asparagine has been researched along with Mitochondrial Myopathies 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 | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Blakely, E; Gardner, JL; He, L; Hudson, G; Hughes, I; Taylor, RW; Turnbull, DM; Walter, J | 1 |
| Eriksson, S; Saada, A; Wang, L | 1 |
| De Meirleir, L; De Paepe, B; Lagae, L; Lissens, W; Meulemans, A; Seneca, S; Smet, J; Van Coster, R | 1 |
3 other study(ies) available for asparagine and Mitochondrial Myopathies
| Article | Year |
|---|---|
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathy.
Topics: Asparagine; DNA Mutational Analysis; DNA, Mitochondrial; Family Health; Female; Glutamine; Humans; Infant; Male; Mitochondrial Myopathies; Multienzyme Complexes; Muscle, Skeletal; Mutation; Serine; Thymidine Kinase | 2008 |
Kinetic properties of mutant human thymidine kinase 2 suggest a mechanism for mitochondrial DNA depletion myopathy.
Topics: Adenosine Triphosphate; Amino Acid Sequence; Asparagine; Binding, Competitive; Chromatography, Gel; Cloning, Molecular; DNA Mutational Analysis; DNA, Complementary; DNA, Mitochondrial; Electrophoresis, Polyacrylamide Gel; Histidine; Humans; Isoleucine; Kinetics; Mitochondrial Myopathies; Models, Biological; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Plasmids; Point Mutation; Sequence Homology, Amino Acid; Thymidine Kinase | 2003 |
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure.
Topics: Adolescent; Asparagine; Base Sequence; Cells, Cultured; DNA, Mitochondrial; Humans; Male; Mitochondrial Myopathies; Molecular Sequence Data; Multiple Organ Failure; Point Mutation; RNA, Transfer, Asn | 2006 |