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Characterisation of the biochemical and cellular roles of native and pathogenic amelogenesis imperfecta mutants of FAM83H

The majority of mutations identified in patients with amelogenesis imperfecta have been mapped to FAM83H. As FAM83H expression is not limited to the enamel, how FAM83H contributes to amelogenesis is still largely unknown. We previously reported that members of the FAM83 family of proteins interact w...

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Detalles Bibliográficos
Autores principales: Tachie-Menson, Theresa, Gázquez-Gutiérrez, Ana, Fulcher, Luke J., Macartney, Thomas J., Wood, Nicola T., Varghese, Joby, Gourlay, Robert, Soares, Renata F., Sapkota, Gopal P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284315/
https://www.ncbi.nlm.nih.gov/pubmed/32289446
http://dx.doi.org/10.1016/j.cellsig.2020.109632