Cargando…
Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMD
MicroRNAs (miRNAs) are short non-coding RNAs that modulate gene expression post-transcriptionally. Current evidence suggests that miR-21 plays a significant role in the progression of fibrosis in muscle diseases. Laminin-deficient congenital muscular dystrophy (LAMA2-CMD) is a severe form of congeni...
Autores principales: | Moreira Soares Oliveira, Bernardo, Durbeej, Madeleine, Holmberg, Johan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542641/ https://www.ncbi.nlm.nih.gov/pubmed/28771630 http://dx.doi.org/10.1371/journal.pone.0181950 |
Ejemplares similares
-
Exploratory Profiling of Urine MicroRNAs in the
dy(2J)/dy(2J) Mouse Model
of LAMA2-CMD: Relation to Disease Progression
por: Moreira Soares Oliveira, Bernardo, et al.
Publicado: (2018) -
A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD
por: Gawlik, Kinga I., et al.
Publicado: (2020) -
Bortezomib Does Not Reduce Muscular Dystrophy in the dy(2J)/dy(2J) Mouse Model of Laminin α2 Chain-Deficient Muscular Dystrophy
por: Körner, Zandra, et al.
Publicado: (2016) -
Antioxidants Reduce Muscular Dystrophy in the dy(2J)/dy(2J) Mouse Model of Laminin α2 Chain-Deficient Muscular Dystrophy
por: Harandi, Vahid M., et al.
Publicado: (2020) -
Gene Therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD) by Trans-Splicing
por: Azibani, Feriel, et al.
Publicado: (2015)