Cargando…
Antisense Oligonucleotides Reduce RNA Foci in Spinocerebellar Ataxia 36 Patient iPSCs
Spinocerebellar ataxia type 36 is a late-onset, slowly progressive cerebellar syndrome with motor neuron degeneration that is caused by expansions of a hexanucleotide repeat (GGCCTG) in the noncoding region of NOP56 gene, with a histopathological feature of RNA foci formation in postmortem tissues....
Autores principales: | Matsuzono, Kosuke, Imamura, Keiko, Murakami, Nagahisa, Tsukita, Kayoko, Yamamoto, Takuya, Izumi, Yuishin, Kaji, Ryuji, Ohta, Yasuyuki, Yamashita, Toru, Abe, Koji, Inoue, Haruhisa |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504081/ https://www.ncbi.nlm.nih.gov/pubmed/28918022 http://dx.doi.org/10.1016/j.omtn.2017.06.017 |
Ejemplares similares
-
Proteasome impairment in neural cells derived from HMSN-P patient iPSCs
por: Murakami, Nagahisa, et al.
Publicado: (2017) -
Antisense oligonucleotide therapy for spinocerebellar ataxia type 2
por: Scoles, Daniel R., et al.
Publicado: (2017) -
Antisense Oligonucleotide-Mediated Removal of the Polyglutamine Repeat in Spinocerebellar Ataxia Type 3 Mice
por: Toonen, Lodewijk J.A., et al.
Publicado: (2017) -
Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
por: Chuang, Ching-Yu, et al.
Publicado: (2019) -
Modeling Alexander disease with patient iPSCs reveals cellular and molecular pathology of astrocytes
por: Kondo, Takayuki, et al.
Publicado: (2016)