Controlling the fluorescence of benzofuran-modified uracil residues in oligonucleotides by triple-helix formation.

Controlling the fluorescence of benzofuran-modified uracil residues in oligonucleotides by triple-helix formation.

Item
http://www.wikidata.org/entity/Q41732856
Responsive Fluorescent PNA Analogue as a Tool for Detecting G-quadruplex Motifs of Oncogenes and Activity of Toxic Ribosome-Inactivating Proteins.Development of bright fluorescent quadracyclic adenine analogues: TDDFT-calculation supported rational design.Vinyluridine as a Versatile Chemoselective Handle for the Post-transcriptional Chemical Functionalization of RNA.Fluorescence enhancement of oligodeoxynucleotides modified with green fluorescent protein chromophore mimics upon triplex formation.7-(Benzofuran-2-yl)-7-deazadeoxyguanosine as a fluorescence turn-ON probe for single-strand DNA binding protein.Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes.Polymerase synthesis of DNA labelled with benzylidene cyanoacetamide-based fluorescent molecular rotors: fluorescent light-up probes for DNA-binding proteins.
P2860

Controlling the fluorescence of benzofuran-modified uracil residues in oligonucleotides by triple-helix formation.

Item
http://www.wikidata.org/entity/Q41732856
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
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2014年论文
@zh-cn
name
Controlling the fluorescence o ...... des by triple-helix formation.
@en
type
label
Controlling the fluorescence o ...... des by triple-helix formation.
@en
prefLabel
Controlling the fluorescence o ...... des by triple-helix formation.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
Controlling the fluorescence o ...... des by triple-helix formation.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698