Literature DB >> 10228638

Excision repair defect in Rothmund Thomson syndrome.

F Vasseur1, E Delaporte, M T Zabot, M N Sturque, D Barrut, J B Savary, L Thomas, P Thomas.   

Abstract

Rothmund Thomson syndrome is a rare autosomal recessive skin disorder. The main clinical feature is poikiloderma appearing in early childhood associated with skeletal abnormalities. Early occurrence of malignancies is another relevant feature. Here we describe the clinical features of 2 patients with Rothmund Thomson syndrome who were investigated for the in vitro DNA repair capacities of blood cells following UVC radiation exposure. DNA excision repair, assessed with unscheduled DNA synthesis following UVC exposure, was decreased in both patients. Such a defect might explain the patients' sensitivity to sunlight and the relatively high risk of cancer associated with this syndrome.

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Year:  1999        PMID: 10228638     DOI: 10.1080/000155599750011417

Source DB:  PubMed          Journal:  Acta Derm Venereol        ISSN: 0001-5555            Impact factor:   4.437


  7 in total

1.  The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases.

Authors:  P Mohaghegh; J K Karow; R M Brosh; V A Bohr; I D Hickson
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

2.  Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome.

Authors:  S G Grant; S L Wenger; J J Latimer; D Thull; L W Burke
Journal:  Clin Genet       Date:  2000-09       Impact factor: 4.438

Review 3.  Rothmund-Thomson syndrome.

Authors:  Lidia Larizza; Gaia Roversi; Ludovica Volpi
Journal:  Orphanet J Rare Dis       Date:  2010-01-29       Impact factor: 4.123

4.  RecQ4 facilitates UV light-induced DNA damage repair through interaction with nucleotide excision repair factor xeroderma pigmentosum group A (XPA).

Authors:  Wei Fan; Jianyuan Luo
Journal:  J Biol Chem       Date:  2008-08-07       Impact factor: 5.157

5.  Activation of p38 MAP kinase and stress signalling in fibroblasts from the progeroid Rothmund-Thomson syndrome.

Authors:  Terence Davis; Hannah S E Tivey; Amy J C Brook; Julia W Grimstead; Michal J Rokicki; David Kipling
Journal:  Age (Dordr)       Date:  2012-09-22

6.  Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents.

Authors:  Weidong Jin; Hao Liu; Yiqun Zhang; Subhendu K Otta; Sharon E Plon; Lisa L Wang
Journal:  Hum Genet       Date:  2008-05-27       Impact factor: 4.132

Review 7.  Role and Regulation of the RECQL4 Family during Genomic Integrity Maintenance.

Authors:  Thong T Luong; Kara A Bernstein
Journal:  Genes (Basel)       Date:  2021-11-29       Impact factor: 4.096

  7 in total

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