NAD+ biosynthesis ameliorates a zebrafish model of muscular dystrophy.
Muscular dystrophies are common, currently incurable diseases. A subset of dystrophies result from genetic disruptions in complexes that attach muscle fibers to their surrounding extracellular matrix microenvironment. Cell-matrix adhesions are exquisite sensors of physiological conditions and mediat...
Guardado en:
Autores principales: | Michelle F Goody, Meghan W Kelly, Christine J Reynolds, Andre Khalil, Bryan D Crawford, Clarissa A Henry |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2012
|
Materias: | |
Acceso en línea: | https://doaj.org/article/a7b034ea753c49c2a647df6f4d468327 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Targeting a therapeutic LIF transgene to muscle via the immune system ameliorates muscular dystrophy
por: Steven S. Welc, et al.
Publicado: (2019) -
MiR-199-3p enhances muscle regeneration and ameliorates aged muscle and muscular dystrophy
por: Masashi Fukuoka, et al.
Publicado: (2021) -
Evaluation of muscular changes by ultrasound Nakagami imaging in Duchenne muscular dystrophy
por: Wen-Chin Weng, et al.
Publicado: (2017) -
Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
por: Niclas E. Bengtsson, et al.
Publicado: (2017) -
PABPN1 gene therapy for oculopharyngeal muscular dystrophy
por: A. Malerba, et al.
Publicado: (2017)