Enzyme replacement therapy: conception, chaos and culmination (Q35153236)

6 August 2017

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title

Enzyme replacement therapy: conception, chaos and culmination (English)

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enzyme replacement therapy

6 August 2017

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author name string

Roscoe O Brady

series ordinal

1

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PubMed ID

12803925

6 August 2017

language of work or name

English

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publication date

1 May 2003

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6 August 2017

5

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Philosophical Transactions of the Royal Society B

inferred from page(s)

published in

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6 August 2017

358

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6 August 2017

1433

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6 August 2017

915-919

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METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE.

6 August 2017

1 reference

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The chemical structure of normal human brain and Tay-Sachs gangliosides

28 July 2018

1 reference

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Cerebroside synthesis in Gaucher's disease

28 July 2018

1 reference

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Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease

28 July 2018

1 reference

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Enzyme replacement therapy in Fabry disease: a randomized controlled trial

28 July 2018

1 reference

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Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial

28 July 2018

1 reference

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Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease

28 July 2018

1 reference

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Delivery, distribution, and neuronal uptake of exogenous mannose-terminal glucocerebrosidase in the intact rat brain.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1693186

Enhanced macrophage uptake of synthetically glycosylated human placental beta-glucocerebrosidase

28 July 2018

1 reference

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Demonstration of an alteration of ganglioside metabolism in Tay-Sachs disease

28 July 2018

1 reference

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Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher's disease

28 July 2018

1 reference

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The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick diseae

28 July 2018

1 reference

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The metabolism of Tay-Sachs ganglioside: catabolic studies with lysosomal enzymes from normal and Tay-Sachs brain tissue

28 July 2018

1 reference

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Intravenous injection of purified hexosaminidase A into a patient with Tay-Sachs disease

28 July 2018

1 reference

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The role of surface carbohydrates in the hepatic recognition and transport of circulating glycoproteins.

28 July 2018

1 reference

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Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1693186

Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1693186

Solubilization of glucocerebrosidase from human placenta and demonstration of a phospholipid requirement for its catalytic activity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1693186

Enzyme replacement therapy in Gaucher's disease: large-scale purification of glucocerebrosidase suitable for human administration

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1693186

THE METABOLISM OF GLUCOCEREBROSIDES. I. PURIFICATION AND PROPERTIES OF A GLUCOCEREBROSIDE-CLEAVING ENZYME FROM SPLEEN TISSUE

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1693186

Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry

27 September 2018

1 reference

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Enzyme-replacement therapy in mucopolysaccharidosis I.

27 September 2018

1 reference

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Enzymatic Defect in Fabry's Disease

27 September 2018

1 reference

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Lysosomal hydrolases as glycoproteins

1 reference

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Fabry's Disease: Antenatal Detection

1 reference

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Identification of heterozygous carriers of lipid storage diseases. Current status and clinical applications

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Replacement Therapy for Inherited Enzyme Deficiency

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Isolation and Characterization of Glucocerebrosidase from Human Placental Tissue

1 reference

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Biochemical, morphological, and ultrastructural studies on the uptake of liposomes by murine macrophages

1 reference

12 December 2020

Uptake and distribution of placental glucocerebrosidase in rat hepatic cells and effects of sequential deglycosylation

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12 December 2020

Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease

1 reference

12 December 2020

Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources

1 reference

12 December 2020

FABRY'S DISEASE: CLASSIFICATION AS A SPHINGOLIPIDOSIS AND PARTIAL CHARACTERIZATION OF A NOVEL GLYCOLIPID

1 reference

12 December 2020

FROM CYTASES TO LYSOSOMES

1 reference

12 December 2020

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12 December 2020

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Diagnosis of gaucher's disease and niemann-pick disease with small samples of venous blood

1 reference

12 December 2020

The lysosomal localization of sphingolipid hydrolases

1 reference

12 December 2020

Identifiers

DOI

10.1098/RSTB.2003.1269

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6 August 2017

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6 August 2017

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PubMed ID

12803925