Synthesis, in vitro and in vivo evaluation of new 99mTc-labeled cyclic RGDfK peptide monocationic complexes (Contributo in atti di convegno)

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  • Synthesis, in vitro and in vivo evaluation of new 99mTc-labeled cyclic RGDfK peptide monocationic complexes (Contributo in atti di convegno) (literal)
Anno
  • 2012-01-01T00:00:00+01:00 (literal)
Alternative label
  • Calderan A.; Biondi B.; Bolzati C.; Refosco F.; Morellato N.; Salvarese N.; Ruzza, P (2012)
    Synthesis, in vitro and in vivo evaluation of new 99mTc-labeled cyclic RGDfK peptide monocationic complexes
    in European Peptide Symposium, Athens, Greece, September 2-7, 2012
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Calderan A.; Biondi B.; Bolzati C.; Refosco F.; Morellato N.; Salvarese N.; Ruzza, P (literal)
Pagina inizio
  • S157 (literal)
Pagina fine
  • S158 (literal)
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  • 18 (literal)
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  • 1S (literal)
Note
  • ISI Web of Science (WOS) (literal)
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  • 1,2,5,7 : CNR, Inst Biomol Chem, Padua Unit, Padua, Italy 3,4 : CNR, Inst Inorgan Chem & Surface, Padua, Italy 6 : Univ Padua, Dept Pharmaceut & Pharmacol Sci, Padua, Italy (literal)
Titolo
  • Synthesis, in vitro and in vivo evaluation of new 99mTc-labeled cyclic RGDfK peptide monocationic complexes (literal)
Abstract
  • Synthetic peptides represent first choice biomelecules, with respect to proteins and mAb, for the monitoring of population variability and receptor functionality associated to a tumor pathology due to their favorable pharmacokinetic profile. It has been demonstrated that the surface molecule integrin alfa-V beta-3 could be an ideal target for the interaction with melanoma directed radiolabeled peptides..... (literal)
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