Page last updated: 2024-08-22

mannose and alpha-Galactosidase A Deficiency

mannose has been researched along with alpha-Galactosidase A Deficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19903 (75.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Edmunds, T; Honey, D; Hou, L; Kyazike, J; Pan, CQ; Park, A; Stefano, JE; Zhou, Q1
Hultberg, B; Sjöblad, S1
De Wit-Verbeek, E; Galjaard, H; Hoogeveen, A; Keijzer, W; Vlek-Noot, C1
Robinson, D1

Reviews

1 review(s) available for mannose and alpha-Galactosidase A Deficiency

ArticleYear
Multiple forms of glycosidases in the normal and pathological states.
    Enzyme, 1974, Volume: 18, Issue:1

    Topics: Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography, Gel; Diffuse Cerebral Sclerosis of Schilder; Fabry Disease; Fucose; Galactosidases; Gangliosides; Gaucher Disease; Glycogen Storage Disease; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoenzymes; Lactose Intolerance; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Mucopolysaccharidoses

1974

Other Studies

3 other study(ies) available for mannose and alpha-Galactosidase A Deficiency

ArticleYear
In vitro and in vivo evaluation of a non-carbohydrate targeting platform for lysosomal proteins.
    Journal of controlled release : official journal of the Controlled Release Society, 2009, Apr-17, Volume: 135, Issue:2

    Topics: alpha-Galactosidase; Amino Acid Motifs; Animals; Cell Line, Tumor; Dimerization; Fabry Disease; Female; Half-Life; Humans; Kinetics; Liver; Lysosomes; Male; Mannose; Mice; Mice, Knockout; Oligosaccharides; Peptides; Polyethylene Glycols; Proteins; Rats; Receptor, IGF Type 2; Recombinant Proteins; Tissue Distribution

2009
Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases.
    Clinica chimica acta; international journal of clinical chemistry, 1977, Oct-01, Volume: 80, Issue:1

    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
The use of quantiatative cytochemical analyses in rapid prenatal detection and somatic cell genetic studies of metabolic diseases.
    The Histochemical journal, 1974, Volume: 6, Issue:5

    Topics: Amniocentesis; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fabry Disease; Female; Galactosidases; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glucosidases; Glycogen Storage Disease; Glycoside Hydrolases; Hexosaminidases; Histocytochemistry; Humans; Hybrid Cells; Mannose; Microchemistry; Pregnancy; Spectrometry, Fluorescence; Uronic Acids

1974