Page last updated: 2024-08-22

mannose and Lipidoses

mannose has been researched along with Lipidoses in 16 studies

Research

Studies (16)

TimeframeStudies, this research(%)All Research%
pre-199016 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hultberg, B; Sjöblad, S1
Ng Kin Kin, NM; Wolfe, LS1
Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI1
Creagan, RP; Darlington, GJ; Gilbert, F; Kucherlapati, R; Murnane, MJ; Ruddle, FH1
Brady, RO; Kolodny, EH; Tallman, JF1
Ockerman, PA1
Brown, B; Brunngraber, EG; Haberland, C; Witting, LA1
Robinson, D1
Touster, O1
Hultbery, B; Ockerman, PA1
Brady, RO; Tallman, JF1
Aro, A; Brown, BD; Brunngraber, EG1
Lalley, PA; Rattazzi, MC; Shows, TB1
Hultberg, B; Nordén, NE; Ockerman, PA1
Montreuil, J; Strecker, G1
Brady, RO; Kanfer, JN; Kolodny, EH; Quirk, JM1

Reviews

3 review(s) available for mannose and Lipidoses

ArticleYear
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
    Advances in experimental medicine and biology, 1976, Volume: 68

    Topics: Adolescent; Binding Sites; Brain; Child; Concanavalin A; Fucose; Galactose; Gangliosidoses; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Middle Aged; Protein Binding; Sialic Acids; Sphingolipidoses

1976
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
Some aspects of the cellular biochemistry of lysosomal and related glycosidases.
    Molecular and cellular biochemistry, 1973, Dec-15, Volume: 2, Issue:2

    Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Diffuse Cerebral Sclerosis of Schilder; Fucose; Galactosamine; Galactosidases; Gangliosides; Gaucher Disease; Glucosidases; Glucuronidase; Glycoside Hydrolases; Golgi Apparatus; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoenzymes; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Neuraminidase; Serine; Xylose

1973

Other Studies

13 other study(ies) available for mannose and Lipidoses

ArticleYear
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
Storage and excretion of oligosaccharides and glycopeptides in the gangliosidoses.
    Advances in experimental medicine and biology, 1976, Volume: 68

    Topics: Galactose; Gangliosidoses; Glucosamine; Glycopeptides; Humans; Infant; Lipidoses; Liver; Mannose; Molecular Conformation; Molecular Weight; Oligosaccharides

1976
Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes.
    Proceedings of the National Academy of Sciences of the United States of America, 1975, Volume: 72, Issue:1

    Topics: Animals; Carbohydrate Epimerases; Cell Line; Chromosome Mapping; Chromosomes, Human, 4-5; Clone Cells; Female; Genes; Genetic Linkage; Hexosaminidases; Humans; Hybrid Cells; Lipidoses; Male; Mannose; Mice; Pyruvate Kinase

1975
The preparation of Tay-Sachs ganglioside specifically labeled in either the N-acetylneuraminosyl or N-acetylgalactosaminyl portion of the molecule.
    Methods in enzymology, 1975, Volume: 35

    Topics: Animals; Brain; Galactosamine; Galactosidases; Gangliosides; Hexosamines; Humans; Isotope Labeling; Lipidoses; Liver; Mannose; Methods; Neuraminidase; Rats; Sialic Acids; Tritium; Vibrio cholerae

1975
Diseases of glycoprotein storage.
    Lancet (London, England), 1969, Apr-05, Volume: 1, Issue:7597

    Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Lipidoses; Liver; Mannose; Mucopolysaccharidoses

1969
Glycoproteins in Tay-sachs disease: isolation and carbohydrate composition of glycopeptides.
    Brain research, 1972, Mar-10, Volume: 38, Issue:1

    Topics: Brain; Brain Stem; Cerebellum; Cerebral Cortex; Child; Chromatography, Paper; Electrophoresis; Female; Galactose; Gangliosides; Glucose; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosaminidases; Humans; Infant; Lipidoses; Mannose; Peptides

1972
Artificial substrates in the assay of acid glycosidases.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 39, Issue:1

    Topics: Chlorides; Chromatography, Gel; Enzyme Activation; Galactosidases; Gaucher Disease; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoelectric Focusing; Lipidoses; Liver; Lysosomes; Macromolecular Substances; Mannose; Methods; Mucopolysaccharidoses; Osmolar Concentration; Retinitis Pigmentosa

1972
The catabolism of Tay-Sachs ganglioside in rat brain lysosomes.
    The Journal of biological chemistry, 1972, Dec-10, Volume: 247, Issue:23

    Topics: Acetates; Animals; Brain; Carbon Isotopes; Chromatography, Thin Layer; Cytosol; Gangliosides; Hexosamines; Hexosaminidases; Hydrogen-Ion Concentration; Kinetics; Lipid Metabolism; Lipidoses; Lysosomes; Male; Mannose; Neuraminidase; Rats; Subcellular Fractions; Surface-Active Agents; Tritium

1972
Glycoproteins in brain tissue of the O-variant of GM2 gangliosidosis.
    Journal of neurochemistry, 1974, Volume: 22, Issue:1

    Topics: Acetamides; Brain; Brain Chemistry; Child, Preschool; Chromatography, Gel; Electrophoresis; Female; Fucose; Galactose; Gangliosides; Glucosamine; Glycoproteins; Hexosamines; Hexosaminidases; Humans; Lipidoses; Male; Mannose; Neuraminic Acids

1974
Proceedings: Synteny relationships of beta-D-N-acetylhexosaminidase A and B in somatic cell hybrids.
    Cytogenetics and cell genetics, 1974, Volume: 13, Issue:1

    Topics: Animals; Carbohydrate Epimerases; Chromosome Mapping; Chromosomes, Human, 6-12 and X; Clone Cells; Hexosaminidases; Humans; Hybrid Cells; Isoenzymes; Lipidoses; Lysosomes; Mannose; Mice

1974
Isoenzymes of four acid hydrolases in human kidney and urine.
    Clinica chimica acta; international journal of clinical chemistry, 1974, Volume: 52, Issue:2

    Topics: Chromatography, Gel; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Isoelectric Focusing; Isoenzymes; Kidney; Lipidoses; Mannose

1974
[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
Preparation of radioactive Tay-Sachs ganglioside labeled in the sialic acid moiety.
    Journal of lipid research, 1970, Volume: 11, Issue:2

    Topics: Animals; Brain; Chemical Phenomena; Chemistry; Chromatography, Thin Layer; Dialysis; Galactosidases; Gangliosides; Hexosamines; Humans; Lipidoses; Liver; Mannose; Methods; Neuraminic Acids; Neuraminidase; Rats; Tritium; Vibrio

1970