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Hexosaminidase
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
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
GM2 Gangliosidoses: Clinical Features, Pathophysiological Aspects, and Current Therapies
Pompe Disease
Glycosphingolipids Are Modulators of Disease Pathogenesis in Amyotrophic Lateral Sclerosis
ZHOU-THESIS-2018.Pdf (2.307Mb)
Tay-Sachs Disease with Altered P-Hexosaminidase B: a New Variant?
New Approaches to Correcting Metabolic Errors in Tay-Sachs
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
Carrier Detection for Tay-Sachs Disease: a Model for Genetic Disease Prevention
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
Tay-Sachs Disease Testing
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
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)
Johanlarsbrinkthesis
Upregulating Beta-Hexosaminidase Activity in Rodents Prevents Alpha
Differential Polysaccharide Utilization Is the Basis for a 10 Nanohaloarchaeon : Haloarchaeon Symbiosis
MK-8719, a Novel and Selective O-Glcnacase Inhibitor That Reduces the Formation of Pathological Tau and Ameliorates Neurodegeneration in a Mouse Model of Tauopathy S
Prenatal Diagnosis of Enzyme Defects
(O-Glcnacase) Activity in Thyroid Cancers
Krabbe Disease Successfully Treated Via Monotherapy of Intrathecal Gene Therapy
Interrelationship of Hexosaminidases a and B: Confirmation Of
Human P-Hexosaminidase
Identification and Characterisation of Endoglycosidase Activities Towards Dermatan Sulphate by Tandem Mass Spectrometry
Agaricus Bisporus Crude Extract: Characterization and Analytical Application
Mucolipidosis IIIC)
Is It Fabry Disease?
(12) United States Patent (10) Patent No.: US 8,232,073 B2 Crawford Et Al
Enzymatic Identification of Mannose 6-Phosphate on the Recognition Marker for Receptor-Mediated Pinocytosis of F3-Glucuronidase
Emerging Novel Concept of Chaperone Therapies for Protein Misfolding Diseases
The Efficacy of Gene Therapy to Treat Fabry Disease
Biochi~Ic~A Et Biophysica A~Ta ELSEVIER Biochimica Et Biophysica Acta 1272 (1995) 1-13
Lysosomal Enzymes in Ataxia: Discovery of Two New Cases of Late Onset Hexosaminidase a and B Deficiency (Adult Sandhoff Disease) in French Canadians A
Pharmacological Chaperones for Human Α-N-Acetylgalactosaminidase
A Chemical Approach for Identifying O-Glcnac- Modified Proteins in Cells
Carbohydrate-Active Enzymes
Genomic Diversification of Giant Enteric Symbionts Reflects Host Dietary Lifestyles
Datasheet for Β-N-Acetyl-Hexosaminidase (P0721
Discovering Novel Carbohydrate-Active Enzymes in the Cellulosome of Anaerobic Bacteria
Glycobiology
(12) United States Patent (10) Patent No.: US 9,340,822 B2 Crawford Et Al