Compounds > adenosine
Page last updated: 2024-08-24

adenosine and MELAS Syndrome

adenosine has been researched along with MELAS Syndrome in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chiang, MF; Shih, BF; Thajeb, P; Tzen, CY; Wu, MC; Yuan, RY1
Holt, IJ; Jacobs, HT; Kirino, Y; Marjavaara, SK; Suzuki, T; Watanabe, K; Yasukawa, T1
Booker, JK; Civalier, C; Fan, H; Farber, RA; Gulley, ML; Prior, TW1
Hol, FA; Janssen, AJ; Lucke, B; Morava, E; Rodenburg, RJ; Schuelke, M; Sengers, RC; Siers, MH; Smeitink, JA; Smits, BW; Ter Laak, H; Trijbels, FJ; van den Heuvel, LP; van der Knaap, MS; van Engelen, BG; Van Spronsen, FJ; Wintjes, LT1
Akiba, Y; Enomoto, H; Fujiuchi, S; Kikuchi, K; Nakano, H; Ohsaki, Y; Osanai, S; Satoh, N; Takahashi, T; Yahara, O1

Other Studies

5 other study(ies) available for adenosine and MELAS Syndrome

ArticleYear
Brain single photon emission computed tomography in patients with A3243G mutation in mitochondrial DNA tRNA.
    Annals of the New York Academy of Sciences, 2005, Volume: 1042

    Topics: Adenosine; Adolescent; Adult; Brain; DNA, Mitochondrial; Humans; Male; MELAS Syndrome; Migraine Disorders; Mutation; RNA, Transfer; Tomography, Emission-Computed, Single-Photon

2005
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
Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase ch
    The Journal of molecular diagnostics : JMD, 2006, Volume: 8, Issue:2

    Topics: Adenosine; Base Sequence; DNA, Mitochondrial; Guanosine; Humans; MELAS Syndrome; MERRF Syndrome; Mutation; Polymerase Chain Reaction; RNA, Transfer, Leu; RNA, Transfer, Lys; Time Factors; Transition Temperature

2006
Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
    Annals of neurology, 2008, Volume: 63, Issue:4

    Topics: Adenosine; Adolescent; Adult; Child; Child, Preschool; DNA, Mitochondrial; Electron Transport; Energy Metabolism; Female; Guanine; Humans; Infant; Male; MELAS Syndrome; Middle Aged; Mitochondria, Muscle; Muscle, Skeletal; Mutation

2008
Hypoxic ventilatory depression in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Respirology (Carlton, Vic.), 2001, Volume: 6, Issue:2

    Topics: Adenosine; Adult; Humans; Hypoventilation; Hypoxia; Male; MELAS Syndrome; Theophylline; Vital Capacity

2001