Ancient origin of a Japanese xeroderma pigmentosum founder mutation-Reference-Cited by-同舟云学术

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Ancient origin of a Japanese xeroderma pigmentosum founder mutation

Published:2013-02 Issue:2 Volume:69 Page:175-176
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Imoto Kyoko,Nadem Carine,Moriwaki Shin-Ichi,Nishigori Chikako,Oh Kyu-Seon,Khan Sikandar G.,Goldstein Alisa M.,Kraemer Kenneth H.

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference10 articles.

1. Shining a light on xeroderma pigmentosum;DiGiovanna;J Invest Dermatol,2012

2. Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum. Cockayne syndrome and trichothiodystrophy;Kleijer;DNA Repair (Amst),2008

3. Xeroderma pigmentosum—bridging a gap between clinic and laboratory;Moriwaki;Photodermatol Photoimmunol Photomed,2001

4. Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair;Bradford;J Med Genet,2011

5. Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population;Hirai;Mutat Res,2006

Cited by 11 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. Revealing the UV response of melanocytes in xeroderma pigmentosum group A using patient-derived induced pluripotent stem cells;Journal of Dermatological Science;2024-06

2. Cell migration is impaired in XPA ‐deficient cells;FASEB BioAdvances;2022-12-12

3. Progressive length‐dependent polyneuropathy in xeroderma pigmentosum group A;Muscle & Nerve;2020-08-10

4. Frequent retrotransposition of endogenous genes in ERCC2-deficient cells derived from a patient with xeroderma pigmentosum;Stem Cell Research & Therapy;2019-08-27

5. Epidemiological Study of Xeroderma Pigmentosum in Japan: Genotype-Phenotype Relationship;DNA Repair Disorders;2018-12-31

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