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

Como Citar

Vainzof, M., Kossugue, P. M., Ayub, D., Onofre, P. C., Zilberztajn, D. D., Sell, K., Yamamoto, L. U., Martins, P. C., Maia, L. S., Zatz, M., Silva, H. C., Miglino, M. A., Ambrosio, C. E., & Neto, J. X. (2006). Modelos animais para doenças neuromusculares humanas. Revista Neurociências, 14, 48–51. https://doi.org/10.34024/rnc.2006.v14.8770

Edição

v. 14 (2006): V SIMPÓSIO BRASILEIRO DE DNM/ELA - I SIMPÓSIO VERDE VIDA SAÚDE

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Artigos Originais
Recebido: 2019-02-28
Publicado: 2006-10-31

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