Teeft.i
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Serveur d'exploration MERS - Exploration (Accueil)

Index « Teeft.i » - entrée « Nucleoside »
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Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.
Nucleoprotein residues < Nucleoside < Nucleoside analog  Facettes :

List of bibliographic references indexed by Nucleoside

Number of relevant bibliographic references: 30.
[0-20] [0 - 20][0 - 30][20-29][20-40]
Ident.Authors (with country if any)Title
002335 (2012) Julie A. Keating [États-Unis] ; Rob Striker [États-Unis]Phosphorylation events during viral infections provide potential therapeutic targets
002338 (2012) Irina Kira Astakhova [Danemark] ; Evgeniya Samokhina [Russie] ; B. Ravindra Babu [Danemark] ; Jesper Wengel [Danemark]Novel (Phenylethynyl)pyrene–LNA Constructs for Fluorescence SNP Sensing in Polymorphic Nucleic Acid Targets
002657 (2010) Xianbin Yang [États-Unis] ; Ellen Mierzejewski [États-Unis]Synthesis of nucleoside and oligonucleoside dithiophosphates
002720 (2010) François Morvan ; Françoise Debart ; Jean-Jacques Vasseur [France]From Anionic to Cationic α‐Anomeric Oligodeoxynucleotides
002E12 (2006) Marcelo Farías [Chili] ; Rody San Martín [Chili] ; Carlos Puebla [Chili] ; Jeremy D. Pearson [Royaume-Uni] ; Javier F. Casado [Espagne] ; Marçal Pastor-Anglada [Espagne] ; Paola Casanello [Chili] ; Luis Sobrevia [Chili]Nitric oxide reduces adenosine transporter ENT1 gene (SLC29A1) promoter activity in human fetal endothelium from gestational diabetes
002E21 (2006) Gonzalo Mu Oz [Chili] ; Rody San Martín [Chili] ; Marcelo Farías [Chili] ; Luis Cea [Chili] ; Andrea Vecchiola [Chili] ; Paola Casanello [Chili] ; Luis Sobrevia [Chili]Insulin restores glucose inhibition of adenosine transport by increasing the expression and activity of the equilibrative nucleoside transporter 2 in human umbilical vein endothelium
002F64 (2005) J B Opalinska [Pologne] ; A M Gewirtz [États-Unis]Rationally Targeted, Conformationally Constrained, Oxetane‐Modified Oligonucleotides Demonstrate Efficient Gene‐Silencing Activity in a Cellular System
003020 (2005) An V. Willems ; Dieter L. Deforce ; Carlos H. Van Peteghem [Belgique] ; Jan F. Van Bocxlaer [Belgique]Analysis of nucleic acid constituents by on‐line capillary electrophoresis‐mass spectrometry
003118 (2004) Astrid E. Klöpffer ; Joachim W. Engels [Allemagne]Synthesis of 2′‐Aminoalkyl‐Substituted Fluorinated Nucleobases and Their Influence on the Kinetic Properties of Hammerhead Ribozymes
003284 (2003) Alexander Berchanski [Israël] ; Miriam Eisenstein [Israël]Construction of molecular assemblies via docking: Modeling of tetramers with D2 symmetry
003292 (2003) Zbigniew J. Lesnikowski [Pologne]Boron Clusters − A New Entity for DNA‐Oligonucleotide Modification
003571 (2001) Jennifer L. Beck [Australie] ; Michelle L. Colgrave [Australie] ; Stephen F. Ralph [Australie] ; Margaret M. Sheil [Australie]Electrospray ionization mass spectrometry of oligonucleotide complexes with drugs, metals, and proteins
003681 (2000) Hong-Qiang Gao [États-Unis] ; Paul L. Boyer [États-Unis] ; Stefan G. Sarafianos [États-Unis] ; Edward Arnold [États-Unis] ; Stephen H. Hughes [États-Unis]The role of steric hindrance in 3TC resistance of human immunodeficiency virus type-1 reverse transcriptase
003907 (1999) Dana Hocková [République tchèque] ; Miloš Bud Nsk [République tchèque] ; Radek Marek [République tchèque] ; Jaromír Marek [République tchèque] ; Antonín Hol [République tchèque]Regioselective Preparation of N7‐ and N9‐Alkyl Derivatives of N6‐[(Dimethylamino)methylene]adenine Bearing an Active Methylene Group and Their Further Derivatization Leading to α‐Branched Acyclic Nucleoside Analogues
003C95 (1997) Guobing Xiang [États-Unis] ; Larry W. Mclaughlin [États-Unis]A cytosine analogue containing a conformationally flexible acyclic linker for triplex formation at sites with contiguous G-C base pairs
003F66 (1996) Karin R. Hagerman [États-Unis] ; Paul J. Hagerman [États-Unis]Helix Rigidity of DNA: The Meroduplex as an Experimental Paradigm
004076 (1995) Kenneth Due Nielsen [Danemark] ; Finn Kirpekar [Danemark] ; Peter Roepstorff [Danemark] ; Jesper Wengel [Danemark]Oligonucleotide analogues containing 4′- C -(Hydroxymethyl)uridine: Synthesis, evaluation and mass spectrometric analysis
004312 (1994) J. A. Grasby [Royaume-Uni] ; M. J. Gait [Royaume-Uni]Synthetic oligoribonucleotides carrying site-specific modifications for RNA structure-function analysis
004534 (1993) Serge L. Beaucage [États-Unis] ; Radhakrishnan P. Iyer [États-Unis]The synthesis of modified oligonucleotides by the phosphoramidite approach and their applications
004758 (1992) C. A. Stein [États-Unis] ; John L. Tonkinson [États-Unis] ; Leonid Yakubov [Russie]Phosphorothioate oligodeoxynucleotides—anti-sense inhibitors of gene expression?
004797 (1992) Frank Oertel [Allemagne] ; Holger Winter [Allemagne] ; Zygmunt Kazimierczuk [Allemagne] ; J. A. Vilpo [Finlande] ; Peter Richter [Allemagne] ; Frank Seela [Allemagne]Synthesis and Properties of Methylthiopyrazolo[3,4‐d]pyrimidine 2′‐Deoxy‐β‐D‐ribonucleosides

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