Modelos animais ajudando a decifrar doenças neuromusculares humanas

Autores

  • Mariz Vainzof Centro de Estudos do Genoma Humano, IBUSP
  • Lydia U Yamamoto Centro de Estudos do Genoma Humano, IBUSP
  • Patrícia M Kossugue Centro de Estudos do Genoma Humano, IBUSP
  • Luciana LQ Fogaça Centro de Estudos do Genoma Humano, IBUSP
  • Fernando Z Velloso Centro de Estudos do Genoma Humano, IBUSP
  • Danielle Ayub Centro de Estudos do Genoma Humano, IBUSP
  • Viviane P Muniz Centro de Estudos do Genoma Humano, IBUSP
  • Mayana Zatz Centro de Estudos do Genoma Humano, IBUSP
  • Helga CA Silva Centro de Estudos do Genoma Humano, IBUSP
  • Silvia MG Massironi ICB, USP
  • Maria Angélica Miglino FMVZ, USP
  • Carlos Eduardo Ambrosio FMVZ, USP
  • Ligia G Miyazato FCAV-UNESP, Jaboticabal
  • Julieta RE Moraes FCAV-UNESP, Jaboticabal
  • Fernando HF D’Angeles FCAV-UNESP, Jaboticabal
  • Joaquim C Lacerda Neto FCAV-UNESP, Jaboticabal
  • Ana Carolina Mortari FMVZ e FM-UNESP, Botucatu, SP
  • Alexandre S Borges FMVZ e FM-UNESP, Botucatu, SP
  • Luiz Antonio L Rezende FMVZ e FM-UNESP, Botucatu, SP
  • Sheila C Rahal FMVZ e FM-UNESP, Botucatu, SP

DOI:

https://doi.org/10.34024/rnc.2005.v13.8800

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Referências

Allamand V, Campbell KP. Animal models for muscular dystrophy: valuable tools for the development of therapies. Human Mol Genet 2000; 9: 2459-2467.

Barone V, Bertocchini F, Bottinelli R, et al. Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors. FEBS Lett 1998;422:160-164.

Cooper BJ, Winand NJ, Stedman H, et al. The homologue of the Duchenne locus is defective in Xlinked muscular dystrophy of dogs. Nature 1988; 334: 154-156.

Fujii J, Otsu K, Zorzato F, et al. Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia. Science 1991; 253: 448-451.

Gussoni E, Yko S, Strickland CD, et al. Dystrophin expression in the mdx mouse restored by stem cell transplantation. Nature 1999; 401: 390-394.

Pastoret C, Sebille A. Mdx mice show progressive weakness and muscle deterioration with age. J Neurol Sci 1995; 129: 97-105.

Vainzof M, Yamamoto LU, Gouveia TLF, Zatz M. The contribution of protein analysis in the diagnosis of neuromuscular diseases. In: Burgess VN, Trends in Muscular Dystrophy Research. USA: Nova Publisher, 2005.

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Publicado

2005-09-30

Como Citar

1.
Vainzof M, Yamamoto LU, Kossugue PM, Fogaça LL, Velloso FZ, Ayub D, et al. Modelos animais ajudando a decifrar doenças neuromusculares humanas. Rev Neurocienc [Internet]. 30º de setembro de 2005 [citado 16º de julho de 2025];13:18-20. Disponível em: https://periodicos.unifesp.br/index.php/neurociencias/article/view/8800