asparagine has been researched along with Carbohydrate-Deficient Glycoprotein Syndrome in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 4 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Beahm, B; Cowan, T; Crawford, BE; Dwight, S; Mak, J; Mueller, WF; Pritchett, J; Tan, B; Taylor, E; Wechsler, T; Wilsey, M; Zhu, L | 1 |
| Candelo, E; Pachajoa, H; Ramírez-Montaño, D | 1 |
| Chen, H; Lu, G; Miao, X; Wu, J | 1 |
| Ceylan, AC; Erdal, AE; Gücüyener, K; Kasapkara, ÇS; Kıreker Köylü, O; Öktem, RM | 1 |
| Hayashi, H; Yamashita, Y | 1 |
| Campbell, RM; Dell, A; Ditto, D; Jaeken, J; Le, D; Levinson, SR; Long, JM; Marth, JD; Morris, HR; Panico, M; Schachter, H; Sutton-Smith, M; Tan, J; Varki, NM; Wang, Y; Wynshaw-Boris, A | 1 |
2 review(s) available for asparagine and Carbohydrate-Deficient Glycoprotein Syndrome
| Article | Year |
|---|---|
Comprehensive Analysis of the Structure and Function of Peptide:N-Glycanase 1 and Relationship with Congenital Disorder of Deglycosylation.
Topics: Asparagine; Congenital Disorders of Glycosylation; Humans; Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase; Peptides; Solute Carrier Family 12, Member 2 | 2022 |
ALG11-CDG: novel variant and review of the literature.
Topics: Asparagine; Child, Preschool; Congenital Disorders of Glycosylation; Glycosylation; Humans; Male; Mannosyltransferases; Mutation; Seizures | 2023 |
4 other study(ies) available for asparagine and Carbohydrate-Deficient Glycoprotein Syndrome
| Article | Year |
|---|---|
GlcNAc-Asn is a biomarker for NGLY1 deficiency.
Topics: Asparagine; Biomarkers; Congenital Disorders of Glycosylation; Humans; Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase | 2022 |
[New variant in the ALG13 gene responsible for the congenital disorder of Is-type glycosylation in a male patient].
Topics: Asparagine; Child; Congenital Disorders of Glycosylation; Exome Sequencing; Genes, X-Linked; Glycosylation; Humans; Male; N-Acetylglucosaminyltransferases | 2021 |
Role of N-glycosylation in cell surface expression and protection against proteolysis of the intestinal anion exchanger SLC26A3.
Topics: Amino Acid Substitution; Animals; Asparagine; Cell Membrane; Chloride-Bicarbonate Antiporters; CHO Cells; Congenital Disorders of Glycosylation; Cricetinae; Cricetulus; Glutamine; Glycoside Hydrolases; Glycosylation; Humans; Hydrogen-Ion Concentration; Intestinal Absorption; Intestinal Mucosa; Mutagenesis, Site-Directed; Oligosaccharides; Proteolysis; Sulfate Transporters | 2012 |
Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis.
Topics: Abnormalities, Multiple; Animals; Asparagine; Bone Diseases, Metabolic; Congenital Disorders of Glycosylation; Disease Models, Animal; Glomerulonephritis; Glycosylation; Humans; Male; Mice; Mice, Inbred ICR; Mice, Mutant Strains; Mutation; N-Acetylglucosaminyltransferases; Polysaccharides; Species Specificity; Testis; Tissue Distribution | 2001 |