C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

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Substrate specificity and kinetic framework of a DNAzyme with an expanded chemical repertoire: a putative RNaseA mimic that catalyzes RNA hydrolysis independent of a divalent metal cation.

P2860

Q38332536-6513549B-D927-4560-AE64-A8CEEF9FCE24

P2860

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

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http://www.wikidata.org/entity/Q44528648

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2003 nî lūn-bûn

@nan

2003年の論文

@ja

2003年学术文章

@wuu

2003年学术文章

@zh

2003年学术文章

@zh-cn

2003年学术文章

@zh-hans

2003年学术文章

@zh-my

2003年学术文章

@zh-sg

2003年學術文章

@yue

2003年學術文章

@zh-hant

name

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@en

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@nl

type

Item

label

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@en

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@nl

prefLabel

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@en

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@nl

P1476

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

@en

P2093

Abhijit Roychowdhury

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

Heike A Held

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

P2860

Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis

Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes.

Expanding the catalytic repertoire of nucleic acid catalysts: simultaneous incorporation of two modified deoxyribonucleoside triphosphates bearing ammonium and imidazolyl functionalities.

Quantitative analysis of receptors for adenosine nucleotides obtained via in vitro selection from a library incorporating a cationic nucleotide analog.

Functionalized nucleoside 5'-triphosphates for in vitro selection of new catalytic ribonucleic acids.

In vitro selection of a ligase ribozyme carrying alkylamino groups in the side chains.

Very High Affinity DNA Recognition by Bicyclic and Cross-Linked Oligonucleotides.

Letter: Synthesis of C-5 substituted pyrimidine nucleosides via organopalladium intermediates.

Challenging artificial genetic systems: thymidine analogs with 5-position sulfur functionality.

A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides.

P304

391-404

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

P31

scholarly article

P356

10.1081/NCN-120022030

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

P433

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

P478

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

P50

Steven A. Benner

P577

2003-04-01T00:00:00Z

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

P698

12885121

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

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

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P2860

P2860

C-5 modified nucleosides: direct insertion of alkynyl-thio functionality in pyrimidines.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698