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Conformationally restricted carbohydrate-modified nucleic acids and antisense technology
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Conformationally restricted carbohydrate-modified nucleic acids and antisense technology
(English)
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stated in
Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
author
Piet Herdewijn
object named as
P Herdewijn
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1
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language of work or name
English
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publication date
1 December 1999
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Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
published in
Biochimica et Biophysica Acta
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stated in
Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
volume
1489
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stated in
Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
issue
1
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Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
page(s)
167-179
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Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
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DNA-Binding Ligands from Peptide Libraries Containing Unnatural Amino Acids
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Targeting RNA with Conformationally Restricted Oligonucleotides
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DNA structure from A to Z.
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Synthesis of 2′-O,3′-C-linked bicyclic nucleosides and bicyclic oligonucleotides
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Crossref
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A Novel Class of Oligonucleotide Analogues Containing 2‘-O,3‘-C-Linked [3.2.0]Bicycloarabinonucleoside Monomers: Synthesis, Thermal Affinity Studies, and Molecular Modeling
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Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides?
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2'-Deoxy-2'(S)-ethinyl oligonucleotides: a modification which selectively stabilizes oligoadenylate pairing to DNA complements
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Homo-N-nucleosides: Incorporation into oligonucleotides and antiviral activity
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Bicyclo[3.2.1]-DNA, a new DNA analog with a rigid backbone and flexibly linked bases: pairing properties with complementary DNA.
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1′, 5′ -Anhydrohexitol Oligonucleotides: Synthesis, Base Pairing and Recognition by Regular Oligodeoxyribonucleotides and Oligoribonucleotides
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Biological activity of hexitol nucleic acids targeted at Ha-ras and intracellular adhesion molecule-1 mRNA
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Warum pentose-und nicht hexose-nucleinsäuren? Teil III. Oligo(2′,3′-dideoxy-β-D-glucopyranosyl) nucleotide (‘homo-DNS’): Paarungesigenschaften
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Synthesis, Biological Evaluation, and Structure Analysis of a Series of New 1,5-Anhydrohexitol Nucleosides
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5-Substituted pyrimidines with a 1,5-anhydro-2, 3-dideoxy-D-arabino-hexitol moiety at N-1: synthesis, antiviral activity, conformational analysis, and interaction with viral thymidine kinase
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Synthesis and Pairing Properties of Oligonucleotides Containing 3-Hydroxy-4-hydroxymethyl-1-cyclohexanyl Nucleosides
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Oligonucleotides Composed of 2‘-Deoxy-1‘,5‘-anhydro-d-mannitol Nucleosides with a Purine Base Moiety
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D-Altritol Nucleic Acids (ANA): Hybridisation Properties, Stability, and Initial Structural Analysis
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Nature of Nucleic Acid−Base Stacking: Nonempirical ab Initio and Empirical Potential Characterization of 10 Stacked Base Dimers. Comparison of Stacked and H-Bonded Base Pairs
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Easy Synthesis and Different Conformational Behavior of Purine and Pyrimidine .beta.-D-glycero-Pent-2'-enopyranosyl Nucleosides
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Synthesis and Conformational Study of 3-Hydroxy-4-(Hydroxymethyl)-1-Cyclohexanyl Purines and Pyrimidines
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Synthesis of 3′-Deoxy-3′-C-Hydroxymethyl-aldopentopyranosyl Nucleosides and their Incorporation in Oligonucleotides. Part II 1
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3′-Deoxy-3′-hydroxymethyl-aldopentopyranosyl nucleoside synthesis. Part I
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0167-4781%2899%2900152-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0167-4781(99)00152-9
1 reference
stated in
Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
PubMed ID
10807006
1 reference
stated in
Europe PubMed Central
PubMed ID
10807006
retrieved
30 July 2017
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