Tat peptide-mediated cellular delivery: back to basics.

By H. Brooks, B. Lebleu, E. Vivés. Advanced Drug Delivery Reviews, 2005

657 citations recorded by the source corpus.

Subfields: Genetics, Molecular Biology, Virology

View Paper: https://www.semanticscholar.org/paper/cf4b4a34ec0d12904da7b2aada7a57b253a3bfc4

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Genetics

1. S. Jin
2. T. R. Pisanic
3. V. Shubayev

In Molecular Biology

1. S. Jin
2. T. R. Pisanic
3. V. Shubayev

In Virology

1. S. Jin
2. T. R. Pisanic
3. V. Shubayev

Citations in the corpus

• Magnetic nanoparticles for theragnostics (2009, methodology): “For example, the HIV-derived TAT peptide conjugated to ultrasmall iron oxide MNP allows efficient T cell labeling within 5 minutes [57].”
• Uptake Pathways and Subsequent Intracellular Trafficking in Nonviral Gene Delivery (2006, background): “A class of cationic peptides, the PTDs, such as the TAT, penetratin, and VP22 peptides, may have the ability to be taken up by cells without endocytosis events (Vives et al., 1997; Thoren et al., 2003; Nakase et al., 2004; Brooks et al., 2005; Gupta et al., 2005).”