Page last updated: 2024-08-22

mannose and Lipid Metabolism, Inborn Error

mannose has been researched along with Lipid Metabolism, Inborn Error in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	10 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Jolly, RD	1
Dawson, G; Tsay, GC	1
Robinson, D	1
Ng-Ying-Kin, NM; Wolfe, LS	1
Berra, B; Brunngraber, EG; Di Palma, S	1
Lalley, PA; Rattazzi, MC; Shows, TB	1
Batt, RD; Hocking, JD; Jolly, RD	1
Dahlqvist, A; Hultberg, B; Ockerman, PA	1
Cotlier, E; Hindman, J	1
Montreuil, J; Strecker, G	1

Reviews

1 review(s) available for mannose and Lipid Metabolism, Inborn Error

Article	Year
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

Article

Year

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

9 other study(ies) available for mannose and Lipid Metabolism, Inborn Error

Article	Year
Two model lysosomal storage diseases. Progress in clinical and biological research, 1982, Volume: 94 Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Cattle; Cattle Diseases; Ceroid; Disease Models, Animal; Lipid Metabolism, Inborn Errors; Lipofuscin; Mannose; Sheep; Sheep Diseases	1982
Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolism. Biochemical and biophysical research communications, 1975, Apr-07, Volume: 63, Issue:3 Topics: alpha-L-Fucosidase; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Fucose; Galactose; Galactosidases; Glucosamine; Glycopeptides; Hexosaminidases; Humans; Lipid Metabolism, Inborn Errors; Mannose; Mannosidases; Metabolism, Inborn Errors; Sialic Acids; Skin	1975
Oligosaccharides accumulating in the liver from a patient with GM2-gangliosidosis variant O (Sandhoff-Jatzkewitz disease). Biochemical and biophysical research communications, 1974, Aug-05, Volume: 59, Issue:3 Topics: Binding Sites; Child, Preschool; Chromatography, Gas; Chromatography, Gel; Computers; Deuterium; Gangliosides; Glucosamine; Humans; Lipid Metabolism, Inborn Errors; Liver; Magnetic Resonance Spectroscopy; Mannose; Mass Spectrometry; Methylation; Molecular Conformation; Oligosaccharides; Oxidation-Reduction	1974
Altered levels of tissue gangliosides and glycoproteins in the infantile form of GM1-gangliosidosis. Clinica chimica acta; international journal of clinical chemistry, 1974, Dec-17, Volume: 57, Issue:3 Topics: Brain; Cerebrosides; Chromatography, Thin Layer; Female; Fucose; Galactose; Galactosidases; Gangliosides; Glycoproteins; Hexosamines; Humans; Infant; Kidney; Lipid Metabolism, Inborn Errors; Liver; Lung; Male; Mannose; Phospholipids; Spleen; Sulfoglycosphingolipids	1974
Human beta-D-N-acetylhexosaminidases A and B: expression and linkage relationships in somatic cell hybrids. Proceedings of the National Academy of Sciences of the United States of America, 1974, Volume: 71, Issue:4 Topics: Animals; Carbohydrate Epimerases; Clone Cells; Electrophoresis, Starch Gel; Fibroblasts; Genes; Genetic Linkage; Hexosaminidases; Humans; Hybrid Cells; Immune Sera; Lipid Metabolism, Inborn Errors; Lung; Lysosomes; Mannose; Mice; Phenotype; Pyruvate Kinase	1974
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease. The Biochemical journal, 1972, Volume: 128, Issue:1 Topics: Animals; Brain; Cattle; Cattle Diseases; Chick Embryo; Chromatography, Paper; Female; Glucosamine; Hexosaminidases; Hexoses; Lipid Metabolism, Inborn Errors; Liver; Lymph Nodes; Lysosomes; Male; Mannose	1972
Gargoylism: hydrolysis of beta-galactosides and tissure accumulation of galactose- and mannose-containing compounds. The Journal of clinical investigation, 1970, Volume: 49, Issue:2 Topics: Brain; Child; Chromatography; Chromatography, Gas; Galactose; Galactosidases; Glucose; Humans; Inositol; Lipid Metabolism, Inborn Errors; Liver; Mannose; Mucopolysaccharidoses	1970
Glycosidases in normal human leukocytes and abnormalities in G M1 -gangliosidosis. Clinical chemistry, 1972, Volume: 18, Issue:9 Topics: Adolescent; Adult; Aged; Carrier State; Child; Clinical Enzyme Tests; Female; Fucose; Galactosidases; Glycoside Hydrolases; Heterozygote; Hexosaminidases; Homozygote; Humans; Infant; Leukocytes; Lipid Metabolism, Inborn Errors; Male; Mannose; Middle Aged	1972
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency]. Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 33, Issue:2 Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Chromatography; Chromatography, Ion Exchange; Chromatography, Paper; Colorimetry; Ethanol; Fucose; Galactose; Gangliosides; Glucosamine; Glucose; Glycoproteins; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Monosaccharides; Neuraminic Acids; Oligosaccharides; Uronic Acids	1971