Slow Intrathecal Injection of rAAVrh10 Enhances its Transduction of Spinal Cord and Therapeutic Efficacy in a Mutant SOD1 Model of ALS
Year: 2017
Type: article
Source: Neuroscience
Language: German
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Funders: Hebei Provincial Department of Human Resources and Social Security, Natural Science Foundation of Hebei Province, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Allergy and Infectious Diseases, National Institute of Neurological Disorders and Stroke
Awards: New Approaches to Gene Therapy for Alpha-1 Antitrypsin Deficiency, A new approach to modeling ALS based on TBK1 mutation in mice, G4826372969, A Gene therapeutic approach to stable suppression of HIV-1 replication, An in vivo approach to understanding mutant PFN1 toxicity on motor neurons, Oligodendrocyte-focused rAAV gene therapy strategies for Canavan disease and Leukodystrophies
OpenAlex ID: W2761044458
