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Neurophysiological, behavioral and morphological abnormalities in the Fabry knockout mice

Neurobiology of disease, 2009-01, Vol.33 (1), p.48-56

2009

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Toxicity of glucosylsphingosine (glucopsychosine) to cultured neuronal cells: a model system for assessing neuronal damage in Gaucher disease type 2 and 3

Neurobiology of disease, 2003-12, Vol.14 (3), p.595-601

2003

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Dynamic intervention-based biomarkers may reduce heterogeneity and motivate targeted interventions in clinical high risk for psychosis

Schizophrenia research, 2022-08, Vol.246, p.60-62

2022

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Deficiencies in sex-regulated expression and levels of two hepatic sterol carrier proteins in a murine model of Niemann-Pick type C disease

The Journal of biological chemistry, 1992-08, Vol.267 (22), p.15902-15908

1992

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High-Level Production of Recombinant Human Lysosomal Acid α -Glucosidase in Chinese Hamster Ovary Cells which Targets to Heart Muscle and Corrects Glycogen Accumulation in Fibroblasts from Patients with Pompe Disease

Proceedings of the National Academy of Sciences - PNAS, 1996-01, Vol.93 (1), p.65-70

1996

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Comparative Efficacy of Dose Regimens in Enzyme Replacement Therapy of Type I Gaucher Disease

Blood cells, molecules, & diseases, 2000-08, Vol.26 (4), p.285-290

2000

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Therapeutic Use of Butyrylcholinesterase for Cocaine Intoxication

Toxicology and applied pharmacology, 1997-08, Vol.145 (2), p.372-380

1997

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A Contemporary View of Intracellular Cholesterol Movement

Trends in Glycoscience and Glycotechnology, 1994/01/02, Vol.6(27), pp.75-91

1994

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Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patients

American journal of human genetics, 1993-10, Vol.53 (4), p.921-930

1993

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A defect in cholesterol esterification in Niemann-Pick disease (type C) patients

Proceedings of the National Academy of Sciences - PNAS, 1985-12, Vol.82 (23), p.8247-8251

1985

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Type-C Niemann-Pick Disease: Low Density Lipoprotein Uptake is Associated with Premature Cholesterol Accumulation in the Golgi Complex and Excessive Cholesterol Storage in Lysosomes

Proceedings of the National Academy of Sciences - PNAS, 1988-11, Vol.85 (21), p.8022-8026

1988

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Outcome of partial splenectomy for type I Gaucher disease

The Journal of pediatrics, 1995-04, Vol.126 (4), p.596-597

1995

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Correction of Glucocerebrosidase Deficiency after Retroviral-Mediated Gene Transfer into Hematopoietic Progenitor Cells from Patients with Gaucher Disease

Proceedings of the National Academy of Sciences - PNAS, 1990-03, Vol.87 (6), p.2334-2338

1990

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Preparation of radioactive Tay-Sachs ganglioside labeled in the sialic acid moiety

Journal of lipid research, 1970-03, Vol.11 (2), p.144-149

1970

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Molecular Cloning and Chromosomal Mapping of the Mouse Cyclin-Dependent Kinase 5 Gene

Genomics (San Diego, Calif.), 1995-08, Vol.28 (3), p.585-588

1995

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Biliary excretion of glycolipid in induced or inherited glucosylceramide lipidosis

Biochimica et biophysica acta, 1981-09, Vol.665 (3), p.615-618

1981

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Comparison of the Chromosomal Localization of Murine and Human Glucocerebrosidase Genes and of the Deduced Amino Acid Sequences

Proceedings of the National Academy of Sciences - PNAS, 1989-07, Vol.86 (13), p.5049-5053

1989

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Production of Human Glucocerebrosidase in Mice after Retroviral Gene Transfer into Multipotential Hematopoietic Progenitor Cells

Proceedings of the National Academy of Sciences - PNAS, 1989-11, Vol.86 (22), p.8912-8916

1989

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Comparison of the effects of Δ9-tetrahydrocannabinol, 11-hydroxy-Δ9-tetrahydrocannabinol, and ethanol on the electrophysiological activity of the giant axon of the squid

Neuropharmacology, 1973-06, Vol.12 (6), p.601-605

1973

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Comparison of the effects of Δ9-tetrahydrocannabinol, 11-hydroxy-Δ 9-tetrahydrocannabinol, and ethanol on the electrophysiological activity of the giant axon of the squid

Neuropharmacology, 1973, Vol.12 (6), p.601-605

1973

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Alteration of Glycolipids in ras-Transfected NIH 3T3 Cells

Proceedings of the National Academy of Sciences - PNAS, 1987-09, Vol.84 (17), p.6065-6068

1987

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Influence of oxygen on the photolysis of coenzyme B 12

Biochemical and biophysical research communications, 1961, Vol.4 (5), p.373-378

1961

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Purification and properties of the two major isozymes of alpha-galactosidase from human placenta

The Journal of biological chemistry, 1978-01, Vol.253 (1), p.184-190

1978

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Biosynthesis of bovine thyroid gangliosides

The Journal of biological chemistry, 1978-08, Vol.253 (16), p.5839-5846

1978

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Impaired cholesterol esterification in primary brain cultures of the lysosomal cholesterol storage disorder (LCSD) mouse mutant

Biochemical and biophysical research communications, 1987-02, Vol.143 (1), p.233-240

1987

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Neurophysiological, behavioral and morphological abnormalities in the Fabry knockout mice

Toxicity of glucosylsphingosine (glucopsychosine) to cultured neuronal cells: a model system for assessing neuronal damage in Gaucher disease type 2 and 3

Dynamic intervention-based biomarkers may reduce heterogeneity and motivate targeted interventions in clinical high risk for psychosis

Deficiencies in sex-regulated expression and levels of two hepatic sterol carrier proteins in a murine model of Niemann-Pick type C disease

High-Level Production of Recombinant Human Lysosomal Acid α -Glucosidase in Chinese Hamster Ovary Cells which Targets to Heart Muscle and Corrects Glycogen Accumulation in Fibroblasts from Patients with Pompe Disease

Comparative Efficacy of Dose Regimens in Enzyme Replacement Therapy of Type I Gaucher Disease

Therapeutic Use of Butyrylcholinesterase for Cocaine Intoxication

A Contemporary View of Intracellular Cholesterol Movement

Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patients

A defect in cholesterol esterification in Niemann-Pick disease (type C) patients

Type-C Niemann-Pick Disease: Low Density Lipoprotein Uptake is Associated with Premature Cholesterol Accumulation in the Golgi Complex and Excessive Cholesterol Storage in Lysosomes

Outcome of partial splenectomy for type I Gaucher disease

Correction of Glucocerebrosidase Deficiency after Retroviral-Mediated Gene Transfer into Hematopoietic Progenitor Cells from Patients with Gaucher Disease

Preparation of radioactive Tay-Sachs ganglioside labeled in the sialic acid moiety

Molecular Cloning and Chromosomal Mapping of the Mouse Cyclin-Dependent Kinase 5 Gene

Biliary excretion of glycolipid in induced or inherited glucosylceramide lipidosis

Comparison of the Chromosomal Localization of Murine and Human Glucocerebrosidase Genes and of the Deduced Amino Acid Sequences

Production of Human Glucocerebrosidase in Mice after Retroviral Gene Transfer into Multipotential Hematopoietic Progenitor Cells

Comparison of the effects of Δ9-tetrahydrocannabinol, 11-hydroxy-Δ9-tetrahydrocannabinol, and ethanol on the electrophysiological activity of the giant axon of the squid

Comparison of the effects of Δ9-tetrahydrocannabinol, 11-hydroxy-Δ 9-tetrahydrocannabinol, and ethanol on the electrophysiological activity of the giant axon of the squid

Alteration of Glycolipids in ras-Transfected NIH 3T3 Cells

Influence of oxygen on the photolysis of coenzyme B 12

Purification and properties of the two major isozymes of alpha-galactosidase from human placenta

Biosynthesis of bovine thyroid gangliosides

Impaired cholesterol esterification in primary brain cultures of the lysosomal cholesterol storage disorder (LCSD) mouse mutant

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