A rapid non-radioactive technique for measurement of repair synthesis in primary human fibroblasts by incorporation of ethynyl deoxyuridine (EdU)
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/37/4/e31/7179658/gkp023.pdf
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1. Molecular Mechanisms of Mammalian Global Genome Nucleotide Excision Repair
2. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: A complex genotype–phenotype relationship
3. Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
4. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η
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