A rapidly photo-activatable light-up fluorescent nucleoside and its application in DNA base variation sensing.

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Vinyluridine as a Versatile Chemoselective Handle for the Post-transcriptional Chemical Functionalization of RNA.

P2860

Q48279591-655A2A35-693C-457E-BB8C-682EC0BE0AC8

P2860

A rapidly photo-activatable light-up fluorescent nucleoside and its application in DNA base variation sensing.

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http://www.wikidata.org/entity/Q52982285

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2016 nî lūn-bûn

@nan

2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

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2016年学术文章

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2016年學術文章

@yue

2016年學術文章

@zh-hant

name

A rapidly photo-activatable li ...... in DNA base variation sensing.

@en

A rapidly photo-activatable li ...... in DNA base variation sensing.

@nl

type

Item

label

A rapidly photo-activatable li ...... in DNA base variation sensing.

@en

A rapidly photo-activatable li ...... in DNA base variation sensing.

@nl

prefLabel

A rapidly photo-activatable li ...... in DNA base variation sensing.

@en

A rapidly photo-activatable li ...... in DNA base variation sensing.

@nl

P1476

A rapidly photo-activatable li ...... in DNA base variation sensing

@en

P2093

Boshi Fu

http://www.w3.org/2001/XMLSchema#string

Jiaqi Wang

http://www.w3.org/2001/XMLSchema#string

Jing Mo

http://www.w3.org/2001/XMLSchema#string

Xiang Zhou

http://www.w3.org/2001/XMLSchema#string

Yafen Wang

http://www.w3.org/2001/XMLSchema#string

Yuhao Du

http://www.w3.org/2001/XMLSchema#string

Yuqi Chen

http://www.w3.org/2001/XMLSchema#string

Zijing Wang

http://www.w3.org/2001/XMLSchema#string

P2860

Structures of KlenTaq DNA polymerase caught while incorporating C5-modified pyrimidine and C7-modified 7-deazapurine nucleoside triphosphates

Fluorescent analogs of biomolecular building blocks: design, properties, and applications.

Rapid, photoactivatable turn-on fluorescent probes based on an intramolecular photoclick reaction

Conquering 2-aminopurine's deficiencies: highly emissive isomorphic guanosine surrogate faithfully monitors guanosine conformation and dynamics in DNA

Photoinducible bioorthogonal chemistry: a spatiotemporally controllable tool to visualize and perturb proteins in live cells.

Genetically encoded cyclopropene directs rapid, photoclick-chemistry-mediated protein labeling in mammalian cells.

Postsynthetic DNA modification through the copper-catalyzed azide-alkyne cycloaddition reaction.

Fast alkene functionalization in vivo by Photoclick chemistry: HOMO lifting of nitrile imine dipoles.

Enzymatic interconversion of isomorphic fluorescent nucleosides: adenosine deaminase transforms an adenosine analogue into an inosine analogue.

Cation-mediated energy transfer in G-quadruplexes revealed by an internal fluorescent probe.

P304

8545-8548

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P31

scholarly article

P356

10.1039/C6CC03098J

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Zhiyong He

P577

2016-06-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27315545

http://www.w3.org/2001/XMLSchema#string

A rapidly photo-activatable light-up fluorescent nucleoside and its application in DNA base variation sensing.

about

P2860

P2860

A rapidly photo-activatable light-up fluorescent nucleoside and its application in DNA base variation sensing.

description

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type

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prefLabel

P1433

P1476

P2093

P2860

P304

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P356

P407

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P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698