Xeroderma Pigmentosum Complementation Group A Protein Acts as a Processivity Factor

By Lambert M.W.   Yang L.  

Biochemical and Biophysical Research Communications, Vol. 271, Iss. 3, 2000-05 ,pp. : 782-787

Elsevier

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Oxidative damage-induced PCNA complex formation is efficient in xeroderma pigmentosum group A but reduced in Cockayne syndrome group B cells

By Balajee Adayabalam S.   Dianova Irina   Bohr Vilhelm A.  

Nucleic Acids Research, Vol. 27, Iss. 22, 1999-10 ,pp. : 4476-4482

Oxford University Press

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Localization of xeroderma pigmentosum group A protein and replication protein A on damaged DNA in nucleotide excision repair

By Krasikova Yuliya S.   Rechkunova Nadejda I.   Maltseva Ekaterina A.   Petruseva Irina O.   Lavrik Olga I.  

Nucleic Acids Research, Vol. 38, Iss. 22, 2010-12 ,pp. : 8083-8094

Oxford University Press

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A low content of ERCC1 and a 120 kDa protein is a frequent feature of group F xeroderma pigmentosum fibroblast cells

By Yagi Takashi  

Mutagenesis, Vol. 12, Iss. 1, 1997-01 ,pp. : 41-44

Oxford University Press

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Ubiquitylation-independent degradation of Xeroderma pigmentosum group C protein is required for efficient nucleotide excision repair

By Wang Qi-En  

Nucleic Acids Research, Vol. 35, Iss. 16, 2007-08 ,pp. : 5338-5350

Oxford University Press

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