NMR imaging comparison of dystrophic mouse models: mdx, Large, mdx/Large (2013)
- Authors:
- USP affiliated authors: TANNUS, ALBERTO - IFSC ; VAINZOF, MARIZ - IB
- Unidades: IFSC; IB
- DOI: 10.1016/j.nmd.2013.06.402
- Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR; DISTROFIA MUSCULAR; MODELOS ANIMAIS DE DOENÇAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 23, n. 9/10, p. 747, abstr. P.1.18, Oct. 2013
- Conference titles: International World Muscle Society Congress
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
BACH, A. B. Martins et al. NMR imaging comparison of dystrophic mouse models: mdx, Large, mdx/Large. Neuromuscular Disorders. London: Elsevier. Disponível em: https://doi.org/10.1016/j.nmd.2013.06.402. Acesso em: 20 abr. 2024. , 2013 -
APA
Bach, A. B. M., Malheiros, J., Machado, P. C. M., Almeida, C. F., Matot, B., Sousa, P. L., et al. (2013). NMR imaging comparison of dystrophic mouse models: mdx, Large, mdx/Large. Neuromuscular Disorders. London: Elsevier. doi:10.1016/j.nmd.2013.06.402 -
NLM
Bach ABM, Malheiros J, Machado PCM, Almeida CF, Matot B, Sousa PL, Tannus A, Carlier PG, Vainzof M. NMR imaging comparison of dystrophic mouse models: mdx, Large, mdx/Large [Internet]. Neuromuscular Disorders. 2013 ; 23( 9/10): 747.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1016/j.nmd.2013.06.402 -
Vancouver
Bach ABM, Malheiros J, Machado PCM, Almeida CF, Matot B, Sousa PL, Tannus A, Carlier PG, Vainzof M. NMR imaging comparison of dystrophic mouse models: mdx, Large, mdx/Large [Internet]. Neuromuscular Disorders. 2013 ; 23( 9/10): 747.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1016/j.nmd.2013.06.402 - Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies
- 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
- Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta]
- Reduction of acethylcolinesterase activity in the brain of mdx mice
- Motor Chip: A comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders
- 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
- Osteopontin expression during chronic and acute muscle injury
Informações sobre o DOI: 10.1016/j.nmd.2013.06.402 (Fonte: oaDOI API)
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