beta-methylcrotonylglycine has been researched along with biotin in 10 studies
| Studies (beta-methylcrotonylglycine) | Trials (beta-methylcrotonylglycine) | Recent Studies (post-2010) (beta-methylcrotonylglycine) | Studies (biotin) | Trials (biotin) | Recent Studies (post-2010) (biotin) |
|---|---|---|---|---|---|
| 27 | 0 | 4 | 14,847 | 95 | 3,882 |
| Protein | Taxonomy | beta-methylcrotonylglycine (IC50) | biotin (IC50) |
|---|---|---|---|
| nonstructural protein 1 | Influenza A virus (A/California/07/2009(H1N1)) | 0.2 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (60.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 3 (30.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Holme, E; Jacobson, CE; Kristiansson, B | 1 |
| Mock, DM; Mock, NI; Weintraub, S | 1 |
| Baker, H; Baswell, DL; Holman, RT; Mock, DM; Sweetman, L | 1 |
| Greter, J; Holme, E; Koivikko, M; Lindstedt, S | 1 |
| Bartlett, K; Leonard, JV; Ng, H | 1 |
| Baker, H; Nyhan, WL; Peterson, RM; Surh, L; Sweetman, L | 1 |
| Berry, SA; Nyhan, WL; Thuy, LP; Tuchman, M | 1 |
| Mock, DM; Mock, NI | 1 |
| Almashanu, S; Baumgartner, ER; Baumgartner, MR; Dantas, MF; Fowler, B; Friebel, D; Gebhardt, B; Giunta, C; Hoffmann, GF; Suormala, T; Valle, D | 1 |
| Kluijtmans, LAJ; Koene, S; Mock, D; Morava, E; Pasch, M; Wevers, R | 1 |
10 other study(ies) available for beta-methylcrotonylglycine and biotin
| Article | Year |
|---|---|
Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities.
Topics: Amidohydrolases; Biotin; Biotinidase; Carbon-Nitrogen Ligases; Child; Fibroblasts; Glycine; Humans; Kinetics; Ligases; Male; Multiple Carboxylase Deficiency; Valerates | 1988 |
Abnormal organic aciduria in biotin deficiency: the rat is similar to the human.
Topics: Animals; Biotin; Disease Models, Animal; Gas Chromatography-Mass Spectrometry; Glycine; Male; Random Allocation; Rats; Rats, Inbred Strains; Valerates | 1988 |
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment.
Topics: Alopecia; Biotin; Citrates; Diagnosis, Differential; Erythema; Fatty Acids, Essential; Female; Glycine; Humans; Infant; Isomerism; Lactates; Lactic Acid; Male; Nervous System Diseases; Parenteral Nutrition; Valerates; Zinc | 1985 |
Biotin-responsive 3-methylcrotonylglycinuria with biotinidase deficiency.
Topics: Amidohydrolases; Biotin; Biotinidase; Carbon-Carbon Ligases; Child, Preschool; Glycine; Humans; Ligases; Male | 1985 |
A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
Topics: Acidosis; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Biotin; Butyrates; Carbon Dioxide; Carboxy-Lyases; Child, Preschool; Crotonates; Female; Fibroblasts; Glycine; Humans; Hydroxy Acids; Ligases; Mitochondria; Propionates; Pyruvate Carboxylase Deficiency Disease; Valerates | 1980 |
Clinical and metabolic abnormalities in a boy with dietary deficiency of biotin.
Topics: Alopecia; Biotin; Carbon-Carbon Ligases; Carboxy-Lyases; Child; Citrates; Diet; Egg Proteins; Facial Dermatoses; Glycine; Humans; Hydroxy Acids; Ligases; Male; Methylmalonyl-CoA Decarboxylase; Propionates; Skin Diseases | 1981 |
Partial methylcrotonyl-coenzyme A carboxylase deficiency in an infant with failure to thrive, gastrointestinal dysfunction, and hypertonia.
Topics: Biotin; Carbon-Carbon Ligases; Failure to Thrive; Gastrointestinal Diseases; Glycine; Humans; Infant; Ligases; Male; Metabolism, Inborn Errors; Muscle Hypertonia; Valerates | 1993 |
Lymphocyte propionyl-CoA carboxylase is an early and sensitive indicator of biotin deficiency in rats, but urinary excretion of 3-hydroxypropionic acid is not.
Topics: Animals; Biomarkers; Biotin; Carboxy-Lyases; Deficiency Diseases; Glycine; Lactic Acid; Lymphocytes; Male; Methylmalonyl-CoA Decarboxylase; Rats; Rats, Sprague-Dawley; Sensitivity and Specificity | 2002 |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy.
Topics: Alleles; Base Sequence; Biotin; Carbon-Carbon Ligases; DNA Mutational Analysis; Dose-Response Relationship, Drug; Fibroblasts; Gene Expression; Genetic Vectors; Germany; Glycine; Greece; Humans; Infant, Newborn; Male; Mitochondrial Diseases; Molecular Sequence Data; Mutation; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Transfection; Valerates | 2004 |
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay.
Topics: Abnormalities, Multiple; Aging, Premature; Biotin; Child, Preschool; Developmental Disabilities; Ectoderm; Female; Glycine; Growth Disorders; Humans; Metabolism, Inborn Errors | 2008 |