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Genetic and Molecular Insights Into Genotype-Phenotype Relationships in Osteopathia Striata With Cranial Sclerosis (OSCS) Through the Analysis of Novel Mouse Wtx Mutant Alleles.
Comai G, Boutet A, Tanneberger K, Massa F, Rocha AS, Charlet A, Panzolini C, Jian Motamedi F, Brommage R, Hans W, Funck-Brentano T, Hrabe de Angelis M, Hartmann C, Cohen-Solal M, Behrens J, Schedl A. Comai G, et al. Among authors: massa f. J Bone Miner Res. 2018 May;33(5):875-887. doi: 10.1002/jbmr.3387. Epub 2018 Mar 1. J Bone Miner Res. 2018. PMID: 29329488 Free article.
Alternatively spliced isoforms of WT1 control podocyte-specific gene expression.
Lefebvre J, Clarkson M, Massa F, Bradford ST, Charlet A, Buske F, Lacas-Gervais S, Schulz H, Gimpel C, Hata Y, Schaefer F, Schedl A. Lefebvre J, et al. Among authors: massa f. Kidney Int. 2015 Aug;88(2):321-31. doi: 10.1038/ki.2015.140. Epub 2015 May 20. Kidney Int. 2015. PMID: 25993318 Free article.
Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
Neirijnck Y, Reginensi A, Renkema KY, Massa F, Kozlov VM, Dhib H, Bongers EMHF, Feitz WF, van Eerde AM, Lefebvre V, Knoers NVAM, Tabatabaei M, Schulz H, McNeill H, Schaefer F, Wegner M, Sock E, Schedl A. Neirijnck Y, et al. Among authors: massa f. Kidney Int. 2018 May;93(5):1142-1153. doi: 10.1016/j.kint.2017.11.026. Epub 2018 Feb 17. Kidney Int. 2018. PMID: 29459093 Free article.
Developmental Renal Glomerular Defects at the Origin of Glomerulocystic Disease.
Fiorentino A, Christophorou A, Massa F, Garbay S, Chiral M, Ramsing M, Rasmussen M, Gubler MC, Bessieres B, Heidet L, Fischer E, Pontoglio M. Fiorentino A, et al. Among authors: massa f. Cell Rep. 2020 Oct 27;33(4):108304. doi: 10.1016/j.celrep.2020.108304. Cell Rep. 2020. PMID: 33113370 Free article.
226 results