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

nork 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
Argitaratua 2009

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

nork 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
Argitaratua izan da Front Genet (2018)

Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers

nork 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.
Argitaratua izan da JCI Insight (2018)

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

nork 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
Argitaratua izan da Dis Model Mech (2020)

Development of a comprehensive noninvasive prenatal test

nork 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
Argitaratua izan da Genet Mol Biol (2018)