Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients

Author:

Khan Sikandar G.,Oh Kyu-Seon,Shahlavi Tala,Ueda Takahiro,Busch David B.,Inui Hiroki,Emmert Steffen,Imoto Kyoko,Muniz-Medina Vanessa,Baker Carl C.,DiGiovanna John J.,Schmidt Deborah,Khadavi Arash,Metin Ahmet,Gozukara Engin,Slor Hanoch,Sarasin Alain,Kraemer Kenneth H.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,General Medicine

Reference61 articles.

1. Bootsma,D., Kraemer,K.H., Cleaver,J.E. and Hoeijmakers,J.H.J. ( 2002 ) Nucleotide excision repair syndromes: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. In Vogelstein,B. and Kinzler,K.W. (eds) The Genetic Basis of Human Cancer, 2nd edn . McGraw-Hill, New York, pp. 211–237.

2. Kraemer,K.H. ( 2003 ) Heritable diseases with increased sensitivity to cellular injury. In Freedberg,I.M., Eisen,A.Z., Wolff,K., Austen,K.F., Goldsmith,L.A. and Katz,S.I. (eds) Fitzpatrick's Dermatology in General Medicine. McGraw-Hill, New York, pp. 1508–1521.

3. Sugasawa,K., Ng,J.M., Masutani,C., Iwai,S., Van der Spek,P.J., Eker,A.P., Hanaoka,F., Bootsma,D. and Hoeijmakers,J.H. ( 1998 ) Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair. Mol. Cell , 2 , 223 –232.

4. Yokoi,M., Masutani,C., Maekawa,T., Sugasawa,K., Ohkuma,Y. and Hanaoka,F. ( 2000 ) The Xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA. J. Biol. Chem. , 275 , 9870 –9875.

5. Okuda,Y., Nishi,R., Ng,J.M., Vermeulen,W., van der Horst,G.T., Mori,T., Hoeijmakers,J.H., Hanaoka,F. and Sugasawa,K. ( 2004 ) Relative levels of the two mammalian Rad23 homologs determine composition and stability of the Xeroderma pigmentosum group C protein complex. DNA Repair (Amst) , 3 , 1285 –1295.

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