proline and Kidney Tubular Transport, Inborn Error

proline has been researched along with Kidney Tubular Transport, Inborn Error in 15 studies

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-199013 (86.67)18.7374
1990's1 (6.67)18.2507
2000's0 (0.00)29.6817
2010's1 (6.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Netto, CA; Wyse, AT1
Scriver, CR2
Goodman, SI; McIntyre, CA; O'Brien, D1
Palmieri, MJ; Segal, S; States, B1
Ohura, T1
Lasley, L; Scriver, CR1
Kissane, JM1
Kitagawa, T1
Alpers, DH; Thier, SO1
Buravina, TA; Iur'eva, EA; Koroleva, IA; Lebedev, VP; Mukhina, IuG1
Procopis, PG; Turner, B1
Durant, JL; Elsas, LJ; Rosenberg, LE1
Blattner, RJ1
Ando, T; Minagawa, A; Morikawa, T; Tada, K; Yoshida, T1

Reviews

7 review(s) available for proline and Kidney Tubular Transport, Inborn Error

ArticleYear
Behavioral and neurochemical effects of proline.
    Metabolic brain disease, 2011, Volume: 26, Issue:3

    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].
    Ryoikibetsu shokogun shirizu, 1998, Issue:19 Pt 2

    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.
    Perspectives in pediatric pathology, 1973, Volume: 1

    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].
    Shinkei kenkyu no shimpo. Advances in neurological sciences, 1968, Volume: 12, Issue:1

    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.
    American journal of diseases of children (1960), 1969, Volume: 117, Issue:1

    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.
    American journal of diseases of children (1960), 1969, Volume: 117, Issue:1

    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)].
    Voprosy okhrany materinstva i detstva, 1970, Volume: 15, Issue:11

    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

Other Studies

8 other study(ies) available for proline and Kidney Tubular Transport, Inborn Error

ArticleYear
Membrane transport in disorders of imino-acid metabolism.
    American journal of diseases of children (1960), 1967, Volume: 113, Issue:1

    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.
    The Journal of pediatrics, 1967, Volume: 71, Issue:2

    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.
    Biochemical and biophysical research communications, 1982, Nov-30, Volume: 109, Issue:2

    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.
    Pediatric research, 1979, Volume: 13, Issue:1

    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.
    The Journal of pediatrics, 1971, Volume: 79, Issue:3

    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.
    The New England journal of medicine, 1968, Jun-27, Volume: 278, Issue:26

    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.
    The Journal of pediatrics, 1969, Volume: 74, Issue:1

    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.
    The Tohoku journal of experimental medicine, 1965, Nov-25, Volume: 87, Issue:2

    Topics: Child; Female; Glycine; Humans; In Vitro Techniques; Infant; Male; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Urine

1965