Literature DB >> 749755

[Photosensitization and DNA repair. Possible nosologic relationship between Xeroderma pigmentosum and Cockayne's syndrome].

D Lafforet, J M Dupuy.   

Abstract

UV-sensitivity is a common feature of several diseases including Xeroderma pigmentosum (XP), Cockayne syndrome (CS) and Bloom syndrome (BS). In 12 children with such diseases, cell viability and DNA repair following UV-irradiation as well as PHA transformation of lymphocytes were studied. In 5 of 6 XP cases, in 1 child with CS and in 1 of 2 children with BS, DNA repair and PHA transformation of lymphocytes showed extremely depressed values. A similar study was performed in 2 children with a rare association of XP and CS. Results suggest a relationship between these 2 diseases

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Year:  1978        PMID: 749755

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  8 in total

1.  Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D.

Authors:  J H Robbins
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

2.  No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H.

Authors:  J H Robbins
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

3.  Slowly progressing nucleotide excision repair in trichothiodystrophy group A patient fibroblasts.

Authors:  Arjan F Theil; Julie Nonnekens; Nils Wijgers; Wim Vermeulen; Giuseppina Giglia-Mari
Journal:  Mol Cell Biol       Date:  2011-07-05       Impact factor: 4.272

4.  Lack of complementation between xeroderma pigmentosum complementation groups D and H.

Authors:  R T Johnson; G C Elliott; S Squires; V C Joysey
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

Review 5.  Cockayne syndrome and xeroderma pigmentosum.

Authors:  I Rapin; Y Lindenbaum; D W Dickson; K H Kraemer; J H Robbins
Journal:  Neurology       Date:  2000-11-28       Impact factor: 9.910

6.  UV damage causes uncontrolled DNA breakage in cells from patients with combined features of XP-D and Cockayne syndrome.

Authors:  M Berneburg; J E Lowe; T Nardo; S Araújo; M I Fousteri; M H Green; J Krutmann; R D Wood; M Stefanini; A R Lehmann
Journal:  EMBO J       Date:  2000-03-01       Impact factor: 11.598

7.  Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

Authors:  W Vermeulen; J Jaeken; N G Jaspers; D Bootsma; J H Hoeijmakers
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

Review 8.  Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.

Authors:  B C Broughton; A F Thompson; S A Harcourt; W Vermeulen; J H Hoeijmakers; E Botta; M Stefanini; M D King; C A Weber; J Cole
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

  8 in total

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