asparagine has been researched along with Inborn Errors of Metabolism in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 8 (80.00) | 18.7374 |
1990's | 2 (20.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fujii, H; Krietsch, WK; Yoshida, A | 1 |
Fukushima, K; Ideo, H; Ohkura, T; Ohno, K; Takeshita, K; Yamashita, K; Yuasa, I | 1 |
Tuchman, M; Yudkoff, M | 1 |
Alla, P; Funakoshi, I; Funakoshi, S; Sugahara, K; Yamashina, I | 1 |
Akasaki, M; Aula, P; Funakoshi, I; Sugahara, K; Yamashina, I | 2 |
Lundblad, A; Masson, PK; Nordén, NE | 1 |
Aula, P; Funakoshi, I; Funakoshi, S; Sugahara, K; Yamashina, I | 1 |
Jenner, FA; Merskey, H; Pollitt, RJ | 1 |
Pollitt, RJ; Pretty, KM | 1 |
10 other study(ies) available for asparagine and Inborn Errors of Metabolism
Article | Year |
---|---|
A single amino acid substitution (Asp leads to Asn) in a phosphoglycerate kinase variant (PGK München) associated with enzyme deficiency.
Topics: Amino Acid Sequence; Amino Acids; Asparagine; Aspartic Acid; Erythrocytes; Genetic Variation; Humans; Metabolism, Inborn Errors; Peptides; Phosphoglycerate Kinase | 1980 |
Sugar chains of serum transferrin from patients with carbohydrate deficient glycoprotein syndrome. Evidence of asparagine-N-linked oligosaccharide transfer deficiency.
Topics: Asparagine; Carbohydrate Metabolism, Inborn Errors; Carbohydrate Sequence; Carbohydrates; Chromatography, Affinity; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Humans; Isoelectric Point; Lectins; Metabolism, Inborn Errors; Molecular Sequence Data; Oligosaccharides; Syndrome; Transferrin | 1993 |
Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
Topics: Adolescent; Adult; Alanine; Amino Acids; Ammonia; Asparagine; Carbon-Nitrogen Ligases; Child; Child, Preschool; Data Interpretation, Statistical; Female; Glutamine; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Retrospective Studies | 1999 |
Characterization of one neutral and two acidic glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU).
Topics: Asparagine; Clostridium perfringens; Glycopeptides; Humans; Metabolism, Inborn Errors; Molecular Conformation; Neuraminidase | 1976 |
Structure of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU).
Topics: Asparagine; Carbohydrates; Chromatography, Gas; Humans; Kinetics; Metabolism, Inborn Errors; Neuraminidase; Oligosaccharides | 1977 |
Structural studies of glycoasparagines from urine of a patient with aspartylglycosylaminuria (AGU).
Topics: Acetylglucosamine; Aminoglycosides; Asparagine; Galactose; Humans; Metabolism, Inborn Errors; Sialic Acids | 1977 |
Structural determination of three glycoasparagines isolated from the urine of a patient with aspartylglycosaminuria.
Topics: Acetylglucosamine; Adult; Asparagine; Female; Galactose; Humans; Mannose; Metabolism, Inborn Errors; Molecular Conformation; Oligosaccharides; Optical Rotation | 1976 |
Characterization of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU).
Topics: Amidohydrolases; Asparagine; Aspartylglucosaminuria; Galactose; Galactosidases; Glucosamine; Metabolism, Inborn Errors; Neuraminidase; Sialic Acids | 1975 |
Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.
Topics: Adult; Asparagine; Aspartic Acid; Female; Glucosamine; Glucosidases; Glycoproteins; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Oligosaccharides; Peptide Hydrolases | 1968 |
The glycoasparagines in urine of a patient with aspartylglycosaminuria.
Topics: Asparagine; Aspartic Acid; Chromatography, Gas; Chromatography, Gel; Chromatography, Ion Exchange; Electrophoresis, Paper; Female; Glucosamine; Glycopeptides; Glycosuria; Humans; Hydrogen-Ion Concentration; Metabolism, Inborn Errors; Models, Chemical | 1974 |