Mitochondrial respiratory chain and creatine kinase activities in mdx mouse brain (2010)
- Authors:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.1002/mus.21559
- Subjects: MITOCÔNDRIAS; ENERGIA (METABOLISMO)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Muscle & Nerve
- ISSN: 0148-639X
- Volume/Número/Paginação/Ano: v. 41, n. 2, p. 257-260, Feb. 2010
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
TUON, Lisiane; COMIM, Clarissa M; FRAGA, Daine B; et al. Mitochondrial respiratory chain and creatine kinase activities in mdx mouse brain. Muscle & Nerve, Hoboken, v. 41, n. 2, p. 257-260, 2010. Disponível em: < http://dx.doi.org/10.1002/mus.21559 > DOI: 10.1002/mus.21559. -
APA
Tuon, L., Comim, C. M., Fraga, D. B., Scaini, G., Rezin, G. T., Baptista, B. R., et al. (2010). Mitochondrial respiratory chain and creatine kinase activities in mdx mouse brain. Muscle & Nerve, 41( 2), 257-260. doi:10.1002/mus.21559 -
NLM
Tuon L, Comim CM, Fraga DB, Scaini G, Rezin GT, Baptista BR, Streck EL, Vainzof M, Quevedo J. Mitochondrial respiratory chain and creatine kinase activities in mdx mouse brain [Internet]. Muscle & Nerve. 2010 ; 41( 2): 257-260.Available from: http://dx.doi.org/10.1002/mus.21559 -
Vancouver
Tuon L, Comim CM, Fraga DB, Scaini G, Rezin GT, Baptista BR, Streck EL, Vainzof M, Quevedo J. Mitochondrial respiratory chain and creatine kinase activities in mdx mouse brain [Internet]. Muscle & Nerve. 2010 ; 41( 2): 257-260.Available from: http://dx.doi.org/10.1002/mus.21559 - Estudo da atividade de quatro enzimas em tecido muscular de heterozigotas certas e afetadas por distrofias musculares progressivas: correlação com achados histológicos
- 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
- Achados histológicos em biópsia muscular de eqüino com alterações neuromusculares
- The contribution of muscle protein analysis in the diagnosis of genetic myopathies and in the understanding of the organization and maintenance of muscle fiber integrity
- Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients
- Behavioral responses in animal model of congenital muscular dystrophy 1D
- The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes
- Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies
- Consensus statement on standard of care for congenital myopathies
- Effects of steroid hormones on myostatin expression and on genes of muscle regeneration pathway
Informações sobre o DOI: 10.1002/mus.21559 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
