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Results: 1-7 |
Results: 7
Characterization of a 2 ',5 '-oligoadenylate (2-5A)-dependent 37-kDa RNaseL. Azido photoaffinity labeling and 2-5A-dependent activation. (vol 276, pg 23707, 2001)
Authors: Shetzline, SE Suhadolnik, RJ
Citation: Se. Shetzline et Rj. Suhadolnik, Characterization of a 2 ',5 '-oligoadenylate (2-5A)-dependent 37-kDa RNaseL. Azido photoaffinity labeling and 2-5A-dependent activation. (vol 276, pg 23707, 2001), J BIOL CHEM, 276(34), 2001, pp. 32392-32392
Characterization of a 2 ',5 '-oligoadenylate (2-5A)-dependent 37-kDa RNaseL - Azido photoaffinity labeling and 2-5A-dependent activation
Authors: Shetzline, SE Suhadolnik, RJ
Citation: Se. Shetzline et Rj. Suhadolnik, Characterization of a 2 ',5 '-oligoadenylate (2-5A)-dependent 37-kDa RNaseL - Azido photoaffinity labeling and 2-5A-dependent activation, J BIOL CHEM, 276(26), 2001, pp. 23707-23711
Synthesis and biological activity of 2 ',5 '-oligoadenylate trimers containing 5 '-terminal 5 '-amino-5 '-deoxy- and 5 '-amino-3 ',5 '-dideoxyadenosine derivatives
Authors: Kvasyuk, EI Mikhailopulo, IA Suhadolnik, RJ Henderson, EE Muto, NF Iacono, KT Homon, J Pfleiderer, W
Citation: Ei. Kvasyuk et al., Synthesis and biological activity of 2 ',5 '-oligoadenylate trimers containing 5 '-terminal 5 '-amino-5 '-deoxy- and 5 '-amino-3 ',5 '-dideoxyadenosine derivatives, NUCLEOS NUC, 18(6-7), 1999, pp. 1483-1484
Inhibition of replication of reactivated human immunodeficiency virus type1 (HIV-1) in latently infected U1 cells transduced with an HIV-1 long terminal repeat-driven PKR cDNA construct
Authors: Muto, NF Martinand-Mari, C Adelson, ME Suhadolnik, RJ
Citation: Nf. Muto et al., Inhibition of replication of reactivated human immunodeficiency virus type1 (HIV-1) in latently infected U1 cells transduced with an HIV-1 long terminal repeat-driven PKR cDNA construct, J VIROLOGY, 73(11), 1999, pp. 9021-9028
Nucleotides - Part LIX - Synthesis, characterization, and biological activities of new potential antiviral agents: (2 '-5 ')adenylate trimer analogs containing 3 '-deoxy-3 '(hexadecanoylamino)adenosine at the 2 '-terminus
Authors: Schirmeister-Tichy, H Iacono, KT Muto, NF Homan, JW Suhadolnik, RJ Pfleiderer, W
Citation: H. Schirmeister-tichy et al., Nucleotides - Part LIX - Synthesis, characterization, and biological activities of new potential antiviral agents: (2 '-5 ')adenylate trimer analogs containing 3 '-deoxy-3 '(hexadecanoylamino)adenosine at the 2 '-terminus, HELV CHIM A, 82(4), 1999, pp. 597-613
Nucleotides - Part LVIII - Synthesis and biological activity of (2 '-5 ')oligoadenylate trimers containing a 5 '-terminal 5 '-amino-5 '-deoxy- or 5 '-amino-3 ',5 '-dideoxyadenosine derivative
Authors: Kvasyuk, EI Mikhailopulo, IA Homan, JW Iacono, KT Muto, NF Suhadolnik, RJ Pfleiderer, W
Citation: Ei. Kvasyuk et al., Nucleotides - Part LVIII - Synthesis and biological activity of (2 '-5 ')oligoadenylate trimers containing a 5 '-terminal 5 '-amino-5 '-deoxy- or 5 '-amino-3 ',5 '-dideoxyadenosine derivative, HELV CHIM A, 82(1), 1999, pp. 19-29
Inhibition of human immunodeficiency virus (HIV-1) replication in SupT1 cells transduced with an HIV-1 LTR-driven PKR cDNA construct
Authors: Adelson, ME Martinand-Mari, C Iacono, KT Muto, NF Suhadolnik, RJ
Citation: Me. Adelson et al., Inhibition of human immunodeficiency virus (HIV-1) replication in SupT1 cells transduced with an HIV-1 LTR-driven PKR cDNA construct, EUR J BIOCH, 264(3), 1999, pp. 806-815
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