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

4 Jul 2022

Abstract excerpt

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 the molecular function of this gene’s protein product and mutational dysfunction in fibrosis and cancer based on...

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PMID: 35860584
DOI: 10.3389/fonc.2022.932167

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Proposed Cellular Function of the Human FAM111B Protein and Dysregulation in Fibrosis and CancerPMID 35860584Read ↗

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