(Q40035578)

16 September 2017

title

Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts (English)

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16 September 2017

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xeroderma pigmentosum

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Arlett CF

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16 September 2017

Green MH

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16 September 2017

Rogers PB

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16 September 2017

Lehmann AR

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16 September 2017

Plowman PN

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16 September 2017

language of work or name

English

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publication date

1 January 2008

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British Journal of Radiology

16 September 2017

published in

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16 September 2017

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16 September 2017

issue

961

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16 September 2017

page(s)

51-58

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describes a project that uses

16 September 2017

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Four radiation hypersensitivity cases and their implications for clinical radiotherapy

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

8-oxoguanine (8-hydroxyguanine) DNA glycosylase and its substrate specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Nucleotide excision repair in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Replication of damaged DNA by translesion synthesis in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Radiation-induced chromatid aberrations in Cockayne syndrome and xeroderma pigmentosum group C fibroblasts in relation to cancer predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Molecular analysis of glioma and skin-tumour alterations in a xeroderma-pigmentosum child

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Transcription-coupled repair: a complex affair

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

The role of CSA in the response to oxidative DNA damage in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Comparative Human Cellular Radiosensitivity: III. γ-radiation Survival of Cultured Skin Fibroblasts and Resting T-lymphocytes from the Peripheral Blood of the Same Individual

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

Characteristics of a human diploid cell designated MRC-5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1259%2FBJR%2F27072321

21 January 2018

Identifiers

DOI

10.1259/BJR/27072321

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16 September 2017

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