glucose-1,6-bisphosphate has been researched along with Congenital Disorders of Glycosylation in 2 studies
*Congenital Disorders of Glycosylation: A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Allocca, M; Andreotti, G; Cubellis, MV; Liguori, L; Monticelli, M | 1 |
| Andreotti, G; Citro, V; Cubellis, MV; Monti, MC | 1 |
2 other study(ies) available for glucose-1,6-bisphosphate and Congenital Disorders of Glycosylation
| Article | Year |
|---|---|
β-Glucose-1,6-Bisphosphate Stabilizes Pathological Phophomannomutase2 Mutants In Vitro and Represents a Lead Compound to Develop Pharmacological Chaperones for the Most Common Disorder of Glycosylation, PMM2-CDG.
Topics: Congenital Disorders of Glycosylation; Glucose-6-Phosphate; Humans; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Conformation; Mutation; Phosphotransferases (Phosphomutases); Protein Binding | 2019 |
Heterodimerization of Two Pathological Mutants Enhances the Activity of Human Phosphomannomutase2.
Topics: Alleles; Congenital Disorders of Glycosylation; Dimerization; Glucose-6-Phosphate; Glycosylation; Heterozygote; Humans; Mutation; Phosphorylation; Phosphotransferases (Phosphomutases); Protein Structure, Quaternary | 2015 |