De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining (Q34426629)

2 August 2017

title

De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining (English)

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2 August 2017

Martin F Arlt

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2 August 2017

Sountharia Rajendran

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2 August 2017

Shanda R Birkeland

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2 August 2017

Thomas E Wilson

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2 August 2017

Thomas W Glover

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2 August 2017

publication date

20 September 2012

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2 August 2017

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2 August 2017

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2 August 2017

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2 August 2017

page(s)

e1002981

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Creative Commons Attribution 4.0 International

2 August 2017

start time

20 September 2012

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April 2022 Public Data File from Crossref

copyrighted

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6 July 2018

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6 July 2018

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6 July 2018

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Dormant origins licensed by excess Mcm2-7 are required for human cells to survive replicative stress.

6 July 2018

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IgH class switching and translocations use a robust non-classical end-joining pathway

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Segmental duplications and copy-number variation in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Rejoining of DNA double-strand breaks as a function of overhang length

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Genomic disorders: genome architecture results in susceptibility to DNA rearrangements causing common human traits

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Detection of large-scale variation in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Large-scale copy number polymorphism in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

The role of late/slow replication of the FRA16D in common fragile site induction

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis

6 July 2018

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Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447954

Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms

27 October 2018

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12 December 2020

Recurrent DNA copy number variation in the laboratory mouse

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12 December 2020

Low joining efficiency and non-conservative repair of two distant double-strand breaks in mouse embryonic stem cells

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12 December 2020

Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†

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12 December 2020

10.1371/JOURNAL.PGEN.1002981

Identifiers

DOI

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2 August 2017

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2 August 2017

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