n-isobutyrylglycine has been researched along with glycine 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 | 0 (0.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brimacombe, KR; Dulcey, AE; Goldsborough, AS; Gottesman, MM; Griffiths, G; Hall, MD; Handley, MD; Kannan, P; Pluchino, KM | 1 |
Christensen, E; Gregersen, N; Kølvraa, S | 1 |
Brandt, NJ; Gregersen, N; Kølvraa, S | 1 |
Bykov, IL; Shigematsu, E | 1 |
Fernando, M; Lindner, M; Popek, M; Sass, JO; Schwab, KO; Walter, M | 1 |
5 other study(ies) available for n-isobutyrylglycine and glycine
Article | Year |
---|---|
Collateral sensitivity of multidrug-resistant cells to the orphan drug tiopronin.
Topics: Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 1; Cell Line, Tumor; Doxorubicin; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; HEK293 Cells; Humans; Multidrug Resistance-Associated Proteins; Orphan Drug Production; Paclitaxel; RNA Stability; RNA, Messenger; Structure-Activity Relationship; Tiopronin | 2011 |
In vivo studies on the metabolic derangement in a patient with D-glyceric acidaemia and hyperglycinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Dehydrogenases; Child, Preschool; Diet; Fructose; Glyceric Acids; Glycine; Humans; Male; Proline; Propionates; Riboflavin; Serine | 1984 |
Excretion of short-chain N-acylglycines in the urine of a patient with D-glyceric acidemia.
Topics: Amino Acid Metabolism, Inborn Errors; Butyrates; Caproates; Caprylates; Child, Preschool; Glyceric Acids; Glycine; Humans; Hydrolysis; Models, Chemical | 1980 |
[Effect of l-carnitine on the expression of glycine conjugates in rats in experimental B2-hypovitaminosis].
Topics: Animals; Carnitine; Glycine; Rats; Rats, Wistar; Riboflavin Deficiency | 1997 |
Two inborn errors of metabolism in a newborn: glutaric aciduria type I combined with isobutyrylglycinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Base Sequence; Brain Diseases, Metabolic; DNA Mutational Analysis; Female; Follow-Up Studies; Glutaryl-CoA Dehydrogenase; Glycine; Humans; Infant, Newborn; Male; Molecular Diagnostic Techniques | 2010 |