Peripheral neuropathy via mutant tRNA synthetases: Inhibition of protein translation provides a possible explanation-Reference-Cited by-同舟云学术

Peripheral neuropathy via mutant tRNA synthetases: Inhibition of protein translation provides a possible explanation

Published:2016-06-28 Issue:9 Volume:38 Page:818-829
ISSN:0265-9247
Container-title:BioEssays
language:en
Short-container-title:BioEssays

Author:

Storkebaum Erik¹²

Affiliation:

1. Molecular Neurogenetics LaboratoryMax Planck Institute for Molecular BiomedicineMünsterGermany

2. Faculty of MedicineUniversity of MünsterMünsterGermany

Funder

Max Planck Society

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bies.201600052

Reference108 articles.

1. AMINOACYL tRNA SYNTHETASES: GENERAL SCHEME OF STRUCTURE-FUNCTION RELATIONSHIPS IN THE POLYPEPTIDES AND RECOGNITION OF TRANSFER RNAS

2. Aminoacyl-tRNA Synthesis

3. Processivity of translation in the eukaryote cell: Role of aminoacyl-tRNA synthetases

4. One of two genes encoding glycyl‐tRNA synthetase in Saccharomyces cerevisiae provides mitochondrial and cytoplasmic functions;Turner RJ;J Biol Chem,2000

5. Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. tRNA Dysregulation in Neurodevelopmental and Neurodegenerative Diseases;Annual Review of Cell and Developmental Biology;2023-10-16

2. Lost in local translation: TDP-43 and FUS in axonal/neuromuscular junction maintenance and dysregulation in amyotrophic lateral sclerosis;Neuron;2023-05

3. Messenger RNA Translation Defects in Neurodegenerative Diseases;New England Journal of Medicine;2023-03-16

4. Heterozygous Seryl‐tRNA Synthetase 1 Variants Cause Charcot–Marie–Tooth Disease;Annals of Neurology;2022-09-28

5. Clinical characteristics and proteome modifications in two Charcot-Marie-Tooth families with the AARS1 Arg326Trp mutation;BMC Neurology;2022-08-15