Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers

Por Arashiro, Patricia, Eisenberg, Iris, Kho, Alvin T., Cerqueira, Antonia M. P., Canovas, Marta, Silva, Helga C. A., Pavanello, Rita C. M., Verjovski-Almeida, Sergio, Kunkel, Louis M., Zatz, Mayana
Publicado em 2009

Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development

Por Hsia, Gabriella S. P., Musso, Camila M., Alvizi, Lucas, Brito, Luciano A., Kobayashi, Gerson S., Pavanello, Rita C. M., Zatz, Mayana, Gardham, Alice, Wakeling, Emma, Zechi-Ceide, Roseli M., Bertola, Debora, Passos-Bueno, Maria Rita
Publicado no Front Genet (2018)

Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers

Por Wyatt, Eugene J., Demonbreun, Alexis R., Kim, Ellis Y., Puckelwartz, Megan J., Vo, Andy H., Dellefave-Castillo, Lisa M., Gao, Quan Q., Vainzof, Mariz, Pavanello, Rita C. M., Zatz, Mayana, McNally, Elizabeth M.
Publicado no JCI Insight (2018)

Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy

Por Fernandes, Stephanie A., Almeida, Camila F., Souza, Lucas S., Lazar, Monize, Onofre-Oliveira, Paula, Yamamoto, Guilherme L., Nogueira, Letícia, Tasaki, Letícia Y., Cardoso, Rafaela R., Pavanello, Rita C. M., Silva, Helga C. A., Ferrari, Merari F. R., Bigot, Anne, Mouly, Vincent, Vainzof, Mariz
Publicado no Dis Model Mech (2020)

Development of a comprehensive noninvasive prenatal test

Por Malcher, Carolina, Yamamoto, Guilherme L., Burnham, Philip, Ezquina, Suzana A.M., Lourenço, Naila C.V., Balkassmi, Sahilla, Antonio, David S. Marco, Hsia, Gabriella S.P., Gollop, Thomaz, Pavanello, Rita C., Lopes, Marco Antonio, Bakker, Egbert, Zatz, Mayana, Bertola, Débora, Vlaminck, Iwijn De, Passos-Bueno, Maria Rita
Publicado no Genet Mol Biol (2018)