Three novel mutations responsible for Cockayne syndrome group A.-Reference-Cited by-同舟云学术

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Three novel mutations responsible for Cockayne syndrome group A.

Published:2003 Issue:1 Volume:78 Page:93-102
ISSN:1341-7568
Container-title:Genes & Genetic Systems
language:en
Short-container-title:Genes Genet. Syst.

Author:

Ren Yan¹,Saijo Masafumi¹²,Nakatsu Yoshimichi¹,Nakai Hiroshi³,Yamaizumi Masaru⁴,Tanaka Kiyoji¹²

Affiliation:

1. Graduate School of Frontier Biosciences, Osaka University

2. Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Corporation

3. Department of Pediatrics, Hachinohe National Hospital

4. Institute of Molecular Embryology and Genetics, Kumamoto University

Publisher

Genetics Society of Japan

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.jstage.jst.go.jp/article/ggs/78/1/78_1_93/_pdf

Reference26 articles.

1. Friedberg, E. C., Walker, G. C., and Siede, W. (1995) DNA Repair and Mutagenesis. American Society for Microbiology, Washington, DC.

2. BRCA1 Required for Transcription-Coupled Repair of Oxidative DNA Damage

3. Transcription-Coupled DNA Repair

4. The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

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1. Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis;Scientific Reports;2024-08-26

2. Clearance of DNA damage-arrested RNAPII is selectively impaired in Cockayne syndrome cells;2024-05-18

3. A universal molecular mechanism driving aging;2024-01-06

4. The landscape of genetic alterations of UVB ‐induced skin tumors in DNA repair‐deficient mice;Experimental Dermatology;2022-07-07

5. Identification of two novel homozygous mutations in ERCC8 gene in two unrelated consanguineous families with Cockayne syndrome from Iran;Clinica Chimica Acta;2021-12

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