Log in to save to my catalogue

Investigations on therapeutic glucocerebrosidases through paired detection with fluorescent activity...

Investigations on therapeutic glucocerebrosidases through paired detection with fluorescent activity...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1869029962

Investigations on therapeutic glucocerebrosidases through paired detection with fluorescent activity-based probes

About this item

Full title

Investigations on therapeutic glucocerebrosidases through paired detection with fluorescent activity-based probes

Publisher

United States: Public Library of Science

Journal title

PloS one, 2017-02, Vol.12 (2), p.e0170268

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Deficiency of glucocerebrosidase (GBA) causes Gaucher disease (GD). In the common non-neuronopathic GD type I variant, glucosylceramide accumulates primarily in the lysosomes of visceral macrophages. Supplementing storage cells with lacking enzyme is accomplished via chronic intravenous administration of recombinant GBA containing mannose-terminate...

Alternative Titles

Full title

Investigations on therapeutic glucocerebrosidases through paired detection with fluorescent activity-based probes

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1869029962

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1869029962

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0170268

How to access this item