Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes (Q34039222)

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scientific article published on October 1, 1979

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English	Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes	scientific article published on October 1, 1979

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scholarly article

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Europe PubMed Central

30 July 2017

Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes (English)

1 reference

Europe PubMed Central

30 July 2017

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Robert J. Desnick

1

object named as

Desnick RJ

1 reference

Europe PubMed Central

30 July 2017

author name string

K. J. Dean

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A228284

18 January 2023

G. Grabowski

3

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18 January 2023

D. F. Bishop

4

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18 January 2023

C. C. Sweeley

5

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18 January 2023

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publication date

1 October 1979

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Europe PubMed Central

30 July 2017

full work available at URL

https://europepmc.org/articles/PMC413135

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Europe PubMed Central

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18 January 2023

https://europepmc.org/articles/PMC413135?pdf=render

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Europe PubMed Central

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Europe PubMed Central

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18 January 2023

https://pnas.org/doi/pdf/10.1073/pnas.76.10.5326

1 reference

10.1073/PNAS.76.10.5326

https://api.crossref.org/works/10.1073/PNAS.76.10.5326

18 January 2023

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

30 July 2017

76

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Europe PubMed Central

30 July 2017

5326-5330

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Europe PubMed Central

30 July 2017

10

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Europe PubMed Central

30 July 2017

The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis

1 reference

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5 July 2018

Fabry's Disease: Alpha-Galactosidase Deficiency

1 reference

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Specific radioactive labeling of terminal n-acetylgalactosamine of glycosphingolipids by the galactose oxidase-sodium borohydride method

1 reference

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5 July 2018

Enzyme Replacement in Fabry's Disease, an Inborn Error of Metabolism

1 reference

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Differences between the N-acetyl hexosaminidase isozymes in serum and tissues.

1 reference

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

1 reference

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

1 reference

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5 July 2018

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

1 reference

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The isolation and properties of a rabbit liver binding protein specific for asialoglycoproteins.

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5 July 2018

The uptake of native and desialylated glucocerebrosidase by rat hepatocytes and Kupffer cells

1 reference

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Enzyme therapy XI: immunologic considerations for replacement therapy with unentrapped, erythrocyte- and liposome-entrapped enzymes

1 reference

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5 July 2018

Clearance of human N-acetyl-β-hexosaminidases from rat circulation

1 reference

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5 July 2018

Fabry disease: Diagnosis by α-galactosidase activities in tears

1 reference

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5 July 2018

Plasma α-galactosidase A: Properties and comparisons with tissue α-galactosidases

1 reference

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5 July 2018

Pilot scale purification of α-galactosidase A from Cohn Fraction IV-1 of human plasma

1 reference

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5 July 2018

Uptake of radiolabeled galactosyl-(α1 → 4)-galactosyl-(β1 → 4)-glucosylceramide by human serum lipoproteins in vitro

1 reference

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5 July 2018

Molecular pathology of Fabry's disease physical and kinetic properties of α-galactosidase a in cultured human endothelial cells

1 reference

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5 July 2018

Rapid, multisample isoelectric focusing in sucrose density gradients using conventional polyacrylamide electrophoresis equipment: A two-peak transient in the approach-to-equilibrium

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A method for the quantitative determination of neutral glycosphingolipids in urine sediment

1 reference

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29 October 2018

Enzymatic Defect in Fabry's Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/228284

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Galactosylgalactosylglucosylceramide: Galactosyl hydrolase in normal human plasma and its absence in patients with fabry's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/228284

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative determination of the neutral glycosyl ceramides in human blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/228284

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Sphingolipid Having a Novel Type of Ceramide and Lacto-N-Fucopentaose III

1 reference

https://pubmed.ncbi.nlm.nih.gov/228284

12 December 2020

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Replacement Therapy for Inherited Enzyme Deficiency

1 reference

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12 December 2020

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Enzyme electrophoresis on cellulose acetate gel. II. Zymogram patterns in man-Chinese hamster somatic cell hybrids

1 reference

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Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis

1 reference

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Clearance of lysosomal hydrolases following intravenous infusion. Kinetic and competition experiments with beta-glucuronidase and N-acetyl-beta-D-glucosaminidase

1 reference

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Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/228284

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Enzyme therapy. Differential in vivo retention of bovine hepatic, renal, and splenic beta-glucuronidases and evidence for enzyme stabilization by intermolecular exchange

1 reference

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1 reference

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Identifiers

10.1073/PNAS.76.10.5326

1 reference

Europe PubMed Central

30 July 2017

1979PNAS...76.5326D

0 references

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

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