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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Publicado no:Cell Signal
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Elsevier Science Ltd 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7284315/
https://ncbi.nlm.nih.gov/pubmed/32289446
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cellsig.2020.109632
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