Log in to save to my catalogue

Cell-autonomous expression of the acid hydrolase galactocerebrosidase

Cell-autonomous expression of the acid hydrolase galactocerebrosidase

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7183170

Cell-autonomous expression of the acid hydrolase galactocerebrosidase

About this item

Full title

Cell-autonomous expression of the acid hydrolase galactocerebrosidase

Publisher

United States: National Academy of Sciences

Journal title

Proceedings of the National Academy of Sciences - PNAS, 2020-04, Vol.117 (16), p.9032-9041

Language

English

Formats

Publication information

Publisher

United States: National Academy of Sciences

More information

Scope and Contents

Contents

Lysosomal storage diseases (LSDs) are typically caused by a deficiency in a soluble acid hydrolase and are characterized by the accumulation of undegraded substrates in the lysosome. Determining the role of specific cell types in the pathogenesis of LSDs is a major challenge due to the secretion and subsequent uptake of lysosomal hydrolases by adja...

Alternative Titles

Full title

Cell-autonomous expression of the acid hydrolase galactocerebrosidase

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7183170

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7183170

Other Identifiers

ISSN

0027-8424

E-ISSN

1091-6490

DOI

10.1073/pnas.1917675117

How to access this item