galactose and Lipidoses
galactose has been researched along with Lipidoses in 48 studies
Research
Studies (48)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 48 (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 |
|---|---|
| GIELEN, W; KLENK, E; LIEDTKE, U | 1 |
| Ng Kin Kin, NM; Wolfe, LS | 1 |
| Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
| Cocquyt, G; Dacremont, G; Kint, JA | 1 |
| Debuch, H; Gielen, W; Kannan, R; Kerènyi, L | 1 |
| Brady, RO | 3 |
| Suzuki, K | 1 |
| Brown, B; Brunngraber, EG; Haberland, C; Witting, LA | 1 |
| Kawamura, N; Taketomi, T | 1 |
| McGuire, EJ; Roseman, S; Schachter, H | 1 |
| Hiatt, W; Sattler, M; Wenger, DA | 1 |
| Dastugue, G; Motta, C; Viallard, JL | 1 |
| Dulaney, JT; Moser, HW; Sugita, M | 1 |
| Makita, A; Takahashi, W; Yokoyama, T | 1 |
| Aro, A; Brown, BD; Brunngraber, EG | 1 |
| Fletcher, TF; Kurtz, HJ | 1 |
| Yip, MC | 1 |
| Montreuil, J; Strecker, G | 1 |
| Tamai, Y; Yamakawa, T | 1 |
| Fredrickson, DS; Jacobson, CB; Sloan, HR; Uhlendorf, BW | 1 |
| Den, H; Kaufman, B; Roseman, S | 1 |
| Dawson, G; Stein, AO | 1 |
| Brady, RO; Kolodny, EH | 1 |
| Dawson, G; Matalon, R; Stein, AO | 1 |
| Kolodny, EH; Stone, AL | 1 |
| Martensson, E; Stoffyn, A; Stoffyn, P | 1 |
| O'Brien, JS; Okada, S | 1 |
| Kennaway, NG; Woolf, LI | 1 |
| Dain, JA; Yip, MC | 2 |
| Krivit, W; Sweeley, CC; Vance, DE | 1 |
| Wagner, A | 1 |
| EDGAR, GW | 1 |
| BRANTE, G | 1 |
| Hooghwinkel, GJ; van Creveld, S | 1 |
| Kaback, MM; Miller, K; Percy, AK; Sonneborn, M | 1 |
| Brown, BD; Brunngraber, EG; Hof, H | 1 |
| Minami, R; Nakao, T; Orii, T; Sukegawa, K | 1 |
| Adelman, LS; Bass, NH; Young, E | 1 |
| Debuch, H; Kannan, R; Tjiong, HB; Wiedemann, HR | 1 |
| Booth, DA; Cumings, JN; Goodwin, H | 1 |
| Borri, PF; Hooghwinkel, GJ | 1 |
| Harzer, K; Jatzkewitz, H; Sandhoff, K; Wässle, W | 1 |
| Bartsch, GG | 1 |
| O'Brien, JS; Okada, S; Veath, ML | 1 |
| Adachi, M; Friedland, J; Schneck, L; Valenti, C; Volk, BW | 1 |
Reviews
2 review(s) available for galactose and Lipidoses
| Article | Year |
|---|---|
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
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 |
Disorders of lipid metabolism.
Topics: Adult; Animals; Bone Marrow; Cell Line; Ceramides; Child; Fabry Disease; Fucose; Galactose; Gangliosides; Gaucher Disease; Genetic Variation; Glycolipids; Glycoside Hydrolases; Humans; Leukemia, Myeloid; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Lipidoses; Mice; Niemann-Pick Diseases; Sulfoglycosphingolipids | 1972 |
Other Studies
46 other study(ies) available for galactose and Lipidoses
| Article | Year |
|---|---|
[BRAIN GANGLIOSIDES IN INFANTILE AMAUROTIC IDIOCY OF THE TAY-SACHS TYPE].
Topics: Brain; Chromatography; Fatty Acids; Galactose; Gangliosides; Glucose; Humans; Intellectual Disability; Lipidoses; Tay-Sachs Disease | 1963 |
Storage and excretion of oligosaccharides and glycopeptides in the gangliosidoses.
Topics: Galactose; Gangliosidoses; Glucosamine; Glycopeptides; Humans; Infant; Lipidoses; Liver; Mannose; Molecular Conformation; Molecular Weight; Oligosaccharides | 1976 |
Brain sphingolipids in I cell disease (mucolipidosis II).
Topics: Abnormalities, Multiple; Ceramides; Cerebrosides; Child, Preschool; Chromatography, Gas; Chromatography, Thin Layer; Cytoplasmic Granules; Fibroblasts; Galactose; Gangliosides; Glucose; Humans; Lactose; Lipidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Neuraminic Acids; Retinitis Pigmentosa; Sphingolipids; Sphingomyelins; Sulfoglycosphingolipids; Syndrome | 1974 |
[A sphingolipidosis with the accumulation of neutral glycosphingolipids, AO2(GM3) and A1(GM2)-ganglioside (author's transl)].
Topics: Brain; Ceramides; Cerebellum; Cerebral Cortex; Child; Fatty Acids; Galactose; Gangliosides; Glucose; Glycolipids; Hexoses; Humans; Lipidoses; Palmitic Acids; Parietal Lobe; Pons; Putamen; Sphingolipidoses; Sphingolipids; Stearic Acids; Thalamus | 1974 |
Cerebral GM1-gangliosidosis: chemical pathology of visceral organs.
Topics: Brain Diseases; Chromatography, Thin Layer; Galactose; Gangliosides; Glycosaminoglycans; Hexosamines; Humans; Lipidoses; Liver; Polysaccharides; Spleen | 1968 |
Glycoproteins in Tay-sachs disease: isolation and carbohydrate composition of glycopeptides.
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 |
Cerebral and visceral glycolipids in a case of Tay-Sachs disease.
Topics: Brain Chemistry; Chromatography, Gas; Chromatography, Thin Layer; Fatty Acids; Female; Galactose; Glucose; Glycolipids; Hexoses; Humans; Infrared Rays; Kidney; Lipidoses; Liver; Silicon Dioxide; Spectrophotometry; Spleen; Time Factors | 1969 |
Sialic acids. 13. A uridine diphosphate D-galactose: mucin galactosyltransferase from porcine submaxillary gland.
Topics: Acetates; Animals; Cadmium; Calcium Chloride; Carbon Isotopes; Chlorides; Chromatography, Paper; Clostridium perfringens; Enzyme Activation; Galactosamine; Galactose; Galactosidases; Gangliosides; Glucosamine; Glucose; Glycoproteins; Hexosaminidases; Hexosyltransferases; Hydrogen-Ion Concentration; Kinetics; Lipidoses; Manganese; Mathematics; Models, Structural; Mucins; Neuraminic Acids; Neuraminidase; Nucleoside Diphosphate Sugars; Oligosaccharides; Ovalbumin; Sheep; Submandibular Gland; Surface-Active Agents; Swine; Uracil Nucleotides; Zinc | 1971 |
The adnormal biochemistry of inherited disorders of lipid metabolism.
Topics: Brain; Ceramides; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Female; Fibroblasts; Galactose; Galactosidases; Gaucher Disease; Glucose; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Humans; Intestines; Kidney; Leukocytes; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Muscles; Niemann-Pick Diseases; Phosphoric Diester Hydrolases; Sphingomyelins; Spleen; Sulfoglycosphingolipids; Syndrome | 1973 |
Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.
Topics: Adult; Brain; Ceramides; Female; Galactose; Galactosidases; Gangliosides; Humans; Infant; Lactose; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Liver; Male; Niemann-Pick Diseases; Skin; Spleen; Syndrome | 1974 |
[Human cerebrospinal fluid hexosaminidases. Activity on N-acetyl-beta-D-glucosaminidic and N-acetyl-beta-galactosaminidic derivatives of 4-methyl-umbelliferone. Evaluation of A and B forms by their thermostability difference].
Topics: Amidines; Cerebrospinal Fluid; Coumarins; Galactose; Glucose; Hexosaminidases; Humans; Lipidoses; Lysosomes | 1972 |
Ceramidase deficiency in Farber's disease (lipogranulomatosis).
Topics: Acid Phosphatase; Adult; Carbon Isotopes; Ceramides; Cerebellum; Cerebrosides; Child; Child, Preschool; Congenital Abnormalities; Female; Galactose; Galactosidases; Glucose; Glycoside Hydrolases; Heart Defects, Congenital; Hexosaminidases; Humans; Hydrolases; Infant; Infant, Newborn; Intellectual Disability; Kidney; Lipidoses; Liver Cirrhosis, Biliary; Male; Metabolism, Inborn Errors; Neuraminidase; Pigmentation Disorders; Respiratory Distress Syndrome, Newborn | 1972 |
Enzymatic degradation of Forssman hapten: a reinvestigation of the chemical structure.
Topics: Animals; Ceramides; Chromatography, Gas; Chromatography, Thin Layer; Forssman Antigen; Galactosamine; Galactose; Glucose; Glycolipids; Hexosaminidases; Horses; Humans; Immunoglobulin M; Kidney; Kinetics; Lipidoses; Mollusca | 1973 |
Glycoproteins in brain tissue of the O-variant of GM2 gangliosidosis.
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 |
Animal model: globoid cell leukodystrophy in the dog.
Topics: Animals; Brain; Cerebrosides; Child; Child, Preschool; Diffuse Cerebral Sclerosis of Schilder; Disease Models, Animal; Dogs; Galactose; Galactosidases; Glycoside Hydrolases; Humans; Lipidoses; Macrophages | 1972 |
The enzymic synthesis of gangliosides: uridine diphosphate galactose: N-acetylgalactosaminyl-(N-acetylneuraminyl)-galactosyl-glucosyl-ceramide galactosyltransferase in rat tissues.
Topics: Age Factors; Animals; Brain; Carbon Isotopes; Chromatography; Chromatography, Thin Layer; Digestive System; Female; Galactose; Gangliosides; Hexosyltransferases; Humans; Kidney; Lipidoses; Liver; Lung; Mammary Glands, Animal; Manganese; Muscles; Myocardium; Rats; Spleen; Uridine Diphosphate Sugars | 1972 |
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency].
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 |
Study on glucocerebroside in Tay-Sachs brain.
Topics: Brain Chemistry; Cerebrosides; Chromatography; Fatty Acids; Galactose; Gangliosides; Glucose; Humans; Infant; Infrared Rays; Lipidoses; Lipids; Spectrophotometry | 1969 |
Beta-galactosidase in tissue culture derived from human skin and bone marrow. Enzyme defect in GM1 gangliosidosis.
Topics: Biopsy; Bone Marrow; Bone Marrow Cells; Brain; Culture Media; Culture Techniques; Fibroblasts; Galactose; Galactosidases; Gangliosides; Glycolipids; Humans; Infant; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Niemann-Pick Diseases; Rheumatic Heart Disease; Skin | 1969 |
Properties of some glycosyltransferases in embryonic chicken brain.
Topics: Aging; Albumins; Amniotic Fluid; Animals; Brain; Carbon Isotopes; Chick Embryo; Cytosine Nucleotides; Detergents; Galactose; Gangliosides; Glucosamine; Glycoproteins; Guinea Pigs; Humans; Lipidoses; Mucins; Neuraminic Acids; Neuraminidase; Oligosaccharides; Serine; Transferases; Uracil Nucleotides; Vitreous Body; Xylose | 1970 |
Lactosyl ceramidosis: catabolic enzyme defect of glycosphingolipid metabolism.
Topics: Bone Marrow; Bone Marrow Cells; Brain; Child, Preschool; Chromatography, Gas; Female; Galactose; Galactosidases; Glycolipids; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Tritium | 1970 |
Further studies on the elucidation of the enzymatic defect in Tay-Sachs disease.
Topics: Freezing; Galactose; Gangliosides; Glycoside Hydrolases; Hexosamines; Humans; Lipidoses; Muscles | 1970 |
Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts.
Topics: Brain Diseases; Cerebrosides; Chromatography, Gas; Chromatography, Thin Layer; Culture Techniques; Fibroblasts; Galactose; Glycoside Hydrolases; Heterozygote; Lactose; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Sphingolipids | 1971 |
Circular dichroism of gangliosides from normal and Tay-Sachs tissues.
Topics: Amino Alcohols; Amino Sugars; Animals; Brain; Brain Chemistry; Cattle; Chemical Phenomena; Chemistry; Circular Dichroism; Cytosine Nucleotides; Fatty Acids; Galactose; Gangliosides; Glucose; Glycols; Hexosamines; Humans; Ketones; Lipidoses; Neuraminic Acids; Rats; Spleen; Transferases; Ultraviolet Rays | 1971 |
Structure of kidney ceramide dihexoside sulfate.
Topics: Cerebrosides; Chemical Phenomena; Chemistry; Chromatography, Thin Layer; Galactose; Hexoses; Humans; Kidney; Lipidoses; Methylation; Sulfates | 1968 |
Generalized gangliosidosis: beta-galactosidase deficiency.
Topics: Acid Phosphatase; Aged; Brain; Carbon Isotopes; Child; Child, Preschool; Chromatography, Paper; Galactose; Galactosidases; Gangliosides; Glucosidases; Glycosides; Humans; Infant; Kidney; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Middle Aged; Molecular Biology; Niemann-Pick Diseases; Nitrophenols; Spleen; Uracil Nucleotides | 1968 |
Splenic lipids in Gaucher's disease.
Topics: Adolescent; Adult; Amino Acids; Carbohydrate Metabolism; Cerebrosides; Child; Child, Preschool; Chromatography; Chromatography, Thin Layer; Colorimetry; Freezing; Galactose; Gaucher Disease; Glucose; Glycolipids; Glycosides; Humans; Infant; Lipid Metabolism; Lipidoses; Methods; Middle Aged; Preservation, Biological; Spleen | 1968 |
The inhibition of galactose oxidase.
Topics: Alcohol Oxidoreductases; Animals; Basidiomycota; Brain; Cattle; Copper; Galactose; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Molecular Weight; Osmotic Pressure | 1968 |
Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis.
Topics: Adolescent; Adult; Cerebrosides; Child; Erythrocytes; Female; Galactose; Gaucher Disease; Glucose; Heterozygote; Humans; Lactose; Lipidoses; Male; Middle Aged | 1969 |
The enzymic synthesis of ganglioside. 1. Brain uridine diphosphate D-galactose: N-acetyl-galactosaminyl-galactosyl-glucosyl-ceramide galactosyl transferase.
Topics: Age Factors; Amino Alcohols; Animals; Anura; Brain; Carbon Isotopes; Centrifugation; Chromatography, Thin Layer; Detergents; Fatty Acids; Galactose; Gangliosides; Glycolipids; Humans; Hydrogen-Ion Concentration; Intestine, Small; Kidney; Kinetics; Lipidoses; Liver; Microscopy, Electron; Models, Biological; Rats; Solubility; Transferases; Uracil Nucleotides | 1969 |
[Concerning brain gangliosides in Tay-Sachs disease].
Topics: Brain Chemistry; Child; Chromatography, Thin Layer; Galactose; Gangliosides; Glucose; Hexosamines; Humans; Lipidoses; Neuraminic Acids; Sphingomyelins; Stearic Acids | 1966 |
[Biochemical approach to types of lipoidosis and leukodystrophy].
Topics: Brain; Brain Diseases; Hexoses; Humans; Lipid Metabolism; Lipidoses; Lysosomal Storage Diseases; Phospholipids | 1955 |
Studies on lipids in morbus Gaucher. I. Qualitative and quantitative determination of the hexose components in normal and Gaucher glycolipids.
Topics: Glycolipids; Hexoses; Humans; Lipidoses; Lipids | 1951 |
Lipids in blood plasma and erythrocytes in juvenile amaurotic idiocy. Cholestyramine therapy.
Topics: Child; Cholesterol; Cholestyramine Resin; Erythrocytes; Hexosamines; Hexoses; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Neuraminic Acids; Phospholipids; Sphingomyelins | 1967 |
Confirmatory studies in the prenatal diagnosis of sphingolipidoses.
Topics: Abortion, Induced; Amniocentesis; Brain Chemistry; Female; Fetus; Galactosidases; Gangliosides; Hexosaminidases; Hexoses; Humans; Isoenzymes; Kidney; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Neuraminic Acids; Phenols; Pregnancy; Sphingolipidoses; Sphingolipids; Sulfoglycosphingolipids | 1973 |
Determination of gangliosides, glycoproteins, and glycosaminoglycans in brain tissue.
Topics: Acetates; Adult; Animals; Brain Chemistry; Brain Diseases; Cattle; Cerebral Cortex; Chemical Precipitation; Child; Child, Preschool; Chloroform; Chromatography, Gel; Dialysis; Electrophoresis; Fucose; Galactosemias; Gangliosides; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosamines; Hexoses; Humans; Hydrogen-Ion Concentration; Lipidoses; Methanol; Methods; Myelin Sheath; Neuraminic Acids; Papain; Peptide Hydrolases; Pyridinium Compounds; Rats; Solubility; Subacute Sclerosing Panencephalitis; Temperature | 1971 |
Hyperglycopeptiduria in genetic mucolipidoses.
Topics: Child; Child, Preschool; Chromatography, Paper; Female; Gangliosides; Gaucher Disease; Glycopeptides; Glycosaminoglycans; Hexoses; Humans; Infant; Lipidoses; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Neuraminic Acids; Sphingolipids; Sulfates; Uronic Acids | 1974 |
Abnormal accumulation of sialoglycoproteins in a case of late infantile amaurotic idiocy.
Topics: Cerebral Cortex; Child, Preschool; Cholesterol; Gangliosides; Glycoproteins; Hexoses; Histocytochemistry; Humans; Inclusion Bodies; Lipid Metabolism; Lipidoses; Male; Microscopy, Electron; Neurons; Pigments, Biological; Sialic Acids | 1974 |
Unusual glycolipids in brain cortex of a visceral lipidosis (Niemann-Pick disease?).
Topics: Brain Chemistry; Ceramides; Cerebral Cortex; Cerebrosides; Child; Cholesterol; Chromatography; Chromatography, Gas; Chromatography, Thin Layer; Fatty Acids; Female; Gangliosides; Glycolipids; Hexoses; Humans; Lipidoses; Lipids; Male; Niemann-Pick Diseases; Sulfoglycosphingolipids | 1974 |
Abnormal gangliosides in Tay-Sachs disease, Niemann-Pick's disease, and gargoylism.
Topics: Amino Alcohols; Brain Chemistry; Cerebral Cortex; Chromatography, Thin Layer; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Mucopolysaccharidoses; Neuraminic Acids; Niemann-Pick Diseases; Sphingomyelins | 1966 |
Comparative studies of glycolipids and carbohydrate moieties in brain and visceral organs in amaurotic idiocy and gargolylism.
Topics: Adolescent; Adult; Aged; Brain Chemistry; Carbohydrate Metabolism; Child; Child, Preschool; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Liver; Middle Aged; Mucopolysaccharidoses; Neuraminic Acids; Spleen | 1968 |
Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.
Topics: Brain; Brain Chemistry; Ceramides; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Galactosamine; Gangliosides; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Hexoses; Hot Temperature; Humans; Hydrogen-Ion Concentration; Infant; Isoelectric Focusing; Kidney; Lipid Metabolism; Lipidoses; Liver | 1971 |
Glycolipid abnormalities in a myoclonic variant of late infantile amaurotic idiocy.
Topics: Brain; Carbohydrates; Cerebrosides; Child; Chromatography, Thin Layer; Gangliosides; Glycolipids; Hexoses; Humans; Lipidoses; Male | 1970 |
Metabolic disorders of sphingolipid metabolism in man.
Topics: Amino Alcohols; Carbon Isotopes; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Esterases; Fatty Acids; Gangliosides; Gaucher Disease; Glycols; Hexoses; Humans; Lipid Metabolism; Lipidoses; Niemann-Pick Diseases; Sphingomyelins; Sulfuric Acids | 1970 |
Juvenile GM2 gangliosidosis: partial deficiency of hexosaminidase A.
Topics: Amidohydrolases; Brain Diseases; Cerebral Cortex; Child, Preschool; Female; Gangliosides; Genes, Recessive; Hexoses; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Skin | 1970 |
Early evolution of cytoplasmic inclusion bodies in Tay-Sachs disease.
Topics: Amidines; Amidohydrolases; Brain; Chromatography; Electrophoresis; Embryo, Mammalian; Fetus; Gangliosides; Hexoses; Humans; Inclusion Bodies, Viral; Infant; Lipidoses; Liver; Microscopy, Electron | 1970 |