FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in Fibroblasts

Por Yeh, Erika, Atique, Rodrigo, Ishiy, Felipe A. A., Fanganiello, Roberto Dalto, Alonso, Nivaldo, Matushita, Hamilton, da Rocha, Katia Maria, Passos-Bueno, Maria Rita
Publicado em 2011

Erratum to: FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells than in Fibroblasts

Por Yeh, Erika, Atique, Rodrigo, Ishiy, Felipe A. A., Fanganiello, Roberto Dalto, Alonso, Nivaldo, Matushita, Hamilton, da Rocha, Katia Maria, Passos-Bueno, Maria Rita
Publicado no Stem Cell Rev (2013)

Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes

Por de Peralta, Mauro S Porcel, Mouguelar, Valeria S, Sdrigotti, María Antonella, Ishiy, Felipe A A, Fanganiello, Roberto D, Passos-Bueno, Maria R, Coux, Gabriela, Calcaterra, Nora B
Publicado no Cell Death Dis (2016)

EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome

Por Miller, Emily E., Kobayashi, Gerson S., Musso, Camila M., Allen, Miranda, Ishiy, Felipe A.A., de Caires, Luiz Carlos, Goulart, Ernesto, Griesi-Oliveira, Karina, Zechi-Ceide, Roseli M., Richieri-Costa, Antonio, Bertola, Debora R., Passos-Bueno, Maria Rita, Silver, Debra L.
Publicado no Hum Mol Genet (2017)