mannose has been researched along with alpha-L-Iduronidase Deficiency in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fujiyama, K; He, X; Kajiura, H; Kermode, AR; McNair, GR; Pierce, OM | 1 |
| Brooks, D; Gloster, TM; Haselhorst, T; He, X; Kermode, AR; Kolarich, D; Packer, NH; Pierce, O; Qian, Y; Vocadlo, DJ; von Itzstein, M | 1 |
| Maita, N; Ohno, K; Saito, S; Sakuraba, H; Taniguchi, H; Taniguchi, T; Tsukimura, T | 1 |
| Cai, SR; Chung, S; Fu, A; Hennig, AK; Herati, RS; Kovacs, A; Lee, D; Liu, Y; Mosinger Ogilvie, J; Parker Ponder, K; Wang, B; Xu, L | 1 |
| Hultberg, B; Sjöblad, S | 1 |
| Miller, CS; Reynolds, LW; Taylor, HA; Thomas, GH | 1 |
| Van Hoof, F | 1 |
| Feleki, V; Gordon, BA | 1 |
1 review(s) available for mannose and alpha-L-Iduronidase Deficiency
| Article | Year |
|---|---|
Mucopolysaccharidoses and mucolipidoses.
Topics: beta-Galactosidase; Cells, Cultured; Child, Preschool; Chondroitin Sulfates; Female; Fucose; Gangliosidoses; Genetic Carrier Screening; Hexosyltransferases; Humans; Iduronidase; Liver; Lysosomes; Mannose; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI | 1974 |
7 other study(ies) available for mannose and alpha-L-Iduronidase Deficiency
| Article | Year |
|---|---|
N-glycan structures and downstream mannose-phosphorylation of plant recombinant human alpha-L-iduronidase: toward development of enzyme replacement therapy for mucopolysaccharidosis I.
Topics: Arabidopsis; Enzyme Replacement Therapy; Glycosylation; Humans; Iduronidase; Kinetics; Mannose; Mucopolysaccharidosis I; Mutation; Phosphorylation; Phosphotransferases; Plants, Genetically Modified; Polysaccharides; Recombinant Proteins; Seeds; Solubility | 2017 |
Characterization and downstream mannose phosphorylation of human recombinant α-L-iduronidase produced in Arabidopsis complex glycan-deficient (cgl) seeds.
Topics: Arabidopsis; Glycosylation; Humans; Iduronidase; Kinetics; Mannose; Mannosephosphates; Mucopolysaccharidosis I; Mutation; Phosphorylation; Plants, Genetically Modified; Polysaccharides; Recombinant Proteins; Seeds; Transgenes | 2013 |
Human α-L-iduronidase uses its own N-glycan as a substrate-binding and catalytic module.
Topics: Amino Acid Sequence; Binding Sites; Biocatalysis; Circular Dichroism; Crystallography, X-Ray; Dermatan Sulfate; Electrophoresis, Polyacrylamide Gel; Heparitin Sulfate; Humans; Iduronidase; Kinetics; Mannose; Models, Molecular; Molecular Sequence Data; Mucopolysaccharidosis I; Mutation; Polysaccharides; Protein Binding; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Substrate Specificity | 2013 |
Liver-directed neonatal gene therapy prevents cardiac, bone, ear, and eye disease in mucopolysaccharidosis I mice.
Topics: Animals; Animals, Newborn; Bone Diseases; DNA; Dogs; Ear Diseases; Eye Diseases; Genetic Therapy; Heart Diseases; Iduronidase; Liver; Mannose; Mice; Mice, Knockout; Mucopolysaccharidosis I; Radiography; Retroviridae; Treatment Outcome | 2005 |
Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fabry Disease; Fibroblasts; Humans; In Vitro Techniques; Lipidoses; Lysosomes; Mannose; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidosis I; Skin | 1977 |
Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.
Topics: Acetamides; Cells, Cultured; Electrophoresis, Starch Gel; Fibroblasts; Fucose; Galactosidases; Glycoside Hydrolases; Hexosaminidases; Humans; In Vitro Techniques; Lysosomes; Mannose; Methods; Mucopolysaccharidosis I; Skin; Spectrophotometry; Sulfatases; Syndrome; Temperature | 1973 |
Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3.
Topics: Acid Phosphatase; Adolescent; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Fucose; Galactosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Liver; Mannose; Mucopolysaccharidosis I; Sulfatases | 1970 |