lysine has been researched along with Diseases, Metabolic in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (33.33) | 18.7374 |
| 1990's | 2 (9.52) | 18.2507 |
| 2000's | 2 (9.52) | 29.6817 |
| 2010's | 6 (28.57) | 24.3611 |
| 2020's | 4 (19.05) | 2.80 |
| Authors | Studies |
|---|---|
| Hoeks, M; Huigen, M; IJzermans, T; Nijenhuis, T; Rennings, A; van der Meijden, W | 1 |
| Chen, H; Chen, T; Fu, B; Fu, X; Xing, Z; Zhang, W | 1 |
| Berska, J; Bugajska, J; Gotfryd-Bugajska, K; Pasternak, A; Sztefko, K; Szura, M | 1 |
| Anwar, A; Faustmann, G; Grabher, J; Hafner-Giessauf, H; Masania, J; Obermayer-Pietsch, B; Rabbani, N; Rajpoot, K; Rajpoot, N; Roob, JM; Thornalley, PJ; Tiran, B; Winklhofer-Roob, BM | 1 |
| Bouchereau, J; Schiff, M | 1 |
| Argmann, C; Bender, A; Dodatko, T; Houten, SM; Leandro, J; Yu, C | 1 |
| Cristea, IM; Rowland, EA; Snowden, CK | 1 |
| Amano, N; Arai, M; Arinami, T; Fukumoto, M; Hashimoto, R; Itokawa, M; Kasai, K; Koike, S; Kushima, I; Miyashita, M; Miyata, T; Niizato, K; Okazaki, Y; Oshima, K; Ozaki, N; Takeda, M; Toyota, T; Ujike, H; Yoshikawa, T; Yuzawa, H | 1 |
| Börsch-Haubold, AG; Haubold, B; Krause, L | 1 |
| Ataei, F; Bakhtiyari, S; Gerayesh-Nejad, S; Gulkho, S; Hanachi, P; Larijani, B; Meshkani, R; Mohammadi, M; Mohammadtaghvaei, N; Parvaneh, L; Saberi, H; Zargari, M | 1 |
| Jakobs, C; Roos, B; Struys, EA; Verhoeven, NM | 1 |
| ROBSON, EB; ROSE, GA | 1 |
| KAZASSIS, C; SCHREIER, K | 1 |
| AVERY, GB; CONE, TE; FLEMING, WH; MORGAN, RI | 1 |
| DONATH, A; RICHTERICH, R; ROSSI, E; SPAHR, A | 1 |
| Lazarevic, G; Milojkovic, M; Stefanovic, V; Sunder-Plassmann, R; Tasic, I; Tasic, NM | 1 |
| Hamada, H; Kubo, T; Takayama, N | 1 |
| Parvy, P | 1 |
| Harper, AE; Tews, JK | 1 |
| Bunting, R; Diamond, S; Hansen, S; Perry, TL; Tischler, B; Weppler, VC | 1 |
| Abdelnour, GM; Gatfield, PD; Haust, MD; Hinton, GG; Taller, E; Wallace, AC | 1 |
2 review(s) available for lysine and Diseases, Metabolic
| Article | Year |
|---|---|
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 |
Protein lipoylation: an evolutionarily conserved metabolic regulator of health and disease.
Topics: Bacteria; Bacterial Proteins; Humans; Lipoylation; Lysine; Mass Spectrometry; Metabolic Diseases; Mitochondrial Proteins; Protein Processing, Post-Translational; Proteins; Proteomics | 2018 |
19 other study(ies) available for lysine and Diseases, Metabolic
| Article | Year |
|---|---|
Improving a Rare Metabolic Disorder Through Kidney Transplantation: A Case Report of a Patient With Lysinuric Protein Intolerance.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Transport System y+L; Arginine; Humans; Kidney Transplantation; Lysine; Metabolic Diseases; Ornithine | 2023 |
[Hyperoxia caused intestinal metabolism disorder in mice].
Topics: Animals; Benzene; Biomarkers; Chlorophyll; Hyperoxia; Lysine; Male; Metabolic Diseases; Mice; Mice, Inbred C57BL; Oxygen; Porphyrins | 2023 |
Characteristics of amino acid profiles and incretin hormones in patients with gallstone disease: a pilot study.
Topics: Adult; Aged; Cholecystolithiasis; Diabetes Mellitus, Type 2; Female; Humans; Incretins; Isoleucine; Leucine; Lysine; Male; Metabolic Diseases; Middle Aged; Pilot Projects; Valine | 2019 |
Urinary Metabolomic Markers of Protein Glycation, Oxidation, and Nitration in Early-Stage Decline in Metabolic, Vascular, and Renal Health.
Topics: Adult; Algorithms; Amino Acids, Branched-Chain; Biomarkers; Body Mass Index; Case-Control Studies; Chromatography, High Pressure Liquid; Female; Glycation End Products, Advanced; Glycosylation; Humans; Kidney; Lysine; Male; Metabolic Diseases; Oxidation-Reduction; Severity of Illness Index; Tandem Mass Spectrometry; Tyrosine; Vascular Diseases | 2019 |
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 |
Replication of enhanced carbonyl stress in a subpopulation of schizophrenia.
Topics: Arginine; Biomarkers; Case-Control Studies; Female; Glycation End Products, Advanced; Humans; Lysine; Male; Metabolic Diseases; Pyridoxal; Schizophrenia; Stress, Physiological | 2014 |
Social exclusion changes histone modifications H3K4me3 and H3K27ac in liver tissue of wild house mice.
Topics: Animals; Chromatin Immunoprecipitation; DNA Methylation; Epigenesis, Genetic; Feeding Behavior; Female; Hierarchy, Social; Histones; Humans; Liver; Lysine; Male; Metabolic Diseases; Mice; Promoter Regions, Genetic | 2015 |
The ENPP1 K121Q polymorphism is not associated with type 2 diabetes and related metabolic traits in an Iranian population.
Topics: Adult; Aged; Amino Acid Substitution; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Genotype; Glutamic Acid; Humans; Insulin Resistance; Iran; Lysine; Male; Metabolic Diseases; Middle Aged; Phosphoric Diester Hydrolases; Polymorphism, Single Nucleotide; Pyrophosphatases; Young Adult | 2011 |
Disease-related metabolites in culture medium of fibroblasts from patients with D-2-hydroxyglutaric aciduria, L-2-hydroxyglutaric aciduria, and combined D/L-2-hydroxyglutaric aciduria.
Topics: Biomarkers; Cell Line; Culture Media; Fibroblasts; Gas Chromatography-Mass Spectrometry; Glutamic Acid; Glutamine; Glutarates; Humans; Ketoglutaric Acids; Lysine; Metabolic Diseases; Stereoisomerism; Succinic Acid | 2003 |
The effect of intravenous lysine on the renal clearances of cystine, arginine and ornithine in normal subjects, in patients with cystinuria and Fanconi syndrome and in their relatives.
Topics: Amino Acids; Arginine; Cystine; Cystinuria; Fanconi Syndrome; Humans; Lysine; Metabolic Diseases; Ornithine | 1957 |
Influence of different types of malnutrition on the 14C-lysine metabolism in young rats.
Topics: Animals; Biochemical Phenomena; Lysine; Malnutrition; Metabolic Diseases; Nutrition Disorders; Nutritional Status; Rats | 1960 |
GASTROINTESTINAL MALABSORPTION ASSOCIATED WITH CYSTINURIA. REPORT OF A CASE IN A NEGRO.
Topics: Adolescent; Anemia; Anemia, Hypochromic; Arginine; Black People; Celiac Disease; Cystine; Cystinuria; Emaciation; Humans; Lysine; Metabolic Diseases; Ornithine; Phosphorus Metabolism Disorders; Proteins; Rickets | 1963 |
CONGENITAL LYSINE INTOLERANCE WITH PERIODIC AMMONIA INTOXICATION.
Topics: Ammonia; Biopsy; Blood Chemical Analysis; Dietary Proteins; Genetics, Medical; Humans; Hyperlysinemias; Infant; Liver; Liver Function Tests; Lysine; Metabolic Diseases; Periodicity; Proteins; Toxicology | 1964 |
The association of PC-1 (ENPP1) K121Q polymorphism with metabolic syndrome in patients with coronary heart disease.
Topics: Alleles; Coronary Disease; Female; Genotype; Glutamine; Humans; Lysine; Male; Metabolic Diseases; Middle Aged; Phosphoric Diester Hydrolases; Polymorphism, Genetic; Pyrophosphatases | 2007 |
Lysinuric protein intolerance in pregnancy: case report with successful outcome.
Topics: Adult; Female; Humans; Lysine; Metabolic Diseases; Pregnancy; Pregnancy Complications; Pregnancy Outcome | 1995 |
[A decision tree for abnormalities of plasma and urine lysine level].
Topics: Decision Trees; Humans; Lysine; Metabolic Diseases | 1991 |
Induction in rats of lysine imbalance by dietary homoarginine.
Topics: Amino Acids; Animals; Arginine; Brain Chemistry; Diet; Growth; Homoarginine; Liver; Lysine; Male; Metabolic Diseases; Muscles; Rats; Rats, Inbred Strains | 1986 |
Unrecognized maternal biochemical disease: an uncommon cause of mental retardation in children.
Topics: Child; Cystinuria; Female; Glycine; Humans; Infant, Newborn; Intellectual Disability; Lysine; Metabolic Diseases; Phenylalanine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1970 |
Hyperpipecolatemia: A new metabolic disorder associated with neuropathy and hepatomegaly: A case study.
Topics: Amino Acids; Brain Chemistry; Central Nervous System Diseases; Cerebellum; Demyelinating Diseases; Diet Therapy; Digestive System; Hepatomegaly; Humans; Infant; Intellectual Disability; Kidney; Liver; Lysine; Male; Medulla Oblongata; Metabolic Diseases; Organ Size; Pipecolic Acids; Pons | 1968 |