Cargando…
Myoblasts generated by lentiviral mediated MyoD transduction of myotonic dystrophy type 1 (DM1) fibroblasts can be used for assays of therapeutic molecules
BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common muscle dystrophy in adults. The disease is caused by a triplet expansion in the 3'end of the myotonic dystrophy protein kinase (DMPK) gene. In order to develop a human cell model for investigation of possible effects of antisense an...
Autores principales: | Larsen, Jan, Pettersson, Olof J, Jakobsen, Maria, Thomsen, Rune, Pedersen, Christina B, Hertz, Jens M, Gregersen, Niels, Corydon, Thomas J, Jensen, Thomas G |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226528/ https://www.ncbi.nlm.nih.gov/pubmed/22078098 http://dx.doi.org/10.1186/1756-0500-4-490 |
Ejemplares similares
-
MyoD, myogenin independent differentiation of primordial myoblasts in mouse somites
Publicado: (1992) -
Loss of MyoD Promotes Fate Transdifferentiation of Myoblasts Into Brown Adipocytes
por: Wang, Chao, et al.
Publicado: (2017) -
Experimental Studies on the Differentiation of Fibroblasts into Myoblasts induced by MyoD Genes in vitro
por: Liu, Zhongmin, et al.
Publicado: (2008) -
Epicatechin elicits MyoD-dependent myoblast differentiation and myogenic conversion of fibroblasts
por: Lee, Sang-Jin, et al.
Publicado: (2017) -
FOXP1 Interacts with MyoD to Repress its Transcription and Myoblast
Conversion
por: Wright, Woodring E., et al.
Publicado: (2021)