Homozygous mice with mutant protein FUS[1-359] overexpression: Innovative possibilities for ALS treatment
Introduction: This study investigates a mouse model with overexpression of the mutant FUS[1-359] protein, which can be used to evaluate the effectiveness of gene therapy and other pharmacological interventions for amyotrophic lateral sclerosis (ALS). The model enhances the deeper understanding of th...
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| Main Author: | |
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| Format: | Article |
| Language: | English |
| Published: |
Belgorod National Research University
2024-12-01
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| Series: | Research Results in Pharmacology |
| Subjects: | |
| Online Access: | https://rrpharmacology.ru/index.php/journal/article/view/554 |
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