Cargando…
Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development
Myotonic dystrophy type 1 (DM1) is caused by an unstable expanded CTG repeat located within the DMPK gene 3’UTR. The nature, severity and age at onset of DM1 symptoms are very variable in patients. Different forms of the disease are described, among which the congenital form (CDM) is the most severe...
Autores principales: | Michel, Lise, Huguet-Lachon, Aline, Gourdon, Geneviève |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560382/ https://www.ncbi.nlm.nih.gov/pubmed/26339785 http://dx.doi.org/10.1371/journal.pone.0137620 |
Ejemplares similares
-
Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 Mice
por: Lo Scrudato, Mirella, et al.
Publicado: (2019) -
DM1 Transgenic Mice Exhibit Abnormal Neurotransmitter Homeostasis and Synaptic Plasticity in Association with RNA Foci and Mis-Splicing in the Hippocampus
por: Potier, Brigitte, et al.
Publicado: (2022) -
Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice
por: Jauvin, Dominic, et al.
Publicado: (2017) -
Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus
por: Brouwer, Judith Rixt, et al.
Publicado: (2013) -
DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1
por: Légaré, Cécilia, et al.
Publicado: (2019)