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Cockayne syndrome: defective repair of transcription?

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The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex.

The Journal of biological chemistry, August 14, 2015, Vol.290(33), pp.20541-20555 [Peer Reviewed Journal]

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A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription.

Journal of Biological Chemistry, 1996, Vol.271(27), pp.15898-15904 [Peer Reviewed Journal]

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DHR6, a Drosophila homolog of the yeast DNA repair gene RAD6.

Proceedings of the National Academy of Sciences of the United States of America, 1991, Vol.88, pp.3832-3836 [Peer Reviewed Journal]

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The second zinc-finger domain of poly(ADP-ribose) polymerase determines specificity for single-stranded breaks in DNA.

Proceedings of the National Academy of Sciences of the United States of America, 1990, Vol.87, pp.2290-2294 [Peer Reviewed Journal]

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Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage-dependent recombination.

EMBO Journal, 2004, Vol.23(17), pp.3548-3558 [Peer Reviewed Journal]

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Interaction of hHR23 with S5a. The ubiquitin-like domain of hHR23 mediates interaction with S5a subunit of 26 S proteasome

Journal of Biological Chemistry, 1999 [Peer Reviewed Journal]

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DNA structural elements required for ERCC1-XPF endonuclease activity

Journal of Biological Chemistry, 1998 [Peer Reviewed Journal]

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Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6.

Proceedings of the National Academy of Sciences of the United States of America, 1991, Vol.88(88), pp.8865-8869 [Peer Reviewed Journal]

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RAD25(SSL2), a yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability.

Proceedings of the National Academy of Sciences of the United States of America, 1992, Vol.89, pp.11416-11420 [Peer Reviewed Journal]

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