isomethyleugenol has been researched along with Mitochondrial Diseases in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Falkous, G; Freyer, C; Gorman, GS; Guha, N; Hopton, S; Lam, A; Lewis, D; Moedas, MF; Moore, D; Poulton, J; Pyle, A; Schober, FA; Sergeant, K; Smith, C; Tang, JX; Taylor, RW; Wredenberg, A; Zierz, CM | 1 |
| Fierke, CA; Karasik, A; Koutmos, M; Wilhelm, CA | 1 |
| Janga, SC; Kadumuri, RV | 1 |
| den Hollander, B; Kankuri, E; Korpi, ER; Mervaala, E; Ojanperä, I; Pelander, A; Siltanen, A; Sundström, M | 1 |
| Blanco, S; Dietmann, S; Durbin, R; Frye, M; Hoffmann, GF; Hussain, S; Kolb-Kokocinski, A; Kotzaeridou, U; Kremer, L; Lantaff, R; Mayr, JA; Memari, Y; Minczuk, M; Pearce, SF; Powell, CA; Prokisch, H; Rorbach, J; Sauer, S; Van Haute, L | 1 |
| Spence, SJ; Zecavati, N | 1 |
| Cambi, F; Haziza, S; Hershkovitz, E; Houtz, R; Magen, S; Magnani, R; Parvari, R | 1 |
2 review(s) available for isomethyleugenol and Mitochondrial Diseases
| Article | Year |
|---|---|
Epitranscriptomic Code and Its Alterations in Human Disease.
Topics: Cardiovascular Diseases; Congenital Abnormalities; Epigenesis, Genetic; High-Throughput Nucleotide Sequencing; Humans; Metabolic Diseases; Methylation; Mitochondrial Diseases; Neoplasms; Nervous System Diseases; Purine Nucleotides; Pyrimidine Nucleotides; RNA; RNA Processing, Post-Transcriptional; Transcriptome | 2018 |
Neurometabolic disorders and dysfunction in autism spectrum disorders.
Topics: Autistic Disorder; Brain Diseases, Metabolic; Humans; Methylation; Mitochondrial Diseases; Oxidation-Reduction; Phenotype | 2009 |
5 other study(ies) available for isomethyleugenol and Mitochondrial Diseases
| Article | Year |
|---|---|
Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease.
Topics: Animals; Methylation; Mice; Mitochondria; Mitochondrial Diseases; S-Adenosylhomocysteine; S-Adenosylmethionine | 2022 |
Disease-associated mutations in mitochondrial precursor tRNAs affect binding, m1R9 methylation, and tRNA processing by mtRNase P.
Topics: Base Pairing; Base Sequence; Humans; Methylation; Methyltransferases; Mitochondria; Mitochondrial Diseases; Mutation; RNA Folding; RNA Precursors; RNA Processing, Post-Transcriptional; RNA, Mitochondrial; RNA, Transfer | 2021 |
Mitochondrial respiratory dysfunction due to the conversion of substituted cathinones to methylbenzamides in SH-SY5Y cells.
Topics: Alkaloids; Benzamides; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Humans; Methylation; Mitochondria; Mitochondrial Diseases; Neurons | 2015 |
Deficient methylation and formylation of mt-tRNA(Met) wobble cytosine in a patient carrying mutations in NSUN3.
Topics: Gene Expression Regulation; HEK293 Cells; HeLa Cells; Humans; Methylation; Methyltransferases; Mitochondria; Mitochondrial Diseases; Mutation; RNA, Transfer | 2016 |
Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence.
Topics: Amino Acid Sequence; Animals; Base Sequence; Benzoquinones; Calmodulin; Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 21; Craniofacial Abnormalities; Cystinuria; Green Fluorescent Proteins; HSP90 Heat-Shock Proteins; Humans; Intellectual Disability; Lactams, Macrocyclic; Methylation; Methyltransferases; Mice; Mice, Inbred ICR; Mitochondrial Diseases; Molecular Sequence Data; Muscle Hypotonia; Protein Binding; Protein Stability; Protein Structure, Tertiary; Protein Transport; Proteolysis; Recombinant Fusion Proteins; Subcellular Fractions; Transcription, Genetic | 2012 |