Cargando…
The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors
The mdx mouse is a good genetic and molecular murine model for Duchenne Muscular Dystrophy (DMD), a progressive and devastating muscle disease. However, this model is inappropriate for testing new therapies due to its mild phenotype. Here, we transferred the mdx mutation to the 129/Sv strain with th...
Autores principales: | Calyjur, Priscila Clara, Almeida, Camila de Freitas, Ayub-Guerrieri, Danielle, Ribeiro, Antonio Fernando, Fernandes, Stephanie de Alcântara, Ishiba, Renata, dos Santos, Andre Luis Fernandes, Onofre-Oliveira, Paula, Vainzof, Mariz |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783004/ https://www.ncbi.nlm.nih.gov/pubmed/26954670 http://dx.doi.org/10.1371/journal.pone.0150748 |
Ejemplares similares
-
Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies
por: Ribeiro, Antonio F., et al.
Publicado: (2019) -
Dmd(mdx)/Large(myd): a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies
por: Martins, Poliana C. M., et al.
Publicado: (2013) -
Apolipoprotein A-IV-Deficient Mice in 129/SvJ Background Are Susceptible to Obesity and Glucose Intolerance
por: Wang, Fei, et al.
Publicado: (2023) -
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, Large(myd) and mdx/Large(myd)
por: Martins-Bach, Aurea B., et al.
Publicado: (2015) -
Characterization of Sv129 Mice as a Susceptible Model to Leishmania amazonensis
por: dos-Santos, Júlio Souza, et al.
Publicado: (2019)