Probing the Role of Alzheimer’s Disease Risk Gene Using Human-Induced Pluripotent Stem Cells and Transgenic Animal Models
A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Neurobiology and Clinical Neuroscience".
Deadline for manuscript submissions: closed (31 December 2023) | Viewed by 2167
Special Issue Editor
Interests: cellular and molecular mechanisms of Alzheimer’s disease (AD) using human induced pluripotent stem cell models; how AD risk genes identified by genome-wide association studies contribute to the regulation of neuronal electrical activity and synaptic plasticity
Special Issue Information
Dear Colleagues,
Alzheimer’s disease (AD) is the leading cause of cognitive impairment and dementia worldwide. Despite the identification of numerous AD risk genes through genome-wide association studies in the last 10 years, a comprehensive understanding of AD pathogenesis remains elusive. Importantly, one out of three AD risk genes is predominantly expressed by a unique cell type of the adult human brain. Therefore, understanding the role of AD risk genes in the pathophysiology of AD requires the use of an appropriate model system allowing the manipulation of gene expression in a cell-type-specific fashion. Therefore, this Special Issue aims to publish original research and review articles focused on the study of AD risk genes using both hiPSC-derived cells and transgenic animal models, with a special emphasis on models harboring genetic modifications in specific cell types.
Dr. Marcos R. Costa
Guest Editor
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Keywords
- Alzheimer’s disease
- human induced pluripotent stem cells (hiPSCs)
- hiPSC-derived neurons (hiNs)
- hiPSC-derived astrocytes (hiAs)
- hiPSC-derived microglia (hiMGs)
- cerebral organoids
- amyloidopathy
- tauopathy
