CRISPR/Cas9-mediated CysLT1R deletion reverses synaptic failure, amyloidosis and cognitive impairment in APP/PS1 mice-Reference-Cited by-同舟云学术

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CRISPR/Cas9-mediated CysLT1R deletion reverses synaptic failure, amyloidosis and cognitive impairment in APP/PS1 mice

Published:2021-02-11 Issue:5 Volume:13 Page:6634-6661
ISSN:1945-4589
Container-title:Aging
language:en
Short-container-title:Aging

Author:

Chen Fang¹²,Fang Shunchang¹,Du Yifeng³,Ghosh Arijit¹,Reed Miranda N.³,Long Yan¹,Suppiramaniam Vishnu³,Tang Susu¹,Hong Hao¹

Affiliation:

1. Department of Pharmacology, China Pharmaceutical University, Nanjing, China

2. Department of Pharmacy, The First Affiliated Hospital of Xiamen University, Xiamen, China

3. Department of Drug Discovery and Development, School of Pharmacy, Auburn University, Auburn, AL 36849, USA

Publisher

Impact Journals, LLC

Subject

Cell Biology,Ageing

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1. In vivo and ex vivo gene therapy for neurodegenerative diseases: a promise for disease modification;Naunyn-Schmiedeberg's Archives of Pharmacology;2024-05-22

2. Nanotechnology-based delivery for CRISPR-Cas 9 cargo in Alzheimer's disease;Alzheimer's Disease and Advanced Drug Delivery Strategies;2024

3. Simvastatin ameliorates synaptic plasticity impairment in chronic mild stress-induced depressed mice by modulating hippocampal NMDA receptor;Psychopharmacology;2023-09-16

4. CRISPR-Cas9 in Alzheimer’s disease: Therapeutic trends, modalities, and challenges;Drug Discovery Today;2023-08

5. Vector enabled CRISPR gene editing – A revolutionary strategy for targeting the diversity of brain pathologies;Coordination Chemistry Reviews;2023-07

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