Cargando…
Cell-type-specific dysregulation of RNA alternative splicing in short tandem repeat mouse knockin models of myotonic dystrophy
Short tandem repeats (STRs) are prone to expansion mutations that cause multiple hereditary neurological and neuromuscular diseases. To study pathomechanisms using mouse models that recapitulate the tissue specificity and developmental timing of an STR expansion gene, we used rolling circle amplific...
Autores principales: | Nutter, Curtis A., Bubenik, Jodi L., Oliveira, Ruan, Ivankovic, Franjo, Sznajder, Łukasz J., Kidd, Benjamin M., Pinto, Belinda S., Otero, Brittney A., Carter, Helmut A., Vitriol, Eric A., Wang, Eric T., Swanson, Maurice S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942047/ https://www.ncbi.nlm.nih.gov/pubmed/31624084 http://dx.doi.org/10.1101/gad.328963.119 |
Ejemplares similares
-
Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy
por: Sznajder, Łukasz J., et al.
Publicado: (2019) -
Autistic traits in myotonic dystrophy type 1 due to MBNL inhibition and RNA mis-splicing
por: Sznajder, Lukasz, et al.
Publicado: (2023) -
Transcriptome alterations in myotonic dystrophy frontal cortex
por: Otero, Brittney A., et al.
Publicado: (2021) -
HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy
por: Li, Moyi, et al.
Publicado: (2020) -
Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1
por: Voellenkle, Christine, et al.
Publicado: (2019)