Bridging the gap: a family of novel DNA polymerases that replicate faulty DNA.
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[1] E. Koonin,et al. Human and mouse homologs of Escherichia coli DinB (DNA polymerase IV), members of the UmuC/DinB superfamily. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[2] J. Epstein,et al. Novel human and mouse homologs of Saccharomyces cerevisiae DNA polymerase eta. , 1999, Genomics.
[3] E. G. Frank,et al. UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[4] J. Wagner,et al. The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis. , 1999, Molecular cell.
[5] Robert E. Johnson,et al. hRAD30 mutations in the variant form of xeroderma pigmentosum. , 1999, Science.
[6] Chikahide Masutani,et al. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η , 1999, Nature.
[7] Robert E. Johnson,et al. Requirement of DNA Polymerase Activity of Yeast Rad30 Protein for Its Biological Function* , 1999, The Journal of Biological Chemistry.
[8] Robert E. Johnson,et al. Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Poleta. , 1999, Science.
[9] R. Quatrano. Genomics , 1998, Plant Cell.
[10] E. G. Frank,et al. Biochemical basis of SOS-induced mutagenesis in Escherichia coli: reconstitution of in vitro lesion bypass dependent on the UmuD'2C mutagenic complex and RecA protein. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[11] Z. Livneh,et al. The mutagenesis proteins UmuD' and UmuC prevent lethal frameshifts while increasing base substitution mutations. , 1998, Molecular cell.
[12] G. Walker,et al. Mutagenesis and more: umuDC and the Escherichia coli SOS response. , 1998, Genetics.
[13] Errol C. Friedberg,et al. Deletion of the Saccharomyces cerevisiae gene RAD30 encoding an Escherichia coli DinB homolog confers UV radiation sensitivity and altered mutability , 1998, Molecular and General Genetics MGG.
[14] W. Kaufmann,et al. Replication Fork Bypass of a Pyrimidine Dimer Blocking Leading Strand DNA Synthesis* , 1997, The Journal of Biological Chemistry.
[15] B. Edgar,et al. Developmental Control of Cell Cycle Regulators: A Fly's Perspective , 1996, Science.
[16] C. Lawrence,et al. Deoxycytidyl transferase activity of yeast REV1 protein , 1996, Nature.
[17] C. Lawrence,et al. Thymine-Thymine Dimer Bypass by Yeast DNA Polymerase ζ , 1996, Science.
[18] H. L. Waters,et al. Ultraviolet hypermutability of a shuttle vector propagated in xeroderma pigmentosum variant cells. , 1993, The Journal of investigative dermatology.
[19] D. Mitchell,et al. Evidence from mutation spectra that the UV hypermutability of xeroderma pigmentosum variant cells reflects abnormal, error-prone replication on a template containing photoproducts , 1993, Molecular and cellular biology.
[20] W. Kaufmann,et al. Similar defects in DNA repair and replication in the pigmented xerodermoid and the xeroderma pigmentosum variants. , 1980, Carcinogenesis.
[21] B. Strauss,et al. A model for replication repair in mammalian cells. , 1976, Journal of molecular biology.
[22] C. Wilde,et al. Exchanges between DNA strands in ultraviolet-irradiated Escherichia coli. , 1971, Journal of molecular biology.
[23] J P McDonald,et al. Is Dna Damage Inducible and Functions in a Novel Error-free Postreplication Repair Mechanism , 1997 .
[24] Y. Bignon,et al. Carcinogenesis , 1979, Current Topics in Pathology.
[25] M. Paterson,et al. Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation. , 1975, Proceedings of the National Academy of Sciences of the United States of America.