Cargando…
Phenotypes induced by NM causing α-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes
BACKGROUND: Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with α-skeletal muscle actin mutations. We previously showed that actin mutations can cause four different biochemical phenotypes and that ex...
Autores principales: | Vandamme, Drieke, Lambert, Ellen, Waterschoot, Davy, Tondeleir, Davina, Vandekerckhove, Joël, Machesky, Laura M, Constantin, Bruno, Rommelaere, Heidi, Ampe, Christophe |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657152/ https://www.ncbi.nlm.nih.gov/pubmed/19284548 http://dx.doi.org/10.1186/1756-0500-2-40 |
Ejemplares similares
-
A method for rapidly screening functionality of actin mutants and tagged actins
por: Rommelaere, Heidi, et al.
Publicado: (2004) -
Phenotypes of Myopathy-related Actin Mutants in differentiated C2C12 Myotubes
por: Bathe, Friederike S, et al.
Publicado: (2007) -
Beta-Actin Is Required for Proper Mouse Neural Crest Ontogeny
por: Tondeleir, Davina, et al.
Publicado: (2014) -
Identification and expression analysis of splice variants of mouse enabled homologue during development and in adult tissues
por: Veniere, Sylvie, et al.
Publicado: (2010) -
Beta-Actin Is Involved in Modulating Erythropoiesis during Development by Fine-Tuning Gata2 Expression Levels
por: Tondeleir, Davina, et al.
Publicado: (2013)