asparagine has been researched along with AGA Deficiency in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (62.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 1 (12.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Guo, HC; Lakshminarasimhan, D; Pande, S | 1 |
| Dunder, U; Kelo, E; Mononen, I | 1 |
| Maury, CP | 1 |
| Maury, CP; Palo, J | 1 |
| Aalto, AM; Arvio, M; Aula, P; Hietala, M; Järvinen, O; Kääriäinen, H; Uutela, A | 1 |
| Borud, O; Torp, KH | 1 |
| Akasaki, M; Aula, P; Funakoshi, I; Sugahara, K; Yamashina, I | 1 |
| Aula, P; Funakoshi, I; Funakoshi, S; Sugahara, K; Yamashina, I | 1 |
8 other study(ies) available for asparagine and AGA Deficiency
| Article | Year |
|---|---|
Crystal structure of a mutant glycosylasparaginase shedding light on aspartylglycosaminuria-causing mechanism as well as on hydrolysis of non-chitobiose substrate.
Topics: Asparagine; Aspartylglucosaminuria; Aspartylglucosylaminase; Biocatalysis; Crystallization; Crystallography, X-Ray; Disaccharides; Glycopeptides; Humans; Hydrolysis; Lysosomes; Models, Molecular; Mutant Proteins; Mutation; Substrate Specificity | 2017 |
Massive accumulation of Man2GlcNAc2-Asn in nonneuronal tissues of glycosylasparaginase-deficient mice and its removal by enzyme replacement therapy.
Topics: Animals; Asparagine; Aspartylglucosaminuria; Aspartylglucosylaminase; Liver; Mice; Mice, Knockout; Neurons; Oligosaccharides | 2005 |
Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria.
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.
Topics: Acetylglucosamine; Adult; Amidohydrolases; Asparagine; Aspartic Acid; Aspartylglucosaminuria; Endocytosis; Female; Glucosamine; Glycoproteins; Humans; Lysosomes; Male; Tissue Distribution | 1980 |
A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria.
Topics: Adolescent; Asparagine; Aspartylglucosaminuria; Child; Child, Preschool; Demography; Female; Genetic Carrier Screening; Genetic Counseling; Glycopeptides; Health Knowledge, Attitudes, Practice; Humans; Infant; Lysosomal Storage Diseases; Male; Retrospective Studies; Sociology, Medical | 2000 |
[Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Finland; Glucosamine; Humans; Infant; Intellectual Disability; Male; Norway | 1978 |
Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU).
Topics: Acetylglucosamine; Amidohydrolases; Asparagine; Aspartylglucosaminuria; Gas Chromatography-Mass Spectrometry; Glucosamine; Hexosaminidases; Humans; Mannose; Mannosidases; Oligosaccharides | 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 |