Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
April 20, 2010Molecular TherapyOpen Access

Engineering of Human Pluripotent Stem Cells by AAV-mediated Gene Targeting

View Full Paper
Ask AI
Bookmark
Share

Authors

IKIram KhanUniversity of Central FloridaRHRoli K. HirataUniversity of WashingtonPWPei-Rong WangUniversity of Washington

Discussion

Loading...

Member takes

Implication

Key Points

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

Cite This Study

Khan et al. (2010) studied this question.

synapsesocial.com/papers/6a63017f6ef2e4c3cf6a6e1chttps://doi.org/10.1038/mt.2010.55
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. 1Adeno-associated virus vectors preferentially transduce cells in S phase.1994 · 277 citations
  2. 2Highly efficient transient gene expression and gene targeting in primate embryonic stem cells with helper-dependent adenoviral vectors2008 · 109 citations
  3. 3Recruitment of wild-type and recombinant adeno-associated virus into adenovirus replication centers1996 · 138 citations
  4. 4Gene Targeting of Mutant COL1A2 Alleles in Mesenchymal Stem Cells From Individuals With Osteogenesis Imperfecta2007 · 85 citations
  5. 5Senescence impairs successful reprogramming to pluripotent stem cells2009 · 643 citations