Identification of Loci Modulating the Cardiovascular and Skeletal Phenotypes of Marfan Syndrome in Mice

por Fernandes, Gustavo R., Massironi, Silvia M. G., Pereira, Lygia V.
Publicado 2016

Early X chromosome inactivation during human preimplantation development revealed by single-cell RNA-sequencing

por Moreira de Mello, Joana C., Fernandes, Gustavo R., Vibranovski, Maria D., Pereira, Lygia V.
Publicado 2017

A New Mouse Model for Marfan Syndrome Presents Phenotypic Variability Associated with the Genetic Background and Overall Levels of Fbn1 Expression

por Lima, Bruno L., Santos, Enrico J. C., Fernandes, Gustavo R., Merkel, Christian, Mello, Marco R. B., Gomes, Juliana P. A., Soukoyan, Marina, Kerkis, Alexandre, Massironi, Silvia M. G., Visintin, José A., Pereira, Lygia V.
Publicado 2010

Insights Into the Somatic Mutation Burden of Hepatoblastomas From Brazilian Patients

por Aguiar, Talita Ferreira Marques, Rivas, Maria Prates, Costa, Silvia, Maschietto, Mariana, Rodrigues, Tatiane, Sobral de Barros, Juliana, Barbosa, Anne Caroline, Valieris, Renan, Fernandes, Gustavo R., Bertola, Debora R., Cypriano, Monica, Caminada de Toledo, Silvia Regina, Major, Angela, Tojal, Israel, Apezzato, Maria Lúcia de Pinho, Carraro, Dirce Maria, Rosenberg, Carla, Lima da Costa, Cecilia Maria, Cunha, Isabela W., Sarabia, Stephen Frederick, Terrada, Dolores-López, Krepischi, Ana Cristina Victorino
Publicado 2020