Cargando…
Analysis of non-human primate models for evaluating prion disease therapeutic efficacy
Prion disease is a fatal neurodegenerative disease caused by the conformational corruption of the prion protein (PrP), encoded by the prion protein gene (PRNP). While no disease-modifying therapy is currently available, genetic and pharmacological proofs of concept support development of therapies t...
Autores principales: | Mortberg, Meredith A., Minikel, Eric Vallabh, Vallabh, Sonia M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436048/ https://www.ncbi.nlm.nih.gov/pubmed/35994510 http://dx.doi.org/10.1371/journal.ppat.1010728 |
Ejemplares similares
-
Disease stages and therapeutic hypotheses in two decades of neurodegenerative disease clinical trials
por: Mortberg, Meredith A., et al.
Publicado: (2022) -
Therapeutic Trial of anle138b in Mouse Models of Genetic Prion Disease
por: Vallabh, Sonia M., et al.
Publicado: (2023) -
Characterization of the Prion Protein Binding Properties of Antisense Oligonucleotides
por: Reidenbach, Andrew G., et al.
Publicado: (2019) -
A single-cell map of antisense oligonucleotide activity in the brain
por: Mortberg, Meredith A, et al.
Publicado: (2023) -
A single-cell map of antisense oligonucleotide activity in the brain
por: Mortberg, Meredith A, et al.
Publicado: (2023)