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Bioorganic & Medicinal Chemistry Letters|October 17, 2009
Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compoundsDaniele Passarella, Daniela Comi, Andrea Vanossi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 13, 2002
Cellular bases of the antitumor activity of the novel taxane IDN 5109 (BAY59-8862) on hormone-refractory prostate cancerGiuliana Cassinelli, Cinzia Lanzi, Rosanna Supino, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 12, 2013
Synergistic antitumor activity of cetuximab and namitecan in human squamous cell carcinoma models relies on cooperative inhibition of EGFR expression and depends on high EGFR gene copy numberMichelandrea De Cesare, Calogero Lauricella, Silvio Marco Veronese, et al.
Cancers|June 10, 2022
Telomere as a Therapeutic Target in Dedifferentiated LiposarcomaIrene Alessandrini, Stefano Percio, Eisa Naghshineh, et al.
Chemmedchem|June 18, 2016
3-Arylidene-N-hydroxyoxindoles: A New Class of Compounds Endowed with Antitumor ActivityLoana Musso, Raffaella Cincinelli, Valentina Zuco, et al.
Biochemical Pharmacology|September 22, 2009
Efficacy of ST1968 (namitecan) on a topotecan-resistant squamous cell carcinomaValentina Zuco, Rosanna Supino, Enrica Favini, et al.
Bioorganic & Medicinal Chemistry|October 21, 2015
New macrocyclic analogs of the natural histone deacetylase inhibitor FK228; design, synthesis and preliminary biological evaluationMinghong Ni, Emiliano Esposito, Victor Paul Raj, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2015
Investigation on the ZBG-functionality of phenyl-4-yl-acrylohydroxamic acid derivatives as histone deacetylase inhibitorsLoana Musso, Raffaella Cincinelli, Valentina Zuco, et al.
Cells|February 20, 2020
miR-1272 Exerts Tumor-Suppressive Functions in Prostate Cancer via HIP1 SuppressionFederica Rotundo, Denis Cominetti, Rihan El Bezawy, et al.
Chemmedchem|March 18, 2009
Synthesis, modelling, and antimitotic properties of tricyclic systems characterised by a 2-(5-Phenyl-1H-pyrrol-3-yl)-1,3,4-oxadiazole moietyGérard A Pinna, Gabriele Murineddu, Caterina Murruzzu, et al.
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