Literature DB >> 7326997

Xeroderma pigmentosum variants.

J E Cleaver, A E Greene, L L Coriell, R A Mulivor.   

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Year:  1981        PMID: 7326997     DOI: 10.1159/000131646

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


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  5 in total

1.  Polymerase eta deficiency in the xeroderma pigmentosum variant uncovers an overlap between the S phase checkpoint and double-strand break repair.

Authors:  C L Limoli; E Giedzinski; W F Morgan; J E Cleaver
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-05       Impact factor: 11.205

2.  Accuracy of lesion bypass by yeast and human DNA polymerase eta.

Authors:  M T Washington; R E Johnson; L Prakash; S Prakash
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

3.  Quantitative measurement of translesion replication in human cells: evidence for bypass of abasic sites by a replicative DNA polymerase.

Authors:  Sharon Avkin; Sheera Adar; Gil Blander; Zvi Livneh
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

4.  Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.

Authors:  G A Greenhaw; A Hebert; M E Duke-Woodside; I J Butler; J T Hecht; J E Cleaver; G H Thomas; W A Horton
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

5.  Xeroderma pigmentosum patients from the Federal Republic of Germany: decrease in post-UV colony-forming ability in 30 xeroderma pigmentosum fibroblast strains is quantitatively correlated with a decrease in DNA-incising capacity.

Authors:  H W Thielmann; L Edler; O Popanda; S Friemel
Journal:  J Cancer Res Clin Oncol       Date:  1985       Impact factor: 4.553

  5 in total

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