Cargando…
AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice
Mutations of the human desmin (DES) gene cause autosomal dominant and recessive myopathies affecting skeletal and cardiac muscle tissue. Desmin knockout mice (DES-KO), which develop progressive myopathy and cardiomyopathy, mirror rare human recessive desminopathies in which mutations on both DES all...
Autores principales: | Heckmann, M B, Bauer, R, Jungmann, A, Winter, L, Rapti, K, Strucksberg, K-H, Clemen, C S, Li, Z, Schröder, R, Katus, H A, Müller, O J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976287/ https://www.ncbi.nlm.nih.gov/pubmed/27101257 http://dx.doi.org/10.1038/gt.2016.40 |
Ejemplares similares
-
AAV-mediated cardiac gene transfer of wild-type desmin in mouse models for recessive desminopathies
por: Ruppert, T., et al.
Publicado: (2020) -
Pregnancy in Desmin-Related Cardiomyopathy
por: Faksh, Arij, et al.
Publicado: (2015) -
The toxic effect of R350P mutant desmin in striated muscle of man and mouse
por: Clemen, Christoph S., et al.
Publicado: (2014) -
Desmin Knock-Out Cardiomyopathy: A Heart on the Verge of Metabolic Crisis
por: Elsnicova, Barbara, et al.
Publicado: (2022) -
Myocardial fibrosis in desmin-related hypertrophic cardiomyopathy
por: He, Yi, et al.
Publicado: (2010)