Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts (Q40946661)

25 September 2017

title

Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts (English)

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Nijmegen breakage syndrome

25 September 2017

main subject

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inferred from title

author name string

Kraakman-van der Zwet M

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25 September 2017

Overkamp WJ

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25 September 2017

Friedl AA

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25 September 2017

Klein B

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25 September 2017

Verhaegh GW

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25 September 2017

Jaspers NG

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25 September 2017

Midro AT

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25 September 2017

Eckardt-Schupp F

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25 September 2017

Lohman PH

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25 September 2017

Zdzienicka MZ

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25 September 2017

language of work or name

English

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publication date

1 May 1999

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25 September 2017

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25 September 2017

volume

434

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25 September 2017

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25 September 2017

page(s)

17-27

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Nijmegen breakage syndrome

25 September 2017

cites work

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Ataxia-telangiectasia and the Nijmegen breakage syndrome: related disorders but genes apart

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7 January 2021

Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation

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7 January 2021

Radiation induction of p53 in cells from Nijmegen breakage syndrome is defective but not similar to ataxia-telangiectasia

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7 January 2021

Chromosomal sensitivity to clastogenic agents and cell cycle perturbations in Nijmegen breakage syndrome lymphoblastoid cell lines.

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Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome

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Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes.

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Hypersensitivity of cells from a new chromosomal-breakage syndrome to DNA-damaging agents

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Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.

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Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

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Positional cloning of the gene for Nijmegen breakage syndrome

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The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response

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hMre11 and hRad50 nuclear foci are induced during the normal cellular response to DNA double-strand breaks

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Mutations in XRS2 and RAD50 delay but do not prevent mating-type switching in Saccharomyces cerevisiae

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7 January 2021

A novel mre11 mutation impairs processing of double-strand breaks of DNA during both mitosis and meiosis

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7 January 2021

The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks

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7 January 2021

Nuclease activities in a complex of human recombination and DNA repair factors Rad50, Mre11, and p95

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7 January 2021

Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing

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Telomere maintenance is dependent on activities required for end repair of double-strand breaks

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Telomeres: moonlighting by DNA repair proteins

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An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability.

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7 January 2021

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

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7 January 2021

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

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7 January 2021

The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species

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7 January 2021

Hypersensitivity of ataxia telangiectasia fibroblasts to ionizing radiation is associated with a repair deficiency of DNA double-strand breaks

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7 January 2021

Comparative human cellular radiosensitivity: I. The effect of SV40 transformation and immortalisation on the gamma-irradiation survival of skin derived fibroblasts from normal individuals and from ataxia-telangiectasia patients and heterozygotes

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Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

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7 January 2021

A new technique for the assay of infectivity of human adenovirus 5 DNA

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7 January 2021

Expression of early genes of origin-defective mutants of simian virus 40

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Transfection with extracellularly UV-damaged DNA induces human and rat cells to express a mutator phenotype towards parvovirus H-1.

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7 January 2021

The rate of DNA synthesis in normal human and ataxia telangiectasia cells after exposure to X-irradiation

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7 January 2021

Two methods for assaying DNA double-strand break repair in mammalian cells by asymmetric field inversion gel electrophoresis

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7 January 2021

An electrophoretic approach to the assessment of the spatial distribution of DNA double-strand breaks in mammalian cells

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7 January 2021

A new chromosomal instability disorder: the Nijmegen breakage syndrome

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7 January 2021

Chromosome instability with bleomycin and X-ray hypersensitivity in a boy with Nijmegen breakage syndrome.

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7 January 2021

DNA topoisomerases: essential enzymes and lethal targets

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7 January 2021

Enhanced sensitivity to camptothecin in ataxia-telangiectasia cells and its relationship with the expression of DNA topoisomerase I.

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7 January 2021

The many interfaces of Mre11

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7 January 2021

Induction and rejoining of DNA double-strand breaks and interphase chromosome breaks after exposure to X rays in one normal and two hypersensitive human fibroblast cell lines

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7 January 2021

Ataxia-telangiectasia: is ATM a sensor of oxidative damage and stress?

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7 January 2021

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

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7 January 2021

10.1016/S0921-8777(99)00009-9

Identifiers

DOI

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25 September 2017

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