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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2014
Matèries:
Research Article
Accés en línia: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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