Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2019 | 1 |
2024 | 0 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
Long-term correction of hemophilia B using adenoviral delivery of CRISPR/Cas9.
J Control Release. 2019 Mar 28;298:128-141. doi: 10.1016/j.jconrel.2019.02.009. Epub 2019 Feb 13.
J Control Release. 2019.
PMID: 30771412
Free PMC article.
Targeted in vivo knock-in of human alpha-1-antitrypsin cDNA using adenoviral delivery of CRISPR/Cas9.
Stephens CJ, Kashentseva E, Everett W, Kaliberova L, Curiel DT.
Stephens CJ, et al.
Gene Ther. 2018 Apr;25(2):139-156. doi: 10.1038/s41434-018-0003-1. Epub 2018 Mar 27.
Gene Ther. 2018.
PMID: 29588497
Free PMC article.
Item in Clipboard
Cite
Cite