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Original Articles

Bent Oligonucleotide Duplexes as HMGB1 Inhibitors: a Comparative Study

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Pages 1447-1450 | Published online: 05 Dec 2007

REFERENCES

  • Bucci , E. M. , Musumeci , D. and Valente , M. 2006 . More than antisense. Targeting extracellular proteins by oligonucleotide analogues . Screening Trends in Drug Discovery , 2 : 32 – 33 .
  • Yang , H. , Wang , H. and Tracey , K. J. 2001 . HMG-1 rediscovered as a cytokine . Shock , 15 : 247 – 253 .
  • Barone , D. G. , Bianchi , M. E. , Bucci , E. M. , Fumero , S. , Valente , M. , Sapio , R. and Musumeci , D. Therapeutic agents comprising synthetic double-stranded nucleic acid with a bent shape structure for the treatment of HMGB1-related pathologies . PCT Int. Appl., WO 2006002971 . 2006 .
  • Kurreck , J. , Wyszko , E. , Gillen , C. and Erdmann , V. A. 2002 . Design of antisense oligonucleotides stabilized by locked nucleic acids . Nucleic Acids Res. , 30 ( 9 ) : 1911 – 1918 .

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