n-acetylglucosaminylasparagine and glucosamine

n-acetylglucosaminylasparagine has been researched along with glucosamine in 28 studies

Compound Research Comparison

Studies (n-acetylglucosaminylasparagine)	Trials (n-acetylglucosaminylasparagine)	Recent Studies (post-2010) (n-acetylglucosaminylasparagine)	Studies (glucosamine)	Trials (glucosamine)	Recent Studies (post-2010) (glucosamine)
111	0	3	10,273	280	1,467

Research

Studies (28)

Timeframe	Studies, this research(%)	All Research%
pre-1990	27 (96.43)	18.7374
1990's	1 (3.57)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Borud, O; Lie, SO; Strömme, JH; Torp, KH	1
Maury, P	1
Kärkkäinen, J; Maury, P	1
Arvio, M; Autio, S; Humaloja, K; Palo, J; Salaspuro, M; Salmela, K	1
Mononen, TK	1
Kaartinen, V; Mononen, I	1
Heino, J; Larjava, H; Näntö-Salonen, K; Pelliniemi, LJ; Penttinen, R; Säämanen, AM; Tammi, M	1
Rudy, JL	1
Alfthan, G; Halme, T; Langevelde, FV; Näntö-Salonen, K; Penttinen, R; Vis, RD	1
Mononen, I; Mononen, T; Parviainen, M; Penttilä, I	1
Aalto, M; Kivimäki, T; Larjava, H; Näntö-Salonen, K	1
Bendiak, B; Cumming, DA	1
Haltia, M; Maury, CP; Palo, J	1
Autio, S; Härö, E; Kivimäki, T; Koskela, SL; Näntö, V; Näntö-Salonen, K; Penttinen, R	1
Ammälä, P; Aula, P; Rapola, J; von Koskull, H	1
Autio, S; Kivimäki, T; Näntö-Salonen, K; Pelliniemi, LJ; Penttinen, R; Rapola, J	1
Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J	2
Maury, CP	3
Näntö-Salonen, K; Penttinen, R	1
Ishihara, H; Sugiyama, K; Takahashi, N; Tejima, S	1
Blumberg, K; Brown, JN; Bush, CA	1
Carter, RJ; Snyder, FF	1
Maury, P; Palo, J	1
Marnela, KM	1
Maury, CP; Palo, J	1

Reviews

1 review(s) available for n-acetylglucosaminylasparagine and glucosamine

Article	Year
Aspartylglycosaminuria: an inborn error of glycoprotein catabolism. Journal of inherited metabolic disease, 1982, Volume: 5, Issue:4 Topics: Acetylglucosamine; Brain; Glucosamine; Glycoproteins; Humans; Liver; Metabolism, Inborn Errors	1982

Other Studies

27 other study(ies) available for n-acetylglucosaminylasparagine and glucosamine

Article	Year
Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet. Journal of inherited metabolic disease, 1978, Volume: 1, Issue:3 Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Creatinine; Dietary Proteins; Female; Glucosamine; Humans; Intellectual Disability; Male; Mucolipidoses	1978
Quantitative determination of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in the urine of patients with aspartylglycosaminuria by gas-liquid chromatography. The Journal of laboratory and clinical medicine, 1979, Volume: 93, Issue:5 Topics: Acetylglucosamine; Adolescent; Adult; Asparagine; Child; Child, Preschool; Chromatography, Gas; Female; Gas Chromatography-Mass Spectrometry; Glucosamine; Humans; Male; Mucolipidoses	1979
Identification of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in biological materials by gas chromatography-mass spectrometry. Clinica chimica acta; international journal of clinical chemistry, 1979, Jan-01, Volume: 91, Issue:1 Topics: Acetylglucosamine; Adult; Asparagine; Chromatography, Gas; Female; Glucosamine; Glycopeptides; Humans; Mass Spectrometry; Mucolipidoses; Ovalbumin	1979
Elevated levels of serum dolichol in aspartylglucosaminuria. Life sciences, 1990, Volume: 47, Issue:7 Topics: Acetylglucosamine; Adult; alpha-Mannosidosis; Dolichols; Female; Glucosamine; Humans; Male; Metabolism, Inborn Errors; Middle Aged	1990
Aspartylglucosamine excretion in heterozygous carriers of aspartylglycosaminuria. Clinica chimica acta; international journal of clinical chemistry, 1989, Mar-15, Volume: 180, Issue:1 Topics: Acetylglucosamine; Amidohydrolases; Aspartylglucosaminuria; Glucosamine; Heterozygote; Humans	1989
Analysis of aspartylglucosamine at the picomole level by high-performance liquid chromatography. Journal of chromatography, 1989, May-30, Volume: 490, Issue:2 Topics: Acetylglucosamine; Adolescent; Adult; Child; Chromatography, High Pressure Liquid; Glucosamine; Humans; Leukocytes; Spectrophotometry, Ultraviolet	1989
Abnormal dermal proteoglycan in aspartylglycosaminuria: a possible mechanism for ultrastructural changes of collagen fibrils in a glycoprotein storage disorder. Connective tissue research, 1987, Volume: 16, Issue:4 Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartylglucosaminuria; Chondroitin Lyases; Chondroitin Sulfates; Collagen; Dermatan Sulfate; Electrophoresis, Polyacrylamide Gel; Female; Glucosamine; Glucuronates; Glucuronic Acid; Heparitin Sulfate; Humans; Male; Microscopy, Electron; Proteoglycans; Skin	1987
Aspartylglycosaminuria diagnosed by routine urine amino acid assay. Clinical chemistry, 1988, Volume: 34, Issue:10 Topics: Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Diagnostic Tests, Routine; Glucosamine; Glycoside Hydrolases; Humans	1988
Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes. Journal of inherited metabolic disease, 1985, Volume: 8, Issue:4 Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartylglucosaminuria; Cells, Cultured; Child; Copper; Female; Fibroblasts; Glucosamine; Hair; Humans; Male; Metabolism, Inborn Errors; Zinc	1985
Liquid-chromatographic detection of aspartylglycosaminuria. Clinical chemistry, 1986, Volume: 32, Issue:3 Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartylglucosaminuria; Child; Child, Preschool; Chromatography, High Pressure Liquid; Female; Glucosamine; Humans; Infant; Male	1986
Urinary glycosaminoglycans in aspartylglycosaminuria: evidence for disturbed proteoglycan metabolism. Clinica chimica acta; international journal of clinical chemistry, 1985, Mar-15, Volume: 146, Issue:2-3 Topics: Acetylglucosamine; Adolescent; Adult; Chromatography, High Pressure Liquid; Chromatography, Thin Layer; Electrophoresis, Cellulose Acetate; Female; Glucosamine; Glycoproteins; Glycosaminoglycans; Humans; Male; Metabolism, Inborn Errors	1985
Hydrazinolysis-N-reacetylation of glycopeptides and glycoproteins. Model studies using 2-acetamido-1-N-(L-aspart-4-oyl)-2-deoxy-beta-D-glucopyranosy lamine. Carbohydrate research, 1985, Nov-15, Volume: 144, Issue:1 Topics: Acetylation; Acetylglucosamine; Chemical Phenomena; Chemistry; Glucosamine; Glycopeptides; Glycoproteins; Hydrazines; Hydrolysis; Indicators and Reagents; Magnetic Resonance Spectroscopy	1985
Regional distribution of glycoasparagine storage material in the brain in aspartylglycosaminuria. Journal of the neurological sciences, 1981, Volume: 50, Issue:2 Topics: Acetylglucosamine; Adult; Asparagine; Aspartic Acid; Axonal Transport; Brain; Capillaries; Endothelium; Glucosamine; Glycopeptides; Humans; Lysosomes; Male; Microscopy, Electron; Nerve Fibers, Myelinated; Neurons	1981
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline. Journal of inherited metabolic disease, 1984, Volume: 7, Issue:3 Topics: Acetylglucosamine; Adolescent; Adult; Age Factors; Child; Child, Preschool; Collagen; Connective Tissue Diseases; Female; Glucosamine; Humans; Hydroxyproline; Infant; Intellectual Disability; Male; Metabolism, Inborn Errors; Middle Aged; Reference Values	1984
Prenatal diagnosis and fetal pathology of aspartylglucosaminuria. American journal of medical genetics, 1984, Volume: 19, Issue:2 Topics: Acetylglucosamine; Amidohydrolases; Amniotic Fluid; Aspartylglucosaminuria; Aspartylglucosylaminase; Cells, Cultured; Chorionic Villi; Female; Fetus; Glucosamine; Heterozygote; Humans; Lysosomes; Male; Pregnancy; Prenatal Diagnosis	1984
Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder. Laboratory investigation; a journal of technical methods and pathology, 1984, Volume: 51, Issue:4 Topics: Acetylglucosamine; Adult; Biopsy; Cells, Cultured; Child; Child, Preschool; Collagen; Female; Fibroblasts; Glucosamine; Glycogen Storage Disease; Humans; Male; Microscopy, Electron; Microscopy, Electron, Scanning; Skin	1984
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family. Helvetica paediatrica acta, 1981, Volume: 36, Issue:2 Topics: Abnormalities, Multiple; Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Fabry Disease; Facial Bones; Female; Glucosamine; Humans; Intellectual Disability; Italy; Male; Pedigree; Skull	1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics. Journal of inherited metabolic disease, 1981, Volume: 4, Issue:4 Topics: Acetylglucosamine; Adult; Amidohydrolases; Aspartylglucosaminuria; Child; Consanguinity; Female; Glucosamine; Humans; Intellectual Disability; Leukocytes; Male; Oligosaccharides; Pedigree	1981
Metabolism of collagen in aspartylglycosaminuria: decreased synthesis by cultured fibroblasts. Journal of inherited metabolic disease, 1982, Volume: 5, Issue:4 Topics: Acetylglucosamine; Aspartylglucosylaminase; Cells, Cultured; Collagen; Culture Media; Fibroblasts; Glucosamine; Humans; Procollagen; Proline	1982
Demonstration of a new glycopeptidase, from jack-bean meal, acting on aspartylglucosylamine linkages. Biochemical and biophysical research communications, 1983, Apr-15, Volume: 112, Issue:1 Topics: Acetylglucosamine; Amidohydrolases; Ammonia; Asparagine; Chemical Phenomena; Chemistry; Fabaceae; Glucosamine; Hydrolysis; Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase; Plants, Medicinal; Structure-Activity Relationship	1983
Crystal structure and solution conformation of 1-N-acetyl-beta-D-glucopyranosyl amine: a model for the glycopeptide linkage. Biopolymers, 1982, Volume: 21, Issue:10 Topics: Acetylglucosamine; Carbohydrate Conformation; Glucosamine; Glycopeptides; Solutions	1982
Detection of aspartylglycosaminuria by gas--liquid chromatography. Clinical chemistry, 1981, Volume: 27, Issue:12 Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Glucosamine; Humans; Middle Aged	1981
Measurement of aspartylglucosamine in physiological fluids with an amino acid analyzer: fused peak analysis with dual photometers. Analytical biochemistry, 1981, Sep-15, Volume: 116, Issue:2 Topics: Acetylglucosamine; Amino Acids; Body Fluids; Glucosamine; Humans; Mathematics; Spectrophotometry; Urea	1981
Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria. Clinical science (London, England : 1979), 1980, Volume: 58, Issue:2 Topics: Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Female; Gas Chromatography-Mass Spectrometry; Glucosamine; Humans; Lymphocytes; Vacuoles	1980
Automated ion-exchange chromatography in the detection of aspartylglucosaminuria. Journal of chromatography, 1980, Jun-13, Volume: 182, Issue:3-4 Topics: Acetylglucosamine; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Autoanalysis; Chromatography, Ion Exchange; Glucosamine; Humans; Microchemistry	1980
Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria. The Journal of laboratory and clinical medicine, 1980, Volume: 96, Issue:5 Topics: Acetylglucosamine; Amidohydrolases; Asparagine; Aspartylglucosaminuria; Glucosamine; Humans; Kidney; Nerve Tissue; Oligosaccharides; Spleen; Thyroid Gland; Tissue Distribution	1980
N-Acetylglucosamine-asparagine levels in tissues of patients with aspartylglycosaminuria. Clinica chimica acta; international journal of clinical chemistry, 1980, Dec-08, Volume: 108, Issue:2 Topics: Acetylglucosamine; Adult; Amidohydrolases; Asparagine; Aspartic Acid; Aspartylglucosaminuria; Endocytosis; Female; Glucosamine; Glycoproteins; Humans; Lysosomes; Male; Tissue Distribution	1980