The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes (2011)
- Authors:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.1016/j.nmd.2011.06.875
- Subjects: DOENÇAS NEUROMUSCULARES; MODELOS ANIMAIS DE DOENÇAS; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 21, n. 9-10, p. 676, res. P2.53, Oct. 2011
- Conference titles: International Congress of the World Muscle Society
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
LANZOTTI, A. A et al. The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.875. Acesso em: 19 abr. 2024. , 2011 -
APA
Lanzotti, A. A., Onofre-Oliveira, P. C. G., Martins-Machado, P. C. M., Martins-Bach, A. B., Feitosa, L. S., & Vainzof, M. (2011). The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.875 -
NLM
Lanzotti AA, Onofre-Oliveira PCG, Martins-Machado PCM, Martins-Bach AB, Feitosa LS, Vainzof M. The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 676.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.875 -
Vancouver
Lanzotti AA, Onofre-Oliveira PCG, Martins-Machado PCM, Martins-Bach AB, Feitosa LS, Vainzof M. The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 676.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.875 - 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
- Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model
- Myostatin expression in different mice models for neuromuscular disorders
Informações sobre o DOI: 10.1016/j.nmd.2011.06.875 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
