Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mayana Zatz"'
Autor:
Michel S, Naslavsky, Marilia O, Scliar, Guilherme L, Yamamoto, Jaqueline Yu Ting, Wang, Stepanka, Zverinova, Tatiana, Karp, Kelly, Nunes, José Ricardo Magliocco, Ceroni, Diego Lima, de Carvalho, Carlos Eduardo, da Silva Simões, Daniel, Bozoklian, Ricardo, Nonaka, Nayane, Dos Santos Brito Silva, Andreia, da Silva Souza, Heloísa, de Souza Andrade, Marília Rodrigues Silva, Passos, Camila Ferreira Bannwart, Castro, Celso T, Mendes-Junior, Rafael L V, Mercuri, Thiago L A, Miller, Jose Leonel, Buzzo, Fernanda O, Rego, Nathalia M, Araújo, Wagner C S, Magalhães, Regina Célia, Mingroni-Netto, Victor, Borda, Heinner, Guio, Carlos P, Rojas, Cesar, Sanchez, Omar, Caceres, Michael, Dean, Mauricio L, Barreto, Maria Fernanda, Lima-Costa, Bernardo L, Horta, Eduardo, Tarazona-Santos, Diogo, Meyer, Pedro A F, Galante, Victor, Guryev, Erick C, Castelli, Yeda A O, Duarte, Maria Rita, Passos-Bueno, Mayana, Zatz
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2022-04-29T08:46:40Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-12-01 National Institute of General Medical Sciences As whole-genome sequencing (WGS) becomes the gold standard tool for studying population genomi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::eee43a010a6ca6a55a0673ada3ebe2e0
https://hdl.handle.net/20.500.12866/11497
https://hdl.handle.net/20.500.12866/11497
Autor:
Mariz Vainzof, Juliana Gurgel Giannetti, Zilda Maria Alves Meira, Carlos H Rassi, Marly Conceição Silva, Carlos E. Rochitte, Roberto Kalil, Mayana Zatz
Publikováno v:
Journal of Cardiovascular Magnetic Resonance
Background Duchenne (DMD) and Becker (BMD) muscular dystrophies (MD) are allelic X-linked recessive disorders, caused by mutation of the dystrophin gene located at locus Xp21 that consists of 79 exons, characterized by progressive skeletal muscle deg
Autor:
Maria Angélica Miglino, Daniele dos Santos Martins, Osvaldo A. Sant'Anna, Carlos Eduardo Ambrósio, Adriana Caroprezo Morini, M. P Brolio, Natássia M. Vieira, Rosa Maria Cabral, Irina Kerkis, Carlos Magno da Costa Maranduba, Alexandre Kerkis, S. A. S. Fonseca, Thaís Peixoto Gaiad, Eder Zucconi, Mayana Zatz
Publikováno v:
Journal of Translational Medicine
Journal of Translational Medicine, Vol 6, Iss 1, p 35 (2008)
Journal of Translational Medicine, Vol 6, Iss 1, p 35 (2008)
Background The golden retriever muscular dystrophy (GRMD) dogs represent the best available animal model for therapeutic trials aiming at the future treatment of human Duchenne muscular dystrophy (DMD). We have obtained a rare litter of six GRMD dogs