Page last updated: 2024-08-17

uridine and MELAS

uridine has been researched along with MELAS in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Nagao, A; Suzuki, T1
Holt, IJ; Jacobs, HT; Kirino, Y; Marjavaara, SK; Suzuki, T; Watanabe, K; Yasukawa, T1
Ishii, N; Ohta, S; Suzuki, T; Ueda, T; Watanabe, K; Yasukawa, T1

Reviews

1 review(s) available for uridine and MELAS

ArticleYear
Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
    Annual review of genetics, 2011, Volume: 45

    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

Other Studies

2 other study(ies) available for uridine and MELAS

ArticleYear
Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
    Human molecular genetics, 2006, Mar-15, Volume: 15, Issue:6

    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.
    FEBS letters, 2000, Feb-11, Volume: 467, Issue:2-3

    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