-
1
-
-
0032742715
-
DNA damage recognition during nucleotide excision repair in mammalian cells
-
Wood R.D. DNA damage recognition during nucleotide excision repair in mammalian cells. Biochimie 81 (1999) 39-44
-
(1999)
Biochimie
, vol.81
, pp. 39-44
-
-
Wood, R.D.1
-
2
-
-
0037031210
-
Xeroderma pigmentosum complementation group E and UV-damaged DNA-binding protein
-
Tang J., and Chu G. Xeroderma pigmentosum complementation group E and UV-damaged DNA-binding protein. DNA Repair (Amst.) 1 (2002) 601-616
-
(2002)
DNA Repair (Amst.)
, vol.1
, pp. 601-616
-
-
Tang, J.1
Chu, G.2
-
3
-
-
0029095126
-
Requirement for TFIIH kinase activity in transcription by RNA polymerase II
-
Akoulitchev S., Makela T.P., Weinberg R.A., and Reinberg D. Requirement for TFIIH kinase activity in transcription by RNA polymerase II. Nature 377 (1995) 557-560
-
(1995)
Nature
, vol.377
, pp. 557-560
-
-
Akoulitchev, S.1
Makela, T.P.2
Weinberg, R.A.3
Reinberg, D.4
-
4
-
-
0034087616
-
Peeling by binding or twisting by cranking: models for promoter opening and transcription initiation by RNA polymerase II
-
Fiedler U., and Marc Timmers H.T. Peeling by binding or twisting by cranking: models for promoter opening and transcription initiation by RNA polymerase II. Bioessays 22 (2000) 316-326
-
(2000)
Bioessays
, vol.22
, pp. 316-326
-
-
Fiedler, U.1
Marc Timmers, H.T.2
-
5
-
-
0040435451
-
TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair
-
Winkler G.S., Araujo S.J., Fiedler U., Vermeulen W., Coin F., Egly J.M., Hoeijmakers J.H., Wood R.D., Timmers H.T., and Weeda G. TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair. J. Biol. Chem. 275 (2000) 4258-4266
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 4258-4266
-
-
Winkler, G.S.1
Araujo, S.J.2
Fiedler, U.3
Vermeulen, W.4
Coin, F.5
Egly, J.M.6
Hoeijmakers, J.H.7
Wood, R.D.8
Timmers, H.T.9
Weeda, G.10
-
6
-
-
34247513888
-
Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair
-
Coin F., Oksenych V., and Egly J.M. Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair. Mol. Cell 26 (2007) 245-256
-
(2007)
Mol. Cell
, vol.26
, pp. 245-256
-
-
Coin, F.1
Oksenych, V.2
Egly, J.M.3
-
7
-
-
0021905437
-
DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall
-
Bohr V.A., Smith C.A., Okumoto D.S., and Hanawalt P.C. DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall. Cell 40 (1985) 359-369
-
(1985)
Cell
, vol.40
, pp. 359-369
-
-
Bohr, V.A.1
Smith, C.A.2
Okumoto, D.S.3
Hanawalt, P.C.4
-
8
-
-
0023663101
-
Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene
-
Mellon I., Spivak G., and Hanawalt P.C. Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene. Cell 51 (1987) 241-249
-
(1987)
Cell
, vol.51
, pp. 241-249
-
-
Mellon, I.1
Spivak, G.2
Hanawalt, P.C.3
-
9
-
-
0037115936
-
Subpathways of nucleotide excision repair and their regulation
-
Hanawalt P.C. Subpathways of nucleotide excision repair and their regulation. Oncogene 21 (2002) 8949-8956
-
(2002)
Oncogene
, vol.21
, pp. 8949-8956
-
-
Hanawalt, P.C.1
-
10
-
-
0942268166
-
DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
-
Lehmann A.R. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. Biochimie 85 (2003) 1101-1111
-
(2003)
Biochimie
, vol.85
, pp. 1101-1111
-
-
Lehmann, A.R.1
-
12
-
-
0030930282
-
Neuropathological findings in eight children with cerebro-oculo-facio-skeletal (COFS) syndrome
-
Del Bigio M.R., Greenberg C.R., Rorke L.B., Schnur R., McDonald-McGinn D.M., and Zackai E.H. Neuropathological findings in eight children with cerebro-oculo-facio-skeletal (COFS) syndrome. J. Neuropathol. Exp. Neurol. 56 (1997) 1147-1157
-
(1997)
J. Neuropathol. Exp. Neurol.
, vol.56
, pp. 1147-1157
-
-
Del Bigio, M.R.1
Greenberg, C.R.2
Rorke, L.B.3
Schnur, R.4
McDonald-McGinn, D.M.5
Zackai, E.H.6
-
13
-
-
24044522541
-
UV-sensitive syndrome
-
Spivak G. UV-sensitive syndrome. Mutat. Res. 577 (2005) 162-169
-
(2005)
Mutat. Res.
, vol.577
, pp. 162-169
-
-
Spivak, G.1
-
14
-
-
34247178359
-
DNA repair in differentiated cells: some new answers to old questions
-
Nouspikel T. DNA repair in differentiated cells: some new answers to old questions. Neuroscience 145 (2007) 1213-1221
-
(2007)
Neuroscience
, vol.145
, pp. 1213-1221
-
-
Nouspikel, T.1
-
15
-
-
0023748941
-
A reduced rate of bulky DNA adduct removal is coincident with differentiation of human neuroblastoma cells induced by nerve growth factor
-
Jensen L., and Linn S. A reduced rate of bulky DNA adduct removal is coincident with differentiation of human neuroblastoma cells induced by nerve growth factor. Mol. Cell. Boil. 8 (1988) 3964-3968
-
(1988)
Mol. Cell. Boil.
, vol.8
, pp. 3964-3968
-
-
Jensen, L.1
Linn, S.2
-
16
-
-
0033961277
-
Terminally differentiated human neurons repair transcribed genes but display attenuated global DNA repair and modulation of repair gene expression
-
Nouspikel T., and Hanawalt P.C. Terminally differentiated human neurons repair transcribed genes but display attenuated global DNA repair and modulation of repair gene expression. Mol. Cell. Biol. 20 (2000) 1562-1570
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 1562-1570
-
-
Nouspikel, T.1
Hanawalt, P.C.2
-
17
-
-
0036012794
-
DNA repair in terminally differentiated cells
-
Nouspikel T., and Hanawalt P.C. DNA repair in terminally differentiated cells. DNA Repair 1 (2002) 59-75
-
(2002)
DNA Repair
, vol.1
, pp. 59-75
-
-
Nouspikel, T.1
Hanawalt, P.C.2
-
18
-
-
0025827017
-
Gene-specific DNA repair in terminally differentiating rat myoblasts
-
Ho L., and Hanawalt P.C. Gene-specific DNA repair in terminally differentiating rat myoblasts. Mutat. Res. DNA Repair 255 (1991) 124-141
-
(1991)
Mutat. Res. DNA Repair
, vol.255
, pp. 124-141
-
-
Ho, L.1
Hanawalt, P.C.2
-
19
-
-
33845429182
-
Nucleotide excision repair phenotype of human acute myeloid leukemia cell lines at various stages of differentiation
-
Hsu P.S., Hanawalt P.C., and Nouspikel T. Nucleotide excision repair phenotype of human acute myeloid leukemia cell lines at various stages of differentiation. Mutat. Res. 614 (2007) 3-15
-
(2007)
Mutat. Res.
, vol.614
, pp. 3-15
-
-
Hsu, P.S.1
Hanawalt, P.C.2
Nouspikel, T.3
-
21
-
-
0020965170
-
UV-induced DNA damage and its repair in human skin in vivo studied by sensitive immunohistochemical methods
-
Eggset G., Volden G., and Krokan H. UV-induced DNA damage and its repair in human skin in vivo studied by sensitive immunohistochemical methods. Carcinogenesis 4 (1983) 745-750
-
(1983)
Carcinogenesis
, vol.4
, pp. 745-750
-
-
Eggset, G.1
Volden, G.2
Krokan, H.3
-
22
-
-
33344478774
-
Non-transcribed strand repair revealed in quiescent cells
-
Bielas J.H. Non-transcribed strand repair revealed in quiescent cells. Mutagenesis 21 (2006) 49-53
-
(2006)
Mutagenesis
, vol.21
, pp. 49-53
-
-
Bielas, J.H.1
-
24
-
-
33750821636
-
Impaired nucleotide excision repair upon macrophage differentiation is corrected by E1 ubiquitin-activating enzyme
-
Nouspikel T., and Hanawalt P.C. Impaired nucleotide excision repair upon macrophage differentiation is corrected by E1 ubiquitin-activating enzyme. Proc. Natl. Acad. Sci. U.S.A. 103 (2006) 16188-16193
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 16188-16193
-
-
Nouspikel, T.1
Hanawalt, P.C.2
-
25
-
-
0035871660
-
DNA replication precedes neuronal cell death in Alzheimer's disease
-
Yang Y., Geldmacher D.S., and Herrup K. DNA replication precedes neuronal cell death in Alzheimer's disease. J. Neurosci. 21 (2001) 2661-2668
-
(2001)
J. Neurosci.
, vol.21
, pp. 2661-2668
-
-
Yang, Y.1
Geldmacher, D.S.2
Herrup, K.3
-
26
-
-
0037322913
-
When parsimony backfires: neglecting DNA repair may doom neurons in Alzheimer's disease
-
Nouspikel T., and Hanawalt P.C. When parsimony backfires: neglecting DNA repair may doom neurons in Alzheimer's disease. BioEssays 25 (2003) 168-173
-
(2003)
BioEssays
, vol.25
, pp. 168-173
-
-
Nouspikel, T.1
Hanawalt, P.C.2
-
27
-
-
0000922826
-
On diseases of the skin, including the exanthemata
-
von Hebra F., and Kaposi M. On diseases of the skin, including the exanthemata. New Sydenham. Soc. 61 (1874) 252-258
-
(1874)
New Sydenham. Soc.
, vol.61
, pp. 252-258
-
-
von Hebra, F.1
Kaposi, M.2
-
29
-
-
0023130695
-
Xeroderma pigmentosum. Cutaneous, ocular, and neurological abnormalities in 830 published cases
-
Kraemer K.H., Lee M.M., and Scotto J. Xeroderma pigmentosum. Cutaneous, ocular, and neurological abnormalities in 830 published cases. Arch. Dermatol. 123 (1987) 241-250
-
(1987)
Arch. Dermatol.
, vol.123
, pp. 241-250
-
-
Kraemer, K.H.1
Lee, M.M.2
Scotto, J.3
-
30
-
-
0021282448
-
DNA repair protects against cutaneous and internal neoplasia: evidence from xeroderma pigmentosum
-
Kraemer K.H., Lee M.M., and Scotto J. DNA repair protects against cutaneous and internal neoplasia: evidence from xeroderma pigmentosum. Carcinogenesis 5 (1984) 511-514
-
(1984)
Carcinogenesis
, vol.5
, pp. 511-514
-
-
Kraemer, K.H.1
Lee, M.M.2
Scotto, J.3
-
31
-
-
0002834557
-
Ueber das xeroderma pigmentosum. Lioderma essentialis cum melanosis et telangectasia
-
Neisser A. Ueber das xeroderma pigmentosum. Lioderma essentialis cum melanosis et telangectasia. Jahrschr. Dermatol. Syphil. 1883 (1883) 47-62
-
(1883)
Jahrschr. Dermatol. Syphil.
, vol.1883
, pp. 47-62
-
-
Neisser, A.1
-
33
-
-
0034727603
-
Cockayne syndrome and xeroderma pigmentosum
-
Rapin I., Lindenbaum Y., Dickson D.W., Kraemer K.H., and Robbins J.H. Cockayne syndrome and xeroderma pigmentosum. Neurology 55 (2000) 1442-1449
-
(2000)
Neurology
, vol.55
, pp. 1442-1449
-
-
Rapin, I.1
Lindenbaum, Y.2
Dickson, D.W.3
Kraemer, K.H.4
Robbins, J.H.5
-
34
-
-
0014421995
-
Defective repair replication of DNA in xeroderma pigmentosum
-
Cleaver J.E. Defective repair replication of DNA in xeroderma pigmentosum. Nature 218 (1968) 652-656
-
(1968)
Nature
, vol.218
, pp. 652-656
-
-
Cleaver, J.E.1
-
35
-
-
0014597052
-
Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA
-
Setlow R.B., Regan J.D., German J., and Carrier W.L. Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. Proc. Natl. Acad. Sci. U.S.A. 64 (1969) 1035-1041
-
(1969)
Proc. Natl. Acad. Sci. U.S.A.
, vol.64
, pp. 1035-1041
-
-
Setlow, R.B.1
Regan, J.D.2
German, J.3
Carrier, W.L.4
-
36
-
-
0033578040
-
The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta
-
Masutani C., Kusumoto R., Yamada A., Dohmae N., Yokoi M., Yuasa M., Araki M., Iwai S., Takio K., and Hanaoka F. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta. Nature 399 (1999) 700-704
-
(1999)
Nature
, vol.399
, pp. 700-704
-
-
Masutani, C.1
Kusumoto, R.2
Yamada, A.3
Dohmae, N.4
Yokoi, M.5
Yuasa, M.6
Araki, M.7
Iwai, S.8
Takio, K.9
Hanaoka, F.10
-
37
-
-
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
-
38
-
-
0038339144
-
A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein
-
Ng J.M., Vermeulen W., van der Horst G.T., Bergink S., Sugasawa K., Vrieling H., and Hoeijmakers J.H. A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein. Genes Dev. 17 (2003) 1630-1645
-
(2003)
Genes Dev.
, vol.17
, pp. 1630-1645
-
-
Ng, J.M.1
Vermeulen, W.2
van der Horst, G.T.3
Bergink, S.4
Sugasawa, K.5
Vrieling, H.6
Hoeijmakers, J.H.7
-
39
-
-
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
-
40
-
-
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
-
41
-
-
34247156564
-
DNA repair, mitochondria, and neurodegeneration
-
Weissman L., de Souza-Pinto N.C., Stevnsner T., and Bohr V.A. DNA repair, mitochondria, and neurodegeneration. Neuroscience 145 (2007) 1318-1329
-
(2007)
Neuroscience
, vol.145
, pp. 1318-1329
-
-
Weissman, L.1
de Souza-Pinto, N.C.2
Stevnsner, T.3
Bohr, V.A.4
-
42
-
-
34247148895
-
The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum
-
Brooks P.J. The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum. Neuroscience 145 (2007) 1407-1417
-
(2007)
Neuroscience
, vol.145
, pp. 1407-1417
-
-
Brooks, P.J.1
-
43
-
-
0030893025
-
Repair of propanodeoxyguanosine by nucleotide excision repair in vivo and in vitro
-
Johnson K.A., Fink S.P., and Marnett L.J. Repair of propanodeoxyguanosine by nucleotide excision repair in vivo and in vitro. J. Biol. Chem. 272 (1997) 11434-11438
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 11434-11438
-
-
Johnson, K.A.1
Fink, S.P.2
Marnett, L.J.3
-
44
-
-
33646088615
-
Topoisomerase deficiencies subtly enhance global genomic repair of ultraviolet-induced DNA damage in Saccharomyces cerevisiae
-
Cline S.D., and Hanawalt P.C. Topoisomerase deficiencies subtly enhance global genomic repair of ultraviolet-induced DNA damage in Saccharomyces cerevisiae. DNA Repair (Amst.) 5 (2006) 611-617
-
(2006)
DNA Repair (Amst.)
, vol.5
, pp. 611-617
-
-
Cline, S.D.1
Hanawalt, P.C.2
-
45
-
-
0033590624
-
Inhibition of RNA polymerase II as a trigger for the p53 response
-
Ljungman M., Zhang F., Chen F., Rainbow A.J., and McKay B.C. Inhibition of RNA polymerase II as a trigger for the p53 response. Oncogene 18 (1999) 583-592
-
(1999)
Oncogene
, vol.18
, pp. 583-592
-
-
Ljungman, M.1
Zhang, F.2
Chen, F.3
Rainbow, A.J.4
McKay, B.C.5
-
46
-
-
0001051767
-
Xeroderma pigmentosum with neurological complications
-
Reed W.B., May S.B., and Nickel W.R. Xeroderma pigmentosum with neurological complications. Arch. Derm. 91 (1965) 224-226
-
(1965)
Arch. Derm.
, vol.91
, pp. 224-226
-
-
Reed, W.B.1
May, S.B.2
Nickel, W.R.3
-
47
-
-
0025088298
-
Peripheral neuropathy in xeroderma pigmentosum
-
Kanda T., Oda M., Yonezawa M., Tamagawa K., Isa F., Hanakago R., and Tsukagoshi H. Peripheral neuropathy in xeroderma pigmentosum. Brain 113 Pt 4 (1990) 1025-1044
-
(1990)
Brain
, vol.113
, Issue.PART 4
, pp. 1025-1044
-
-
Kanda, T.1
Oda, M.2
Yonezawa, M.3
Tamagawa, K.4
Isa, F.5
Hanakago, R.6
Tsukagoshi, H.7
-
48
-
-
0030060577
-
Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype
-
Itoh T., Cleaver J.E., and Yamaizumi M. Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype. Hum. Genet. 97 (1996) 176-179
-
(1996)
Hum. Genet.
, vol.97
, pp. 176-179
-
-
Itoh, T.1
Cleaver, J.E.2
Yamaizumi, M.3
-
49
-
-
0034192532
-
Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum
-
Colella S., Nardo T., Botta E., Lehmann A.R., and Stefanini M. Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum. Hum. Mol. Genet. 9 (2000) 1171-1175
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1171-1175
-
-
Colella, S.1
Nardo, T.2
Botta, E.3
Lehmann, A.R.4
Stefanini, M.5
-
50
-
-
0002362694
-
Dwarfism with retinal atrophy and deafness
-
Cockayne A.E. Dwarfism with retinal atrophy and deafness. Arch. Dis. Child. 11 (1936) 1-8
-
(1936)
Arch. Dis. Child.
, vol.11
, pp. 1-8
-
-
Cockayne, A.E.1
-
51
-
-
0026508774
-
Cockayne syndrome: review of 140 cases
-
Nance M.A., and Berry S.A. Cockayne syndrome: review of 140 cases. Am. J. Med. Genet. 42 (1992) 68-84
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 68-84
-
-
Nance, M.A.1
Berry, S.A.2
-
52
-
-
0020265071
-
Early onset of Cockayne syndrome
-
Lowry R.B. Early onset of Cockayne syndrome. Am. J. Med. Genet. 13 (1982) 209-210
-
(1982)
Am. J. Med. Genet.
, vol.13
, pp. 209-210
-
-
Lowry, R.B.1
-
53
-
-
0025341294
-
The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA
-
Venema J., Mullenders L.H., Natarajan A.T., van Zeeland A.A., and Mayne L.V. The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. Proc. Natl. Acad. Sci. U.S.A. 87 (1990) 4707-4711
-
(1990)
Proc. Natl. Acad. Sci. U.S.A.
, vol.87
, pp. 4707-4711
-
-
Venema, J.1
Mullenders, L.H.2
Natarajan, A.T.3
van Zeeland, A.A.4
Mayne, L.V.5
-
54
-
-
0020066520
-
Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum
-
Mayne L.V., and Lehmann A.R. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum. Cancer Res. 42 (1982) 1473-1478
-
(1982)
Cancer Res.
, vol.42
, pp. 1473-1478
-
-
Mayne, L.V.1
Lehmann, A.R.2
-
55
-
-
33744546833
-
Translesion synthesis DNA polymerases and control of genome stability
-
Shcherbakova P.V., and Fijalkowska I.J. Translesion synthesis DNA polymerases and control of genome stability. Front. Biosci. 11 (2006) 2496-2517
-
(2006)
Front. Biosci.
, vol.11
, pp. 2496-2517
-
-
Shcherbakova, P.V.1
Fijalkowska, I.J.2
-
56
-
-
0034723161
-
Distinct roles for the helicases of TFIIH in transcript initiation and promoter escape
-
Bradsher J., Coin F., and Egly J.M. Distinct roles for the helicases of TFIIH in transcript initiation and promoter escape. J. Biol. Chem. 275 (2000) 2532-2538
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 2532-2538
-
-
Bradsher, J.1
Coin, F.2
Egly, J.M.3
-
57
-
-
0030826732
-
The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex
-
van Gool A.J., Citterio E., Rademakers S., van Os R., Vermeulen W., Constantinou A., Egly J.M., Bootsma D., and Hoeijmakers J.H. The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex. EMBO J. 16 (1997) 5955-5965
-
(1997)
EMBO J.
, vol.16
, pp. 5955-5965
-
-
van Gool, A.J.1
Citterio, E.2
Rademakers, S.3
van Os, R.4
Vermeulen, W.5
Constantinou, A.6
Egly, J.M.7
Bootsma, D.8
Hoeijmakers, J.H.9
-
58
-
-
0030822591
-
Cockayne syndrome group B protein enhances elongation by RNA polymerase II
-
Selby C.P., and Sancar A. Cockayne syndrome group B protein enhances elongation by RNA polymerase II. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 11205-11209
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 11205-11209
-
-
Selby, C.P.1
Sancar, A.2
-
59
-
-
0030902253
-
Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells
-
Balajee A.S., May A., Dianov G.L., Friedberg E.C., and Bohr V.A. Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 4306-4311
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 4306-4311
-
-
Balajee, A.S.1
May, A.2
Dianov, G.L.3
Friedberg, E.C.4
Bohr, V.A.5
-
60
-
-
0030862095
-
Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells
-
Dianov G.L., Houle J.F., Iyer N., Bohr V.A., and Friedberg E.C. Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells. Nucleic Acids Res. 25 (1997) 3636-3642
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 3636-3642
-
-
Dianov, G.L.1
Houle, J.F.2
Iyer, N.3
Bohr, V.A.4
Friedberg, E.C.5
-
61
-
-
0029931026
-
Xeroderma pigmentosum Cockayne syndrome and trichothiodystrophy: do the genes explain the diseases?
-
Chu G., and Mayne L. Xeroderma pigmentosum Cockayne syndrome and trichothiodystrophy: do the genes explain the diseases?. Trends Genet. 12 (1996) 187-192
-
(1996)
Trends Genet.
, vol.12
, pp. 187-192
-
-
Chu, G.1
Mayne, L.2
-
62
-
-
0028934977
-
Mechanisms of DNA demethylation in chicken embryos. Purification and properties of a 5-methylcytosine-DNA glycosylase
-
Jost J.P., Siegmann M., Sun L., and Leung R. Mechanisms of DNA demethylation in chicken embryos. Purification and properties of a 5-methylcytosine-DNA glycosylase. J. Biol. Chem. 270 (1995) 9734-9739
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 9734-9739
-
-
Jost, J.P.1
Siegmann, M.2
Sun, L.3
Leung, R.4
-
63
-
-
0033567059
-
A chicken embryo protein related to the mammalian DEAD box protein p68 is tightly associated with the highly purified protein-RNA complex of 5-MeC-DNA glycosylase
-
Jost J.P., Schwarz S., Hess D., Angliker H., Fuller-Pace F.V., Stahl H., Thiry S., and Siegmann M. A chicken embryo protein related to the mammalian DEAD box protein p68 is tightly associated with the highly purified protein-RNA complex of 5-MeC-DNA glycosylase. Nucleic Acids Res. 27 (1999) 3245-3252
-
(1999)
Nucleic Acids Res.
, vol.27
, pp. 3245-3252
-
-
Jost, J.P.1
Schwarz, S.2
Hess, D.3
Angliker, H.4
Fuller-Pace, F.V.5
Stahl, H.6
Thiry, S.7
Siegmann, M.8
-
64
-
-
0027255962
-
Complementation of the DNA repair defect in xeroderma pigmenstosum group G cells by a human cDNA related to yeast RAD2
-
Scherly D., Nouspikel T., Corlet J., Ucla C., Bairoch A., and Clarkson S.G. Complementation of the DNA repair defect in xeroderma pigmenstosum group G cells by a human cDNA related to yeast RAD2. Nature 363 (1993) 182-184
-
(1993)
Nature
, vol.363
, pp. 182-184
-
-
Scherly, D.1
Nouspikel, T.2
Corlet, J.3
Ucla, C.4
Bairoch, A.5
Clarkson, S.G.6
-
65
-
-
34247256517
-
XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients
-
Ito S., Kuraoka I., Chymkowitch P., Compe E., Takedachi A., Ishigami C., Coin F., Egly J.M., and Tanaka K. XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients. Mol. Cell 26 (2007) 231-243
-
(2007)
Mol. Cell
, vol.26
, pp. 231-243
-
-
Ito, S.1
Kuraoka, I.2
Chymkowitch, P.3
Compe, E.4
Takedachi, A.5
Ishigami, C.6
Coin, F.7
Egly, J.M.8
Tanaka, K.9
-
66
-
-
0030990434
-
A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function
-
Nouspikel T., Lalle P., Leadon S.A., Cooper P.K., and Clarkson S.G. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 3116-3121
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 3116-3121
-
-
Nouspikel, T.1
Lalle, P.2
Leadon, S.A.3
Cooper, P.K.4
Clarkson, S.G.5
-
67
-
-
33846252240
-
Genome-wide atlas of gene expression in the adult mouse brain
-
Lein E.S., Hawrylycz M.J., Ao N., Ayres M., Bensinger A., Bernard A., Boe A.F., Boguski M.S., Brockway K.S., Byrnes E.J., Chen L., Chen L., Chen T.M., Chin M.C., Chong J., Crook B.E., Czaplinska A., Dang C.N., Datta S., Dee N.R., Desaki A.L., Desta T., Diep E., Dolbeare T.A., Donelan M.J., Dong H.W., Dougherty J.G., Duncan B.J., Ebbert A.J., Eichele G., Estin L.K., Faber C., Facer B.A., Fields R., Fischer S.R., Fliss T.P., Frensley C., Gates S.N., Glattfelder K.J., Halverson K.R., Hart M.R., Hohmann J.G., Howell M.P., Jeung D.P., Johnson R.A., Karr P.T., Kawal R., Kidney J.M., Knapik R.H., Kuan C.L., Lake J.H., Laramee A.R., Larsen K.D., Lau C., Lemon T.A., Liang A.J., Liu Y., Luong L.T., Michaels J., Morgan J.J., Morgan R.J., Mortrud M.T., Mosqueda N.F., Ng L.L., Ng R., Orta G.J., Overly C.C., Pak T.H., Parry S.E., Pathak S.D., Pearson O.C., Puchalski R.B., Riley Z.L., Rockett H.R., Rowland S.A., Royall J.J., Ruiz M.J., Sarno N.R., Schaffnit K., Shapovalova N.V., Sivisay T., Slaughterbeck C.R., Smith S.C., Smith K.A., Smith B.I., Sodt A.J., Stewart N.N., Stumpf K.R., Sunkin S.M., Sutram M., Tam A., Teemer C.D., Thaller C., Thompson C.L., Varnam L.R., Visel A., Whitlock R.M., Wohnoutka P.E., Wolkey C.K., Wong V.Y., Wood M., Yaylaoglu M.B., Young R.C., Youngstrom B.L., Yuan X.F., Zhang B., Zwingman T.A., and Jones A.R. Genome-wide atlas of gene expression in the adult mouse brain. Nature 445 (2007) 168-176
-
(2007)
Nature
, vol.445
, pp. 168-176
-
-
Lein, E.S.1
Hawrylycz, M.J.2
Ao, N.3
Ayres, M.4
Bensinger, A.5
Bernard, A.6
Boe, A.F.7
Boguski, M.S.8
Brockway, K.S.9
Byrnes, E.J.10
Chen, L.11
Chen, L.12
Chen, T.M.13
Chin, M.C.14
Chong, J.15
Crook, B.E.16
Czaplinska, A.17
Dang, C.N.18
Datta, S.19
Dee, N.R.20
Desaki, A.L.21
Desta, T.22
Diep, E.23
Dolbeare, T.A.24
Donelan, M.J.25
Dong, H.W.26
Dougherty, J.G.27
Duncan, B.J.28
Ebbert, A.J.29
Eichele, G.30
Estin, L.K.31
Faber, C.32
Facer, B.A.33
Fields, R.34
Fischer, S.R.35
Fliss, T.P.36
Frensley, C.37
Gates, S.N.38
Glattfelder, K.J.39
Halverson, K.R.40
Hart, M.R.41
Hohmann, J.G.42
Howell, M.P.43
Jeung, D.P.44
Johnson, R.A.45
Karr, P.T.46
Kawal, R.47
Kidney, J.M.48
Knapik, R.H.49
Kuan, C.L.50
Lake, J.H.51
Laramee, A.R.52
Larsen, K.D.53
Lau, C.54
Lemon, T.A.55
Liang, A.J.56
Liu, Y.57
Luong, L.T.58
Michaels, J.59
Morgan, J.J.60
Morgan, R.J.61
Mortrud, M.T.62
Mosqueda, N.F.63
Ng, L.L.64
Ng, R.65
Orta, G.J.66
Overly, C.C.67
Pak, T.H.68
Parry, S.E.69
Pathak, S.D.70
Pearson, O.C.71
Puchalski, R.B.72
Riley, Z.L.73
Rockett, H.R.74
Rowland, S.A.75
Royall, J.J.76
Ruiz, M.J.77
Sarno, N.R.78
Schaffnit, K.79
Shapovalova, N.V.80
Sivisay, T.81
Slaughterbeck, C.R.82
Smith, S.C.83
Smith, K.A.84
Smith, B.I.85
Sodt, A.J.86
Stewart, N.N.87
Stumpf, K.R.88
Sunkin, S.M.89
Sutram, M.90
Tam, A.91
Teemer, C.D.92
Thaller, C.93
Thompson, C.L.94
Varnam, L.R.95
Visel, A.96
Whitlock, R.M.97
Wohnoutka, P.E.98
Wolkey, C.K.99
Wong, V.Y.100
Wood, M.101
Yaylaoglu, M.B.102
Young, R.C.103
Youngstrom, B.L.104
Yuan, X.F.105
Zhang, B.106
Zwingman, T.A.107
Jones, A.R.108
more..
-
68
-
-
0029941444
-
The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes
-
van Oosterwijk M.F., Versteeg A., Filon R., van Zeeland A.A., and Mullenders L.H. The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes. Mol. Cell. Biol. 16 (1996) 4436-4444
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 4436-4444
-
-
van Oosterwijk, M.F.1
Versteeg, A.2
Filon, R.3
van Zeeland, A.A.4
Mullenders, L.H.5
-
69
-
-
0029803732
-
The sensitivity of human fibroblasts to N-acetoxy-2-acetylaminofluorene is determined by the extent of transcription-coupled repair, and/or their capability to counteract RNA synthesis inhibition
-
van Oosterwijk M.F., Filon R., Kalle W.H., Mullenders L.H., and van Zeeland A.A. The sensitivity of human fibroblasts to N-acetoxy-2-acetylaminofluorene is determined by the extent of transcription-coupled repair, and/or their capability to counteract RNA synthesis inhibition. Nucleic Acids Res. 24 (1996) 4653-4659
-
(1996)
Nucleic Acids Res.
, vol.24
, pp. 4653-4659
-
-
van Oosterwijk, M.F.1
Filon, R.2
Kalle, W.H.3
Mullenders, L.H.4
van Zeeland, A.A.5
-
70
-
-
0032577452
-
Lack of transcription-coupled repair of acetylaminofluorene DNA adducts in human fibroblasts contrasts their efficient inhibition of transcription
-
van Oosterwijk M.F., Filon R., de Groot A.J., van Zeeland A.A., and Mullenders L.H. Lack of transcription-coupled repair of acetylaminofluorene DNA adducts in human fibroblasts contrasts their efficient inhibition of transcription. J. Biol. Chem. 273 (1998) 13599-13604
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 13599-13604
-
-
van Oosterwijk, M.F.1
Filon, R.2
de Groot, A.J.3
van Zeeland, A.A.4
Mullenders, L.H.5
-
71
-
-
0033588105
-
Structural characterization of RNA polymerase II complexes arrested by a cyclobutane pyrimidine dimer in the transcribed strand of template DNA
-
Tornaletti S., Reines D., and Hanawalt P.C. Structural characterization of RNA polymerase II complexes arrested by a cyclobutane pyrimidine dimer in the transcribed strand of template DNA. J. Biol. Chem. 274 (1999) 24124-24130
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 24124-24130
-
-
Tornaletti, S.1
Reines, D.2
Hanawalt, P.C.3
-
72
-
-
0033555926
-
Rad26, the yeast homolog of the cockayne syndrome B gene product, counteracts inhibition of DNA repair due to RNA polymerase II transcription
-
Tijsterman M., and Brouwer J. Rad26, the yeast homolog of the cockayne syndrome B gene product, counteracts inhibition of DNA repair due to RNA polymerase II transcription. J. Biol. Chem. 274 (1999) 1199-1202
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 1199-1202
-
-
Tijsterman, M.1
Brouwer, J.2
-
73
-
-
0036363646
-
Mechanisms of transcription-coupled DNA repair
-
Svejstrup J.Q. Mechanisms of transcription-coupled DNA repair. Nat. Rev. Mol. Cell. Biol. 3 (2002) 21-29
-
(2002)
Nat. Rev. Mol. Cell. Biol.
, vol.3
, pp. 21-29
-
-
Svejstrup, J.Q.1
-
74
-
-
33747194740
-
Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo
-
Fousteri M., Vermeulen W., van Zeeland A.A., and Mullenders L.H. Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo. Mol. Cell 23 (2006) 471-482
-
(2006)
Mol. Cell
, vol.23
, pp. 471-482
-
-
Fousteri, M.1
Vermeulen, W.2
van Zeeland, A.A.3
Mullenders, L.H.4
-
75
-
-
26944448202
-
Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome
-
Sarker A.H., Tsutakawa S.E., Kostek S., Ng C., Shin D.S., Peris M., Campeau E., Tainer J.A., Nogales E., and Cooper P.K. Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome. Mol. Cell 20 (2005) 187-198
-
(2005)
Mol. Cell
, vol.20
, pp. 187-198
-
-
Sarker, A.H.1
Tsutakawa, S.E.2
Kostek, S.3
Ng, C.4
Shin, D.S.5
Peris, M.6
Campeau, E.7
Tainer, J.A.8
Nogales, E.9
Cooper, P.K.10
-
76
-
-
0029859295
-
UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells
-
Bregman D.B., Halaban R., van Gool A.J., Henning K.A., Friedberg E.C., and Warren S.L. UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells. Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 11586-11590
-
(1996)
Proc. Natl. Acad. Sci. U.S.A.
, vol.93
, pp. 11586-11590
-
-
Bregman, D.B.1
Halaban, R.2
van Gool, A.J.3
Henning, K.A.4
Friedberg, E.C.5
Warren, S.L.6
-
77
-
-
0037509859
-
The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage
-
Groisman R., Polanowska J., Kuraoka I., Sawada J., Saijo M., Drapkin R., Kisselev A.F., Tanaka K., and Nakatani Y. The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage. Cell 113 (2003) 357-367
-
(2003)
Cell
, vol.113
, pp. 357-367
-
-
Groisman, R.1
Polanowska, J.2
Kuraoka, I.3
Sawada, J.4
Saijo, M.5
Drapkin, R.6
Kisselev, A.F.7
Tanaka, K.8
Nakatani, Y.9
-
78
-
-
33744795969
-
CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome
-
Groisman R., Kuraoka I., Chevallier O., Gaye N., Magnaldo T., Tanaka K., Kisselev A.F., Harel-Bellan A., and Nakatani Y. CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome. Genes Dev. 20 (2006) 1429-1434
-
(2006)
Genes Dev.
, vol.20
, pp. 1429-1434
-
-
Groisman, R.1
Kuraoka, I.2
Chevallier, O.3
Gaye, N.4
Magnaldo, T.5
Tanaka, K.6
Kisselev, A.F.7
Harel-Bellan, A.8
Nakatani, Y.9
-
79
-
-
0034437623
-
Transcription-coupled repair of oxidative DNA damage in human cells: mechanisms and consequences
-
Tsutakawa S.E., and Cooper P.K. Transcription-coupled repair of oxidative DNA damage in human cells: mechanisms and consequences. Cold Spring Harb. Symp. Quant. Biol. 65 (2000) 201-215
-
(2000)
Cold Spring Harb. Symp. Quant. Biol.
, vol.65
, pp. 201-215
-
-
Tsutakawa, S.E.1
Cooper, P.K.2
-
80
-
-
0034713078
-
DNA repair. The bases for Cockayne syndrome
-
Hanawalt P.C. DNA repair. The bases for Cockayne syndrome. Nature 405 (2000) 415-416
-
(2000)
Nature
, vol.405
, pp. 415-416
-
-
Hanawalt, P.C.1
-
81
-
-
24044438505
-
Transcription-coupled repair: a complex affair
-
Mellon I. Transcription-coupled repair: a complex affair. Mutat. Res. 577 (2005) 155-161
-
(2005)
Mutat. Res.
, vol.577
, pp. 155-161
-
-
Mellon, I.1
-
82
-
-
0032973211
-
Base excision repair of oxidative DNA damage activated by XPG protein
-
Klungland A., Höss M., Gunz D., Constantinou A., Clarkson S.G., Doetsch P.W., Bolton P.H., Wood R.D., and Lindahl T. Base excision repair of oxidative DNA damage activated by XPG protein. Mol. Cell 3 (1999) 33-42
-
(1999)
Mol. Cell
, vol.3
, pp. 33-42
-
-
Klungland, A.1
Höss, M.2
Gunz, D.3
Constantinou, A.4
Clarkson, S.G.5
Doetsch, P.W.6
Bolton, P.H.7
Wood, R.D.8
Lindahl, T.9
-
83
-
-
2442590835
-
Transcriptional mutagenesis induced by uracil and 8-oxoguanine in Escherichia coli
-
Bregeon D., Doddridge Z.A., You H.J., Weiss B., and Doetsch P.W. Transcriptional mutagenesis induced by uracil and 8-oxoguanine in Escherichia coli. Mol. Cell 12 (2003) 959-970
-
(2003)
Mol. Cell
, vol.12
, pp. 959-970
-
-
Bregeon, D.1
Doddridge, Z.A.2
You, H.J.3
Weiss, B.4
Doetsch, P.W.5
-
84
-
-
29244483920
-
Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts
-
Spivak G., and Hanawalt P.C. Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts. DNA Repair (Amst.) 5 (2006) 13-22
-
(2006)
DNA Repair (Amst.)
, vol.5
, pp. 13-22
-
-
Spivak, G.1
Hanawalt, P.C.2
-
85
-
-
24044476230
-
Transcription arrest at DNA damage sites
-
Tornaletti S. Transcription arrest at DNA damage sites. Mutat. Res. 577 (2005) 131-145
-
(2005)
Mutat. Res.
, vol.577
, pp. 131-145
-
-
Tornaletti, S.1
-
86
-
-
33751559420
-
RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors
-
Charlet-Berguerand N., Feuerhahn S., Kong S.E., Ziserman H., Conaway J.W., Conaway R., and Egly J.M. RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors. EMBO J. 25 (2006) 5481-5491
-
(2006)
EMBO J.
, vol.25
, pp. 5481-5491
-
-
Charlet-Berguerand, N.1
Feuerhahn, S.2
Kong, S.E.3
Ziserman, H.4
Conaway, J.W.5
Conaway, R.6
Egly, J.M.7
-
87
-
-
0035977062
-
Effect of thymine glycol on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II
-
Tornaletti S., Maeda L.S., Lloyd D.R., Reines D., and Hanawalt P.C. Effect of thymine glycol on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II. J. Biol. Chem. 276 (2001) 45367-45371
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 45367-45371
-
-
Tornaletti, S.1
Maeda, L.S.2
Lloyd, D.R.3
Reines, D.4
Hanawalt, P.C.5
-
88
-
-
1842685197
-
Effect of 8-oxoguanine on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II
-
Tornaletti S., Maeda L.S., Kolodner R.D., and Hanawalt P.C. Effect of 8-oxoguanine on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II. DNA Repair (Amst.) 3 (2004) 483-494
-
(2004)
DNA Repair (Amst.)
, vol.3
, pp. 483-494
-
-
Tornaletti, S.1
Maeda, L.S.2
Kolodner, R.D.3
Hanawalt, P.C.4
-
89
-
-
0027165306
-
Effects of abasic sites and DNA single-strand breaks on prokaryotic RNA polymerases
-
Zhou W., and Doetsch P.W. Effects of abasic sites and DNA single-strand breaks on prokaryotic RNA polymerases. Proc. Natl. Acad. Sci. U.S.A. 90 (1993) 6601-6605
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, pp. 6601-6605
-
-
Zhou, W.1
Doetsch, P.W.2
-
90
-
-
33644530369
-
Transcriptional inhibition by an oxidized abasic site in DNA
-
Wang Y., Sheppard T.L., Tornaletti S., Maeda L.S., and Hanawalt P.C. Transcriptional inhibition by an oxidized abasic site in DNA. Chem. Res. Toxicol. 19 (2006) 234-241
-
(2006)
Chem. Res. Toxicol.
, vol.19
, pp. 234-241
-
-
Wang, Y.1
Sheppard, T.L.2
Tornaletti, S.3
Maeda, L.S.4
Hanawalt, P.C.5
-
91
-
-
34247148449
-
Base excision repair and the central nervous system
-
Wilson III D.M., and McNeill D.R. Base excision repair and the central nervous system. Neuroscience 145 (2007) 1187-1200
-
(2007)
Neuroscience
, vol.145
, pp. 1187-1200
-
-
Wilson III, D.M.1
McNeill, D.R.2
-
92
-
-
34247127167
-
Mitochondrial DNA repair: a critical player in the response of cells of the CNS to genotoxic insults
-
LeDoux S.P., Druzhyna N.M., Hollensworth S.B., Harrison J.F., and Wilson G.L. Mitochondrial DNA repair: a critical player in the response of cells of the CNS to genotoxic insults. Neuroscience 145 (2007) 1249-1259
-
(2007)
Neuroscience
, vol.145
, pp. 1249-1259
-
-
LeDoux, S.P.1
Druzhyna, N.M.2
Hollensworth, S.B.3
Harrison, J.F.4
Wilson, G.L.5
-
93
-
-
7444270518
-
The many faces of Cockayne syndrome
-
Spivak G. The many faces of Cockayne syndrome. Proc. Natl. Acad. Sci. U.S.A. 101 (2004) 15273-15274
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 15273-15274
-
-
Spivak, G.1
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