Deletion of 5′ sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome-Reference-Cited by-同舟云学术

Deletion of 5′ sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome

Published:2008-01-09 Issue:3 Volume:16 Page:320-327
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Laugel Vincent,Dalloz Cecile,Stary Anne,Cormier-Daire Valerie,Desguerre Isabelle,Renouil Michel,Fourmaintraux Alain,Velez-Cruz Renier,Egly Jean-Marc,Sarasin Alain,Dollfus Helene

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5201991.pdf

Reference23 articles.

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2. Lehmann AR : DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. Biochimie 2003; 85: 1101–1111.

3. Laine JP, Egly JM : When transcription and repair meet: a complex system. Trends Genet 2006; 22: 430–436.

4. Sarasin A, Stary A : New insights for understanding the transcription-coupled repair pathway. DNA Repair (Amst) 2007; 6: 265–269.

5. Troelstra C, van Gool A, de Wit J, Vermeulen W, Bootsma D, Hoeijmakers JH : ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell 1992; 71: 939–953.

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