Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sara M. Lopes"'
Autor:
Rui Jorge Nobre, Diana D. Lobo, Carina Henriques, Sonia P. Duarte, Sara M. Lopes, Ana C. Silva, Miguel M. Lopes, Fanny Mariet, Lukas K. Schwarz, M.S. Baatje, Valerie Ferreira, Astrid Vallès, Luis Pereira de Almeida, Melvin M. Evers, Lodewijk J.A. Toonen
Publikováno v:
Nucleic Acid Therapeutics. 32:194-205
Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder caused by the expansion of a CAG repeat in the
Autor:
Miguel M. Lopes, Jacques Paysan, José Rino, Sara M. Lopes, Luís Pereira de Almeida, Luísa Cortes, Rui Jorge Nobre
Publikováno v:
Gene therapy. 29(12)
© The Author(s), under exclusive licence to Springer Nature Limited 2022
Recombinant adeno-associated virus (rAAV) has become one of the most promising gene delivery systems for both in vitro and in vivo applications. However, a key challenge i
Recombinant adeno-associated virus (rAAV) has become one of the most promising gene delivery systems for both in vitro and in vivo applications. However, a key challenge i
Autor:
Sara M, Lopes, Rosário, Faro, Miguel M, Lopes, Isabel, Onofre, Nuno, Mendonça, Joana, Ribeiro, Cristina, Januário, Rui Jorge, Nobre, Luís, Pereira de Almeida
Publikováno v:
The Journal of molecular diagnostics : JMD. 22(6)
Polyglutamine spinocerebellar ataxias (SCAs) constitute a group of autosomal dominantly inherited neurodegenerative disorders with considerable phenotypic overlap. Definitive diagnoses rely on the detection of a mutation in each associated locus, com