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  • Mihail S. Iordanov, David Pribnow, +4 authors Bruce E. Magun
  • Medicine, Biology
  • Molecular and cellular biology
  • 1997 (First Published: 1 June 1997)
  • Inhibition of protein synthesis per se does not potentiate the stress-activated protein kinases (SAPKs; also known as cJun NH2-terminal kinases [JNKs]). The protein synthesis inhibitor anisomycin,Continue Reading
  • Mihail S. Iordanov, Olga P Ryabinina, +4 authors Bruce E. Magun
  • Biology, Medicine
  • Cancer research
  • 2000 (First Published: 1 April 2000)
  • Cytotoxic endoribonucleases (RNases) possess a potential for use in cancer therapy. However, the molecular determinants of RNase-induced cell death are not well understood. In this work, we identifyContinue Reading
  • Karin D Rodland, Leslie L. Muldoon, T H Dinh, Bruce E. Magun
  • Biology, Medicine
  • Molecular and cellular biology
  • 1988 (First Published: 1 May 1988)
  • A single VL30 element present in the RVL-3 cell line was transcriptionally induced by both epidermal growth factor (EGF) and the protein kinase C (pkC) activators 12-O-tetradecanoylphorbol-13-acetateContinue Reading
  • Muriel Delepierre, C Milhé, Abdelkader Namane, T H Dinh, Bernard Pierre Roques
  • Chemistry, Medicine
  • Biopolymers
  • 1991 (First Published: 15 February 1991)
  • The structures of the complexes formed in aqueous solution between ditercalinium, a bis-intercalating drug, and both the self-complementary tetranucleotide d(GCGC)2 and octanucleotide d(CCTATAGG)2,Continue Reading
  • Peter Allard, T H Dinh, Catherine Gouyette, Jean Igolen, Jean Claude Chermann, F. Barré-Sinoussi
  • Chemistry, Medicine
  • Journal of medicinal chemistry
  • 1981 (First Published: 1 November 1981)
  • A series of 2-alpha-L-rhamnopyranosylnitro[1,2,4]triazolo[1,5-a] pyridine C-nucleosides was synthesized from the condensation oa thioiminoether with nitro-2-pyridylhydrazines. Catalytic reductionContinue Reading