» Articles » PMID: 37354903

Antisense Drugs for Rare and Ultra-rare Genetic Neurological Diseases

Overview
Journal Neuron
Publisher Cell Press
Specialty Neurology
Date 2023 Jun 24
PMID 37354903
Authors
Affiliations
Soon will be listed here.
Abstract

The regulatory approvals of nusinersen and tofersen, plus the large body of clinical and preclinical data from other drugs, have significantly de-risked antisense technology for neurological diseases. The platform learnings over the last 2 decades can be applied to subsequent drugs to improve the efficiency of discovering effective neuro-therapeutics.

Citing Articles

Molecular diagnostic approach to rare neurological diseases from a clinician viewpoint.

Lee J Genomics Inform. 2024; 22(1):18.

PMID: 39390516 PMC: 11468364. DOI: 10.1186/s44342-024-00025-0.


Antisense oligonucleotides and their applications in rare neurological diseases.

McDowall S, Aung-Htut M, Wilton S, Li D Front Neurosci. 2024; 18:1414658.

PMID: 39376536 PMC: 11456401. DOI: 10.3389/fnins.2024.1414658.


Therapeutic targeting of RNA for neurological and neuromuscular disease.

Bubenik J, Scotti M, Swanson M Genes Dev. 2024; 38(15-16):698-717.

PMID: 39142832 PMC: 11444190. DOI: 10.1101/gad.351612.124.


Ube3a unsilencer for the potential treatment of Angelman syndrome.

Vihma H, Li K, Welton-Arndt A, Smith A, Bettadapur K, Gilmore R Nat Commun. 2024; 15(1):5558.

PMID: 38977672 PMC: 11231141. DOI: 10.1038/s41467-024-49788-8.


Targeting RNA opens therapeutic avenues for Timothy syndrome.

Velasco S Nature. 2024; 628(8009):730-732.

PMID: 38600188 DOI: 10.1038/d41586-024-00911-1.