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

di 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
Pubblicazione 2009

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

di 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
Pubblicato in Front Genet (2018)

Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers

di 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.
Pubblicato in JCI Insight (2018)

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

di 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
Pubblicato in Dis Model Mech (2020)

Development of a comprehensive noninvasive prenatal test

di 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
Pubblicato in Genet Mol Biol (2018)