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Publications by Balraj Doray

Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy

Molecular Therapy - Methods and Clinical Development

English

Analysis of Gga Null Mice Demonstrates a Non-Redundant Role for Mammalian GGA2 During Development

PLoS ONE

Multidisciplinary

2012

English

Related publications

Promising CNS-directed Enzyme Replacement Therapy for Lysosomal Storage Diseases

Experimental Neurology

Developmental Neuroscience

Neurology

2009

English

Cost-Effectiveness of Enzyme Replacement Therapy for Type 1 Gaucher Disease

Orphanet Journal of Rare Diseases

English

Psy97 - Cost-Effectiveness Analysis of Enzyme Replacement Therapy for Type 1 Gaucher Disease

English

Loss of Lysosomal Enzymes, Inhibition of Enzyme Pinocytosis and Decreased Activity of Lysosomal Enzymes in Chloroquine Treated Fibroblasts

English

Enzyme Replacement Therapy for Late-Onset Pompe Disease

Cochrane Database of Systematic Reviews

2018

English

Early Diagnosis of Infantile-Onset Lysosomal Acid Lipase Deficiency in the Advent of Available Enzyme Replacement Therapy

Orphanet Journal of Rare Diseases

English

Synthesis of the Subterminally 6-O-Phosphorylated Trimannosides Found on Carbohydrate Chains of Lysosomal Enzymes

Canadian Journal of Chemistry

English

An Alternative Hypothesis of Cellular Transport of Lysosomal Enzymes in Fibroblasts. Effect of Inhibitors of Lysosomal Enzyme Endocytosis on Intra- And Extra-Cellular Lysosomal Enzyme Activities

English

Lysosomal Enzyme Phosphorylation in Human Fibroblasts. Kinetic Parameters Offer a Biochemical Rationale for Two Distinct Defects in the Uridine Diphospho-N-Acetylglucosamine:lysosomal Enzyme Precursor N-Acetylglucosamine-1-Phosphotransferase.

Journal of Clinical Investigation

Medicine

1985

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Balraj Doray

Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy

Analysis of Gga Null Mice Demonstrates a Non-Redundant Role for Mammalian GGA2 During Development

Related publications

Promising CNS-directed Enzyme Replacement Therapy for Lysosomal Storage Diseases

Cost-Effectiveness of Enzyme Replacement Therapy for Type 1 Gaucher Disease

Psy97 - Cost-Effectiveness Analysis of Enzyme Replacement Therapy for Type 1 Gaucher Disease

Loss of Lysosomal Enzymes, Inhibition of Enzyme Pinocytosis and Decreased Activity of Lysosomal Enzymes in Chloroquine Treated Fibroblasts

Enzyme Replacement Therapy for Late-Onset Pompe Disease

Early Diagnosis of Infantile-Onset Lysosomal Acid Lipase Deficiency in the Advent of Available Enzyme Replacement Therapy

Synthesis of the Subterminally 6-O-Phosphorylated Trimannosides Found on Carbohydrate Chains of Lysosomal Enzymes

An Alternative Hypothesis of Cellular Transport of Lysosomal Enzymes in Fibroblasts. Effect of Inhibitors of Lysosomal Enzyme Endocytosis on Intra- And Extra-Cellular Lysosomal Enzyme Activities

Lysosomal Enzyme Phosphorylation in Human Fibroblasts. Kinetic Parameters Offer a Biochemical Rationale for Two Distinct Defects in the Uridine Diphospho-N-Acetylglucosamine:lysosomal Enzyme Precursor N-Acetylglucosamine-1-Phosphotransferase.