Modelos animais para doenças neuromusculares humanas

Autores

  • Mariz Vainzof Centro de Estudos do Genoma Humano, IBUSP
  • Patrícia M Kossugue Centro de Estudos do Genoma Humano, IBUSP
  • Danielle Ayub Centro de Estudos do Genoma Humano, IBUSP
  • Paula CG Onofre Centro de Estudos do Genoma Humano, IBUSP
  • Dinorah Dinorah Zilberztajn Centro de Estudos do Genoma Humano, IBUSP
  • Karen Sell Centro de Estudos do Genoma Humano, IBUSP
  • Lydia U Yamamoto Centro de Estudos do Genoma Humano, IBUSP
  • Poliana CM Martins Centro de Estudos do Genoma Humano, IBUSP
  • Lucas S Maia 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
  • Maria A Miglino FMVZ, USP
  • Carlos E Ambrosio FMVZ, USP
  • José Xavier Neto Incor, FMUSP

DOI:

https://doi.org/10.34024/rnc.2006.v14.8770

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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, Protasi F, Allen PD, Franzini Armstrong C, 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, Valentine BA, Hoffman EP, Kunkel LM, et al. The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs. Nature 1988; 334: 154-156.

Drachman DB, Frank K, Dykes-Hoberg M, Teismann P, Almer G, Przedborski S, et al. Cyclooxygenase 2 inhibition protects motor neurons and prolongs survival in a transgenic mouse model of ALS. Ann. Neurol 2002; 52: 771 778.

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

Gussoni E, Soneoka Y, Strickland CD, Buzney EA, Khan MK, Flint AF, 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.

Wong PC, Pardo CA, Borchelt DR, Lee MK, Copeland NG, Jenkins NA, et al. An adverse property of familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 1995; 14:1105-1116.

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Publicado

2006-10-31

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1.
Vainzof M, Kossugue PM, Ayub D, Onofre PC, Zilberztajn DD, Sell K, et al. Modelos animais para doenças neuromusculares humanas. Rev Neurocienc [Internet]. 31º de outubro de 2006 [citado 14º de dezembro de 2025];14:48-51. Disponível em: https://periodicos.unifesp.br/index.php/neurociencias/article/view/8770