serine has been researched along with Encephalomyopathies, Mitochondrial in 4 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wang, Y | 1 |
| Zhou, XL | 1 |
| Ruan, ZR | 1 |
| Liu, RJ | 1 |
| Eriani, G | 1 |
| Wang, ED | 1 |
| Pulkes, T | 1 |
| Liolitsa, D | 1 |
| Eunson, LH | 1 |
| Rose, M | 1 |
| Nelson, IP | 1 |
| Rahman, S | 1 |
| Poulton, J | 1 |
| Marchington, DR | 1 |
| Landon, DN | 1 |
| Debono, AG | 1 |
| Morgan-Hughes, JA | 1 |
| Hanna, MG | 1 |
| Horváth, R | 1 |
| Schoser, BG | 1 |
| Müller-Höcker, J | 1 |
| Völpel, M | 1 |
| Jaksch, M | 1 |
| Lochmüller, H | 1 |
| Fernandez-Moreira, D | 1 |
| Ugalde, C | 1 |
| Smeets, R | 1 |
| Rodenburg, RJ | 1 |
| Lopez-Laso, E | 1 |
| Ruiz-Falco, ML | 1 |
| Briones, P | 1 |
| Martin, MA | 1 |
| Smeitink, JA | 1 |
| Arenas, J | 1 |
4 other studies available for serine and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
A Human Disease-causing Point Mutation in Mitochondrial Threonyl-tRNA Synthetase Induces Both Structural and Functional Defects.
Topics: Adenosine Monophosphate; Alternative Splicing; Amino Acid Sequence; Enzyme Activation; Enzyme Stabil | 2016 |
New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.
Topics: Adolescent; Adult; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex IV; Elect | 2005 |
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy.
Topics: Adult; DNA Mutational Analysis; Electron Transport Complex IV; Glutamic Acid; Humans; Immunohistoche | 2005 |
X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.
Topics: Animals; Arginine; DNA Mutational Analysis; Electron Transport Complex I; Electrophoresis, Gel, Two- | 2007 |