Quantifying DNA double-strand breaks induced by site-specific endonucleases in living cells by ligation-mediated purification. (Q45807486)

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7 March 2020

title

Quantifying DNA double-strand breaks induced by site-specific endonucleases in living cells by ligation-mediated purification (English)

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7 March 2020

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7 March 2020

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7 March 2020

Catherine Chailleux

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7 March 2020

François Aymard

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7 March 2020

Virginie Daburon

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7 March 2020

Céline Courilleau

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7 March 2020

Yvan Canitrot

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7 March 2020

Gaëlle Legube

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7 March 2020

publication date

6 February 2014

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7 March 2020

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7 March 2020

volume

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issue

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7 March 2020

page(s)

517-528

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DNA repair pathways as targets for cancer therapy

7 March 2020

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Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks

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MRE11-RAD50-NBS1 is a critical regulator of FANCD2 stability and function during DNA double-strand break repair

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Robust chromosomal DNA repair via alternative end-joining in the absence of X-ray repair cross-complementing protein 1 (XRCC1)

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Methylation of histone H3 lysine 36 enhances DNA repair by nonhomologous end-joining

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Essential role of Tip60-dependent recruitment of ribonucleotide reductase at DNA damage sites in DNA repair during G1 phase

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BRCA1 tumor suppression depends on BRCT phosphoprotein binding, but not its E3 ligase activity

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The block in immunoglobulin class switch recombination caused by activation-induced cytidine deaminase deficiency occurs prior to the generation of DNA double strand breaks in switch mu region

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Live imaging of induced and controlled DNA double-strand break formation reveals extremely low repair by homologous recombination in human cells

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I-SceI-mediated double-strand break does not increase the frequency of homologous recombination at the Dct locus in mouse embryonic stem cells

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Measuring the formation and repair of UV damage at the DNA sequence level by ligation-mediated PCR

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Genome-wide mapping of DNA strand breaks

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Detection of DNA double-strand breaks and chromosome translocations using ligation-mediated PCR and inverse PCR

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I-SceI endonuclease, a new tool for studying DNA double-strand break repair mechanisms in Drosophila

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PubMed

https://pubmed.ncbi.nlm.nih.gov/24504477

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Targeted chromosomal cleavage and mutagenesis in Drosophila using zinc-finger nucleases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24504477

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NPROT.2014.031

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24504477%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

7 March 2020

1010396170

0 references

1 reference

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