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  1. Antimicrobial and Structural Properties of Metal Ions Complexes with Thiosemicarbazide Motif and Related Heterocyclic Compounds
  2. Guanosine in a Single Stranded Region of Anticodon Stem-Loop tRNA Models is Prone to Oxidatively Generated Damage Resulting in Dehydroguanidinohydantoin and Spiroiminodihydantoin Lesions
  3. LNA units present in the (2′-OMe)-RNA strand stabilize parallel duplexes (2′-OMe)-RNA/[All-RP-PS]-DNA and parallel triplexes (2′-OMe)-RNA/[All-RP-PS]-DNA/RNA. An improved tool for the inhibition of reverse transcription
  4. Thermal stability and conformation of antiparallel duplexes formed by P-stereodefined phosphorothioate DNA/LNA chimeric oligomers with DNA and RNA matrices
  5. Unexpected Loss of Stereoselectivity in Ring-Opening Reaction of 2-Alkoxy-2-Thio-1,3,2-Oxathiaphospholanes With a Pyrophosphate Anion
  6. Selenium and Tellurium Derivatives of Carbohydrates and Nucleotides
  7. ChemInform Abstract: Phosphorothioate Nucleotides and Oligonucleotides-Recent Progress in Synthesis and Application
  8. A Single Nuclease-Resistant Linkage in DNA as a Versatile Tool for the Characterization of DNA Lesions: Application to the Guanine Oxidative Lesion “G+34” Generated by Metalloporphyrin/KHSO 5 Reagent
  9. ChemInform Abstract: Phosphorothioate Nucleotides and Oligonucleotides - Recent Progress in Synthesis and Application
  10. Phosphorothioate Nucleotides and Oligonucleotides - Recent Progress in Synthesis and Application
  11. Diastereomerically pure nucleoside-5′-O-(2-thio-4,4-pentamethylene-1,3,2-oxathiaphospholane)s-Substrates for synthesis of P-chiral derivatives of nucleoside-5′-O-phosphorothioates
  12. ChemInform Abstract: Oligo(nucleoside Phosphorothioate)s
  13. ChemInform Abstract: Nucleoside 3′-O-(2-oxo-“spiro”-4.4-Pentamethylene-1.3.2-oxathiaphospholane)s: Monomers for Stereocontrolled Synthesis of Oligo(Nucleoside Phosphorothioate/Phosphate)s.
  14. Restoration of catalytic functions in Cre recombinase mutants by electrostatic compensation between active site and DNA substrate
  15. ChemInform Abstract: Recent Advances in Stereocontrolled Synthesis of P-Chiral Analogues of Biophosphates.
  16. Electrostatic Suppression Allows Tyrosine Site-specific Recombination in the Absence of a Conserved Catalytic Arginine
  17. Stereoselective formation of a P–P bond in the reaction of 2-alkoxy-2-thio-1,3,2-oxathiaphospholanes with O,O-dialkyl H-phosphonates and H-thiophosphonates
  18. Reactions of Cre with Methylphosphonate DNA: Similarities and Contrasts with Flp and Vaccinia Topoisomerase
  19. Active site electrostatics protect genome integrity by blocking abortive hydrolysis during DNA recombination
  20. ChemInform Abstract: 1,3,2-Oxathiaphospholane Approach to the Synthesis of P-Chiral Stereodefined Analogues of Oligonucleotides and Biologically Relevant Nucleoside Polyphosphates
  21. Selenium-Derivatized Oligonucleotides
  22. 1,3,2-Oxathiaphospholane approach to the synthesis of P-chiral stereodefined analogs of oligonucleotides and biologically relevant nucleoside polyphosphates
  23. Hoogsteen-Paired Homopurine [RP-PS]-DNA and Homopyrimidine RNA Strands Form a Thermally Stable Parallel Duplex
  24. P-Chiral Oligonucleotides in Biological Recognition Processes
  25. Unusual Thermal Stability of RNA/[RP-PS]-DNA/RNA Triplexes Containing a Homopurine DNA Strand
  26. Cyclization versus oligomerization of SP- and RP-5′-OH-N4-benzoyl-2′-deoxycytidine-3′-O-(2-thio-4,4-pentamethylene-1,3,2-oxathiaphospholane)s
  27. Enhanced P-stereodependent stability of complexes formed by phosphorothioate oligonucleotides due to involvement of sulfur as strong hydrogen bond acceptor
  28. Oxathiaphospholane Approach to the Synthesis of Oligodeoxyribonucleotides Containing Stereodefined Internucleotide Phosphoroselenoate Function †
  29. Effect of Phosphorothioate Chirality on i-Motif Structure and Stability †
  30. Comparison of the cleavage profiles of oligonucleotide duplexes with or without phosphorothioate linkages by using a chemical nuclease probe
  31. P-Chirality-Dependent Immune Activation by Phosphorothioate CpG Oligodeoxynucleotides
  32. Dynamic NMR Structures of [Rp]- and [Sp]-Phosphorothioated DNA-RNA Hybrids: Is Flexibility Required for RNase H Recognition?
  33. Synthesis of Phosphorothioate Oligonucleotides with Stereodefined Phosphorothioate Linkages
  34. Stereodefined Phosphorothioate Analogues of DNA:  Relative Thermodynamic Stability of the Model PS-DNA/DNA and PS-DNA/RNA Complexes †
  35. Inhibition of human immunodeficiency virus type 1 replication by P-stereodefined oligo(nucleoside phosphorothioate)s in a long-term infection model
  36. Synthesis of P-Chiral [ 18 O]-Labeled Isotopomeric Oligo(deoxyribonucleoside Phosphorothioate)s and Phosphates
  37. Retention of Configuration in the Action of Human Plasma 3‘-Exonuclease on Oligo(deoxynucleoside phosphorothioate). A New Method for Assignment of Absolute Configuration at Phosphorus in Isotopomeric Deoxyadenosine 5‘- O -[ 18 O]Phosphorothioate
  38. Recent Advances in Stereocontrolled Synthesis of P-Chiral Analogues of Biophosphates
  39. Oxathiaphospholane Approach to the Synthesis of P-Chiral, Isotopomeric Deoxy(ribonucleoside phosphorothioate)s and Phosphates Labeled with an Oxygen Isotope
  40. Oxathiaphospholane Approach to the Synthesis of P-Chiral, Isotopomeric Deoxy(ribonucleoside phosphorothioate)s and Phosphates Labeled with an Oxygen Isotope
  41. Oxathiaphospholane Approach to the Synthesis of P-Chiral, Isotopomeric Deoxy(ribonucleoside phosphorothioate)s and Phosphates Labeled with an Oxygen Isotope
  42. Effect of P-Chirality of Internucleotide Bonds on B−Z Conversion of Stereodefined Self-Complementary Phosphorothioate Oligonucleotides of the [PS]-d(CG) 4 and [PS]-d(GC) 4 Series †
  43. Nucleoside 3′-O-(2-Oxo-“Spiro”-4.4-Pentamethylene-1.3.2-Oxathiaphospholane)S: Monomers For Stereocontrolled Synthesis Of Oligo(Nucleoside Phosphorothioate/Phosphate)S
  44. Deoxyribonucleoside 3‘- O -(2-Thio- and 2-Oxo-“spiro”-4,4-pentamethylene-1,3,2-oxathiaphospholane)s:  Monomers for Stereocontrolled Synthesis of Oligo(deoxyribonucleoside phosphorothioate)s and Chimeric PS/PO Oligonucleotides §
  45. Stability of Stereoregular Oligo(nucleoside Phosphorothioate)s in Human Plasma: Diastereoselectivity of Plasma 3‵-Exonuclease
  46. Stereochemistry of Dbu-Assisted Reaction of Nucleoside 3'-O-(2-Thiono-1.3.2-Oxathiaphospholanes) with 5'-Hydroxynucleosides
  47. Stereochemistry of Dbu-Assisted Reaction of Nucleoside 3'-O-(2-Thiono-1.3.2-Oxathiaphospholanes) with 5'-Hydroxynucleosides
  48. Diastereomers of Nucleoside 3'-O-(2-Thio-1,3,2-oxathia(selena)phospholanes): Building Blocks for Stereocontrolled Synthesis of Oligo(nucleoside phosphorothioate)s
  49. Activation of the Carboxy Terminus of a Peptide for Carboxy-Terminal Sequencing
  50. Binding of phosphorothioate oligodeoxynucleotides to basic fibroblast growth factor, recombinant soluble CD4, laminin and fibronectin is P-chirality independent
  51. The effects of tumor necrosis factor (TNF) derivatives on TNF receptors
  52. The effect of tumour necrosis factor-α (TNF-α) muteins on human neutrophilsin vitro
  53. Synthesis of a gene encoding bovine substance P precursors and its expression in Escherichia coli
  54. Stereochemistry of the reaction of ribonucleoside cyclic 3?,5?-phosphorothioates with oxiranes
  55. Mechanism of Formation of Ribonucleoside Cyclic 2′,3′-Phosphates in the Reaction of Appropriate 3′,5′-Phos-Phorothioates with Epoxides
  56. Mechanism of Formation of Ribonucleoside Cyclic 2',3'-Phosphates in the Reaction of Appropriate 3',5'-Phosphorothioates with Epoxides
  57. Novel approach to the synthesis of isotopomeric monoalkyl [16O,17O,18O]phosphates. The stereospecific one-pot conversion of (RP)-thymidine 3′-(4-nitrophenyl)phosphorothioate into (RP)-thymidine 3′-...
  58. DNA-Triesters - The Synthesis and Absolute Configuration Assignments at P-Stereogenic Centres
  59. Direct transformation of ribonucleoside cyclic 3′,5′-phosphorothioates into cyclic 2′,3′-phosphates
  60. Stereoretentive conversion of dialkyl [18O]-phosphoranilidates into dialkyl hydrogen [18O]-phosphates
  61. Synthesis and absolute configuration of P-chiral -isopropyl oligonucleotide triesters
  62. Stereospecific conversion of P-chiral nucleoside phosphorothioates into [18O]phosphates
  63. Stereoretentive conversion of dialkyl phosphorothioates into [18O]-phosphates