glutaric acid has been researched along with lysine in 29 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (10.34) | 18.7374 |
| 1990's | 4 (13.79) | 18.2507 |
| 2000's | 9 (31.03) | 29.6817 |
| 2010's | 8 (27.59) | 24.3611 |
| 2020's | 5 (17.24) | 2.80 |
| Authors | Studies |
|---|---|
| Bennett, MJ; Goodman, SI; Hale, DE; Pollitt, RJ; Vamecq, J | 1 |
| Horn, L; Jellum, E; Kvittingen, EA; Nilsen, E; Seip, R; Stokke, O; Thoresen, O | 1 |
| Bennett, MJ; Curnock, DA; Engel, PC; Gray, RG; Hull, D; Patrick, AD; Pollitt, RJ; Shaw, L | 1 |
| Rohr, F; Warman, ML; Yannicelli, S | 1 |
| Dalton, RN; Howard, RS; Olpin, SE; Prevett, MC | 1 |
| Emons, D; Haverkamp, F; Kreft, B; Woelfle, J | 1 |
| Crnic, LS; Koeller, DM; Woontner, M | 1 |
| Manoj, N; Saraswathi, NT; Vijayan, M | 1 |
| Prats Viñas, J | 1 |
| Christensen, E; de Koning, TJ; Dorland, L; Hoffmann, GF; Knerr, I; Müller, P; Rascher, W; Trautmann, U; Trefz, FK; Wündisch, GF; Zschocke, J | 1 |
| Andresen, BS; Campistol, J; Curcoy, A; Gregersen, N; Olsen, RK; Osorio, JH; Ribes, A; Trenchs, V; Vilaseca, MA | 1 |
| HAIGHT, RD; MATTOON, JR | 1 |
| Alderson, NL; Baynes, JW; Januszewski, AS; Jenkins, AJ; Thorpe, SR | 1 |
| Antonetti, DA; Cheng, KC; Connor, JR; Goodman, SI; Lazovic, J; Smith, MB; Wolpert, EB; Woontner, M; Zinnanti, WJ | 1 |
| Hoffmann, GF; Koeller, DM; Kölker, S; Okun, JG; Sauer, SW | 1 |
| Cheng, KC; Connor, JR; Goodman, SI; Housman, C; Jacobs, RE; LaNoue, K; Lazovic, J; O'Callaghan, JP; Simpson, I; Woontner, M; Zinnanti, WJ | 1 |
| Blank, AE; Burgard, P; Koeller, DM; Kölker, S; Komatsuzaki, S; Mittelbronn, M; Okun, JG; Opp, S; Sauer, SW | 1 |
| Huang, H; Li, Q; Wang, G; Xie, J; Xie, L; Yu, Z; Zhou, M | 1 |
| Cho, JS; Choi, JW; Jeong, KJ; Joo, JC; Lee, MH; Lee, SY; Oh, YH; Park, SH; Park, SJ; Shin, JH; Yu, J | 1 |
| Assmann, B; Boy, N; Burgard, P; Dixon, M; Fleissner, S; Greenberg, CR; Harting, I; Heringer, J; Hoffmann, GF; Karall, D; Koeller, DM; Kölker, S; Krawinkel, MB; Maier, EM; Mühlhausen, C; Okun, JG; Opladen, T; Posset, R; Sahm, K; Zschocke, J | 1 |
| He, JJ; Ju, Z | 1 |
| Baritugo, KA; Hyun, SM; Joo, JC; Jung, SH; Kang, KH; Khang, TU; Kim, GB; Kim, HT; Kim, HU; Lee, SY; Oh, MK; Park, K; Park, SJ; Song, BK | 1 |
| Ahn, JO; Bhatia, SK; Choi, TR; Hong, YG; Joo, JC; Jung, HR; Kim, YG; Lee, YK; Moon, YM; Park, K; Yang, SY; Yang, YH | 1 |
| Hsu, JB; Huang, KY; Kao, HJ; Lee, TY; Weng, SL | 1 |
| Bhatia, SK; Choi, TR; Choi, YK; Gurav, R; Han, YH; Kim, HJ; Kim, W; Park, K; Park, SH; Park, YL; Song, HS; Yang, YH | 1 |
| Ahmad, MW; Arafat, ME; Dehzangi, A; Dipta, SR; Hasan, MAM; Sharma, A; Shatabda, S; Shovan, SM; Taherzadeh, G | 1 |
| Bouchereau, J; Schiff, M | 1 |
| Han, T; Kim, GB; Lee, SY | 1 |
| Argmann, C; Bender, A; Dodatko, T; Houten, SM; Leandro, J; Yu, C | 1 |
3 review(s) available for glutaric acid and lysine
| Article | Year |
|---|---|
Nutrition support for glutaric acidemia type I.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Dietary Proteins; Female; Food, Formulated; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Infant, Newborn; Lysine; Male; Mitochondria; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Tryptophan | 1994 |
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Dietary Supplements; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine | 2017 |
Inherited Disorders of Lysine Metabolism: A Review.
Topics: 2-Aminoadipic Acid; Aldehyde Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Arginine; Brain; Brain Diseases, Metabolic; Brain Diseases, Metabolic, Inborn; Carnitine; Epilepsy; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Metabolic Diseases; Pyridoxal Phosphate; Pyridoxine | 2020 |
26 other study(ies) available for glutaric acid and lysine
| Article | Year |
|---|---|
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.
Topics: Acyl-CoA Oxidase; Cells, Cultured; Child, Preschool; Fatty Acids; Female; Fibroblasts; Gas Chromatography-Mass Spectrometry; Glutarates; Humans; Lysine; Microbodies; Oxidation-Reduction; Oxidoreductases; Riboflavin | 1991 |
Advances in the use of computerized gas chromatography-mass spectrometry and high-performance liquid chromatography with rapid scanning detection for clinical diagnosis.
Topics: Acids; Alkaptonuria; Child; Chromatography, High Pressure Liquid; Clinical Laboratory Techniques; Female; Gas Chromatography-Mass Spectrometry; Glutarates; Humans; Infant; Lysine; Pharmaceutical Preparations | 1989 |
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally.
Topics: Adipates; Carbon Dioxide; Fatty Acid Desaturases; Fatty Acids; Female; Fibroblasts; Glutarates; Humans; Infant, Newborn; Liver; Lysine; Pregnancy; Prenatal Diagnosis; Sarcosine | 1984 |
Glutaric aciduria type 1 in adulthood.
Topics: Amino Acid Metabolism, Inborn Errors; Dystonia; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Middle Aged; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Tryptophan | 1996 |
Subdural hemorrhage as an initial sign of glutaric aciduria type 1: a diagnostic pitfall.
Topics: Amino Acid Metabolism, Inborn Errors; Atrophy; Cisterna Magna; Developmental Disabilities; Diagnosis, Differential; Female; Frontal Lobe; Glutarates; Glutaryl-CoA Dehydrogenase; Hematoma, Subdural; Humans; Infant; Lysine; Magnetic Resonance Imaging; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Psychomotor Performance; Temporal Lobe; Tomography, X-Ray Computed; Tryptophan | 1996 |
Analysis of the expression of murine glutaryl-CoA dehydrogenase: in vitro and in vivo studies.
Topics: 3T3 Cells; 5' Untranslated Regions; Animals; Base Sequence; Blotting, Western; Brain; Glutarates; Glutaryl-CoA Dehydrogenase; Kidney; Liver; Lysine; Mice; Mice, Inbred C57BL; Molecular Sequence Data; Organ Specificity; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Promoter Regions, Genetic; Reverse Transcriptase Polymerase Chain Reaction; Sequence Alignment; Transfection | 2000 |
X-ray studies on crystalline complexes involving amino acids and peptides. XXXVII. Novel aggregation patterns and effect of chirality in the complexes of DL- and L-lysine with glutaric acid.
Topics: Crystallography, X-Ray; Electrochemistry; Glutarates; Lysine; Macromolecular Substances; Models, Molecular; Stereoisomerism | 2001 |
[Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders].
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Carnitine; Child, Preschool; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Lysine; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; Tryptophan | 2001 |
Glutaric aciduria type III: a distinctive non-disease?
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromosome Deletion; Diarrhea; Fasting; Female; Glutarates; Humans; Liver; Lysine; Male; Pipecolic Acids; Riboflavin | 2002 |
Late-onset form of beta-electron transfer flavoprotein deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Carnitine; Cysteine; DNA Mutational Analysis; Electron-Transferring Flavoproteins; Electrons; Exons; Female; Fibroblasts; Gas Chromatography-Mass Spectrometry; Gene Deletion; Glutarates; Humans; Infant, Newborn; Iron-Sulfur Proteins; Lysine; Mutation, Missense; Oxidoreductases Acting on CH-NH Group Donors; Oxygen; Phenotype | 2003 |
Glutaric acid accumulation by a lysine-requiring yeast mutant.
Topics: Glutarates; Humans; Lysine; Saccharomyces cerevisiae; Yeasts | 1962 |
Chemical modification of proteins during peroxidation of phospholipids.
Topics: Adult; Blood Proteins; Catalysis; Copper Sulfate; Diabetes Mellitus, Type 1; Dicarboxylic Acids; Female; Glutarates; Glycation End Products, Advanced; Humans; Lipid Peroxidation; Lipoproteins, LDL; Lysine; Lysophosphatidylcholines; Male; Oxidation-Reduction; Phospholipids; Ribonuclease, Pancreatic | 2005 |
A diet-induced mouse model for glutaric aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Blood-Brain Barrier; Capillary Permeability; Corpus Striatum; Diet; Dietary Proteins; Disease Models, Animal; Female; Glutarates; Lysine; Magnetic Resonance Imaging; Male; Mice; Mice, Inbred C57BL; Neurons; Survival Analysis; Tissue Culture Techniques | 2006 |
Lysine intake and neurotoxicity in glutaric aciduria type I: towards a rationale for therapy?
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Diet; Disease Models, Animal; Glutarates; Lysine; Mice | 2006 |
Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I.
Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child; Diet; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glucose; Glutamic Acid; Glutarates; Glutaryl-CoA Dehydrogenase; Homoarginine; Humans; Lysine; Mice; Mice, Knockout; Mitochondria; Neurons; Nuclear Magnetic Resonance, Biomolecular; Tryptophan | 2007 |
Multifactorial modulation of susceptibility to l-lysine in an animal model of glutaric aciduria type I.
Topics: Aconitate Hydratase; Amino Acid Metabolism, Inborn Errors; Animals; Brain; Brain Diseases, Metabolic; Diet; Disease Models, Animal; Dose-Response Relationship, Drug; Energy Metabolism; Female; Genetic Predisposition to Disease; Glutarates; Glutaryl-CoA Dehydrogenase; Glyceraldehyde-3-Phosphate Dehydrogenases; Ketoglutarate Dehydrogenase Complex; Lysine; Male; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Risk Factors; Sex Factors; Spectrophotometry | 2015 |
Proteome-wide Lysine Glutarylation Profiling of the Mycobacterium tuberculosis H37Rv.
Topics: Acetylation; Acyltransferases; Amino Acid Sequence; Antigens, Bacterial; Bacterial Proteins; Chromatography, Liquid; Escherichia coli; Escherichia coli Proteins; Gene Expression; Gene Expression Profiling; Glutarates; Lysine; Mass Spectrometry; Mycobacterium tuberculosis; Peptide Elongation Factor Tu; Protein Processing, Post-Translational; Proteome; Ribosomal Proteins; Succinic Acid | 2016 |
Metabolic engineering of Corynebacterium glutamicum for enhanced production of 5-aminovaleric acid.
Topics: Amidohydrolases; Amino Acids, Neutral; Batch Cell Culture Techniques; Corynebacterium glutamicum; Escherichia coli; Fermentation; Glucose; Glutarates; Lysine; Metabolic Engineering; Mixed Function Oxygenases; Pseudomonas putida | 2016 |
Prediction of lysine glutarylation sites by maximum relevance minimum redundancy feature selection.
Topics: Acylation; Glutarates; Lysine; Protein Processing, Post-Translational; Proteins; Sequence Analysis, Protein; Software; Support Vector Machine | 2018 |
Metabolic engineering of Corynebacterium glutamicum for the production of glutaric acid, a C5 dicarboxylic acid platform chemical.
Topics: Codon; Corynebacterium glutamicum; Dicarboxylic Acids; DNA, Bacterial; Fermentation; Glucose; Glutarates; Lysine; Metabolic Engineering; Plasmids; Pseudomonas putida; Vasotocin | 2019 |
Enhanced production of glutaric acid by NADH oxidase and GabD-reinforced bioconversion from l-lysine.
Topics: Bacillus subtilis; Biotransformation; Escherichia coli; Escherichia coli Proteins; Glutarates; Lysine; Metabolic Engineering; Multienzyme Complexes; NADH, NADPH Oxidoreductases; Recombinant Proteins; Succinate-Semialdehyde Dehydrogenase | 2019 |
Characterization and identification of lysine glutarylation based on intrinsic interdependence between positions in the substrate sites.
Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Computational Biology; Databases, Protein; Glutarates; Lysine; Mice; Proteins; Reproducibility of Results; ROC Curve; Substrate Specificity; Support Vector Machine; User-Computer Interface | 2019 |
Simultaneous monitoring of the bioconversion from lysine to glutaric acid by ethyl chloroformate derivatization and gas chromatography-mass spectrometry.
Topics: Chromatography, High Pressure Liquid; Fermentation; Formic Acid Esters; Gas Chromatography-Mass Spectrometry; Glutarates; Lysine; Molecular Structure | 2020 |
Accurately Predicting Glutarylation Sites Using Sequential Bi-Peptide-Based Evolutionary Features.
Topics: Algorithms; Amino Acid Sequence; Animals; Computational Biology; Evolution, Molecular; Glutarates; Lysine; Machine Learning; Mice; Mycobacterium tuberculosis; Peptide Fragments; Protein Processing, Post-Translational; Proteins; Support Vector Machine | 2020 |
Glutaric acid production by systems metabolic engineering of an l-lysine-overproducing
Topics: Batch Cell Culture Techniques; Biosynthetic Pathways; Corynebacterium glutamicum; Fermentation; Glutarates; Lysine; Metabolic Engineering; Metabolic Flux Analysis; Systems Biology; Transcriptome | 2020 |
Glutaric aciduria type 3 is a naturally occurring biochemical trait in inbred mice of 129 substrains.
Topics: Acyltransferases; Amino Acid Metabolism, Inborn Errors; Animals; Disease Models, Animal; Glutarates; Humans; Lysine; Metabolic Diseases; Mice; Mice, Inbred Strains; Oxidoreductases; Phenotype; Transferases | 2021 |