uridine has been researched along with MELAS in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Nagao, A; Suzuki, T | 1 |
Holt, IJ; Jacobs, HT; Kirino, Y; Marjavaara, SK; Suzuki, T; Watanabe, K; Yasukawa, T | 1 |
Ishii, N; Ohta, S; Suzuki, T; Ueda, T; Watanabe, K; Yasukawa, T | 1 |
1 review(s) available for uridine and MELAS
Article | Year |
---|---|
Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
Topics: Amino Acyl-tRNA Synthetases; Aminoacylation; Animals; Humans; Mammals; MELAS Syndrome; Mitochondria; Mitochondrial Diseases; Mutation; Oxidative Phosphorylation; Protein Conformation; RNA; RNA Processing, Post-Transcriptional; RNA, Mitochondrial; RNA, Transfer; Thiouridine; Transcription, Genetic; Uridine | 2011 |
2 other study(ies) available for uridine and MELAS
Article | Year |
---|---|
Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
Topics: Adenosine; Anticodon; Base Sequence; Cell Line, Tumor; Guanosine; Humans; MELAS Syndrome; Molecular Sequence Data; Nucleic Acid Conformation; Point Mutation; RNA; RNA, Mitochondrial; RNA, Transfer, Leu; Suppression, Genetic; Uridine | 2006 |
Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.
Topics: Anticodon; Cell Line; HeLa Cells; Humans; MELAS Syndrome; MERRF Syndrome; Mitochondria; Mitochondrial Myopathies; Mutation; Point Mutation; RNA, Transfer, Leu; RNA, Transfer, Lys; Uridine | 2000 |