tryptophan and Cystinuria

tryptophan has been researched along with Cystinuria in 12 studies

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-199011 (91.67)18.7374
1990's0 (0.00)18.2507
2000's1 (8.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
MILNE, MD1
GANIS, FM; HENDRICKSON, MW; HOWLAND, JW1
Bröer, A; Bröer, S; Gelpí, JL; Kaltenbach, S; Lang, F; Martín Del Río, R; Palacín, M; Pineda, M; Stehberger, PA; Wagner, CA; Zorzano, A1
Caspary, WF1
Clifton, JA1
Francois, J1
Houpt, JB; Hunt, M; Ogryzlo, MA1
Alpers, DH; Thier, SO1
Groth, U; Rosenberg, LE1
Gibbs, DA; Watts, RW1
Abdel Kader, MM; Abdel Wahab, F; Ata, AA; Emara, SH; Soliman, L1
Martin, GM; Platter, H1

Reviews

4 review(s) available for tryptophan and Cystinuria

ArticleYear
[RENAL TUBULAR DISEASES, WITH SPECIAL REFERENCE TO AMINOACIDURIA].
    Recenti progressi in medicina, 1964, Volume: 36

    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].
    Zeitschrift fur Gastroenterologie. Verhandlungsband, 1979, Volume: 16

    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.
    International ophthalmology clinics, 1968,Winter, Volume: 8, Issue:4

    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.
    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

Other Studies

8 other study(ies) available for tryptophan and Cystinuria

ArticleYear
AMINO ACID EXCRETION IN HUMAN PATIENTS ACCIDENTALLY EXPOSED TO LARGE DOSES OF PARTIAL-BODY IONIZING RADIATION. (THE LOCKPORT INCIDENT).
    Radiation research, 1965, Volume: 24

    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.
    The Biochemical journal, 2004, Feb-01, Volume: 377, Issue:Pt 3

    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].
    Der Internist, 1976, Volume: 17, Issue:7

    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).
    Seminars in arthritis and rheumatism, 1973, Volume: 2, Issue:4

    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.
    The Journal of clinical investigation, 1972, Volume: 51, Issue:8

    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.
    Clinical science, 1969, Volume: 36, Issue:1

    Topics: Adolescent; Adult; Child; Cystinuria; Female; Humans; Kynurenine; Male; ortho-Aminobenzoates; Penicillamine; Pyridoxine; Tryptophan

1969
Urinary amino acid patterns in simple and complicated bilharziasis.
    The Journal of tropical medicine and hygiene, 1969, Volume: 72, Issue:7

    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.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1966, Volume: 123, Issue:1

    Topics: Biological Transport; Culture Techniques; Cystinuria; Fibroblasts; Hartnup Disease; Humans; Kinetics; Tryptophan

1966