methionine has been researched along with cobamamide in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (40.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 2 (40.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Garovic-Kocic, V; Rosenblatt, DS | 1 |
Blackmore, JA; Laurence, AS; Parry, TE; Roberts, B | 1 |
Bishop, AJ; Cooper, BA; Haworth, JC; Rosenblatt, DS; Schroeder, ML; Schuh, S; Seargeant, LE | 1 |
Baumgartner, MR; BerghaĆ¼ser, M; Burlina, A; Coelho, D; Fowler, B; Herwig, J; Koch, HG; Kozich, V; Sewell, A; Suormala, T; Wraith, JE; Zavadakova, P | 1 |
Barrick, JE; Block, KF; Breaker, RR; Hammond, MC; Roth, A; Sudarsan, N; Welz, R | 1 |
5 other study(ies) available for methionine and cobamamide
Article | Year |
---|---|
Methionine auxotrophy in inborn errors of cobalamin metabolism.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Cell Division; Cell Line; Cobamides; Fibroblasts; Homocysteine; Humans; Metabolism, Inborn Errors; Methionine; Vitamin B 12; Vitamin B 12 Deficiency | 1992 |
Serum valine, methionine and isoleucine levels in patients anaesthetized with and without nitrous oxide.
Topics: Adolescent; Adult; Aged; Anesthesia; Cobamides; Female; Humans; Isoleucine; Male; Methionine; Methylmalonyl-CoA Mutase; Middle Aged; Nitrous Oxide; Valine | 1985 |
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Amino Acid Metabolism, Inborn Errors; Anemia, Macrocytic; Anemia, Megaloblastic; Cobamides; Fibroblasts; Homocystinuria; Humans; Hydroxocobalamin; Infant, Newborn; Male; Methionine; Propionates; Tetrahydrofolates; Vitamin B 12 | 1984 |
The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adolescent; Alkyl and Aryl Transferases; Child; Child, Preschool; Cobamides; DNA, Complementary; Fibroblasts; Genetic Complementation Test; Homocysteine; Homocystinuria; Humans; Male; Methionine; Methylmalonyl-CoA Mutase; Models, Biological; Mutation; Phenotype; Vitamin B 12; Vitamin B 12 Deficiency | 2004 |
Tandem riboswitch architectures exhibit complex gene control functions.
Topics: 5' Untranslated Regions; Aptamers, Nucleotide; Bacillus; Base Sequence; Cobamides; Gene Expression Regulation, Bacterial; Genes, Bacterial; Ligands; Methionine; Molecular Sequence Data; Nucleic Acid Conformation; RNA, Bacterial; RNA, Messenger; S-Adenosylmethionine; Transcription, Genetic | 2006 |