s-adenosylmethionine has been researched along with riboflavin in 22 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (9.09) | 18.7374 |
| 1990's | 1 (4.55) | 18.2507 |
| 2000's | 4 (18.18) | 29.6817 |
| 2010's | 13 (59.09) | 24.3611 |
| 2020's | 2 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Mitsuda, H; Nadamoto, T; Nakajima, K | 1 |
| Bell, IR; Berkes, S; Morrow, FD; Perrone, G; Read, M | 1 |
| Srinoot, P; Thithapandha, A | 1 |
| Graham, DE; White, RH; Xu, H | 1 |
| Alberto, JM; Audonnet-Blaise, S; Blaise, SA; Daval, JL; Guéant, JL | 1 |
| Bandarian, V | 1 |
| Begley, TP; Benjdia, A; Berteau, O; Decamps, L; Philmus, B; White, R | 1 |
| Cole, D; Cox, SE; da Costa, KA; Dominguez-Salas, P; Dyer, RA; Fulford, AJ; Hennig, BJ; Innis, SM; Moore, SE; Prentice, AM; Waterland, RA; Zeisel, SH | 1 |
| Gruber, K; Jankowitsch, F; Macheroux, P; Mack, M; Tongsook, C; Uhl, MK | 1 |
| Allen, KD; White, RH | 1 |
| Andersen, O; Andresen, BS; Beresford, MW; Cornelius, N; Dean, JC; Frerman, FE; Gregersen, N; Holme, E; Merinero, B; Miedzybrodzka, ZH; Morris, AA; Oldfors, A; Olpin, SE; Olsen, RK; Pourfarzam, M; Turnbull, DM | 1 |
| Berger, R; de Sain-van der Velden, MG; Dorland, L; Ruiter, JP; Spliet, WG; Testerink, N; van der Kolk, JH; Votion, DM; Wanders, RJ; Westermann, CM; Wijnberg, ID | 1 |
| Acquaviva-Bourdain, C; Brivet, M; Eymard, B; Jardel, C; Laforêt, P; Lombès, A; Maillart, E; Rigal, O; Vianey-Saban, C | 1 |
| Hogan, J; Holzman, T; Lampe, JW; Levy, L; May, DH; McIntosh, MW; Navarro, SL; Ogata, Y; Ruczinski, I; Schwarz, Y | 1 |
| Abrams, AJ; Al-Odaib, A; Antony, J; Baxter, PS; Brandner, S; Broomfield, A; Burns, J; Carpenter, K; Christodoulou, J; Clayton, P; Farrell, MO; Foley, AR; Forman, E; Gold, W; Gonzalez, MA; Hargreaves, I; Horvath, R; Houlden, H; Hughes, I; Jungbluth, H; King, MD; Land, JM; Lek, M; Lim, MJ; Lin, JP; Manzur, AY; Mathew, AA; Matsubara, K; McCullagh, BG; McGarvey, ML; Megarbane, A; Menezes, MP; Muntoni, F; Ng, J; O'Brien, K; O'Byrne, JJ; Olpin, S; Oppenheim, M; Ouvrier, RA; Pandraud, A; Phadke, R; Prasad, M; Rahman, S; Reilly, MM; Scherer, SS; Scoto, M; Shah, AH; Straub, V; Sugano, K; Urtizberea, JA; Wang, MX; Webster, R; Yonezawa, A; Züchner, S | 1 |
| Fukuda, T; Hiroki, M; Ishii, A; Shigematsu, Y; Shioya, A; Sugie, H; Takuma, H; Tamaoka, A; Yamaguchi, S | 1 |
| Kim, YJ; Ko, JM; Lee, KA; Song, J | 1 |
| Fukuda, S; Hasegawa, Y; Ito, M; Kobayashi, H; Taketani, T; Yamada, K; Yamaguchi, S | 1 |
| Künnapas, K; Lilleväli, H; Mosegaard, S; Muru, K; Nochi, Z; Olsen, RKJ; Õunap, K; Pajusalu, S; Reinson, K | 1 |
| Han, J; Ji, G; Lu, S; Song, X; Wu, H; Xie, Y | 1 |
| Chen, L; Cheng, L; Deepak, RNVK; Deng, H; Fan, H; Jiao, Y; Kee, K; Kuang, W; Lan, Z; Li, W; Liu, C; Liu, X; Luo, Q; Ma, Z; Meng, X; Meng, Z; Wang, W; Wang, X; Xu, L; Zhang, J; Zhao, X | 1 |
| Chen, D; Chen, Y; Fu, Q; Huang, C; Lin, Y; Peng, W; Zheng, W | 1 |
1 review(s) available for s-adenosylmethionine and riboflavin
| Article | Year |
|---|---|
Radical SAM enzymes involved in the biosynthesis of purine-based natural products.
Topics: Bacterial Proteins; Biocatalysis; Biological Products; Free Radicals; Iron-Sulfur Proteins; Nucleoside Q; Nucleosides; Oxidation-Reduction; Riboflavin; RNA, Transfer; S-Adenosylmethionine | 2012 |
1 trial(s) available for s-adenosylmethionine and riboflavin
| Article | Year |
|---|---|
Metabolomic profiling of urine: response to a randomised, controlled feeding study of select fruits and vegetables, and application to an observational study.
Topics: Adult; Biomarkers; Brassicaceae; Carnitine; Citrus; Cross-Sectional Studies; Diet; Diet Records; Fatty Acids; Feeding Behavior; Female; Fruit; Glycine max; Humans; Ions; Male; Metabolome; Metabolomics; Niacin; Nutrition Assessment; Phytochemicals; Proline; Riboflavin; Surveys and Questionnaires; Vegetables; Young Adult | 2013 |
20 other study(ies) available for s-adenosylmethionine and riboflavin
| Article | Year |
|---|---|
The relation between purine metabolism and flavinogenesis in Eremothecium ashbyii. The identification of S-adenosylmethionine and S-adenosylhomocysteine accumulated in non-growing cells of E. ashbyii.
Topics: Adenine; Ascomycota; Culture Media; Dose-Response Relationship, Drug; Homocysteine; Riboflavin; S-Adenosylhomocysteine; S-Adenosylmethionine; Saccharomycetales | 1977 |
Low thyroxine levels in female psychiatric inpatients with riboflavin deficiency: implications for folate-dependent methylation.
Topics: Adult; Female; Folic Acid; Folic Acid Deficiency; Hospitalization; Humans; Male; Mental Disorders; Middle Aged; Pyridoxine; Riboflavin; Riboflavin Deficiency; S-Adenosylmethionine; Thiamine; Thyroid Function Tests; Thyroxine; Vitamin B 12 | 1992 |
Comparative inhibitory effects of vitamins on methylating enzymes.
Topics: Animals; Ascorbic Acid; Carbon Isotopes; Catechol O-Methyltransferase Inhibitors; Cats; Dose-Response Relationship, Drug; Female; Histamine; In Vitro Techniques; Kidney; Kinetics; Magnesium; Male; Methyltransferases; Proteins; Pyridoxine; Rats; Riboflavin; S-Adenosylmethionine; Thiamine; Vitamin E; Vitamin K; Vitamins | 1972 |
Identification of the 7,8-didemethyl-8-hydroxy-5-deazariboflavin synthase required for coenzyme F(420) biosynthesis.
Topics: Actinobacteria; Amino Acid Sequence; Archaeal Proteins; Cloning, Molecular; Cyanobacteria; DNA, Archaeal; Evolution, Molecular; Methanococcus; Molecular Sequence Data; Mycobacterium smegmatis; Phylogeny; Protein Subunits; Recombinant Proteins; Riboflavin; Riboflavin Synthase; S-Adenosylmethionine; Sequence Alignment; Sequence Homology, Amino Acid | 2003 |
Influence of preconditioning-like hypoxia on the liver of developing methyl-deficient rats.
Topics: Animals; Animals, Newborn; Apoptosis; Cell Proliferation; Choline Deficiency; Cystathionine beta-Synthase; Female; Folic Acid; Folic Acid Deficiency; Food, Formulated; Glutathione; Homocysteine; Hypoxia; Liver; Nitric Oxide Synthase Type II; Pregnancy; Rats; Rats, Wistar; Riboflavin; Riboflavin Deficiency; S-Adenosylhomocysteine; S-Adenosylmethionine; Vitamin B 12; Vitamin B 12 Deficiency; Vitamin B Deficiency | 2007 |
Biosynthesis of F0, precursor of the F420 cofactor, requires a unique two radical-SAM domain enzyme and tyrosine as substrate.
Topics: Actinomycetales; Methanococcus; Nostoc; Protein Structure, Tertiary; Riboflavin; Riboflavin Synthase; S-Adenosylmethionine; Tyrosine | 2012 |
DNA methylation potential: dietary intake and blood concentrations of one-carbon metabolites and cofactors in rural African women.
Topics: Adolescent; Adult; Betaine; Biomarkers; Choline; Cysteine; Diet; Diet Records; Dietary Carbohydrates; Dietary Fats; Dietary Proteins; DNA Methylation; Feeding Behavior; Female; Folic Acid; Gambia; Homocysteine; Humans; Linear Models; Methionine; Middle Aged; Nutrition Assessment; Prospective Studies; Riboflavin; Rural Population; S-Adenosylhomocysteine; S-Adenosylmethionine; Sarcosine; Vitamin B 12; Vitamin B 6; Young Adult | 2013 |
Structural and kinetic studies on RosA, the enzyme catalysing the methylation of 8-demethyl-8-amino-d-riboflavin to the antibiotic roseoflavin.
Topics: Anti-Bacterial Agents; Binding Sites; Catalysis; Crystallography, X-Ray; Kinetics; Methylation; Methyltransferases; Models, Molecular; Protein Conformation; Riboflavin; S-Adenosylhomocysteine; S-Adenosylmethionine; Streptomyces | 2016 |
Identification of the Radical SAM Enzymes Involved in the Biosynthesis of Methanopterin and Coenzyme F
Topics: Alkyl and Aryl Transferases; Amino Acid Sequence; Archaeal Proteins; Cloning, Molecular; Enzyme Assays; Methanocaldococcus; Pterins; Recombinant Proteins; Riboflavin; S-Adenosylmethionine | 2018 |
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acids; Female; Humans; Iron-Sulfur Proteins; Male; Metabolism, Inborn Errors; Mitochondria, Muscle; Mitochondrial Myopathies; Muscle, Skeletal; Mutation; Oxidation-Reduction; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin | 2007 |
Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Animals; Butyric Acid; Butyryl-CoA Dehydrogenase; Carnitine; Chromatography, High Pressure Liquid; Female; Gas Chromatography-Mass Spectrometry; Glutarates; Horse Diseases; Horses; Isovaleryl-CoA Dehydrogenase; Lactic Acid; Male; Microscopy, Electron; Microscopy, Fluorescence; Muscles; Muscular Diseases; Riboflavin | 2008 |
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis].
Topics: Acyl-CoA Dehydrogenases; Adult; Biopsy; Brain Diseases, Metabolic; Carnitine; Coloring Agents; DNA Mutational Analysis; Electron Transport; Electron-Transferring Flavoproteins; Female; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Middle Aged; Muscle Weakness; Muscle, Skeletal; Riboflavin; Tandem Mass Spectrometry; Young Adult | 2010 |
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
Topics: Adolescent; Brain; Bulbar Palsy, Progressive; Carnitine; Child; Child, Preschool; Exome; Female; Genotype; Hearing Loss, Sensorineural; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Microarray Analysis; Motor Neuron Disease; Mutation; Neurologic Examination; Pedigree; Receptors, G-Protein-Coupled; Riboflavin; RNA; Sequence Analysis, DNA; Sural Nerve; Vitamins; Young Adult | 2014 |
Amelioration of acylcarnitine profile using bezafibrate and riboflavin in a case of adult-onset glutaric acidemia type 2 with novel mutations of the electron transfer flavoprotein dehydrogenase (ETFDH) gene.
Topics: Adult; Bezafibrate; Carnitine; Drug Therapy, Combination; Electron-Transferring Flavoproteins; Humans; Hypolipidemic Agents; Iron-Sulfur Proteins; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Mutation; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin; Treatment Outcome | 2014 |
Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases.
Topics: Asian People; Base Sequence; Carnitine; Dietary Supplements; DNA Mutational Analysis; Electron-Transferring Flavoproteins; Gene Deletion; Humans; Infant, Newborn; Iron-Sulfur Proteins; Male; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Oxidoreductases Acting on CH-NH Group Donors; Pedigree; Republic of Korea; Riboflavin; Tandem Mass Spectrometry | 2018 |
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report.
Topics: Acyl Coenzyme A; Carnitine; Child, Preschool; Codon, Nonsense; Electron-Transferring Flavoproteins; Flavin-Adenine Dinucleotide; Humans; Male; Membrane Transport Proteins; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Mutation; Receptors, G-Protein-Coupled; Riboflavin | 2019 |
FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening.
Topics: Carnitine; Female; Humans; Infant, Newborn; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Mutation; Nucleotidyltransferases; Riboflavin | 2019 |
Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study.
Topics: Adolescent; Adult; Carnitine; Child; China; Electron-Transferring Flavoproteins; Female; Humans; Hyperuricemia; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Male; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Muscular Dystrophies; Oxidoreductases Acting on CH-NH Group Donors; Quality of Life; Riboflavin; Young Adult | 2019 |
SLC22A14 is a mitochondrial riboflavin transporter required for sperm oxidative phosphorylation and male fertility.
Topics: Animals; Carnitine; Citric Acid Cycle; Diet; Fatty Acids; Female; Fertility; Fertilization in Vitro; Gene Expression; Humans; Infertility, Male; Male; Metabolome; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondria; Mitochondrial Membranes; Models, Molecular; Organic Cation Transport Proteins; Oxidative Phosphorylation; Riboflavin; Sperm Motility; Spermatozoa | 2021 |
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency.
Topics: Electron-Transferring Flavoproteins; Genetic Testing; Humans; Infant, Newborn; Iron-Sulfur Proteins; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Mutation; Neonatal Screening; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin | 2022 |