Xeroderma pigmentosum patients from Germany: Clinical symptoms and DNA repair characteristics-Reference-Cited by-同舟云学术

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Xeroderma pigmentosum patients from Germany: Clinical symptoms and DNA repair characteristics

Published:1982-12 Issue:3-4 Volume:274 Page:229-247
ISSN:0340-3696
Container-title:Archives of Dermatological Research
language:en
Short-container-title:Arch Dermatol Res

Author:

Fischer Elisabeth,Thielmann Heinz Walter,Neund�rfer Bernhard,Rentsch Friedrich Johannes,Edler Lutz,Jung Ernst Gustav

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00403726.pdf

Reference28 articles.

1. Andrews AD, Barrett SF, Robbins JH (1978) Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation. Proc Natl Acad Sci USA 75:1984?1988

2. Arase S, Kozuka T, Tanaka K, Ikenaga M, Takebe H (1979) A sixth complementation group in xeroderma pigmentosum. Mutat Res 59:143?146

3. Barrett SF, Tarone RE, Moshell AN, Ganges MB, Robbins JH (1981) The post-UV colony-forming ability of normal fibroblast strains and of the xeroderma pigmentosum group G strain. J Invest Dermatol 76:59?62

4. Bohnert E, Humbel WG (1980) DNA repair of lymphocytes during PUVA-treatment. Arch Dermatol Res 267:175?178

5. Bootsma D, Zelle B, Keijzer W (1979) Deficient DNA repair in xeroderma pigmentosum. Stud Biophys 76:177?184

Cited by 53 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Xeroderma Pigmentosum: Relato de Dois Casos;Revista Brasileira de Cancerologia;2023-08-07

2. XPG: a multitasking genome caretaker;Cellular and Molecular Life Sciences;2022-03

3. Rare exon 10 deletion in POLH gene in a family with xeroderma pigmentosum variant correlating with protein expression by immunohistochemistry;Giornale Italiano di Dermatologia e Venereologia;2020-07

4. An unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP / CS complex phenotype;British Journal of Dermatology;2014-07-26

5. Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta;European Journal of Human Genetics;2012-01-11

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