isomethyleugenol has been researched along with Brain Diseases in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (30.00) | 18.7374 |
| 1990's | 3 (30.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kožich, V; Stabler, S | 1 |
| Hara, A; Imakita, N; Ito, T; Kasahara, K; Kitabatake, M; Matsukawa, A; Mikasa, K; Morita-Takemura, S; Ouji-Sageshima, N; Wanaka, A | 1 |
| Doi, H; Hosoya, T; Koyama, H; Onoe, H; Suzuki, M; Watanabe, Y; Zhang, Z | 1 |
| Boespflug-Tanguy, O; Fogli, A; Merle, C; Roussel, V; Schiffmann, R; Theisen, M; Ughetto, S | 1 |
| Franke, L; Uebelhack, R; Zschenderlein, R | 1 |
| Bottiglieri, T; Hyland, K; Reynolds, EH | 1 |
| Surtees, R | 1 |
| Bottiglieri, T; Charles, HC; Gray, L; Hyland, K; Jaeken, J; Kahler, SG; Lazeyras, F; Van Hove, JL; Zeisel, SH | 1 |
| Chanarin, I; Deacon, R; Green, R; Lumb, M; Perry, J; Purkiss, P | 1 |
3 review(s) available for isomethyleugenol and Brain Diseases
| Article | Year |
|---|---|
Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
Topics: Amino Acids, Sulfur; Animals; Brain Diseases; Cysteine; Glutathione; Homocysteine; Homocystinuria; Humans; Hydrogen Sulfide; Liver; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Methylation; S-Adenosylmethionine; Sulfites; Sulfur; Sulfur Compounds | 2020 |
The clinical potential of ademetionine (S-adenosylmethionine) in neurological disorders.
Topics: AIDS Dementia Complex; Animals; Brain Diseases; Dementia; Disease Models, Animal; Epilepsy; Humans; Metabolism, Inborn Errors; Methotrexate; Methylation; Multiple Sclerosis; Neurotransmitter Agents; Parkinson Disease; Receptors, Neurotransmitter; S-Adenosylmethionine; Spinal Cord Diseases | 1994 |
Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brain.
Topics: Brain Diseases; Demyelinating Diseases; Humans; Metabolism, Inborn Errors; Methylation; Nerve Degeneration; Spinal Cord Diseases; Vitamin B 12; Vitamin B 12 Deficiency | 1993 |
7 other study(ies) available for isomethyleugenol and Brain Diseases
| Article | Year |
|---|---|
Abrogated Caveolin-1 expression via histone modification enzyme Setdb2 regulates brain edema in a mouse model of influenza-associated encephalopathy.
Topics: Animals; Blood-Brain Barrier; Brain Diseases; Brain Edema; Caveolin 1; Cytokines; Disease Models, Animal; Histone-Lysine N-Methyltransferase; Interferon Type I; Lipopolysaccharides; Methylation; Mice; Orthomyxoviridae; Orthomyxoviridae Infections | 2019 |
Pd0-mediated rapid cross-coupling reactions, the rapid C-[11C]methylations, revolutionarily advancing the syntheses of short-lived PET molecular probes.
Topics: Brain Diseases; Carbon Radioisotopes; Catalysis; Humans; Hydrocarbons, Iodinated; Isotope Labeling; Methylation; Molecular Probes; Palladium; Positron-Emission Tomography; Radiopharmaceuticals | 2014 |
CSF N-glycan profiles to investigate biomarkers in brain developmental disorders: application to leukodystrophies related to eIF2B mutations.
Topics: Biomarkers; Brain Diseases; Calibration; Cerebrospinal Fluid; Child, Preschool; Developmental Disabilities; Eukaryotic Initiation Factor-2B; Female; Glycosylation; Hereditary Central Nervous System Demyelinating Diseases; Humans; Infant; Male; Methylation; Mutation; Polysaccharides; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 2012 |
The methyl-folate trap and the supply of S-adenosylomethionine.
Topics: Brain; Brain Diseases; Folic Acid; Methionine; Methylation; S-Adenosylmethionine; Vitamin B 12 Deficiency | 1981 |
[Determination of arteriovenous differences of methylated indoleamines in brain stem lesions].
Topics: 5-Methoxytryptamine; Adult; Brain Diseases; Brain Stem; Female; Humans; Intracranial Embolism and Thrombosis; Male; Methoxydimethyltryptamines; Methylation; Middle Aged; N,N-Dimethyltryptamine; Pons; Tryptamines; Vertebrobasilar Insufficiency | 1983 |
One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levels.
Topics: Amino Acid Metabolism, Inborn Errors; Benzoic Acid; Brain Diseases; Choline; Coma; Female; Glycine; Homocysteine; Humans; Infant; Infant, Newborn; Male; Methionine; Methylation; Phosphatidylcholines; S-Adenosylmethionine; Seizures; Serine; Tetrahydrofolates | 1998 |
Vitamin B12 neuropathy is not due to failure to methylate myelin basic protein.
Topics: Animals; Arginine; Brain Diseases; Chiroptera; Cycloleucine; Disease Models, Animal; Liver; Methylation; Myelin Basic Protein; Rats; Rats, Inbred Strains; Vitamin B 12; Vitamin B 12 Deficiency | 1986 |