Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
October 26, 1999Proceedings of the National Academy of SciencesOpen Access

Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons

View Full Paper
Ask AI
Bookmark
Share

Authors

NMNúria MorralIndiana University – Purdue University IndianapolisWOWanda K. O’NealUniversity of North Carolina at Chapel HillKRKaren RiceUCB Pharma (United States)

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Morral et al. (1999) studied this question.

synapsesocial.com/papers/6a8999464c30e1095aec80b7https://doi.org/10.1073/pnas.96.22.12816
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: Implications for gene therapy1998 · 245 citations
  2. 2Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression.1995 · 596 citations
  3. 3Persistence in muscle of an adenoviral vector that lacks all viral genes1997 · 293 citations
  4. 4Innate Immune Mechanisms Dominate Elimination of Adenoviral Vectors Following In Vivo Administration1997 · 497 citations
  5. 5In Vivo Expression of Full-Length Human Dystrophin from Adenoviral Vectors Deleted of All Viral Genes1996 · 147 citations