Guanine-rich sequences inhibit proofreading DNA polymerases. - Wikidata - awgldk - TriplyDB

Guanine-rich sequences inhibit proofreading DNA polymerases.

Guanine-rich sequences inhibit proofreading DNA polymerases.

http://www.wikidata.org/entity/Q37044511

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TT(N)mGCCTC inhibits archaeal family B DNA polymerases.

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Guanine-rich sequences inhibit proofreading DNA polymerases.

http://www.wikidata.org/entity/Q37044511

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 28 June 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Guanine-rich sequences inhibit proofreading DNA polymerases.

@en

Guanine-rich sequences inhibit proofreading DNA polymerases.

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Guanine-rich sequences inhibit proofreading DNA polymerases.

@en

Guanine-rich sequences inhibit proofreading DNA polymerases.

@nl

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Guanine-rich sequences inhibit proofreading DNA polymerases.

@en

Guanine-rich sequences inhibit proofreading DNA polymerases.

@nl

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Scientific Reports

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Guanine-rich sequences inhibit proofreading DNA polymerases

@en

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Binghua Xie

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

Mengsheng Qiu

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

Shuhui Sun

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

Xiao-Jing Zhu

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

Xuemei Hu

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

Zunyi Zhang

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

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DNA polymerases as useful reagents for biotechnology - the history of developmental research in the field

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Effective amplification of long targets from cloned inserts and human genomic DNA

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

Recent developments in the optimization of thermostable DNA polymerases for efficient applications

Aptamer selection based on inhibitory activity using an evolution-mimicking algorithm.

PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates.

G-quadruplex formation at the 3' end of telomere DNA inhibits its extension by telomerase, polymerase and unwinding by helicase.

A novel strategy to engineer DNA polymerases for enhanced processivity and improved performance in vitro

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28769

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scholarly article

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10.1038/SREP28769

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6

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2016-06-28T00:00:00Z

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4923904

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