The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells (Q41963195)

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scientific article published on 10 January 2014

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English	The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells	scientific article published on 10 January 2014

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scholarly article

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Europe PubMed Central

PMC publication ID

14 October 2017

The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells (English)

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Europe PubMed Central

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14 October 2017

2

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31 May 2020

Arianna Montanari

4

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31 May 2020

Antonio F Campese

5

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31 May 2020

7

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31 May 2020

8

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31 May 2020

Patrizio Di Micco

11

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31 May 2020

14

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31 May 2020

Silvia Francisci

15

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31 May 2020

16

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31 May 2020

Robert William Taylor

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Robert W Taylor

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31 May 2020

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Elena Perli

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31 May 2020

Annalinda Pisano

3

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31 May 2020

Aurelio Reyes

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31 May 2020

Helen A Tuppen

9

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31 May 2020

Maurizia Orlandi

10

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31 May 2020

Elena Poser

12

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31 May 2020

Laura Frontali

17

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31 May 2020

Giulia d'Amati

19

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31 May 2020

Massimo Zeviani

18

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31 May 2020

publication date

10 January 2014

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14 October 2017

EMBO Molecular Medicine

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31 May 2020

6

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31 May 2020

2

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31 May 2020

169-182

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Peptides from aminoacyl-tRNA synthetases can cure the defects due to mutations in mt tRNA genes

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Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes

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Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene

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The role of aminoacyl-tRNA synthetases in genetic diseases

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Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation

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https://pubmed.ncbi.nlm.nih.gov/24413190

12 December 2020

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10.1002/EMMM.201303198

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31 May 2020

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24 November 2022

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31 May 2020

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31 May 2020

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