-
1
-
-
0031023182
-
Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex
-
Bessho T., Sancar A., Thompson L.H., and Thelen M.P. Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex. J. Biol. Chem. 272 (1997) 3833-3837
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 3833-3837
-
-
Bessho, T.1
Sancar, A.2
Thompson, L.H.3
Thelen, M.P.4
-
2
-
-
0034675930
-
Role of ERCC1 in removal of long non-homologous tails during targeted homologous recombination
-
Adair G.M., Rolig R.L., Moore-Faver D., Zabelshansky M., Wilson J.H., and Nairn R.S. Role of ERCC1 in removal of long non-homologous tails during targeted homologous recombination. EMBO J. 19 (2000) 5552-5561
-
(2000)
EMBO J.
, vol.19
, pp. 5552-5561
-
-
Adair, G.M.1
Rolig, R.L.2
Moore-Faver, D.3
Zabelshansky, M.4
Wilson, J.H.5
Nairn, R.S.6
-
3
-
-
0035890270
-
The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells
-
Niedernhofer L.J., Essers J., Weeda G., Beverloo B., de Wit J., Muijtjens M., Odijk H., Hoeijmakers J.H., and Kanaar R. The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells. EMBO J. 20 (2001) 6540-6549
-
(2001)
EMBO J.
, vol.20
, pp. 6540-6549
-
-
Niedernhofer, L.J.1
Essers, J.2
Weeda, G.3
Beverloo, B.4
de Wit, J.5
Muijtjens, M.6
Odijk, H.7
Hoeijmakers, J.H.8
Kanaar, R.9
-
4
-
-
12644303223
-
Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1
-
Sargent R.G., Rolig R.L., Kilburn A.E., Adair G.M., Wilson J.H., and Nairn R.S. Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 13122-13127
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 13122-13127
-
-
Sargent, R.G.1
Rolig, R.L.2
Kilburn, A.E.3
Adair, G.M.4
Wilson, J.H.5
Nairn, R.S.6
-
5
-
-
0034307734
-
Role of the nucleotide excision repair gene ERCC1 in formation of recombination-dependent rearrangements in mammalian cells
-
Sargent R.G., Meservy J.L., Perkins B.D., Kilburn A.E., Intody Z., Adair G.M., Nairn R.S., and Wilson J.H. Role of the nucleotide excision repair gene ERCC1 in formation of recombination-dependent rearrangements in mammalian cells. Nucleic Acids Res. 28 (2000) 3771-3778
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 3771-3778
-
-
Sargent, R.G.1
Meservy, J.L.2
Perkins, B.D.3
Kilburn, A.E.4
Intody, Z.5
Adair, G.M.6
Nairn, R.S.7
Wilson, J.H.8
-
6
-
-
0347416975
-
ERCC1/XPF removes the 3′ overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes
-
Zhu X.D., Niedernhofer L., Kuster B., Mann M., Hoeijmakers J.H., and de Lange T. ERCC1/XPF removes the 3′ overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes. Mol. Cell 12 (2003) 1489-1498
-
(2003)
Mol. Cell
, vol.12
, pp. 1489-1498
-
-
Zhu, X.D.1
Niedernhofer, L.2
Kuster, B.3
Mann, M.4
Hoeijmakers, J.H.5
de Lange, T.6
-
7
-
-
33846210498
-
XPF with mutations in its conserved nuclease domain is defective in DNA repair but functions in TRF2-mediated telomere shortening
-
Wu Y., Zacal N.J., Rainbow A.J., and Zhu X.D. XPF with mutations in its conserved nuclease domain is defective in DNA repair but functions in TRF2-mediated telomere shortening. DNA Repair 6 (2007) 157-166
-
(2007)
DNA Repair
, vol.6
, pp. 157-166
-
-
Wu, Y.1
Zacal, N.J.2
Rainbow, A.J.3
Zhu, X.D.4
-
8
-
-
0021143604
-
Molecular cloning of a human DNA repair gene
-
Westerveld A., Hoeijmakers J.H., van Duin M., de Wit J., Odijk H., Pastink A., Wood R.D., and Bootsma D. Molecular cloning of a human DNA repair gene. Nature 310 (1984) 425-429
-
(1984)
Nature
, vol.310
, pp. 425-429
-
-
Westerveld, A.1
Hoeijmakers, J.H.2
van Duin, M.3
de Wit, J.4
Odijk, H.5
Pastink, A.6
Wood, R.D.7
Bootsma, D.8
-
9
-
-
10244256322
-
ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs
-
Brookman K.W., Lamerdin J.E., Thelen M.P., Hwang M., Reardon J.T., Sancar A., Zhou Z.Q., Walter C.A., Parris C.N., and Thompson L.H. ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs. Mol. Cell. Biol. 16 (1996) 6553-6562
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 6553-6562
-
-
Brookman, K.W.1
Lamerdin, J.E.2
Thelen, M.P.3
Hwang, M.4
Reardon, J.T.5
Sancar, A.6
Zhou, Z.Q.7
Walter, C.A.8
Parris, C.N.9
Thompson, L.H.10
-
10
-
-
16044373761
-
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease
-
Sijbers A.M., de Laat W.L., Ariza R.R., Biggerstaff M., Wei Y.F., Moggs J.G., Carter K.C., Shell B.K., Evans E., de Jong M.C., Rademakers S., de Rooij J., Jaspers N.G., Hoeijmakers J.H., and Wood R.D. Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease. Cell 86 (1996) 811-822
-
(1996)
Cell
, vol.86
, pp. 811-822
-
-
Sijbers, A.M.1
de Laat, W.L.2
Ariza, R.R.3
Biggerstaff, M.4
Wei, Y.F.5
Moggs, J.G.6
Carter, K.C.7
Shell, B.K.8
Evans, E.9
de Jong, M.C.10
Rademakers, S.11
de Rooij, J.12
Jaspers, N.G.13
Hoeijmakers, J.H.14
Wood, R.D.15
-
11
-
-
0019828282
-
Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells
-
Thompson L.H., Busch D.B., Brookman K., Mooney C.L., and Glaser D.A. Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells. Proc. Natl. Acad. Sci. U.S.A. 78 (1981) 3734-3737
-
(1981)
Proc. Natl. Acad. Sci. U.S.A.
, vol.78
, pp. 3734-3737
-
-
Thompson, L.H.1
Busch, D.B.2
Brookman, K.3
Mooney, C.L.4
Glaser, D.A.5
-
12
-
-
0024415769
-
Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening
-
Busch D., Greiner C., Lewis K., Ford R., Adair G., and Thompson L. Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening. Mutagenesis 4 (1989) 349-354
-
(1989)
Mutagenesis
, vol.4
, pp. 349-354
-
-
Busch, D.1
Greiner, C.2
Lewis, K.3
Ford, R.4
Adair, G.5
Thompson, L.6
-
13
-
-
0027473181
-
Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics
-
Collins A.R. Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics. Mutat. Res. 293 (1993) 99-118
-
(1993)
Mutat. Res.
, vol.293
, pp. 99-118
-
-
Collins, A.R.1
-
14
-
-
17744411864
-
Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4
-
Busch D.B., van Vuuren H., de Wit J., Collins A., Zdzienicka M.Z., Mitchell D.L., Brookman K.W., Stefanini M., Riboni R., Thompson L.H., Albert R.B., van Gool A.J., and Hoeijmakers J. Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4. Mutat. Res. 383 (1997) 91-106
-
(1997)
Mutat. Res.
, vol.383
, pp. 91-106
-
-
Busch, D.B.1
van Vuuren, H.2
de Wit, J.3
Collins, A.4
Zdzienicka, M.Z.5
Mitchell, D.L.6
Brookman, K.W.7
Stefanini, M.8
Riboni, R.9
Thompson, L.H.10
Albert, R.B.11
van Gool, A.J.12
Hoeijmakers, J.13
-
15
-
-
0024763821
-
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19
-
Thompson L.H., Bachinski L.L., Stallings R.L., Dolf G., Weber C.A., Westerveld A., and Siciliano M.J. Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics 5 (1989) 670-679
-
(1989)
Genomics
, vol.5
, pp. 670-679
-
-
Thompson, L.H.1
Bachinski, L.L.2
Stallings, R.L.3
Dolf, G.4
Weber, C.A.5
Westerveld, A.6
Siciliano, M.J.7
-
16
-
-
0030758096
-
Survival, mutagenesis, and host cell reactivation in a Chinese hamster ovary cell ERCC1 knock-out mutant
-
Rolig R.L., Layher S.K., Santi B., Adair G.M., Gu F., Rainbow A.J., and Nairn R.S. Survival, mutagenesis, and host cell reactivation in a Chinese hamster ovary cell ERCC1 knock-out mutant. Mutagenesis 12 (1997) 277-283
-
(1997)
Mutagenesis
, vol.12
, pp. 277-283
-
-
Rolig, R.L.1
Layher, S.K.2
Santi, B.3
Adair, G.M.4
Gu, F.5
Rainbow, A.J.6
Nairn, R.S.7
-
17
-
-
0031822921
-
Characterization and analysis of Chinese hamster ovary cell ERCC1 mutant alleles
-
Rolig R.L., Lowery M.P., Adair G.M., and Nairn R.S. Characterization and analysis of Chinese hamster ovary cell ERCC1 mutant alleles. Mutagenesis 13 (1998) 357-365
-
(1998)
Mutagenesis
, vol.13
, pp. 357-365
-
-
Rolig, R.L.1
Lowery, M.P.2
Adair, G.M.3
Nairn, R.S.4
-
18
-
-
38349098477
-
The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells
-
Al-Minawi A.Z., Saleh-Gohari N., and Helleday T. The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells. Nucleic Acids Res. 36 (2008) 1-9
-
(2008)
Nucleic Acids Res.
, vol.36
, pp. 1-9
-
-
Al-Minawi, A.Z.1
Saleh-Gohari, N.2
Helleday, T.3
-
19
-
-
0037090816
-
The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif
-
Enzlin J.H., and Scharer O.D. The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif. EMBO J. 21 (2002) 2045-2053
-
(2002)
EMBO J.
, vol.21
, pp. 2045-2053
-
-
Enzlin, J.H.1
Scharer, O.D.2
-
20
-
-
34547810916
-
From broken to old: DNA damage, IGF1 endocrine suppression and aging
-
Monnat R.J. From broken to old: DNA damage, IGF1 endocrine suppression and aging. DNA Repair 6 (2007) 1386-1390
-
(2007)
DNA Repair
, vol.6
, pp. 1386-1390
-
-
Monnat, R.J.1
-
21
-
-
0029552525
-
Efficient modification of the APRT gene by FLP/FRT site-specific targeting
-
Merrihew R.V., Sargent R.G., and Wilson J.H. Efficient modification of the APRT gene by FLP/FRT site-specific targeting. Somat. Cell Mol. Genet. 21 (1995) 299-307
-
(1995)
Somat. Cell Mol. Genet.
, vol.21
, pp. 299-307
-
-
Merrihew, R.V.1
Sargent, R.G.2
Wilson, J.H.3
-
22
-
-
0021195801
-
Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7
-
Adair G.M., Stallings R.L., and Siciliano M.J. Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7. Somat. Cell Mol. Genet. 10 (1984) 283-295
-
(1984)
Somat. Cell Mol. Genet.
, vol.10
, pp. 283-295
-
-
Adair, G.M.1
Stallings, R.L.2
Siciliano, M.J.3
-
24
-
-
1542309071
-
Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF
-
Tian M., Shinkura R., Shinkura N., and Alt F.W. Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF. Mol. Cell. Biol. 24 (2004) 1200-1205
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 1200-1205
-
-
Tian, M.1
Shinkura, R.2
Shinkura, N.3
Alt, F.W.4
-
25
-
-
0034621854
-
Frequent chromosomal translocations induced by DNA double-strand breaks
-
Richardson C., and Jasin M. Frequent chromosomal translocations induced by DNA double-strand breaks. Nature 405 (2000) 697-700
-
(2000)
Nature
, vol.405
, pp. 697-700
-
-
Richardson, C.1
Jasin, M.2
-
26
-
-
0034600975
-
Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells
-
Johnson R.D., and Jasin M. Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells. EMBO J. 19 (2000) 3398-3407
-
(2000)
EMBO J.
, vol.19
, pp. 3398-3407
-
-
Johnson, R.D.1
Jasin, M.2
-
27
-
-
0035801472
-
Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences
-
Tutt A., Bertwistle D., Valentine J., Gabriel A., Swift S., Ross G., Griffin C., Thacker J., and Ashworth A. Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences. EMBO J. 20 (2001) 4704-4716
-
(2001)
EMBO J.
, vol.20
, pp. 4704-4716
-
-
Tutt, A.1
Bertwistle, D.2
Valentine, J.3
Gabriel, A.4
Swift, S.5
Ross, G.6
Griffin, C.7
Thacker, J.8
Ashworth, A.9
-
28
-
-
0742323558
-
Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics
-
Maquat L.E. Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics. Nat. Rev. Mol. Cell. Biol. 5 (2004) 89-99
-
(2004)
Nat. Rev. Mol. Cell. Biol.
, vol.5
, pp. 89-99
-
-
Maquat, L.E.1
-
29
-
-
0025944309
-
Direct-repeat analysis of chromatid interactions during intrachromosomal recombination in mouse cells
-
Bollag R.J., and Liskay R.M. Direct-repeat analysis of chromatid interactions during intrachromosomal recombination in mouse cells. Mol. Cell. Biol. 11 (1991) 4839-4845
-
(1991)
Mol. Cell. Biol.
, vol.11
, pp. 4839-4845
-
-
Bollag, R.J.1
Liskay, R.M.2
-
30
-
-
0024372735
-
Yeast intrachromosomal recombination: long gene conversion tracts are preferentially associated with reciprocal exchange and require the RAD1 and RAD3 gene products
-
Aguilera A., and Klein H.L. Yeast intrachromosomal recombination: long gene conversion tracts are preferentially associated with reciprocal exchange and require the RAD1 and RAD3 gene products. Genetics 123 (1989) 683-694
-
(1989)
Genetics
, vol.123
, pp. 683-694
-
-
Aguilera, A.1
Klein, H.L.2
-
31
-
-
0035871341
-
Loss of Werner syndrome protein function promotes aberrant mitotic recombination
-
Prince P.R., Emond M.J., and Monnat Jr. R.J. Loss of Werner syndrome protein function promotes aberrant mitotic recombination. Genes Dev. 15 (2001) 933-938
-
(2001)
Genes Dev.
, vol.15
, pp. 933-938
-
-
Prince, P.R.1
Emond, M.J.2
Monnat Jr., R.J.3
-
32
-
-
0037530653
-
Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process
-
Opresko P.L., Cheng W.-H., von Kobbe C., Harrigan J.A., and Bohr V. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process. Carcinogenesis 24 (2003) 791-802
-
(2003)
Carcinogenesis
, vol.24
, pp. 791-802
-
-
Opresko, P.L.1
Cheng, W.-H.2
von Kobbe, C.3
Harrigan, J.A.4
Bohr, V.5
-
33
-
-
33845914051
-
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis
-
Niedernhofer L.J., Garinis G.A., Raams A., Lalai A.S., Robinson A.R., Appeldoorn E., Odijk H., Oostendorp R., Ahmad A., van Leeuwen W., Theil A.F., Vermeulen W., van der Horst G.T., Meinecke P., Kleijer W.J., Vijg J., Jaspers N.G., and Hoeijmakers J.H. A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis. Nature 444 (2006) 1038-1043
-
(2006)
Nature
, vol.444
, pp. 1038-1043
-
-
Niedernhofer, L.J.1
Garinis, G.A.2
Raams, A.3
Lalai, A.S.4
Robinson, A.R.5
Appeldoorn, E.6
Odijk, H.7
Oostendorp, R.8
Ahmad, A.9
van Leeuwen, W.10
Theil, A.F.11
Vermeulen, W.12
van der Horst, G.T.13
Meinecke, P.14
Kleijer, W.J.15
Vijg, J.16
Jaspers, N.G.17
Hoeijmakers, J.H.18
-
34
-
-
33847056347
-
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure
-
Jaspers N.G., Raams A., Silengo M.C., Wijgers N., Niedernhofer L.J., Robinson A.R., Giglia-Mari G., Hoogstraten D., Kleijer W.J., Hoeijmakers J.H., and Vermeulen W. First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure. Am. J. Hum. Genet. 80 (2007) 457-466
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 457-466
-
-
Jaspers, N.G.1
Raams, A.2
Silengo, M.C.3
Wijgers, N.4
Niedernhofer, L.J.5
Robinson, A.R.6
Giglia-Mari, G.7
Hoogstraten, D.8
Kleijer, W.J.9
Hoeijmakers, J.H.10
Vermeulen, W.11
-
35
-
-
84993881991
-
New syndrome reconciles theories of ageing
-
Goymer P. New syndrome reconciles theories of ageing. Nat. Rev. Genet. 8 (2007) 90
-
(2007)
Nat. Rev. Genet.
, vol.8
, pp. 90
-
-
Goymer, P.1
-
36
-
-
12644266319
-
Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence
-
Weeda G., Donker I., de Wit J., Morreau H., Janssens R., Vissers C.J., Nigg A., van Steeg H., Bootsma D., and Hoeijmakers J.H. Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence. Curr. Biol. 7 (1997) 427-439
-
(1997)
Curr. Biol.
, vol.7
, pp. 427-439
-
-
Weeda, G.1
Donker, I.2
de Wit, J.3
Morreau, H.4
Janssens, R.5
Vissers, C.J.6
Nigg, A.7
van Steeg, H.8
Bootsma, D.9
Hoeijmakers, J.H.10
|