Error-prone nonhomologous end joining repair operates in human pluripotent stem cells during late G2. (Q38274084)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21685510%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

Error-prone nonhomologous end joining repair operates in human pluripotent stem cells during late G2 (English)

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5 February 2020

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Aleksandra Bogomazova

1

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5 February 2020

Leyla Tskhovrebova

3

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5 February 2020

5

Sergey L Kiselev

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5 February 2020

author name string

Maria A Lagarkova

2

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5 February 2020

Maria V Shutova

4

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5 February 2020

publication date

1 June 2011

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5 February 2020

number of pages

13

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inferred from page(s)

published in

Aging

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volume

3

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5 February 2020

issue

6

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5 February 2020

page(s)

584-596

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Generation of induced pluripotent stem cell lines from 3 distinct laminopathies bearing heterogeneous mutations in lamin A/C

5 February 2020

cites work

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6 September 2017

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Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture

6 September 2017

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Chromatin dynamics during cell cycle mediate conversion of DNA damage into chromatid breaks and affect formation of chromosomal aberrations: biological and clinical significance

6 September 2017

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A human genome structural variation sequencing resource reveals insights into mutational mechanisms

6 September 2017

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Homologous recombination conserves DNA sequence integrity throughout the cell cycle in embryonic stem cells

6 September 2017

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Dynamic dependence on ATR and ATM for double-strand break repair in human embryonic stem cells and neural descendants

6 September 2017

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ATM and Artemis promote homologous recombination of radiation-induced DNA double-strand breaks in G2

6 September 2017

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Mechanisms of change in gene copy number

6 September 2017

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Ionizing radiation induces ataxia telangiectasia mutated-dependent checkpoint signaling and G(2) but not G(1) cell cycle arrest in pluripotent human embryonic stem cells

6 September 2017

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Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells.

6 September 2017

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Survival responses of human embryonic stem cells to DNA damage

6 September 2017

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Advances in the biophysical and molecular bases of radiation cytogenetics

6 September 2017

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Comparison of nonhomologous end joining and homologous recombination in human cells.

6 September 2017

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Chromosome breakage after G2 checkpoint release

6 September 2017

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Homologous and non-homologous recombination differentially affect DNA damage repair in mice

6 September 2017

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Human embryonic stem cell lines isolation, cultivation, and characterization

6 September 2017

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gammaH2AX foci analysis for monitoring DNA double-strand break repair: strengths, limitations and optimization

14 September 2017

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Explanation for excessive DNA single-strand breaks and endogenous repair foci in pluripotent mouse embryonic stem cells

14 September 2017

1 reference

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Human embryonic stem cells reveal recurrent genomic instability at 20q11.21.

14 September 2017

1 reference

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Enhanced use of backup pathways of NHEJ in G2 in Chinese hamster mutant cells with defects in the classical pathway of NHEJ.

14 September 2017

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Human ESCs predisposition to karyotypic instability: Is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?

14 September 2017

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Chromosomal integrity maintained in five human embryonic stem cell lines after prolonged in vitro culture

14 September 2017

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Radiation-induced genomic rearrangements formed by nonhomologous end-joining of DNA double-strand breaks

14 September 2017

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ATM-independent, high-fidelity nonhomologous end joining predominates in human embryonic stem cells

27 September 2017

1 reference

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Induction of pluripotency in human endothelial cells resets epigenetic profile on genome scale.

31 August 2018

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Modeling disease in human ESCs using an efficient BAC-based homologous recombination system

31 August 2018

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Chromosome instability is common in human cleavage-stage embryos.

31 August 2018

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Activation of DNA damage response signaling in mouse embryonic stem cells

31 August 2018

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Checkpoint abrogation in G2 compromises repair of chromosomal breaks in ataxia telangiectasia cells

31 August 2018

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Radiosensitization and DNA repair inhibition by the combined use of novel inhibitors of DNA-dependent protein kinase and poly(ADP-ribose) polymerase-1.

31 August 2018

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From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalities

31 August 2018

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12 December 2020

Chromatid break rejoining and exchange aberration formation following gamma-ray exposure: analysis in G2 human fibroblasts by chemically induced premature chromosome condensation

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12 December 2020

A protocol for isolation and culture of human umbilical vein endothelial cells.

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12 December 2020

Cultures of hESM human embryonic stem cells: chromosomal aberrations and karyotype stability

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12 December 2020

High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity

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12 December 2020

Chromosomally abnormal cells are not selected for the extra-embryonic compartment of the human preimplantation embryo at the blastocyst stage

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12 December 2020

Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

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12 December 2020

The G2 chromosomal radiosensitivity assay

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12 December 2020

Identifiers

DOI

10.18632/AGING.100336

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21685510%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

1 reference

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5 February 2020

PubMed publication ID

21685510

1 reference