mannose has been researched along with Muscular Dystrophy in 19 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (5.26) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (21.05) | 29.6817 |
| 2010's | 13 (68.42) | 24.3611 |
| 2020's | 1 (5.26) | 2.80 |
| Authors | Studies |
|---|---|
| Chompoopong, P; Milone, M | 1 |
| Endo, T; Manya, H | 2 |
| Halmo, SM; Sheikh, MO; Wells, L | 1 |
| Boons, GJ; Live, D; Wells, L | 1 |
| Panin, VM; Wells, L | 1 |
| Hu, W; Li, ZF; Lv, F; Wu, X | 1 |
| Campbell, KP; Davis, S; Kunz, S; Madson, M; Oldstone, MB; Schachter, H; Stalnaker, SH; Wells, L; Yoshida-Moriguchi, T; Yu, L | 1 |
| Lyalin, D; Nakamura, N; Panin, VM | 1 |
| Aoki, K; Buskirk, S; Campbell, KP; Hu, H; Lim, JM; Liu, M; Live, D; Porterfield, M; Satz, JS; Stalnaker, SH; Tiemeyer, M; Wells, L; Xiong, Y; Zhang, P | 1 |
| Stalnaker, SH; Stuart, R; Wells, L | 1 |
| Lim, JM; Liu, M; Live, D; Stalnaker, SH; Ten Hagen, KG; Tran, DT; Wells, L | 1 |
| Aiello, C; Barone, R; Bertini, E; Carella, M; Concolino, D; Fiumara, A; Foulquier, F; Garozzo, D; Jaeken, J; Lefeber, DJ; Matthijs, G; Mercuri, E; Messina, S; Morava, E; Passarelli, C; Race, V; Riemersma, M; Santorelli, F; Sturiale, L; Vleugels, W; Wevers, RA | 1 |
| Dobson, CM; Hempel, SJ; Stalnaker, SH; Stuart, R; Wells, L | 1 |
| Wells, L | 1 |
| Cruces, J; Strahl, S; Tanner, W; Valero, MC; Willer, T | 1 |
| Endo, T | 2 |
| Atkins, L; Kanvfer, JN; Kolodny, EH; Littlefield, JW; Milunsky, A; Shih, VE | 1 |
13 review(s) available for mannose and Muscular Dystrophy
| Article | Year |
|---|---|
GDP-Mannose Pyrophosphorylase B (
Topics: Acetylcholinesterase; Dystroglycans; Humans; Mannose; Muscle Weakness; Muscular Dystrophies; Muscular Dystrophies, Limb-Girdle | 2023 |
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 |
Recent advancements in understanding mammalian O-mannosylation.
Topics: Animals; Arenavirus; Dystroglycans; Evolution, Molecular; Glycosylation; Glycosyltransferases; Humans; Mammals; Mannose; Muscular Dystrophies; Neoplasms; Protein Processing, Post-Translational; Receptors, Virus | 2017 |
Dissecting the molecular basis of the role of the O-mannosylation pathway in disease: α-dystroglycan and forms of muscular dystrophy.
Topics: Amino Acid Sequence; Animals; Carbohydrate Sequence; Dystroglycans; Glycoconjugates; Glycopeptides; Humans; Mannose; Molecular Sequence Data; Muscular Dystrophies | 2013 |
Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypes.
Topics: Animals; Carbohydrate Conformation; Carbohydrate Sequence; Drosophila; Dystroglycans; Dystrophin; Glycosylation; Humans; Mannose; Mannosyltransferases; Molecular Sequence Data; Muscular Dystrophies; Phenotype; Polysaccharides | 2010 |
Mammalian O-mannosylation: unsolved questions of structure/function.
Topics: Animals; Brain; Dystroglycans; Dystrophin; Glycosylation; Humans; Mammals; Mannose; Mannosyltransferases; Membrane Proteins; Muscular Dystrophies; Mutation; Polysaccharides; Protein Processing, Post-Translational; Structure-Activity Relationship | 2011 |
O-Mannosylation and human disease.
Topics: Animals; Arenaviridae Infections; Dystroglycans; Glycosylation; Humans; Mannose; Muscular Dystrophies; Neoplasm Metastasis; Neoplasms | 2013 |
The o-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy.
Topics: Animals; Genetic Predisposition to Disease; Glycoproteins; Glycosylation; Glycosyltransferases; Humans; Mannose; Muscular Dystrophies; Mutation; Signal Transduction | 2013 |
O-mannosyl glycans: from yeast to novel associations with human disease.
Topics: Animals; Glycoproteins; Humans; Mammals; Mannose; Mannosyltransferases; Molecular Conformation; Molecular Structure; Muscular Dystrophies; Polysaccharides; Saccharomyces cerevisiae; Species Specificity; Structure-Activity Relationship; Yeasts | 2003 |
Structure, function and pathology of O-mannosyl glycans.
Topics: Animals; Glycoproteins; Glycosylation; Humans; Mannose; Models, Biological; Muscular Dystrophies; Mutation; Peptides; Polysaccharides | 2004 |
[Defective O-mannosyl glycosylation causes congenital muscular dystrophies].
Topics: Abnormalities, Multiple; Animals; Brain; Dystroglycans; Eye Abnormalities; Glycosylation; Humans; Mannose; Mannosyltransferases; Muscular Dystrophies; Mutation; N-Acetylglucosaminyltransferases; Syndrome | 2004 |
[Regulation of glycosylation and muscular dystrophies].
Topics: Amino Acid Sequence; Animals; Carbohydrates; Dystroglycans; Glycosylation; Humans; Mannose; Molecular Sequence Data; Muscular Dystrophies; N-Acetylglucosaminyltransferases | 2007 |
Prenatal genetic diagnosis. 3.
Topics: Abortion, Induced; Acid Phosphatase; Adrenal Hyperplasia, Congenital; Amnion; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Congenital Abnormalities; Counseling; Culture Techniques; Cystic Fibrosis; Economics, Medical; Ethics, Medical; Female; Fetal Diseases; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Heterozygote; Homozygote; Humans; Lysosomes; Mannose; Marfan Syndrome; Methods; Mucopolysaccharidoses; Muscular Dystrophies; Porphyrias; Pregnancy; Punctures; Xeroderma Pigmentosum | 1970 |
6 other study(ies) available for mannose and Muscular Dystrophy
| Article | Year |
|---|---|
Protein O-mannosylation in metazoan organisms.
Topics: Blotting, Western; Chromatography, Affinity; Dystroglycans; Glycosylation; Humans; Mannose; Mass Spectrometry; Muscular Dystrophies | 2014 |
Small molecules enhance functional O-mannosylation of Alpha-dystroglycan.
Topics: Animals; Cell Line; CHO Cells; Cricetulus; Drug Evaluation, Preclinical; Dystroglycans; Glycosylation; High-Throughput Screening Assays; Humans; Mannose; Mice; Muscular Dystrophies; Small Molecule Libraries | 2015 |
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.
Topics: Animals; Carbohydrate Conformation; Cell Line; Dystroglycans; Glycosylation; Humans; Laminin; Magnetic Resonance Spectroscopy; Mannose; Mass Spectrometry; Membrane Proteins; Mice; Mice, Inbred C57BL; Muscle, Skeletal; Muscular Dystrophies; Muscular Dystrophy, Animal; N-Acetylglucosaminyltransferases; Phosphorylation; Protein Binding; Recombinant Proteins | 2010 |
Glycomic analyses of mouse models of congenital muscular dystrophy.
Topics: Animals; Brain; Carbohydrates; Disease Models, Animal; Dystroglycans; Galactosyltransferases; Glycomics; Glycosylation; Mannose; Mice; Mice, Knockout; Muscular Dystrophies; Mutation; N-Acetylglucosaminyltransferases; Polysaccharides | 2011 |
Glycosylation of α-dystroglycan: O-mannosylation influences the subsequent addition of GalNAc by UDP-GalNAc polypeptide N-acetylgalactosaminyltransferases.
Topics: Acetylgalactosamine; Animals; Cell Line; Dystroglycans; Endoplasmic Reticulum; Glycosylation; Humans; Mannose; Mice; Multienzyme Complexes; Muscular Dystrophies; N-Acetylgalactosaminyltransferases; Uridine Diphosphate N-Acetylgalactosamine | 2012 |
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Coagulation Protein Disorders; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Drug Resistance; Dystroglycans; Electromyography; Endoplasmic Reticulum; Epilepsy; Female; Fibroblasts; Glycosylation; Humans; Infant; Isoelectric Focusing; Liver Diseases; Male; Mannose; Mannosyltransferases; Microcephaly; Middle Aged; Molecular Sequence Data; Muscular Dystrophies; Mutation; Mutation, Missense; Pregnancy; Vision Disorders; Young Adult | 2012 |