Cockayne syndrome B

Flohr C, Burkle A, Radicella JP et al. Poly(ADP-ribosyl)ation accelerates DNA repair in a pathway dependent on Cockayne syndrome B protein. Nucl Acids Res 2003 31 5332-5337. 

Kim, N., Kage, K., Matsuda, F., Lefranc, M.-P., Storb, U. (1997). B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. J. Exp. Med. 186,413-419. 

Tuo, J., Jaruga, P., Rodriguez, H., Dizdaroglu, M., and Bohr, V.A. (2002) The Cockayne syndrome group B gene product is involved in cellular repair of 8-hydroxyadenine in DNA. J. Biol. 

Bootsma, D Kraemer, K.H., Cleaver, J.E., and Hoeijmakers, J.H.J. (1998) Nucleotide excision repair syndromes xeroderma pigmentosum, cockayne syndrome, and trichothiodystrophy, in The Genetic Basis of Cancer (eds B. Vogelstein and K.W. Kinzler), McGraw-Hill, New York, pp. 245-274. 

Kraemer, K.H., Patronas, N.J., Schiffmann, R., Brooks, B.P., Tamura, D., and DiGiovanna, J.J. (2007) Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome a complex genotype-phenotype relationship. Neuroscience, 145,1388-1396. 

Iyer, N., Reagan, M. S., Wu, K.-J., Canagarajah, B., and Friedberg, E. C. (1996). Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein. Biochemistry 35, 2157-2167. 

Selby, C. P., and Sancar, A. (1997b). Cockayne syndrome group B protein enhances elongation by RNA polymerase II. Proc. Natl. Acad. Sci. USA 94, 11205-11209. 

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