Proposed Cellular Function of the Human FAM111B Protein and Dysregulation in Fibrosis and Cancer

FAM111B gene mutations are associated with a hereditary fibrosing poikiloderma known to cause poikiloderma, tendon contracture, myopathy, and pulmonary fibrosis (POIKTMP). In addition, the overexpression of FAM111B has been associated with cancer progression and poor prognosis. This review inferred...

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Detalles Bibliográficos
Autores principales: Arowolo, Afolake, Malebana, Moses, Sunda, Falone, Rhoda, Cenza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293052/
https://www.ncbi.nlm.nih.gov/pubmed/35860584
http://dx.doi.org/10.3389/fonc.2022.932167

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293052/
https://www.ncbi.nlm.nih.gov/pubmed/35860584
http://dx.doi.org/10.3389/fonc.2022.932167

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