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Pedersen Erik B.
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http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_4/101021jm040845b/authorship/6
http://hub.abes.fr/oup/periodical/nar/2008/volume_36/issue_10/101093nargkn242/authorship/5
http://hub.abes.fr/oup/periodical/nar/1998/volume_26/issue_21/101093nar26214919/authorship/2
http://hub.abes.fr/oup/periodical/nar/2005/volume_33/issue_22/101093nargki1019/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_42/101021ja053645d/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_2/101021jm970443m/authorship/2
http://hub.abes.fr/acs/periodical/bcches/2006/volume_17/issue_4/101021bc060058o/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_26/101021jm020949r/authorship/5
http://hub.abes.fr/acs/periodical/bcches/2004/volume_15/issue_2/101021bc0341932/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39/issue_12/101021jm9600499/authorship/3
http://hub.abes.fr/acs/periodical/bcches/1997/volume_8/issue_6/101021bc970067k/authorship/2
http://hub.abes.fr/acs/periodical/bcches/1999/volume_10/issue_1/101021bc980073w/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_22/101021jo00074a028/authorship/3
http://hub.abes.fr/springer/periodical/706/1994/volume_125/issue_5/B8CEC1B32BDF3A9AE053120B220A9C63/authorship/3
http://hub.abes.fr/springer/periodical/706/1994/volume_125/issue_6_7/B8CEC1B32C383A9AE053120B220A9C63/authorship/2
http://hub.abes.fr/springer/periodical/706/1993/volume_124/issue_1/B8CF348974F26FEEE053120B220A2124/authorship/5
http://hub.abes.fr/springer/periodical/706/1994/volume_125/issue_8_9/B8CEC1B32BAF3A9AE053120B220A9C63/authorship/3
http://hub.abes.fr/springer/periodical/706/1995/volume_126/issue_5/B8CF006202D17E97E053120B220A3B7C/authorship/3
http://hub.abes.fr/springer/periodical/706/1995/volume_126/issue_6_7/B8CF006203257E97E053120B220A3B7C/authorship/3
http://hub.abes.fr/springer/periodical/706/1992/volume_123/issue_4/B8CE95BE6E5A3A8CE053120B220AD92C/authorship/4
http://hub.abes.fr/springer/periodical/706/1995/volume_126/issue_11/B8CF006202CB7E97E053120B220A3B7C/authorship/2
http://hub.abes.fr/springer/periodical/706/1993/volume_124/issue_1/B8CF348974F16FEEE053120B220A2124/authorship/4
http://hub.abes.fr/springer/periodical/706/1992/volume_123/issue_4/B8CE95BE6E5C3A8CE053120B220AD92C/authorship/3
http://hub.abes.fr/springer/periodical/706/1991/volume_122/issue_1_2/B8CEC1B32E973A9AE053120B220A9C63/authorship/2
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Synthesis of 5-dialkylaminomethyl-3′-azido and 3′-fluoro-2′,3′-dideoxyuridines for evaluation as anti-HIV agents
Targeting of nucleic acid junctions: addressing to a branch point an oligodeoxynucleotide conjugated with an intercalator
Synthesis and reactions of 2-deoxy-β-D-ribofuranosyl derivatives of 3-aryl-4H-pyrrolo[2,3-d]pyrimidin-4-imines
Synthesis of 2-O-ethyl analogues of 3′-azido- and 3′-fluoro-2′,3′-dideoxyuridines and evaluation of their biological activity against HIV
Hydantoin analogs of thymidine
NMR Structure Determination of a Modified DNA OligonucleotideContaining a New Intercalating Nucleic Acid
Stable and Selective Formation of Hoogsteen-Type Triplexesand Duplexes Using Twisted Intercalating Nucleic Acids(TINA) Prepared via Postsynthetic Sonogashira Solid-PhaseCoupling Reactions
Synthesis and Evaluation of Double-Prodrugs against HIV. Conjugation of D4Twith 6-Benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, Emivirine)-TypeReverse Transcriptase Inhibitors via the SATE Prodrug Approach
Purine twisted-intercalating nucleic acids: a new class of anti-gene molecules resistant to potassium-induced aggregation
Bisintercalation of Homodimeric Thiazole Orange Dyes in DNA: Effect of Modifying the Linker
Bis-Intercalation of Homodimeric Thiazole Orange Dye Derivativesin DNA
Easily denaturing nucleic acids derived from intercalating nucleic acids: thermal stability studies, dual duplex invasion and inhibition of transcription start
Synthesis of Twisted Intercalating Nucleic Acids Possessing Acridine Derivatives.Thermal Stability Studies
Synthesis and Anti-HIV-1 Activity of Novel2,3-Dihydro-7H-thiazolo[3,2-a]pyrimidin-7-ones
Synthesis of Novel N-1 (Allyloxymethyl) Analogues of6-Benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, Emivirine) withImproved Activity Against HIV-1 and Its Mutants
New route for the synthesis of 2-thiouracil analogues of 3′-azido-2′,3′-dideoxy nucleosides
Synthesis and Potent Anti-HIV-1 Activity of Novel 6-Benzyluracil Analogues of1-[(2-Hydroxyethoxy)methyl]-6-(phenylthio)thymine
Synthesis and evaluation of antiviral activity of 2′-deoxyuridines with 5-methylene-2-thiohydantoin substituents in the 5-position
Synthesis of 5′-amino- and 5′-azido-2′,5′-dideoxy nucleosides from thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
Convergent synthesis of 2′,3′-dideoxy-3′-mercapto nucleosides — Potential anti-HIV agents
Convergent synthesis of 2′,3′-dideoxy-3′-methylthio and 2′,3′-dideoxy-3′-mercapto nucleosides and their disulfide analogues — Potential anti-HIV agents
Synthesis of 1-(3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-L-arabino-hexofuranosyl)uracils via an α,β-unsaturated aldehydrohexose
Synthesis of 2′,3′-dideoxynucleosides from 5-alkoxymethyluracils
Synthesis and investigation of antiviral activity of 3′-O-(aminoalkyl)-thymidines and their quaternary ammonium salts
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