Mice models deficient for two muscle proteins helping to understand protein complexes organization and function (2010)
- Autores:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- Assuntos: MODELOS ANIMAIS DE DOENÇAS; DOENÇAS NEUROMUSCULARES; PROTEÍNAS
- Idioma: Inglês
- Imprenta:
- Local: Ospedaletto
- Data de publicação: 2010
- Fonte:
- Título do periódico: Acta Myologica
- ISSN: 1128-2460
- Volume/Número/Paginação/Ano: v. 29, p. 262, res. S26.L4, 2010
- Nome do evento: International Congress on Neuromuscular Diseases (ICNMD)
-
ABNT
VAINZOF, Mariz et al. Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 29 mar. 2024. , 2010 -
APA
Vainzof, M., Martins-Machado, P. C. M., Onofre-Oliveira, P. C. G., Ayub-Guerrieri, D., Gotlieb, D., Fernandes, A., et al. (2010). Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. -
NLM
Vainzof M, Martins-Machado PCM, Onofre-Oliveira PCG, Ayub-Guerrieri D, Gotlieb D, Fernandes A, Lopes V, Yamamoto LU. Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. 2010 ; 29 262.[citado 2024 mar. 29 ] -
Vancouver
Vainzof M, Martins-Machado PCM, Onofre-Oliveira PCG, Ayub-Guerrieri D, Gotlieb D, Fernandes A, Lopes V, Yamamoto LU. Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. 2010 ; 29 262.[citado 2024 mar. 29 ] - Estudo das enzimas glutamato desidrogenase, isocitrato desidrogenase, 'beta'-glucuronidase e isoenzima MB da creatino quinase no soro sanguineo de afetados por distrofias musculares progressivas
- 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
- Triagem de mutações no gene CLCN1 em pacientes com Miotonia Congênita Hereditária
- Animal models for genetic neuromuscular diseases
- Clinical and molecular characterization of Mcardle’s disease in brazilian patients
- Expression analysis of x-dystroglycosyltransferases in distinct murine muscular dystrophies models
- Approach to the diagnosis of congenital myopathies
- Muscle phenotypic variability in limb girdle muscular dystrophy 2 G
- 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017
- Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas