Charcot Marie Tooth disease-associated mutant tRNA synthetases linked to altered dimer interface and neurite distribution defect
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference15 articles.
1. Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V
2. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations
3. Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutation
4. An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model
5. Functional Analyses of Glycyl-tRNA Synthetase Mutations Suggest a Key Role for tRNA-Charging Enzymes in Peripheral Axons
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3. An Adapted GeneSwitch Toolkit for Comparable Cellular and Animal Models: A Proof of Concept in Modeling Charcot-Marie-Tooth Neuropathy;International Journal of Molecular Sciences;2023-11-09
4. tRNA Dysregulation in Neurodevelopmental and Neurodegenerative Diseases;Annual Review of Cell and Developmental Biology;2023-10-16
5. Aminoacyl‐tRNA synthetase – a molecular multitasker;The FASEB Journal;2023-09-30
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