proline has been researched along with Kidney Tubular Transport, Inborn Error in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 13 (86.67) | 18.7374 |
1990's | 1 (6.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (6.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Netto, CA; Wyse, AT | 1 |
Scriver, CR | 2 |
Goodman, SI; McIntyre, CA; O'Brien, D | 1 |
Palmieri, MJ; Segal, S; States, B | 1 |
Ohura, T | 1 |
Lasley, L; Scriver, CR | 1 |
Kissane, JM | 1 |
Kitagawa, T | 1 |
Alpers, DH; Thier, SO | 1 |
Buravina, TA; Iur'eva, EA; Koroleva, IA; Lebedev, VP; Mukhina, IuG | 1 |
Procopis, PG; Turner, B | 1 |
Durant, JL; Elsas, LJ; Rosenberg, LE | 1 |
Blattner, RJ | 1 |
Ando, T; Minagawa, A; Morikawa, T; Tada, K; Yoshida, T | 1 |
7 review(s) available for proline and Kidney Tubular Transport, Inborn Error
Article | Year |
---|---|
Behavioral and neurochemical effects of proline.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Animals; Antioxidants; Ascorbic Acid; Brain; Brain Diseases, Metabolic; Creatine Kinase; Energy Metabolism; Free Radicals; Glycine; Gyrate Atrophy; Humans; Memory Disorders; Mice; Oxidative Stress; Proline; Proline Oxidase; Rats; Receptors, Cholinergic; Receptors, Purinergic; Renal Tubular Transport, Inborn Errors; Sodium-Potassium-Exchanging ATPase; Vitamin E | 2011 |
[Familial iminoglycinuria].
Topics: Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Genotype; Glycine; Humans; Hydroxyproline; Mutation; Phenotype; Prognosis; Proline; Renal Tubular Transport, Inborn Errors | 1998 |
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 |
[Congenital metabolic inborn errors, with the exception of amino acid metabolism].
Topics: Amino Acids; Carbohydrate Metabolism, Inborn Errors; Galactose; Humans; Hypercalcemia; Intellectual Disability; Kidney Function Tests; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Metal Metabolism, Inborn Errors; Proline; Purine-Pyrimidine Metabolism, Inborn Errors; Renal Tubular Transport, Inborn Errors | 1968 |
Use of human genetic variation to study membrane transport of amino acids in kidney.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Child; Cysteine; Genetics, Medical; Heterozygote; Homozygote; Humans; Kidney; Lysine; Male; Mutation; Proline; Renal Tubular Transport, Inborn Errors | 1969 |
Disorders of intestinal transport of amino acids.
Topics: Amino Acids; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Fructose; Galactosemias; Genes, Recessive; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Lysine; Methionine; Phenylketonurias; Proline; Renal Tubular Transport, Inborn Errors; Tryptophan | 1969 |
[Primary and secondary hyperaminoaciduria in children (review of the literature)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Biological Transport, Active; Cystinuria; Fanconi Syndrome; Glycine; Glycosuria, Renal; Hartnup Disease; Histidine; Humans; Infant, Newborn; Kidney Diseases; Kidney Tubules; Maple Syrup Urine Disease; Phenylketonurias; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Sodium | 1970 |
8 other study(ies) available for proline and Kidney Tubular Transport, Inborn Error
Article | Year |
---|---|
Membrane transport in disorders of imino-acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Hydroxyproline; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Proline; Renal Tubular Transport, Inborn Errors | 1967 |
Impaired intestinal transport of proline in a patient with familial iminoaciduria.
Topics: Adolescent; Female; Glycine; Humans; Imines; Intestinal Absorption; Proline; Renal Tubular Transport, Inborn Errors | 1967 |
Uptake of proline in cultured cells from patients with Lowe's syndrome.
Topics: Amino Acids; Biological Transport; Cells, Cultured; Fibroblasts; Humans; Kinetics; Oculocerebrorenal Syndrome; Proline; Renal Tubular Transport, Inborn Errors; Skin | 1982 |
Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systems.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Glycine; Humans; Imino Acids; Infant, Newborn; Kidney Tubules; Mutation; Proline; Renal Tubular Transport, Inborn Errors; Syndrome | 1979 |
Iminoaciduria: a benign renal tubular defect.
Topics: Australia; Female; Glomerular Filtration Rate; Glycine; Heterozygote; Humans; Hydroxyproline; Infant; Male; Mass Screening; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors | 1971 |
Familial iminoglycinuria. An inborn error of renal tubular transport.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Genotype; Glycine; Heterozygote; Homozygote; Humans; Hydroxyproline; Intellectual Disability; Intestinal Absorption; Kidney Function Tests; Male; Proline; Renal Tubular Transport, Inborn Errors | 1968 |
Iminoaciduria.
Topics: Albinism; Amino Acid Metabolism, Inborn Errors; Audiometry; Biological Transport; Cell Membrane Permeability; Cystinuria; Electrophoresis; Genes, Recessive; Genetics, Medical; Glycine; Homozygote; Humans; Hydroxyproline; Imines; Intestinal Absorption; Kidney; Pentoses; Phenylacetates; Proline; Renal Tubular Transport, Inborn Errors | 1969 |
Prolinuria: a new renal tubular defect in transport of proline and glycine.
Topics: Child; Female; Glycine; Humans; In Vitro Techniques; Infant; Male; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Urine | 1965 |