Identification of a Peptide for Systemic Brain Delivery of a Morpholino Oligonucleotide in Mouse Models of Spinal Muscular Atrophy
Splice-switching antisense oligonucleotides are emerging treatments for neuromuscular diseases, with several splice-switching oligonucleotides (SSOs) currently undergoing clinical trials such as for Duchenne muscular dystrophy (DMD) and spinal muscular atrophy (SMA). However, the development of syst...
Hoofdauteurs: | Shabanpoor, F, Hammond, S, Abendroth, F, Hazell, G, Wood, M, Gait, M |
---|---|
Formaat: | Journal article |
Taal: | English |
Gepubliceerd in: |
Mary Ann Liebert
2017
|
Gelijkaardige items
-
Evaluation of cell-penetrating peptide delivery of antisense oligonucleotides for therapeutic efficacy in spinal muscular atrophy
door: Hammond, S, et al.
Gepubliceerd in: (2019) -
Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy
door: Hammond, S, et al.
Gepubliceerd in: (2016) -
Antibody-oligonucleotide conjugate achieves CNS delivery in animal models for spinal muscular atrophy
door: Suzan M. Hammond, et al.
Gepubliceerd in: (2022-12-01) -
Heteroduplex oligonucleotide technology boosts oligonucleotide splice switching activity of morpholino oligomers in a Duchenne muscular dystrophy mouse model
door: Juri Hasegawa, et al.
Gepubliceerd in: (2024-09-01) -
NOVEL CELL PENETRATING PEPTIDES FOR SKELETAL AND CARDIAC MUSCLE DELIVERY OF PMO ANTISENSE OLIGONUCLEOTIDES FOR THE TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY
door: Hammond, S, et al.
Gepubliceerd in: (2011)