tryptophan has been researched along with Cystinuria in 12 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 11 (91.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (8.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
MILNE, MD | 1 |
GANIS, FM; HENDRICKSON, MW; HOWLAND, JW | 1 |
Bröer, A; Bröer, S; Gelpí, JL; Kaltenbach, S; Lang, F; Martín Del Río, R; Palacín, M; Pineda, M; Stehberger, PA; Wagner, CA; Zorzano, A | 1 |
Caspary, WF | 1 |
Clifton, JA | 1 |
Francois, J | 1 |
Houpt, JB; Hunt, M; Ogryzlo, MA | 1 |
Alpers, DH; Thier, SO | 1 |
Groth, U; Rosenberg, LE | 1 |
Gibbs, DA; Watts, RW | 1 |
Abdel Kader, MM; Abdel Wahab, F; Ata, AA; Emara, SH; Soliman, L | 1 |
Martin, GM; Platter, H | 1 |
4 review(s) available for tryptophan and Cystinuria
Article | Year |
---|---|
[RENAL TUBULAR DISEASES, WITH SPECIAL REFERENCE TO AMINOACIDURIA].
Topics: Cystinosis; Cystinuria; Galactosemias; Genetics, Medical; Glycine; Hepatolenticular Degeneration; Humans; Kidney; Kidney Diseases; Kidney Tubules; Metabolic Diseases; Metabolism; Multiple Myeloma; Nephrotic Syndrome; Pellagra; Renal Aminoacidurias; Tryptophan; Urine | 1964 |
[Nephrolithiasis and the gastrointestinal tract].
Topics: Amino Acids; Biological Transport; Calcium Oxalate; Cystinuria; Dehydration; Digestive System; Glutamine; Hartnup Disease; Humans; Kidney Calculi; Niacinamide; Oxalates; Solubility; Tryptophan | 1979 |
Hereditary chorioretinal degeneration and metabolic disturbances.
Topics: Abetalipoproteinemia; Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Cystinuria; Female; Growth Disorders; Humans; Lipid Metabolism, Inborn Errors; Lipids; Lipoproteins; Metabolism, Inborn Errors; Mice; Mucopolysaccharidoses; Rabbits; Rats; Refsum Disease; Retinal Degeneration; Retinal Pigments; Tryptophan | 1968 |
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 |
8 other study(ies) available for tryptophan and Cystinuria
Article | Year |
---|---|
AMINO ACID EXCRETION IN HUMAN PATIENTS ACCIDENTALLY EXPOSED TO LARGE DOSES OF PARTIAL-BODY IONIZING RADIATION. (THE LOCKPORT INCIDENT).
Topics: Accidents; Accidents, Occupational; Amino Acids; Chromatography; Cystinuria; Fluids and Secretions; Proline; Radiation Injuries; Radiation, Ionizing; Tryptophan; Urine | 1965 |
Cystinuria-specific rBAT(R365W) mutation reveals two translocation pathways in the amino acid transporter rBAT-b0,+AT.
Topics: Amino Acid Substitution; Amino Acid Transport System ASC; Amino Acid Transport Systems; Amino Acid Transport Systems, Basic; Animals; Arginine; Carrier Proteins; Cell Line, Tumor; Cystinuria; Female; HeLa Cells; Humans; Membrane Glycoproteins; Minor Histocompatibility Antigens; Mutation; Oocytes; Transfection; Tryptophan; Xenopus laevis | 2004 |
[Some hereditary disorders of intestinal resorption with renal dysfunction].
Topics: Arginine; Child; Chlorides; Cystine; Cystinuria; Diarrhea; Female; Galactose; Glucose; Hartnup Disease; Humans; Infant, Newborn; Intestinal Absorption; Kidney Diseases; Lysine; Malabsorption Syndromes; Male; Pedigree; Tryptophan | 1976 |
Tryptophan metabolism in man (with special reference to rheumatoid arthritis and scleroderma).
Topics: Arthritis, Rheumatoid; Aspirin; Cystinuria; Drug Synergism; Edetic Acid; Humans; Kynurenic Acid; Kynurenine; Methods; Niacinamide; Penicillamine; Pyridoxine; Scleroderma, Systemic; Tryptophan; Xanthurenates | 1973 |
Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease.
Topics: Adult; Amino Acids; Arginine; Biological Transport; Cell Line; Cells, Cultured; Cystine; Cystinuria; Female; Fibroblasts; Hartnup Disease; Humans; Infant; Lysine; Male; Mutation; Skin; Tryptophan | 1972 |
Studies on the effect of D-penicillamine and N-acetyl-D-penicillamine on the excretion of some tryptophan metabolites in patients with cystinuria.
Topics: Adolescent; Adult; Child; Cystinuria; Female; Humans; Kynurenine; Male; ortho-Aminobenzoates; Penicillamine; Pyridoxine; Tryptophan | 1969 |
Urinary amino acid patterns in simple and complicated bilharziasis.
Topics: Adolescent; Adult; Aged; Alanine; Amino Acids; Ascites; Chromatography, Paper; Cystinuria; Hepatomegaly; Humans; Liver Diseases; Male; Middle Aged; Schistosomiasis; Splenomegaly; Threonine; Tryptophan; Tyrosine | 1969 |
Tryptophane transport in cultures of human fibroblasts.
Topics: Biological Transport; Culture Techniques; Cystinuria; Fibroblasts; Hartnup Disease; Humans; Kinetics; Tryptophan | 1966 |