Replication fork convergence at termination: A multistep process.

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CRISPR-Cas adaptation in Escherichia coli requires RecBCD helicase but not nuclease activity, is independent of homologous recombination, and is antagonized by 5' ssDNA exonucleases

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Replication fork convergence at termination: A multistep process.

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2017 nî lūn-bûn

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Replication fork convergence at termination: A multistep process.

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Replication fork convergence at termination: A multistep process.

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Replication fork convergence at termination: A multistep process.

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Replication fork convergence at termination: A multistep process.

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Replication fork convergence at termination: A multistep process.

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Replication fork convergence at termination: A multistep process.

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P1476

Replication fork convergence at termination: A multistep process.

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P2093

Mike E O'Donnell

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Nina Y Yao

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P2860

Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells

DNA unwinding assay using streptavidin-bound oligonucleotides.

A mechanism of palindromic gene amplification in Saccharomyces cerevisiae.

Completion of DNA replication in Escherichia coli.

Arrest of bacterial DNA replication.

Mre11-Sae2 and RPA Collaborate to Prevent Palindromic Gene Amplification

RecBCD is required to complete chromosomal replication: Implications for double-strand break frequencies and repair mechanisms

Disruption of mRad50 causes embryonic stem cell lethality, abnormal embryonic development, and sensitivity to ionizing radiation.

Principles and concepts of DNA replication in bacteria, archaea, and eukarya.

Chromosome Duplication in Saccharomyces cerevisiae.

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237-239

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scholarly article

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10.1073/PNAS.1719825115

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English

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115

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2017-12-19T00:00:00Z

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29259108

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5777084

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Replication fork convergence at termination: A multistep process.

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P2860

P2860

Replication fork convergence at termination: A multistep process.

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