Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies (2013)
- Authors:
- USP affiliated authors: TANNUS, ALBERTO - IFSC ; VAINZOF, MARIZ - IB
- Unidades: IFSC; IB
- DOI: 10.1242/dmm.011700
- Subjects: DOENÇAS NEUROMUSCULARES; RATOS (EXPERIMENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Disease Models and Mechanisms
- ISSN: 1754-8403
- Volume/Número/Paginação/Ano: v. 6, n. 5, p. 1167-1174, Sept. 2013
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MARTINS, Poliana C. M. et al. Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies. Disease Models and Mechanisms, v. 6, n. 5, p. 1167-1174, 2013Tradução . . Disponível em: https://doi.org/10.1242/dmm.011700. Acesso em: 25 fev. 2026. -
APA
Martins, P. C. M., Ayub-Guerrieri, D., Bach, A. B. M., Oliveira, P. O., Malheiros, J. M., Tannús, A., et al. (2013). Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies. Disease Models and Mechanisms, 6( 5), 1167-1174. doi:10.1242/dmm.011700 -
NLM
Martins PCM, Ayub-Guerrieri D, Bach ABM, Oliveira PO, Malheiros JM, Tannús A, Sousa PL, Carlier PG, Vainzof M. Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies [Internet]. Disease Models and Mechanisms. 2013 ; 6( 5): 1167-1174.[citado 2026 fev. 25 ] Available from: https://doi.org/10.1242/dmm.011700 -
Vancouver
Martins PCM, Ayub-Guerrieri D, Bach ABM, Oliveira PO, Malheiros JM, Tannús A, Sousa PL, Carlier PG, Vainzof M. Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies [Internet]. Disease Models and Mechanisms. 2013 ; 6( 5): 1167-1174.[citado 2026 fev. 25 ] Available from: https://doi.org/10.1242/dmm.011700 - NMR imaging comparison of dystrophic mouse models: mdx, Large, mdx/Large
- Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy: mdx, largemyd and mdx/largemyd
- Therapeutic potential of murine mesenchymal stem cells (MSC) from adipose tissue in the treatment of muscular dystrophy in the new double mutant mouse model for the genes Dystrophin and Large
- Estudo das enzimas glutamato desidrogenase, isocitrato desidrogenase, 'beta'-glucuronidase e isoenzima MB da creatino quinase no soro sanguineo de afetados por distrofias musculares progressivas
- Osteopontin expression during chronic and acute muscle injury
- Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model
- Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophies
- Myogenic differentiation of ES cells for therapies in neuromuscular diseases: progress to date
- Striatum brain-derived neurotrophic factor levels are decreased in dystrophin-deficient mice
- Mitochondrial alterations in dynamin 2-related centronuclear myopathy
Informações sobre o DOI: 10.1242/dmm.011700 (Fonte: oaDOI API)
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