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A natural non-Watson-Crick base pair in human mitochondrial tRNA<sup>Thr</sup> causes structural and functional susceptibility to local mutations.
- Published in:
- Nucleic Acids Research, 2018, v. 46, n. 9, p. 4662, doi. 10.1093/nar/gky243
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- Article
Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 523, doi. 10.1093/hmg/ddab257
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- Article
Selective degradation of tRNASer(AGY) is the primary driver for mitochondrial seryl-tRNA synthetase-related disease.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. 20, p. 11755, doi. 10.1093/nar/gkac1028
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- Article
Nitrosative stress inhibits aminoacylation and editing activities of mitochondrial threonyl-tRNA synthetase by S-nitrosation.
- Published in:
- Nucleic Acids Research, 2020, v. 48, n. 12, p. 6799, doi. 10.1093/nar/gkaa471
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- Article
The G3-U70-independent tRNA recognition by human mitochondrial alanyl-tRNA synthetase.
- Published in:
- Nucleic Acids Research, 2019, v. 47, n. 6, p. 3072, doi. 10.1093/nar/gkz078
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- Article