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Enhancement of TFO Triplex Formation by Conjugation with Pyrene via Click Chemistry.Aminopyridinyl-Pseudodeoxycytidine Derivatives Selectively Stabilize Antiparallel Triplex DNA with Multiple CG Inversion Sites.Wet-dry cycles enable the parallel origin of canonical and non-canonical nucleosides by continuous synthesis.Noncanonical RNA Nucleosides as Molecular Fossils of an Early Earth-Generation by Prebiotic Methylations and Carbamoylations.Nicht-kanonische RNA-Nukleoside als molekulare Fossilien einer frühen Erde - Generierung durch präbiotische Methylierungen und CarbamoylierungenModification of the aminopyridine unit of 2'-deoxyaminopyridinyl-pseudocytidine allowing triplex formation at CG interruptions in homopurine sequencesA Click‐Chemistry Linked 2′3′‐cGAMP AnalogueAn isocytidine derivative with a 2-amino-6-methylpyridine unit for selective recognition of the CG interrupting site in an antiparallel triplex DNAProperties of oligonucleotide with phenyl-substituted carbocyclic nucleoside analogs for the formation of duplex and triplex DNAEffect of the 3-halo substitution of the 2'-deoxy aminopyridinyl-pseudocytidine derivatives on the selectivity and stability of antiparallel triplex DNA with a CG inversion siteStable and Selective Antiparallel Type Triplex DNA Formation by Targeting a GC Base Pair with the TFO Containing One N2-Phenyl-2'-deoxyguanosineProto-Urea-RNA (Wöhler RNA) Containing Unusually Stable Urea NucleosidesUnified prebiotically plausible synthesis of pyrimidine and purine RNA ribonucleotidesA one-pot, water compatible synthesis of pyrimidine nucleobases under plausible prebiotic conditionsSynthesis of 2'-deoxy-4-aminopyridinylpseudocytidine Derivatives for Incorporation Into Triplex Forming Oligonucleotides
P50
Q38823121-E2CDFE5F-C28E-4AE3-BCF7-7E1EE2D84E74Q48088683-1FC453F4-673C-4292-ADA5-905F9EECBCA4Q48263296-482DE51E-273F-41F3-998F-B4722AE429E9Q53837762-F13BFAE2-702D-459D-8F47-8457A01F36B2Q57376659-CC4016A9-059B-4C0F-9E63-950957DA0E88Q58794850-BA3919B2-D932-4CEB-B304-03E144E41048Q63383772-8D06283A-5624-4B30-A347-03A1ED71D118Q85246311-3848FD2F-84D9-4AE0-A500-4AC7B1D114D0Q85624828-114CE80E-F39B-48B8-9AA0-3D093992776DQ88215234-C31DDD83-5E8C-4DD6-A187-27494AAF4041Q88970532-BA1E32A6-4F22-40E1-BE76-0C5110523103Q90411137-A64FC487-26B6-4EAF-81E3-B41F0522720BQ90658864-A0B2B748-836D-40EF-B41F-46D72D422D4CQ91217395-2DECB38D-CB93-421D-91B6-DD00AD0DF010Q92447329-82EE392E-98EA-4C26-BBC4-A9762725A7F3
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-2792-9595
@en
name
Hidenori Okamura
@ast
Hidenori Okamura
@en
Hidenori Okamura
@es
Hidenori Okamura
@nl
type
label
Hidenori Okamura
@ast
Hidenori Okamura
@en
Hidenori Okamura
@es
Hidenori Okamura
@nl
prefLabel
Hidenori Okamura
@ast
Hidenori Okamura
@en
Hidenori Okamura
@es
Hidenori Okamura
@nl
P106
P1153
55489106500
P31
P496
0000-0002-2792-9595