Associated Papers
Using computer-generated protein models to analyze mutations linked to Amelogenesis Imperfecta.
Sharmin N et al.
Plos One, 2025
Molecular-based phenotype variations in amelogenesis imperfecta.
Dong J et al.
Oral Diseases, 2023
Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature.
Sriwattanapong K et al.
Bdj Open, 2023
Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta.
Yoshioka H et al.
International Journal of Molecular Sciences, 2021
33672174 (PubMed )
Supplement: ijms-22-02202-s001.zip › Supplementary_Table_S4-1_Final_021921.xlsx › Table_S3.1
The ITGB6 gene: its role in experimental and clinical biology.
Meecham A et al.
Gene: X, 2020
Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta.
Seymen F et al.
Oral Diseases, 2015
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta.
Poulter JA et al.
Human Molecular Genetics, 2014
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