. . . . . . . "[Loss of Wt1 abrogated the PMC phenotype and showed evidence of mesothelial-to-mesenchymal transition (MMT), with a reduced expression of E-cadherin and an increase in the profibrotic markers ?-smooth muscle actin (?-SMA) and fibronectin, along with increased migration and contractility, compared with that of the control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:12:49+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .