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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2014
Gaiak:
Research Article
Sarrera elektronikoa: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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