Multilineage transduction of resident lung cells in vivo by AAV2/8 for [alpha]1-antitrypsin gene the...
Multilineage transduction of resident lung cells in vivo by AAV2/8 for [alpha]1-antitrypsin gene therapy
About this item
Full title
Author / Creator
Publisher
Milwaukee: Elsevier Limited
Journal title
Language
English
Formats
Publication information
Publisher
Milwaukee: Elsevier Limited
More information
Scope and Contents
Contents
In vivo gene delivery has long represented an appealing potential treatment approach for monogenic diseases such as α1 -antitrypsin deficiency (AATD) but has proven challenging to achieve in practice. Alternate pseudotyping of recombinant adeno-associated virus (AAV) vectors is producing vectors with increasingly heterogeneous tropic specificity, g...
Alternative Titles
Full title
Multilineage transduction of resident lung cells in vivo by AAV2/8 for [alpha]1-antitrypsin gene therapy
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_journals_1800270990
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1800270990
Other Identifiers
E-ISSN
2329-0501
DOI
10.1038/mtm.2016.42
