AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout‐NLS‐lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue‐specificity

BACKGROUND: Ameloblastin (AMBN) is a secreted matrix protein that is critical for the formation of dental enamel and is enamel‐specific with respect to its essential functions. Biallelic AMBN defects cause non‐syndromic autosomal recessive amelogenesis imperfecta. Homozygous Ambn mutant mice express...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Mol Genet Genomic Med
Main Authors: Liang, Tian, Hu, Yuanyuan, Smith, Charles E., Richardson, Amelia S, Zhang, Hong, Yang, Jie, Lin, Brent, Wang, Shih‐Kai, Kim, Jung‐Wook, Chun, Yong‐Hee, Simmer, James P., Hu, Jan C.‐C.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6732285/
https://ncbi.nlm.nih.gov/pubmed/31402633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.929
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