuan, Lu, Yuhe, Smith, Charles E., Lertlam, Rangsiyakorn, Wright, John Timothy, Suggs, Cynthia, McKee, Marc D., Beniash, Elia, Kabir, M. Enamul, Simmer, James P.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3945975/
https://ncbi.nlm.nih.gov/pubmed/24603688
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0089303
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