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Samantha Powers
Samantha Powers
Scientist II, Forge Biologics
在 forgebiologics.com 的电子邮件经过验证
标题
引用次数
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Directly converted astrocytes retain the ageing features of the donor fibroblasts and elucidate the astrocytic contribution to human CNS health and disease
N Gatto, C Dos Santos Souza, AC Shaw, SM Bell, MA Myszczynska, ...
Aging Cell 20 (1), e13281, 2021
472021
Editor's highlight: embryonic exposure to the environmental neurotoxin BMAA negatively impacts early neuronal development and progression of neurodegeneration in the sod1-g93r …
S Powers, S Kwok, E Lovejoy, T Lavin, RB Sher
Toxicological Sciences 157 (1), 129-140, 2017
282017
Rett syndrome gene therapy improves survival and ameliorates behavioral phenotypes in MeCP2 null (S51. 002)
S Powers, C Miranda, C Dennys-Rivers, A Huffenberger, L Braun, ...
Neurology 92 (15_supplement), S51. 002, 2019
82019
Novel MECP2 gene therapy is effective in a multicenter study using two mouse models of Rett syndrome and is safe in non-human primates
S Powers, S Likhite, KK Gadalla, CJ Miranda, AJ Huffenberger, C Dennys, ...
Molecular Therapy 31 (9), 2767-2782, 2023
62023
Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategy
SS Ray, D Dutta, C Dennys, S Powers, F Roussel, P Lisowski, P Glažar, ...
Cell Reports 41 (10), 2022
52022
In vitro modeling as a tool for testing therapeutics for spinal muscular atrophy and IGHMBP2-related disorders
JA Sierra-Delgado, S Sinha-Ray, A Kaleem, M Ganjibakhsh, M Parvate, ...
Biology 12 (6), 867, 2023
42023
Rett syndrome gene therapy improves survival and ameliorates behavioral phenotypes in MeCP2 null
S Powers, C Miranda, C Dennys-Rivers, A Huffenberger, L Braun, ...
Oral presentation, 2019
32019
Environmental and Genetic Interactions in a Zebrafish Model of Amyotrophic Lateral Sclerosis
S Powers
12015
MeCP2 gene therapy ameliorates disease phenotype in mouse model for Pitt Hopkins syndrome
CN Dennys, SAD Vermudez, RJM Deacon, JA Sierra-Delgado, K Rich, ...
Neurotherapeutics, e00376, 2024
2024
A Novel Gene Therapy for Rett Syndrome through Reactivation of the Silent X Chromosome
S Powers, S Lou, S Nardini, S Likhite, J Delgado, A Sierra, M Baird, ...
MOLECULAR THERAPY 30 (4), 395-395, 2022
2022
Advancing Treatment and Understanding of Rett Syndrome
SL Powers
The Ohio State University, 2020
2020
Efficacy and Safety in Mice and Non-Hman Primates of CSF Delivered AVXS-201 for the Treatment of Rett Syndrome
K Foust, G Thomsen, M Fugere, L Braun, K Nguyen, S Solano, E Lang, ...
MOLECULAR THERAPY 27 (4), 188-188, 2019
2019
A Novel In Vitro Modeling System for the Study of MeCP2 Pathology and Treatment Response
SL Powers, K Kinley, R Rodrigo, X Zhang, S Likhite, C Dennys-Rivers, ...
MOLECULAR THERAPY 27 (4), 264-264, 2019
2019
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