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hyaluronoglucosaminidase and Mucopolysaccharidoses

hyaluronoglucosaminidase has been researched along with Mucopolysaccharidoses in 33 studies

Research

Studies (33)

TimeframeStudies, this research(%)All Research%
pre-199021 (63.64)18.7374
1990's3 (9.09)18.2507
2000's4 (12.12)29.6817
2010's4 (12.12)24.3611
2020's1 (3.03)2.80

Authors

AuthorsStudies
Boonen, M; Flamion, B; Gilis, F; Jadot, M; Puissant, E; Tevel, V; Vandeweerd, JM1
Caron, N; Colombaro, V; Declèves, AE; Flamion, B; Giordano, L; Habsch, I; Jadot, I; Malaisse, J; Voisin, V1
Chowdhury, B; Dolinsky, VW; Muggenthaler, M; Triggs-Raine, B; Xiang, B1
Meshach Paul, D; Rajasekaran, R1
Ding, H; Flamion, B; Frost, GI; Jadin, L; Onclinx, C; Triggs-Raine, B; Wu, X1
Nusgens, BV1
Czartoryska, B; Fiszer-Szafarz, B; Tylki-Szymanska, A1
Atmuri, V; Byers, S; Csoka, AB; Farley, J; Hemming, RJ; Hombach-Klonisch, S; Martin, DC; Mort, JS; Stern, R; Triggs-Raine, BL1
Klein, U; von Figura, K1
Czartoryska, B; Fiszer-Szafarz, B; Lityńska, A; Tylki-Szymańska, A; Vannier, P; Zou, L1
Calza, AM; Masouyé, I; Saurat, JH1
Natowicz, MR; Salo, TJ; Triggs-Raine, B; Wicklow, BA; Zhang, H1
Csoka, AB; Frost, GI; Stern, R1
Aranka, L; Lajos, S1
Pereira, S; Toledo, A1
Applegarth, DA; Bozoian, G; Lowry, RB1
Davis, ML; Fluharty, AL; Kihara, H; Stevens, RL; Trammell, DJ1
Forrest, T; Herd, JK; Tschida, J1
Barnes, IC; Pennock, CA1
Hatae, Y; Makita, A1
Dicsö, F; Endreffy, I1
Lamberg, SI; Stoolmiller, AC1
Aronson, NN; Davidson, EA1
Calatroni, A; Di Ferrante, N; Donnelly, PV1
Józsa, L; Szabó, L2
Hall, MO; Heller, J1
Cunningham, WL; Ramage, PR1
Taniguchi, N1
Herd, JK1
Harvey, J; Robertson, WV1
Lee, TY; Schafer, IA1
Di Donato, S; Rimoldi, M; Tettamanti, G; Zambotti, V1

Reviews

3 review(s) available for hyaluronoglucosaminidase and Mucopolysaccharidoses

ArticleYear
[Hyaluronic acid and extracellular matrix: a primitive molecule?].
    Annales de dermatologie et de venereologie, 2010, Volume: 137 Suppl 1

    Topics: Animals; Cell Movement; Cell Proliferation; Chick Embryo; Cutis Laxa; Dogs; Extracellular Matrix; Free Radicals; Glycosaminoglycans; Humans; Hyaluronan Receptors; Hyaluronic Acid; Hyaluronoglucosaminidase; Infant, Newborn; Mice; Mice, Knockout; Mucopolysaccharidoses; Neoplasms; Proteoglycans; Skin

2010
The six hyaluronidase-like genes in the human and mouse genomes.
    Matrix biology : journal of the International Society for Matrix Biology, 2001, Volume: 20, Issue:8

    Topics: Amino Acid Sequence; Animals; Chromosomes, Human, Pair 3; Chromosomes, Human, Pair 7; Evolution, Molecular; Gene Duplication; Genome; Genome, Human; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Mice; Mice, Knockout; Models, Biological; Molecular Sequence Data; Mucopolysaccharidoses; Multigene Family; Neoplasms; Phylogeny; Pseudogenes; Sequence Homology, Amino Acid; Species Specificity

2001
Glycosaminoglycans. A biochemical and clinical review.
    The Journal of investigative dermatology, 1974, Volume: 63, Issue:6

    Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Chondroitin; Cornea; Corneal Opacity; Dermatan Sulfate; Fibroblasts; Galactose; Glucosamine; Glycosaminoglycans; Heparin; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Intellectual Disability; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Proteoglycans; Retinitis Pigmentosa; Skin; Staining and Labeling; Sulfatases; Testis

1974

Other Studies

30 other study(ies) available for hyaluronoglucosaminidase and Mucopolysaccharidoses

ArticleYear
Hyaluronidase 1 deficiency decreases bone mineral density in mice.
    Scientific reports, 2022, 06-16, Volume: 12, Issue:1

    Topics: Animals; Bone Density; Bone Resorption; Cell Differentiation; Hyaluronic Acid; Hyaluronoglucosaminidase; Mice; Mice, Knockout; Mucopolysaccharidoses; Osteoblasts; Osteoclasts

2022
Lack of hyaluronidases exacerbates renal post-ischemic injury, inflammation, and fibrosis.
    Kidney international, 2015, Volume: 88, Issue:1

    Topics: Actins; Acute Kidney Injury; Animals; Chemokine CCL2; Chemokine CXCL2; Collagen Type I; Collagen Type III; Creatinine; Fibrosis; GPI-Linked Proteins; Hyaluronan Receptors; Hyaluronic Acid; Hyaluronoglucosaminidase; Kidney; Kidney Tubules; Leukocyte Count; Male; Mice, Inbred C57BL; Mice, Knockout; Mucopolysaccharidoses; Nephritis; Neutrophils; Reperfusion Injury; RNA, Messenger

2015
Hyaluronidase 2 deficiency is a molecular cause of cor triatriatum sinister in mice.
    International journal of cardiology, 2016, Apr-15, Volume: 209

    Topics: Animals; Cor Triatriatum; GPI-Linked Proteins; Hyaluronic Acid; Hyaluronoglucosaminidase; Mice; Mice, Knockout; Mucopolysaccharidoses

2016
In silico approach to explore the disruption in the molecular mechanism of human hyaluronidase 1 by mutant E268K that directs Natowicz syndrome.
    European biophysics journal : EBJ, 2017, Volume: 46, Issue:2

    Topics: Catalytic Domain; Hyaluronoglucosaminidase; Hydrogen Bonding; Molecular Docking Simulation; Mucopolysaccharidoses; Mutation, Missense; Protein Binding; Static Electricity

2017
Skeletal and hematological anomalies in HYAL2-deficient mice: a second type of mucopolysaccharidosis IX?
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2008, Volume: 22, Issue:12

    Topics: Animals; Female; Genotype; Hematologic Tests; Hyaluronic Acid; Hyaluronoglucosaminidase; Male; Mice; Mucopolysaccharidoses; Musculoskeletal Abnormalities; Phenotype; Polymerase Chain Reaction; Skull; Thrombocytopenia

2008
Serum hyaluronidase aberrations in metabolic and morphogenetic disorders.
    Glycoconjugate journal, 2005, Volume: 22, Issue:7-9

    Topics: Acetylglucosaminidase; Achondroplasia; Adolescent; Bone Diseases, Metabolic; Child; Child, Preschool; Dysostoses; Female; Glucuronidase; Humans; Hyaluronoglucosaminidase; Hypophosphatemia, Familial; Male; Mucolipidoses; Mucopolysaccharidoses

2005
A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritis.
    Human molecular genetics, 2008, Jul-01, Volume: 17, Issue:13

    Topics: Animals; Disease Models, Animal; Female; Gene Targeting; Glycosaminoglycans; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Joints; Male; Mice; Mice, Knockout; Mucopolysaccharidoses; Osteoarthritis; Phenotype

2008
Characterization of dermatan sulfate in mucopolysaccharidosis VI. Evidence for the absence of hyaluronidase-like enzymes in human skin fibroblasts.
    Biochimica et biophysica acta, 1980, Jun-05, Volume: 630, Issue:1

    Topics: Cells, Cultured; Chondroitin; Dermatan Sulfate; Fibroblasts; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis VI; Skin

1980
Hyaluronidase in human somatic tissues and urine: polymorphism and the activity in diseases.
    Acta biochimica Polonica, 1995, Volume: 42, Issue:1

    Topics: Arthritis, Rheumatoid; Child; Female; Humans; Hyaluronoglucosaminidase; Isoenzymes; Male; Mucopolysaccharidoses; Synovial Fluid; Tissue Distribution

1995
An unusual case of infantile dermal mucinosis.
    Pediatric dermatology, 1994, Volume: 11, Issue:3

    Topics: Child; Collagen; Diagnosis, Differential; Fibroblasts; Humans; Hyaluronoglucosaminidase; Infant; Male; Mucinoses; Mucopolysaccharidoses

1994
Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX.
    Proceedings of the National Academy of Sciences of the United States of America, 1999, May-25, Volume: 96, Issue:11

    Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Binding Sites; Chromosome Mapping; Chromosomes, Human, Pair 3; DNA Transposable Elements; Female; Fibroblasts; Humans; Hyaluronoglucosaminidase; Leukocytes; Lysosomes; Male; Molecular Sequence Data; Mucopolysaccharidoses; Multigene Family; Pedigree; Point Mutation; Polymorphism, Single-Stranded Conformational; Sequence Alignment; Sequence Deletion; Sequence Homology, Nucleic Acid; Spermatozoa

1999
[Detection of mucopolysaccharidosis gene carriers by a modified method of toluidine blue staining of the blood smear].
    Orvosi hetilap, 1975, Jan-26, Volume: 116, Issue:4

    Topics: Gene Frequency; Heterozygote; Homozygote; Hyaluronoglucosaminidase; Mucopolysaccharidoses; Staining and Labeling; Tolonium Chloride

1975
Enzyme therapy in inherited enzymatic deficiencies: an approach to mucopolysaccharidoses.
    Revista do Hospital das Clinicas, 1978, Volume: 33, Issue:2

    Topics: Glycoside Hydrolases; Humans; Hyaluronoglucosaminidase; Iduronidase; Immunity, Cellular; Mucopolysaccharidoses

1978
Analysis of urinary mucopolysaccharides using small ion exchange columns.
    Clinical biochemistry, 1975, Volume: 8, Issue:3

    Topics: Chemical Precipitation; Chromatography, Ion Exchange; Galactosamine; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Methods; Mucopolysaccharidoses; Sodium Chloride; Uronic Acids

1975
Mucopolysaccharides synthesized by cultured glial cells derived from a patient with Sanfilippo A syndrome.
    Journal of neurochemistry, 1975, Volume: 25, Issue:4

    Topics: Animals; Autoradiography; Brain; Catalysis; Cattle; Cells, Cultured; Child; Chondroitin; Chromatography, Ion Exchange; Electrophoresis; Female; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Lyases; Male; Mucopolysaccharidoses; Mucopolysaccharidosis III; Neuroglia; Sulfur Radioisotopes; Testis

1975
Separation of dermatan sulfate from heparan sulfate in mucopolysaccharidosis urine by chromatography on Sephadex G-75.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Apr-01, Volume: 68, Issue:1

    Topics: Child; Chondroitin; Chromatography, Gel; Dermatan Sulfate; Female; Glycosaminoglycans; Heparitin Sulfate; Hexosamines; Humans; Hyaluronoglucosaminidase; Indicators and Reagents; Male; Mucopolysaccharidoses; Spectrophotometry; Sulfuric Acids; Testis

1976
The mucopolysaccharidoses.
    Journal of medical genetics, 1976, Volume: 13, Issue:3

    Topics: Acetylglucosaminidase; Chemical Phenomena; Chemistry; Female; Galactosidases; Glucuronidase; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Male; Molecular Conformation; Mucopolysaccharidoses; Prenatal Diagnosis; Sulfatases

1976
Colorimetric determination of hyaluronate degraded by Streptomyces hyaluronidase.
    Analytical biochemistry, 1975, Volume: 64, Issue:1

    Topics: Colorimetry; Glycosaminoglycans; Hexosamines; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Mucopolysaccharidoses; Protein Binding; Streptomyces; Synovial Fluid; Time Factors

1975
Glycosaminoglycan excretion in connective tissue diseases.
    Clinical biochemistry, 1988, Volume: 21, Issue:2

    Topics: Child; Child, Preschool; Connective Tissue Diseases; Female; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Male; Mucopolysaccharidoses

1988
Catabolism of mucopolysaccharides by rat liver lysosomes in vivo.
    The Journal of biological chemistry, 1968, Sep-10, Volume: 243, Issue:17

    Topics: Animals; Centrifugation, Density Gradient; Chick Embryo; Chondroitin; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Liver; Lysosomes; Mucopolysaccharidoses; Rats; Sulfur Isotopes; Swine; Time Factors; Tritium

1968
The glycosaminoglycans of human plasma.
    The Journal of clinical investigation, 1969, Volume: 48, Issue:2

    Topics: Adolescent; Adult; Animals; Child; Child, Preschool; Chondroitin; Chromatography; Collagen Diseases; Female; Glycosaminoglycans; Heparin; Humans; Hyaluronoglucosaminidase; In Vitro Techniques; Keratins; Male; Methods; Mucopolysaccharidoses; Papain; Rabbits; Spectrophotometry; Sulfur Isotopes

1969
Urinary hyaluronidase activity in mucopolysaccharidosis.
    Acta paediatrica Academiae Scientiarum Hungaricae, 1969, Volume: 10, Issue:1

    Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Intellectual Disability; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa

1969
Mucopolysaccharides of the retina.
    UCLA forum in medical sciences, 1969, Volume: 8

    Topics: Animals; Autoradiography; Connective Tissue; Glycosaminoglycans; Histocytochemistry; Humans; Hyaluronoglucosaminidase; Mucopolysaccharidoses; Nerve Tissue Proteins; Photoreceptor Cells; Retina; Sulfur Isotopes

1969
Serum acid hydrolases in the mucopolysaccharidoses.
    The Biochemical journal, 1971, Volume: 125, Issue:2

    Topics: Carbohydrate Metabolism, Inborn Errors; Child; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Humans; Hyaluronoglucosaminidase; Mucopolysaccharidoses; Mucopolysaccharidosis IV

1971
Age differences in the pattern of urinary glycosaminoglycan excretion in normal individuals.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 37

    Topics: Adolescent; Adult; Age Factors; Aged; Child; Child, Preschool; Chondroitin; Chromatography, Gas; Chromatography, Ion Exchange; Diagnosis, Differential; Electrophoresis; Female; Galactose; Glycosaminoglycans; Heparitin Sulfate; Hexosamines; Humans; Hyaluronoglucosaminidase; Lyases; Male; Methods; Middle Aged; Mucopolysaccharidoses; Retinitis Pigmentosa; Serine; Sulfuric Acids; Testis; Xylose

1972
Detection of radioactive acid mucopolysaccharides on electrophoresis membranes.
    Analytical biochemistry, 1972, Volume: 48, Issue:1

    Topics: Carbon Isotopes; Cellulose; Child; Chondroitin; Culture Techniques; Electrophoresis; Evaluation Studies as Topic; Fibroblasts; Glycosaminoglycans; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Male; Membranes, Artificial; Mucopolysaccharidoses; Pronase; Skin; Sulfur Isotopes; Sulfuric Acids; Testis

1972
The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine.
    Biochemical medicine, 1972, Volume: 6, Issue:3

    Topics: Achondroplasia; Adolescent; Adult; Aged; Aging; Arthritis, Rheumatoid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Colorimetry; Dermatomyositis; Female; Galactose; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Infant, Newborn; Intellectual Disability; Lipid Metabolism, Inborn Errors; Male; Methods; Middle Aged; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Sulfuric Acids

1972
Determination of heterozygous carrier state from the urine of the parents of children suffering from mucopolysaccharidosis.
    Acta paediatrica Academiae Scientiarum Hungaricae, 1972, Volume: 13, Issue:1

    Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Child; Female; Glycosaminoglycans; Heterozygote; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Male; Mucopolysaccharidoses

1972
Glycosaminoglycan composition of human amniotic fluid.
    Biochimica et biophysica acta, 1974, Jul-04, Volume: 354, Issue:2

    Topics: Amniocentesis; Amniotic Fluid; Chondroitin; Chromatography, Ion Exchange; Chromatography, Paper; Female; Fetus; Galactosamine; Glucosamine; Glycopeptides; Glycosaminoglycans; Heparitin Sulfate; Hexoses; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Mucopolysaccharidoses; Pregnancy; Sulfates; Sulfuric Acids; Time Factors; Uronic Acids

1974
[Enzymatic diagnosis of glycolipidosis].
    Quaderni Sclavo di diagnostica clinica e di laboratorio, 1972, Volume: 8, Issue:1

    Topics: Diffuse Cerebral Sclerosis of Schilder; Galactosidases; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hyaluronoglucosaminidase; Hydrolases; Leukocytes; Lipid Metabolism, Inborn Errors; Lipidoses; Mucopolysaccharidoses; Phosphoric Monoester Hydrolases; Sulfatases

1972