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Hexosaminidase

  • Hexosaminidase in Mast Β Primary Role of Degranulation Indicator in Mast Cells?

    Hexosaminidase in Mast Β Primary Role of Degranulation Indicator in Mast Cells?

  • Quality Assessment Enzyme Analysis for Lysosomal Storage Diseases ERNDIM / EUGT Meeting 5-6 October 2006, Prague

    Quality Assessment Enzyme Analysis for Lysosomal Storage Diseases ERNDIM / EUGT Meeting 5-6 October 2006, Prague

  • Functional Characterization of Carbohydrate-Active Enzymes from Marine Bacteria

    Functional Characterization of Carbohydrate-Active Enzymes from Marine Bacteria

  • The Metabolism of Tay-Sachs Ganglioside: Catabolic Studies with Lysosomal Enzymes from Normal and Tay-Sachs Brain Tissue

    The Metabolism of Tay-Sachs Ganglioside: Catabolic Studies with Lysosomal Enzymes from Normal and Tay-Sachs Brain Tissue

  • GM2 Gangliosidoses: Clinical Features, Pathophysiological Aspects, and Current Therapies

    GM2 Gangliosidoses: Clinical Features, Pathophysiological Aspects, and Current Therapies

  • Pompe Disease

    Pompe Disease

  • Glycosphingolipids Are Modulators of Disease Pathogenesis in Amyotrophic Lateral Sclerosis

    Glycosphingolipids Are Modulators of Disease Pathogenesis in Amyotrophic Lateral Sclerosis

  • ZHOU-THESIS-2018.Pdf (2.307Mb)

    ZHOU-THESIS-2018.Pdf (2.307Mb)

  • Tay-Sachs Disease with Altered P-Hexosaminidase B: a New Variant?

    Tay-Sachs Disease with Altered P-Hexosaminidase B: a New Variant?

  • New Approaches to Correcting Metabolic Errors in Tay-Sachs

    New Approaches to Correcting Metabolic Errors in Tay-Sachs

  • Impaired Β-Glucocerebrosidase Activity and Processing in Frontotemporal Dementia Due to Progranulin Mutations Andrew E

    Impaired Β-Glucocerebrosidase Activity and Processing in Frontotemporal Dementia Due to Progranulin Mutations Andrew E

  • Mutagenesis of Human Alpha-Galactosidase a for the Treatment of Fabry Disease

    Mutagenesis of Human Alpha-Galactosidase a for the Treatment of Fabry Disease

  • Carrier Detection for Tay-Sachs Disease: a Model for Genetic Disease Prevention

    Carrier Detection for Tay-Sachs Disease: a Model for Genetic Disease Prevention

  • Cherry-Red Spot Myoclonus Syndrome and A-Neuraminidase Deficiency

    Cherry-Red Spot Myoclonus Syndrome and A-Neuraminidase Deficiency

  • Inborn Errors of Metabolism As a Cause of Neurological Disease in Adults: an Approach to Investigation

    Inborn Errors of Metabolism As a Cause of Neurological Disease in Adults: an Approach to Investigation

  • Tay-Sachs Disease Testing

    Tay-Sachs Disease Testing

  • LIMP-2 Expression Is Critical for Β-Glucocerebrosidase Activity and Α-Synuclein Clearance

    LIMP-2 Expression Is Critical for Β-Glucocerebrosidase Activity and Α-Synuclein Clearance

  • Structural and Biochemical Insights Into Biosynthesis and Degradation of and Degradation Into Insights Biosynthesis and Biochemical Structural

    Structural and Biochemical Insights Into Biosynthesis and Degradation of and Degradation Into Insights Biosynthesis and Biochemical Structural

Top View
  • Evidence That Small Molecule Enhancement of Β-Hexosaminidase Activity Corrects the Behavioral Phenotype in Dutch APPE69
  • Krabbe Disease Successfully Treated Via Monotherapy of Intrathecal Gene Therapy
  • Synthesis of Human Milk Oligosaccharides: Protein Engineering Strategies for Improved Enzymatic Transglycosylation
  • Supplementary File 1 (PDF, 225 Kib)
  • Structure and Function of Er Class 1 Alpha Mannosidase
  • Deficiency of the Hexosaminidase a Activator Protein in a Case of GM2 Gangliosidosis; Variant AB
  • Coordinacy of Lysosomal Enzyme Excretion in Human Urine
  • Isolation and Characterization of a Class II A-Mannosidase Cdna from Lepidopteran Insect Cells
  • Beta Hexosaminidase Activity Assay Kit
  • Loss of Acid Sphingomyelinase Ameliorates Disease Progression In
  • Effects of a Chemical Chaperone on Genetic Mutations in Α-Galactosidase a in Korean Patients with Fabry Disease
  • Dase-B: Studies in Tay-Sachs' and Sandho:Ff's Disease
  • Lysosomal Diseases
  • Biochemical Properties of Extracellular A-Mannosidases from the Digestive
  • The Activity of N-Acetyl-Β-D-Hexosaminidase in Serum And
  • Modulation of HSP70 Glcnac-Directed Lectin Activity by Glucose Availability and Utilization
  • High-Level Production of Recombinant Human Lysosomal Acid
  • Downloaded from JGI IMG/M (Table 1)


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