proline has been researched along with Metabolic Diseases in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (16.67) | 29.6817 |
| 2010's | 8 (44.44) | 24.3611 |
| 2020's | 1 (5.56) | 2.80 |
| Authors | Studies |
|---|---|
| Goehring, I; Heidenreich, S; Knauer, M; Krause, E; Muenzner, M; Myllyharju, J; Oster, M; Petricek, KM; Salo, AM; Schumann, A; Schupp, M; Schütte, T; Sommerfeld, M; Stephanowitz, H; Weber, P; Witte, N; Yang, N | 1 |
| de Koning, TJ | 1 |
| Baltar, VT; Barros, CR; Curti, ML; Ferreira, SR; Rogero, MM; Siqueira-Catania, A | 1 |
| Aldámiz-Echevarria, T; Berenguer, J; Fernández-Rodríguez, A; García-Alvarez, M; García-Broncano, P; Jiménez-Sousa, MÁ; López, JC; Micheloud, D; Miralles, P; Pineda-Tenor, D; Resino, S | 1 |
| J, J; K N, S; Sivashanmugam, M; V, U | 1 |
| Carmona-Alvarez, F; Cervera, J; Martínez, AI; Pérez-Arellano, I; Rodríguez-Díaz, J | 1 |
| Area, E; Artuch, R; Cormand, B; Drakaki, K; Garcia-Cazorla, A; Giannakopoulos, A; Kanavakis, E; Orfanou, I; Ormazabal, A; Pons, R; Ribasés, M; Serrano, M; Toma, C; Youroukos, S | 1 |
| Chen, CH; Chen, PY; Chiu, CC; Huang, MC; Kao, CF; Kuo, PH; Lu, ML | 1 |
| Baptista, T; Carrizo, E; Connell, L; Fernández, E | 1 |
| EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D | 1 |
| Chiarani, F; Delwing, D; Wajner, M; Wannmacher, CM; Wyse, AT | 1 |
| Bavaresco, CS; Delwing, D; Matté, C; Monteiro, SC; Netto, CA; Wyse, AT | 1 |
| Merton, WL; Mills, GA; Peters, SA; Walker, V | 1 |
| Kissane, JM | 1 |
| Goodwin, JF | 1 |
| Henneman, DH | 1 |
| Bunting, R; Diamond, S; Hansen, S; Perry, TL; Tischler, B; Weppler, VC | 1 |
| Gjessing, LR; Seip, M; Vellan, EJ | 1 |
4 review(s) available for proline and Metabolic Diseases
| Article | Year |
|---|---|
Amino acid synthesis deficiencies.
Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Brain Diseases; Central Nervous System; Fetal Growth Retardation; Glutamine; High-Throughput Nucleotide Sequencing; Humans; Ichthyosis; Limb Deformities, Congenital; Metabolic Diseases; Mice; Microcephaly; Proline; Serine | 2017 |
Ornithine and its role in metabolic diseases: An appraisal.
Topics: Animals; Humans; Metabolic Diseases; Ornithine; Polyamines; Proline; Protein Binding; Protein Structure, Secondary | 2017 |
Pyrroline-5-carboxylate synthase and proline biosynthesis: from osmotolerance to rare metabolic disease.
Topics: Amino Acid Sequence; Animals; Bacteria; Humans; Metabolic Diseases; Ornithine-Oxo-Acid Transaminase; Osmotic Fragility; Osmotic Pressure; Plants; Proline; Protein Conformation; Sequence Alignment | 2010 |
Hereditary disorders of the kidney. II. Hereditary nephropathies.
Topics: Adolescent; Adult; Aldosterone; Amyloidosis; Bone Resorption; Child; Child, Preschool; Female; Glomerulonephritis; Humans; Infant; Juxtaglomerular Apparatus; Kidney; Kidney Calculi; Kidney Diseases; Kidney Neoplasms; Laurence-Moon Syndrome; Lipodystrophy; Male; Metabolic Diseases; Middle Aged; Muscular Atrophy; Nail-Patella Syndrome; Nephritis; Nephrotic Syndrome; Potassium; Proline; Renal Tubular Transport, Inborn Errors | 1973 |
1 trial(s) available for proline and Metabolic Diseases
| Article | Year |
|---|---|
FTO T/A and peroxisome proliferator-activated receptor-γ Pro12Ala polymorphisms but not ApoA1 -75 are associated with better response to lifestyle intervention in Brazilians at high cardiometabolic risk.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Alpha-Ketoglutarate-Dependent Dioxygenase FTO; Amino Acid Substitution; Apolipoprotein A-I; Brazil; Cardiovascular Diseases; Female; Genetic Association Studies; Humans; Male; Metabolic Diseases; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Promoter Regions, Genetic; Proteins; Risk Factors; Risk Reduction Behavior; Young Adult | 2013 |
13 other study(ies) available for proline and Metabolic Diseases
| Article | Year |
|---|---|
The glucose-sensing transcription factor ChREBP is targeted by proline hydroxylation.
Topics: Animals; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Gene Expression Regulation; Glucose; HEK293 Cells; Humans; Hydroxylation; Liver; Male; Metabolic Diseases; Mice; Mice, Transgenic; Proline; Protein Processing, Post-Translational | 2020 |
PPARγ2 Pro12Ala polymorphism was associated with favorable cardiometabolic risk profile in HIV/HCV coinfected patients: a cross-sectional study.
Topics: Adult; Alanine; Amino Acid Substitution; Cardiovascular Diseases; Coinfection; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Hepatitis C; HIV Infections; HIV-1; Humans; Male; Metabolic Diseases; Metabolome; Middle Aged; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Risk Factors | 2014 |
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.
Topics: Child, Preschool; Dihydroxyphenylalanine; DNA Mutational Analysis; Greece; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Leucine; Metabolic Diseases; Methoxyhydroxyphenylglycol; Mutation; Proline; Tyrosine; Tyrosine 3-Monooxygenase; Young Adult | 2010 |
Gender differences in the effects of peroxisome proliferator-activated receptor γ2 gene polymorphisms on metabolic adversity in patients with schizophrenia or schizoaffective disorder.
Topics: Adult; Alanine; Female; Gene Frequency; Genotype; Humans; Male; Metabolic Diseases; Metabolic Syndrome; Middle Aged; Obesity; Polymorphism, Genetic; PPAR gamma; Proline; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Sex Characteristics | 2011 |
Pro12Ala polymorphism of the PPAR-γ2 gene, metabolic syndrome and response to metformin in clozapine-treated patients.
Topics: Adult; Aged; Alanine; Antipsychotic Agents; Blood Glucose; Clozapine; Enzyme-Linked Immunosorbent Assay; Female; Gene Frequency; Genotype; Humans; Hypoglycemic Agents; Insulin; Leptin; Male; Metabolic Diseases; Metformin; Middle Aged; Polymorphism, Genetic; PPAR gamma; Proline | 2012 |
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine | 1964 |
Effect of hyperprolinemia on acetylcholinesterase and butyrylcholinesterase activities in rat.
Topics: Acetylcholinesterase; Animals; Brain Chemistry; Butyrylcholinesterase; Cerebellar Cortex; Metabolic Diseases; Oxidative Stress; Proline; Rats; Rats, Wistar | 2005 |
alpha-Tocopherol and ascorbic acid prevent memory deficits provoked by chronic hyperprolinemia in rats.
Topics: alpha-Tocopherol; Animals; Animals, Newborn; Antioxidants; Ascorbic Acid; Behavior, Animal; Chronic Disease; Drug Interactions; Male; Maze Learning; Memory Disorders; Metabolic Diseases; Proline; Rats; Rats, Wistar; Reaction Time; Time Factors | 2006 |
Fits, pyridoxine, and hyperprolinaemia type II.
Topics: Female; Genes, Recessive; Humans; Infant; Metabolic Diseases; Proline; Pyrroline Carboxylate Reductases; Seizures; Vitamin B 6 Deficiency | 2000 |
Spectrophotometry of proline in plasma and urine.
Topics: Amino Acids; Benzene; Chemical Phenomena; Chemistry; Creatinine; Evaluation Studies as Topic; Filtration; Humans; Hydrolysis; Hydroxyproline; Indenes; Indicators and Reagents; Infant; Ketones; Malabsorption Syndromes; Metabolic Diseases; Methods; Nitrites; Ornithine; Proline; Proteins; Spectrophotometry; Ultraviolet Rays | 1972 |
Inhibition of the effect of D-penicillamine on collagen solubility in skin by 17-beta-estradiol cypionate; and the effect of D-penicillamine and 17-beta-estradiol on the abnormalities in rat bone produced by a low calcium diet.
Topics: Animals; Aorta; Bone and Bones; Calcium, Dietary; Carbon Isotopes; Carrageenan; Collagen; Deficiency Diseases; Drug Antagonism; Estradiol; Female; Granuloma; Guinea Pigs; Hydroxyproline; In Vitro Techniques; Metabolic Diseases; Penicillamine; Proline; Rats; Skin; Solubility; Stereoisomerism | 1970 |
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 |
Hair amino acids in cystinosis, homocystinuria, Fölling's disease and tyrosinosis.
Topics: Amino Acids; Autoanalysis; Citrulline; Cystine; Cystinosis; Female; Hair; Homocysteine; Homocystinuria; Humans; In Vitro Techniques; Male; Metabolic Diseases; Methionine; Methods; Phenylalanine; Phenylketonurias; Proline; Tyrosine | 1969 |