mannose has been researched along with alpha-Dystroglycanopathies in 5 studies
| 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 | 5 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Endo, T; Manya, H | 1 |
| Bai, L; Kenny, A; Kovach, A; Li, H; You, Q | 1 |
| Adema, GJ; Ashikov, A; Boltje, TJ; Büll, C; Heise, T; Lefeber, DJ; Riemersma, M; Sandrock, J; van Bokhoven, H | 1 |
| Dwyer, CA; Katoh, T; Matthews, RT; Tiemeyer, M | 1 |
| Campbell, KP; Cirak, S; de Bernabe, DB; Dobyns, WB; Lee, H; Loder, AS; Lommel, M; Mathews, KD; Moore, SA; Muntoni, F; Nelson, SF; Schachter, H; Strahl, S; Vajsar, J; Venzke, D; Voit, T; Willer, T; Winder, TL; Yoshida-Moriguchi, T | 1 |
1 review(s) available for mannose and alpha-Dystroglycanopathies
| Article | Year |
|---|---|
Glycosylation with ribitol-phosphate in mammals: New insights into the O-mannosyl glycan.
Topics: Animals; Brain; Carbohydrate Sequence; Dystroglycans; Glycosylation; Humans; Mannose; Models, Molecular; Muscle, Skeletal; Muscular Dystrophies; N-Acetylglucosaminyltransferases; Pentosephosphates; Polysaccharides; Protein Processing, Post-Translational; Walker-Warburg Syndrome | 2017 |
4 other study(ies) available for mannose and alpha-Dystroglycanopathies
| Article | Year |
|---|---|
Structure of the eukaryotic protein O-mannosyltransferase Pmt1-Pmt2 complex.
Topics: Cryoelectron Microscopy; Glycosylation; Humans; Image Processing, Computer-Assisted; Mannose; Mannosyltransferases; Models, Molecular; Multienzyme Complexes; Protein Conformation; Protein Domains; Protein Folding; Protein Processing, Post-Translational; Recombinant Proteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Species Specificity; Substrate Specificity; Walker-Warburg Syndrome | 2019 |
Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acid.
Topics: Cell Line; Cytidine Monophosphate; Dystroglycans; Humans; Mannose; Mutation; N-Acetylneuraminic Acid; Nucleotide Transport Proteins; Walker-Warburg Syndrome | 2015 |
Neurons and glia modify receptor protein-tyrosine phosphatase ζ (RPTPζ)/phosphacan with cell-specific O-mannosyl glycans in the developing brain.
Topics: Amino Sugars; Animals; Animals, Newborn; Antibodies, Monoclonal; Brain; Carbohydrate Sequence; Disease Models, Animal; Gene Expression Regulation, Developmental; Glycosylation; Isoenzymes; Mannose; Mice; Mice, Knockout; Molecular Sequence Data; N-Acetylglucosaminyltransferases; Neuroglia; Neurons; Organ Specificity; Receptor-Like Protein Tyrosine Phosphatases, Class 5; Signal Transduction; Walker-Warburg Syndrome | 2015 |
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome.
Topics: Cells, Cultured; Dystroglycans; Fibroblasts; Genetic Complementation Test; Glycosylation; Humans; Infant; Laminin; Mannose; Mannosyltransferases; Mutation; Nucleotidyltransferases; Polysaccharides; Skin; Walker-Warburg Syndrome | 2012 |