(Q40236887)

18 September 2017

title

The Rothmund-Thomson gene product RECQL4 localizes to the nucleolus in response to oxidative stress (English)

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18 September 2017

Leslie L Woo

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18 September 2017

Kazunobu Futami

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18 September 2017

Akira Shimamoto

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18 September 2017

Yasuhiro Furuichi

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18 September 2017

Karen M Frank

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18 September 2017

language of work or name

English

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publication date

2 August 2006

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Experimental Cell Research

18 September 2017

published in

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18 September 2017

volume

312

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18 September 2017

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18 September 2017

page(s)

3443-3457

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RecQ family members combine strand pairing and unwinding activities to catalyze strand exchange

18 September 2017

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Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

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Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping

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Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases

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Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome

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Clonal lines of aneuploid cells in Rothmund-Thomson syndrome

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Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome

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Growth retardation and skin abnormalities of the Recql4-deficient mouse.

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Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome

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RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway

7 January 2021

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Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome

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Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome

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The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability

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Regulation of the Werner helicase through a direct interaction with a subunit of protein kinase A

7 January 2021

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Requirement of the protein B23 for nucleolar disassembly induced by the FRGY2a family proteins

7 January 2021

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Nucleolar localization of the Werner syndrome protein in human cells

7 January 2021

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A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949-1092.

7 January 2021

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7 January 2021

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DNA damage-induced translocation of the Werner helicase is regulated by acetylation

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Effect of poly(ADP-ribose) polymerase inhibitors on oxidative stress evoked hydroxyl radical level and macromolecules oxidation in cell free system of rat brain cortex.

7 January 2021

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Genotoxicity of streptonigrin: a review

7 January 2021

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Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Two nuclear localization signals present in the basic-helix 1 domains of MyoD promote its active nuclear translocation and can function independently

7 January 2021

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Accumulation of Werner protein at DNA double-strand breaks in human cells

7 January 2021

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7 January 2021

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Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrest

7 January 2021

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Oxidative damage, bleomycin, and gamma radiation induce different types of DNA strand breaks in normal lymphocytes and thymocytes. A comet assay study

7 January 2021

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7 January 2021

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7 January 2021

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Formation, Prevention, and Repair of DNA Damage by Iron/Hydrogen Peroxide

7 January 2021

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RECQL4-deficient cells are hypersensitive to oxidative stress/damage: Insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products

7 January 2021

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DNA damage-dependent nuclear dynamics of the Mre11 complex

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

Repair of oxidative DNA damage in nuclear and mitochondrial DNA, and some changes with aging in mammalian cells

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

Endogenous oxidative stress: relationship to aging, longevity and caloric restriction

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

WRN helicase accelerates the transcription of ribosomal RNA as a component of an RNA polymerase I-associated complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

Poly(ADP-ribose) polymerases: homology, structural domains and functions. Novel therapeutical applications.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.07.023

10.1016/J.YEXCR.2006.07.023

7 January 2021

Identifiers

DOI

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18 September 2017

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