Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds

Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are autosomal dominant neuromuscular diseases caused by microsatellite expansions and belong to the family of RNA-dominant disorders. Availability of cellular models in which the DM mutation is expressed within its natural context is essential to faci...

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Sparad:
Bibliografiska uppgifter
I publikationen:Dis Model Mech
Huvudupphovsmän: Arandel, Ludovic, Polay Espinoza, Micaela, Matloka, Magdalena, Bazinet, Audrey, De Dea Diniz, Damily, Naouar, Naïra, Rau, Frédérique, Jollet, Arnaud, Edom-Vovard, Frédérique, Mamchaoui, Kamel, Tarnopolsky, Mark, Puymirat, Jack, Battail, Christophe, Boland, Anne, Deleuze, Jean-Francois, Mouly, Vincent, Klein, Arnaud F., Furling, Denis
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Company of Biologists Ltd 2017
Ämnen:
Resource Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5399563/
https://ncbi.nlm.nih.gov/pubmed/28188264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.027367
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