期刊
ADVANCED DRUG DELIVERY REVIEWS
卷 191, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.addr.2022.114562
关键词
Neurodevelopmental Disorders; Gene mutation; Genetic engineered animal models; Gene therapy; Functional reversal; Pharmacological targets; Non-human primate models; Gene editing; CRISPR/Cas9; AAV-mediated gene delivery; Translatability
资金
- CIHR/CRC program
- Canada Foundation for Innovation [38264]
- Montreal Neurological Institute-Hospital
- McGill University's Healthy Brains, Healthy Lives (Canada First Research Excellence Fund)
- Azrieli Center for Autism Research (ACAR)
- Azrieli Foundation
- NSERC [RGPIN-2020-04872, DGECR-2020-00030]
- SickKids Foundation [NI22-1106]
- 2021 NARSAD Young Investigator Grant from the Brain & Behavior Research Foundation
- National Research Training Platform in Neurodevelopmental Disorders through Transforming Autism Care Consortium
This article reviews the progress in the diagnosis, etiology discovery, modeling, and mechanistic understanding of neurodevelopmental disorders (NDDs) from both fundamental and clinical research. It introduces breakthroughs in the reversal studies of NDDs using genetically engineered models and discusses the application and challenges of cutting-edge technologies in NDDs therapeutic development.
Neurodevelopmental Disorders (NDDs) encompass a broad spectrum of conditions resulting from atypical brain development. Over the past decades, we have had the fortune to witness enormous progress in diagnosis, etiology discovery, modeling, and mechanistic understanding of NDDs from both fundamental and clinical research. Here, we review recent neurobiological advances from experimental models of NDDs. We introduce several examples and highlight breakthroughs in reversal studies of phenotypes using genetically engineered models of NDDs. The in-depth understanding of brain pathophysiology underlying NDDs and evaluations of reversibility in animal models paves the foundation for discovering novel treatment options. We discuss how the expanding property of cutting-edge technologies, such as gene editing and AAV-mediated gene delivery, are leveraged in animal models for the therapeutic development of NDDs. We envision opportunities and challenges toward faithful modeling and fruitful clinical translation. (c) 2022 Elsevier B.V. All rights reserved.
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