597 results on '"Rosenberg, Ivan"'
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52. A New Analogue of Locked Cyclohexane Nucleic Acids
53. N-Branched acyclic nucleoside phosphonates as monomers for the synthesis of modified oligonucleotides
54. A comparison of the dose distributions from three proton treatment planning systems in the planning of meningioma patients with single-field uniform dose pencil beam scanning
55. Synthesis of locked cyclohexene and cyclohexane nucleic acids (LCeNA and LCNA) with modified adenosine units
56. Structure-based design of a bisphosphonate 5′(3′)-deoxyribonucleotidase inhibitor
57. Structural diversity of nucleoside phosphonic acids as a key factor in the discovery of potent inhibitors of rat T-cell lymphoma thymidine phosphorylase
58. In vivodosimetry for total body irradiation: five‐year results and technique comparison
59. Theoretical and Experimental Study of Charge Transfer through DNA: Impact of Mercury Mediated T-Hg-T Base Pair
60. Imaging Cerenkov emission as a quality assurance tool in electron radiotherapy
61. ChemInform Abstract: A New Class of Phosphanucleosides Containing a 3‐Hydroxy‐1‐hydroxymethylphospholane 1‐Oxide Ring.
62. Structures of human cytosolic and mitochondrial nucleotidases: implications for structure-based design of selective inhibitors
63. Conformationally constrained nucleoside phosphonic acids – potent inhibitors of human mitochondrial and cytosolic 5′(3′)-nucleotidases
64. Novel conformationally locked nucleosides and oligonucleotides based on bicyclo[3.2.1]octane scaffold as a pseudosugar moiety
65. Bi-substrate inhibitors of human pyrimidine 5’-nucleotidases
66. Cerenkov optical emissions in particle radiotherapy
67. Phosphanucleosides containing 1-hydroxymethylphospholane 1-oxide ring
68. Oligonucleotides modified with acyclic nucleoside phosphonate (HPEP) units
69. Sulfur-containing phosphonate monomers for oligonucleotide synthesis
70. Activation of human RNase L by 5’-C-phosphonate-modified oligoadenylates
71. Intensity-modulated arc therapy to improve radiation dose delivery in the treatment of abdominal neuroblastoma
72. Oxidation of Disulfides to Taurine and Sulfanilic Acid Derivatives.
73. Atomic Scissors: A New Method of Tracking the 5-Bromo-2′-Deoxyuridine-Labeled DNA In Situ
74. Most Anti-BrdU Antibodies React with 2′-Deoxy-5-Ethynyluridine — The Method for the Effective Suppression of This Cross-Reactivity
75. Neutron radiotherapy in South Africa: Neutron radiotherapy should continue
76. N-Phosphonocarbonylpyrrolidine Derivatives of Guanine: A New Class of Bi-Substrate Inhibitors of Human Purine Nucleoside Phosphorylase
77. ChemInform Abstract: Synthesis and Properties of ApA Analogues with Shortened Phosphonate Internucleotide Linkage.
78. ChemInform Abstract: Tetrofuranose Nucleoside Phosphonic Acids: Synthesis and Properties.
79. A Ferrier-Type Allylic Rearrangement of 3′-Deoxy-3′,4′-didehydronucleosides Mediated by DMF Dimethyl Acetal: Direct Access to 4′-Alkoxy-2′,3′-didehydro-2′,3′-dideoxynucleosides
80. Synthesis and Properties of ApA Analogues with Shortened Phosphonate Internucleotide Linkage
81. Tetrofuranose nucleoside phosphonic acids: Synthesis and properties
82. Synthesis of new potential inhibitors of 5'-nucleotidases
83. Synthesis and structural assignment of novel 5'-epimeric 3'-deoxy-3',4'-didehydronucleoside-5'-C-phosphonates
84. Synthesis of novel deoxynucleoside S-methylphosphonic acids using S-(diisopropylphosphonomethyl)isothiouronium tosylate, a new equivalent of mercaptomethylphosphonate
85. Synthesis of oligoribonucleotides with phosphonate-modified linkages
86. Miguel Awschalom
87. Straightforward synthesis of 3′-deoxy-3′,4′-didehydronucleoside-5′-aldehydes via 2′,3′-O-orthoester group elimination: a simple route to 3′,4′-didehydronucleosides
88. ChemInform Abstract: Efficient Synthesis of 2′-Deoxynucleoside 3′-C-Phosphonates: Reactivity of Geminal Hydroxyphosphonate Moiety.
89. ChemInform Abstract: Methyl 4‐Toluenesulfonyloxymethylphosphonate, a New and Versatile Reagent for the Convenient Synthesis of Phosphonate‐Containing Compounds.
90. ChemInform Abstract: A Convenient, High‐Yield Synthesis of 1‐Substituted Uracil and Thymine Derivatives.
91. Methyl 4-toluenesulfonyloxymethylphosphonate, a new and versatile reagent for the convenient synthesis of phosphonate-containing compounds
92. Oligomerization of adenosin‐5′‐O‐ylmethylphosphonate, an isopolar AMP analogue: Evaluation of the route to short oligoadenylates
93. A convenient, high-yield synthesis of 1-substituted uracil and thymine derivatives
94. Mapping of HIV-1 integrase preferences for target site selection with various oligonucleotides
95. Structure−Activity Study of New Inhibitors of Human Betaine-Homocysteine S-Methyltransferase
96. Conformational evaluation of labeled C3′‐O‐P‐13CH2‐O‐C4″ phosphonate internucleotide linkage, a phosphodiester isostere
97. Structure and Dynamics of the ApA, ApC, CpA, and CpC RNA Dinucleoside Monophosphates Resolved with NMR Scalar Spin−Spin Couplings
98. Synthesis and hybridization of oligonucleotides modified at AMP sites with adenine pyrrolidine phosphonate nucleotides
99. A primer in automated decision-support systems
100. Surface plasmon resonance study on HIV-1 integrase strand transfer activity
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