Page last updated: 2024-08-17

uridine and MELAS Syndrome

uridine has been researched along with MELAS Syndrome in 3 studies

Research

Studies (3)

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

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

Reviews

1 review(s) available for uridine and MELAS Syndrome

Article	Year
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

Article

Year

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 Syndrome

Article	Year
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

Article

Year

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