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R Legerski
Author PubWeight™ 16.78
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH.
Cell
1995
2.78
2
Inhibition of nucleotide excision repair by the cyclin-dependent kinase inhibitor p21.
J Biol Chem
1995
1.42
3
Nucleotide excision repair genes as determinants of cellular sensitivity to cyclophosphamide analogs.
Cancer Chemother Pharmacol
1996
1.29
4
Isolation of human transcribed sequences from human-rodent somatic cell hybrids.
Science
1989
1.21
5
High-frequency transformation of human repair-deficient cell lines by an Epstein-Barr virus-based cDNA expression vector.
Gene
1991
1.20
6
Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia.
J Invest Dermatol
1998
1.11
7
XPC interacts with both HHR23B and HHR23A in vivo.
Mutat Res
1997
1.04
8
Cloning the Drosophila homolog of the xeroderma pigmentosum complementation group C gene reveals homology between the predicted human and Drosophila polypeptides and that encoded by the yeast RAD4 gene.
Nucleic Acids Res
1994
1.02
9
Sequence of the mouse XPC cDNA and genomic structure of the human XPC gene.
Nucleic Acids Res
1996
0.91
10
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cells.
Somat Cell Mol Genet
1995
0.87
11
Differential processing of UV mimetic and interstrand crosslink damage by XPF cell extracts.
Nucleic Acids Res
2000
0.86
12
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C.
Nature
1992
0.84
13
Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.
Mutagenesis
1993
0.80
14
Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybrids.
Hum Mutat
1997
0.80
15
Genetic complementation of radiation response by 3' untranslated regions (UTR) of RNA.
Int J Radiat Biol
1996
0.79