Literature DB >> 2606486

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

J H Robbins.   

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Year:  1989        PMID: 2606486     DOI: 10.1007/bf00210685

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


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  19 in total

1.  No apparent neurologic defect in a patient with xeroderma pigmentosum complementation group D.

Authors:  M Ichihashi; K Yamamura; T Hiramoto; Y Fujiwara
Journal:  Arch Dermatol       Date:  1988-02

2.  Assignment of three patients with xeroderma pigmentosum to complementation group E and their characteristics.

Authors:  S Kondo; S Fukuro; A Mamada; A Kawada; Y Satoh; Y Fujiwara
Journal:  J Invest Dermatol       Date:  1988-02       Impact factor: 8.551

3.  The relative cytotoxicity of (6-4) photoproducts and cyclobutane dimers in mammalian cells.

Authors:  D L Mitchell
Journal:  Photochem Photobiol       Date:  1988-07       Impact factor: 3.421

4.  Assignment of two Japanese xeroderma pigmentosum patients to complementation group D and their characteristics.

Authors:  Y Fujiwara; Y Satoh
Journal:  Jpn J Cancer Res       Date:  1985-03

5.  Xeroderma pigmentosum complementation group F: more assignments and repair characteristics.

Authors:  Y Fujiwara; Y Uehara; M Ichihashi; K Nishioka
Journal:  Photochem Photobiol       Date:  1985-05       Impact factor: 3.421

6.  Xeroderma pigmentosum groups C and F: additional assignments and a review of the subjects in Japan.

Authors:  Y Fujiwara; M Ichihashi; Y Uehara; A Matsumoto; Y Yamamoto; Y Kano; Y Tanakura
Journal:  J Radiat Res       Date:  1985-12       Impact factor: 2.724

7.  Repair of UV-endonuclease-susceptible sites in the 7 complementation groups of xeroderma pigmentosum A through G.

Authors:  B Zelle; P H Lohman
Journal:  Mutat Res       Date:  1979-09       Impact factor: 2.433

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

Authors:  D Lafforet; J M Dupuy
Journal:  Arch Fr Pediatr       Date:  1978-12

9.  Xeroderma pigmentosum patients from Germany: clinical symptoms and DNA repair characteristics.

Authors:  E Fischer; H W Thielmann; B Neundörfer; F J Rentsch; L Edler; E G Jung
Journal:  Arch Dermatol Res       Date:  1982       Impact factor: 3.017

10.  Xeroderma pigmentosum complementation group E: a case report.

Authors:  A Kawada; Y Satoh; Y Fujiwara
Journal:  Photodermatol       Date:  1986-08
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  2 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.  Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.

Authors:  G Weeda; L B Ma; R C van Ham; A J van der Eb; J H Hoeijmakers
Journal:  Nucleic Acids Res       Date:  1991-11-25       Impact factor: 16.971

  2 in total

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