thymine has been researched along with MELAS in 3 studies
Excerpt | Relevance | Reference |
---|---|---|
"The majority of patients with MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) have an A-->G mutation at nucleotide 3243 in mitochondrial transfer (t)RNA." | 1.30 | Clinical, physiological, and histological features in a kindred with the T3271C melas mutation. ( Applegarth, D; Maguire, J; Myint, T; Robinson, BH; Tarnopolsky, MA, 1998) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Park, H | 1 |
Davidson, E | 1 |
King, MP | 1 |
Tarnopolsky, MA | 1 |
Maguire, J | 1 |
Myint, T | 1 |
Applegarth, D | 1 |
Robinson, BH | 1 |
Gill-Randall, R | 1 |
Sherratt, EJ | 1 |
Thomas, AW | 1 |
Gagg, JW | 1 |
Lee, A | 1 |
Alcolado, JC | 1 |
3 other studies available for thymine and MELAS
Article | Year |
---|---|
The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation.
Topics: Acylation; Adenine; Base Sequence; Cell Line; Cytosine; Guanine; Humans; Leucine-tRNA Ligase; MELAS | 2003 |
Clinical, physiological, and histological features in a kindred with the T3271C melas mutation.
Topics: Adenine; Adult; Biopsy, Needle; Child, Preschool; Cytosine; DNA; DNA, Mitochondrial; Female; Forearm | 1998 |
Analysis of a polycytosine tract and heteroplasmic length variation in the mitochondrial DNA D-loop of patients with diabetes, MELAS syndrome and race-matched controls.
Topics: Adult; Cytosine; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Genetic Variation; Humans; Leukocyte | 2001 |