RNA-Targeting CRISPR/CasRx system relieves disease symptoms in Huntington’s disease models
Abstract Background HD is a devastating neurodegenerative disorder caused by the expansion of CAG repeats in the HTT. Silencing the expression of mutated proteins is a therapeutic direction to rescue HD patients, and recent advances in gene editing technology such as CRISPR/CasRx have opened up new...
Saved in:
Main Authors: | Yingqi Lin, Caijuan Li, Yizhi Chen, Jiale Gao, Jiawei Li, Chunhui Huang, Zhaoming Liu, Wei Wang, Xiao Zheng, Xichen Song, Jianhao Wu, Jiaxi Wu, Oscar Junhong Luo, Zhuchi Tu, Shihua Li, Xiao-Jiang Li, Liangxue Lai, Sen Yan |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2025-01-01
|
Series: | Molecular Neurodegeneration |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13024-024-00794-w |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Application of antisense oligonucleotide drugs in amyotrophic lateral sclerosis and Huntington’s disease
by: Kaili Ou, et al.
Published: (2025-01-01) -
Huntington’s disease modeling on HEK293 cell line
by: D. V. Sharipova, et al.
Published: (2017-12-01) -
Psychological discomfort in carriers and non-carriers of the Huntington disease mutation and its relationship with disease burden
by: Y. Rodríguez-Agudelo, et al.
Published: (2025-01-01) -
Optical Coherence Tomography in Huntington's Disease—A Potential Future Biomarker for Neurodegeneration?
by: Clancy Cerejo, et al.
Published: (2025-01-01) -
Advances in Stem Cell Therapy for Huntington’s Disease: A Comprehensive Literature Review
by: Siddharth Shah, et al.
Published: (2025-01-01)