Synthesis, cellular uptake and HIV-1 Tat-dependent trans-activation inhibition activity of oligonucleotide analogues disulphide-conjugated to cell-penetrating peptides

مواد مشابهة

• Cell-penetrating peptide conjugates of peptide nucleic acids (PNA) as inhibitors of HIV-1 Tat-dependent trans-activation in cells
  بواسطة: Turner, John J., وآخرون
  منشور في: (2005)
• Steric inhibition of human immunodeficiency virus type-1 Tat-dependent trans-activation in vitro and in cells by oligonucleotides containing 2′-O-methyl G-clamp ribonucleoside analogues
  بواسطة: Holmes, Stephen C., وآخرون
  منشور في: (2003)
• Cell penetrating peptide conjugates of steric block oligonucleotides()
  بواسطة: Lebleu, Bernard, وآخرون
  منشور في: (2008)
• Parallel synthesis and splicing redirection activity of cell-penetrating peptide conjugate libraries of a PNA cargo
  بواسطة: Deuss, Peter J., وآخرون
  منشور في: (2013)
• Synthesis and Splice-Redirecting Activity of Branched, Arginine-Rich Peptide Dendrimer Conjugates of Peptide Nucleic Acid Oligonucleotides
  بواسطة: Saleh, Amer F., وآخرون
  منشور في: (2010)