-
3
-
-
33845683300
-
Nucleotide excision repair disorders and the balance between cancer and aging
-
Andressoo J.O., Hoeijmakers J.H., and Mitchell J.R. Nucleotide excision repair disorders and the balance between cancer and aging. Cell Cycle 5 (2006) 2886-2888
-
(2006)
Cell Cycle
, vol.5
, pp. 2886-2888
-
-
Andressoo, J.O.1
Hoeijmakers, J.H.2
Mitchell, J.R.3
-
4
-
-
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
-
5
-
-
0034719453
-
Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis
-
Balajee A.S., Proietti De Santis L., Brosh Jr. R.M., Selzer R., and Bohr V.A. Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis. Oncogene 19 (2000) 477-489
-
(2000)
Oncogene
, vol.19
, pp. 477-489
-
-
Balajee, A.S.1
Proietti De Santis, L.2
Brosh Jr., R.M.3
Selzer, R.4
Bohr, V.A.5
-
6
-
-
14244255484
-
The CSB protein actively wraps DNA
-
Beerens N., Hoeijmakers J.H., Kanaar R., Vermeulen W., and Wyman C. The CSB protein actively wraps DNA. J. Biol. Chem. 280 (2005) 4722-4729
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 4722-4729
-
-
Beerens, N.1
Hoeijmakers, J.H.2
Kanaar, R.3
Vermeulen, W.4
Wyman, C.5
-
7
-
-
0026484396
-
A mammalian cell line deficient in activity of the DNA repair enzyme 5-hydroxymethyluracil-DNA glycosylase is resistant to the toxic effects of the thymidine analog 5-hydroxymethyl-2′-deoxyuridine
-
Boorstein R.J., Chiu L.N., and Teebor G.W. A mammalian cell line deficient in activity of the DNA repair enzyme 5-hydroxymethyluracil-DNA glycosylase is resistant to the toxic effects of the thymidine analog 5-hydroxymethyl-2′-deoxyuridine. Mol. Cell Biol. 12 (1992) 5536-5540
-
(1992)
Mol. Cell Biol.
, vol.12
, pp. 5536-5540
-
-
Boorstein, R.J.1
Chiu, L.N.2
Teebor, G.W.3
-
8
-
-
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
-
9
-
-
0034698033
-
The oxidative DNA lesion 8, 5′-(S)-cyclo-2′-deoxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expression in mammalian cells
-
Brooks P.J., Wise D.S., Berry D.A., Kosmoski J.V., Smerdon M.J., Somers R.L., Mackie H., Spoonde A.Y., Ackerman E.J., Coleman K., Tarone R.E., and Robbins J.H. The oxidative DNA lesion 8, 5′-(S)-cyclo-2′-deoxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expression in mammalian cells. J. Biol. Chem. 275 (2000) 22355-22362
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 22355-22362
-
-
Brooks, P.J.1
Wise, D.S.2
Berry, D.A.3
Kosmoski, J.V.4
Smerdon, M.J.5
Somers, R.L.6
Mackie, H.7
Spoonde, A.Y.8
Ackerman, E.J.9
Coleman, K.10
Tarone, R.E.11
Robbins, J.H.12
-
10
-
-
33646945579
-
Age-related loss of the DNA repair response following exposure to oxidative stress
-
Cabelof D.C., Raffoul J.J., Ge Y., Van Remmen H., Matherly L.H., and Heydari A.R. Age-related loss of the DNA repair response following exposure to oxidative stress. J. Gerontol. A Biol. Sci. Med. Sci. 61 (2006) 427-434
-
(2006)
J. Gerontol. A Biol. Sci. Med. Sci.
, vol.61
, pp. 427-434
-
-
Cabelof, D.C.1
Raffoul, J.J.2
Ge, Y.3
Van Remmen, H.4
Matherly, L.H.5
Heydari, A.R.6
-
11
-
-
0037324344
-
Functional consequences of mutations in the conserved SF2 motifs and post-translational phosphorylation of the CSB protein
-
Christiansen M., Stevnsner T., Modin C., Martensen P.M., Brosh Jr. R.M., and Bohr V.A. Functional consequences of mutations in the conserved SF2 motifs and post-translational phosphorylation of the CSB protein. Nucleic Acids Res. 31 (2003) 963-973
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 963-973
-
-
Christiansen, M.1
Stevnsner, T.2
Modin, C.3
Martensen, P.M.4
Brosh Jr., R.M.5
Bohr, V.A.6
-
12
-
-
24644473682
-
The Cockayne syndrome group B protein is a functional dimmer
-
Christiansen M., Thorslund T., Jochimsen B., Bohr V.A., and Stevnsner T. The Cockayne syndrome group B protein is a functional dimmer. FEBS J. 272 (2005) 4306-4314
-
(2005)
FEBS J.
, vol.272
, pp. 4306-4314
-
-
Christiansen, M.1
Thorslund, T.2
Jochimsen, B.3
Bohr, V.A.4
Stevnsner, T.5
-
13
-
-
0033806183
-
ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor
-
Citterio E., Van Den Boom V., Schnitzler G., Kanaar R., Bonte E., Kingston R.E., Hoeijmakers J.H., and Vermeulen W. ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor. Mol. Cell Biol. 20 (2000) 7643-7653
-
(2000)
Mol. Cell Biol.
, vol.20
, pp. 7643-7653
-
-
Citterio, E.1
Van Den Boom, V.2
Schnitzler, G.3
Kanaar, R.4
Bonte, E.5
Kingston, R.E.6
Hoeijmakers, J.H.7
Vermeulen, W.8
-
14
-
-
0032945313
-
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity
-
Colella S., Nardo T., Mallery D., Borrone C., Ricci R., Ruffa G., Lehmann A.R., and Stefanini M. Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity. Hum. Mol. Genet. 8 (1999) 935-941
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 935-941
-
-
Colella, S.1
Nardo, T.2
Mallery, D.3
Borrone, C.4
Ricci, R.5
Ruffa, G.6
Lehmann, A.R.7
Stefanini, M.8
-
15
-
-
4444332513
-
Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage
-
de Waard H., de Wit J., Andressoo J.O., van Oostrom C.T., Riis B., Weimann A., Poulsen H.E., van Steeg H., Hoeijmakers J.H., and van der Horst G.T. Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage. Mol. Cell Biol. 24 (2004) 7941-7948
-
(2004)
Mol. Cell Biol.
, vol.24
, pp. 7941-7948
-
-
de Waard, H.1
de Wit, J.2
Andressoo, J.O.3
van Oostrom, C.T.4
Riis, B.5
Weimann, A.6
Poulsen, H.E.7
van Steeg, H.8
Hoeijmakers, J.H.9
van der Horst, G.T.10
-
16
-
-
0037413368
-
Cell type-specific hypersensitivity to oxidative damage in CSB and XPA mice
-
de Waard H., de Wit J., Gorgels T.G., van den Aardweg G., Andressoo J.O., Vermeij M., van Steeg H., Hoeijmakers J.H., and van der Horst G.T. Cell type-specific hypersensitivity to oxidative damage in CSB and XPA mice. DNA Repair (Amst) 2 (2003) 13-25
-
(2003)
DNA Repair (Amst)
, vol.2
, pp. 13-25
-
-
de Waard, H.1
de Wit, J.2
Gorgels, T.G.3
van den Aardweg, G.4
Andressoo, J.O.5
Vermeij, M.6
van Steeg, H.7
Hoeijmakers, J.H.8
van der Horst, G.T.9
-
17
-
-
0033105926
-
Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells
-
Dianov G., Bischoff C., Sunesen M., and Bohr V.A. Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells. Nucleic Acids Res. 27 (1999) 1365-1368
-
(1999)
Nucleic Acids Res.
, vol.27
, pp. 1365-1368
-
-
Dianov, G.1
Bischoff, C.2
Sunesen, M.3
Bohr, V.A.4
-
18
-
-
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
-
19
-
-
0029157378
-
Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions
-
Eisen J.A., Sweder K.S., and Hanawalt P.C. Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions. Nucleic Acids Res. 23 (1995) 2715-2723
-
(1995)
Nucleic Acids Res.
, vol.23
, pp. 2715-2723
-
-
Eisen, J.A.1
Sweder, K.S.2
Hanawalt, P.C.3
-
20
-
-
0344443371
-
Poly(ADP-ribosyl)ation accelerates DNA repair in a pathway dependent on Cockayne syndrome B protein
-
Flohr C., Burkle A., Radicella J.P., and Epe B. Poly(ADP-ribosyl)ation accelerates DNA repair in a pathway dependent on Cockayne syndrome B protein. Nucleic Acids Res. 31 (2003) 5332-5337
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 5332-5337
-
-
Flohr, C.1
Burkle, A.2
Radicella, J.P.3
Epe, B.4
-
21
-
-
38049178545
-
Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects
-
Fousteri M., and Mullenders L.H.F. Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects. Cell Res. 18 (2008) 73-84
-
(2008)
Cell Res.
, vol.18
, pp. 73-84
-
-
Fousteri, M.1
Mullenders, L.H.F.2
-
23
-
-
33846923284
-
Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndrome
-
Gorgels T.G., van der Pluijm I., Brandt R.M., Garinis G.A., van Steeg H., van den Aardweg G., Jansen G.H., Ruijter J.M., Bergen A.A., van Norren D., Hoeijmakers J.H., and van der Horst G.T. Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndrome. Mol. Cell Biol. 27 (2007) 1433-1441
-
(2007)
Mol. Cell Biol.
, vol.27
, pp. 1433-1441
-
-
Gorgels, T.G.1
van der Pluijm, I.2
Brandt, R.M.3
Garinis, G.A.4
van Steeg, H.5
van den Aardweg, G.6
Jansen, G.H.7
Ruijter, J.M.8
Bergen, A.A.9
van Norren, D.10
Hoeijmakers, J.H.11
van der Horst, G.T.12
-
24
-
-
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
-
25
-
-
0029088143
-
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH
-
Henning K.A., Li L., Iyer N., McDaniel L.D., Reagan M.S., Legerski R., Schultz R.A., Stefanini M., Lehmann A.R., Mayne L.V., and Friedberg E.C. 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 82 (1995) 555-564
-
(1995)
Cell
, vol.82
, pp. 555-564
-
-
Henning, K.A.1
Li, L.2
Iyer, N.3
McDaniel, L.D.4
Reagan, M.S.5
Legerski, R.6
Schultz, R.A.7
Stefanini, M.8
Lehmann, A.R.9
Mayne, L.V.10
Friedberg, E.C.11
-
26
-
-
0035796025
-
Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death
-
Herceg Z., and Wang Z.Q. Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death. Mutat. Res. 477 (2001) 97-110
-
(2001)
Mutat. Res.
, vol.477
, pp. 97-110
-
-
Herceg, Z.1
Wang, Z.Q.2
-
27
-
-
7444226812
-
Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome
-
Horibata K., Iwamoto Y., Kuraoka I., Jaspers N.G., Kurimasa A., Oshimura M., Ichihashi M., and Tanaka K. Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome. Proc. Natl. Acad. Sci. U.S.A. 101 (2004) 15410-15415
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 15410-15415
-
-
Horibata, K.1
Iwamoto, Y.2
Kuraoka, I.3
Jaspers, N.G.4
Kurimasa, A.5
Oshimura, M.6
Ichihashi, M.7
Tanaka, K.8
-
28
-
-
34548570178
-
Cockayne syndrome protein B interacts with and is phosphorylated by c-Abl tyrosine kinase
-
Imam S.Z., Indig F.E., Cheng W.H., Saxena S.P., Stevnsner T., Kufe D., and Bohr V.A. Cockayne syndrome protein B interacts with and is phosphorylated by c-Abl tyrosine kinase. Nucleic Acids Res. 35 (2007) 4941-4951
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. 4941-4951
-
-
Imam, S.Z.1
Indig, F.E.2
Cheng, W.H.3
Saxena, S.P.4
Stevnsner, T.5
Kufe, D.6
Bohr, V.A.7
-
29
-
-
33744912521
-
Mitochondrial and nuclear DNA-repair capacity of various brain regions in mouse is altered in an age-dependent manner
-
Imam S.Z., Karahalil B., Hogue B.A., Souza-Pinto N.C., and Bohr V.A. Mitochondrial and nuclear DNA-repair capacity of various brain regions in mouse is altered in an age-dependent manner. Neurobiol. Aging 27 (2006) 1129-1136
-
(2006)
Neurobiol. Aging
, vol.27
, pp. 1129-1136
-
-
Imam, S.Z.1
Karahalil, B.2
Hogue, B.A.3
Souza-Pinto, N.C.4
Bohr, V.A.5
-
30
-
-
0033026499
-
Neurodegeneration in hereditary nucleotide repair disorders
-
Itoh M., Hayashi M., Shioda K., Minagawa M., Isa F., Tamagawa K., Morimatsu Y., and Oda M. Neurodegeneration in hereditary nucleotide repair disorders. Brain Dev. 21 (1999) 326-333
-
(1999)
Brain Dev.
, vol.21
, pp. 326-333
-
-
Itoh, M.1
Hayashi, M.2
Shioda, K.3
Minagawa, M.4
Isa, F.5
Tamagawa, K.6
Morimatsu, Y.7
Oda, M.8
-
31
-
-
0038143225
-
Mammalian 8-oxoguanine DNA glycosylase 1 incises 8-oxoadenine opposite cytosine in nuclei and mitochondria, while a different glycosylase incises 8-oxoadenine opposite guanine in nuclei
-
Jensen A., Calvayrac G., Karahalil B., Bohr V.A., and Stevnsner T. Mammalian 8-oxoguanine DNA glycosylase 1 incises 8-oxoadenine opposite cytosine in nuclei and mitochondria, while a different glycosylase incises 8-oxoadenine opposite guanine in nuclei. J. Biol. Chem. 278 (2003) 19541-19548
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 19541-19548
-
-
Jensen, A.1
Calvayrac, G.2
Karahalil, B.3
Bohr, V.A.4
Stevnsner, T.5
-
32
-
-
2442504817
-
Single-stranded breaks in DNA but not oxidative DNA base damages block transcriptional elongation by RNA polymerase II in HeLa cell nuclear extracts
-
Kathe S.D., Shen G.P., and Wallace S.S. Single-stranded breaks in DNA but not oxidative DNA base damages block transcriptional elongation by RNA polymerase II in HeLa cell nuclear extracts. J. Biol. Chem. 279 (2004) 18511-18520
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 18511-18520
-
-
Kathe, S.D.1
Shen, G.P.2
Wallace, S.S.3
-
33
-
-
0037470158
-
Effects of endogenous DNA base lesions on transcription elongation by mammalian RNA polymerase II. Implications for transcription-coupled DNA repair and transcriptional mutagenesis
-
Kuraoka I., Endou M., Yamaguchi Y., Wada T., Handa H., and Tanaka K. Effects of endogenous DNA base lesions on transcription elongation by mammalian RNA polymerase II. Implications for transcription-coupled DNA repair and transcriptional mutagenesis. J. Biol. Chem. 278 (2003) 7294-7299
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 7294-7299
-
-
Kuraoka, I.1
Endou, M.2
Yamaguchi, Y.3
Wada, T.4
Handa, H.5
Tanaka, K.6
-
34
-
-
33644541793
-
Gene expression and DNA repair in progeroid syndromes and human aging
-
Kyng K.J., and Bohr V.A. Gene expression and DNA repair in progeroid syndromes and human aging. Ageing Res. Rev. 4 (2005) 579-602
-
(2005)
Ageing Res. Rev.
, vol.4
, pp. 579-602
-
-
Kyng, K.J.1
Bohr, V.A.2
-
35
-
-
0037468273
-
The transcriptional response after oxidative stress is defective in Cockayne syndrome group B cells
-
Kyng K.J., May A., Brosh Jr. R.M., Cheng W.H., Chen C., Becker K.G., and Bohr V.A. The transcriptional response after oxidative stress is defective in Cockayne syndrome group B cells. Oncogene 22 (2003) 1135-1149
-
(2003)
Oncogene
, vol.22
, pp. 1135-1149
-
-
Kyng, K.J.1
May, A.2
Brosh Jr., R.M.3
Cheng, W.H.4
Chen, C.5
Becker, K.G.6
Bohr, V.A.7
-
36
-
-
31444444611
-
Initiation of DNA repair mediated by a stalled RNA polymerase IIo
-
Laine J.P., and Egly J.M. Initiation of DNA repair mediated by a stalled RNA polymerase IIo. EMBO J. 2 (2006) 387-397
-
(2006)
EMBO J.
, vol.2
, pp. 387-397
-
-
Laine, J.P.1
Egly, J.M.2
-
37
-
-
33746666589
-
When transcription and repair meet: a complex system
-
Laine J.P., and Egly J.M. When transcription and repair meet: a complex system. Trends Genet. 8 (2006) 430
-
(2006)
Trends Genet.
, vol.8
, pp. 430
-
-
Laine, J.P.1
Egly, J.M.2
-
38
-
-
33846613301
-
Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice
-
Laposa R.R., Huang E.J., and Cleaver J.E. Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice. Proc. Natl. Acad. Sci. U.S.A. 104 (2007) 1389-1394
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 1389-1394
-
-
Laposa, R.R.1
Huang, E.J.2
Cleaver, J.E.3
-
39
-
-
4544243741
-
Transcription activities at 8-oxoG lesions in DNA
-
Larsen E., Kwon K., Coin F., Egly J.M., and Klungland A. Transcription activities at 8-oxoG lesions in DNA. DNA Repair (Amst) 3 (2004) 1457-1468
-
(2004)
DNA Repair (Amst)
, vol.3
, pp. 1457-1468
-
-
Larsen, E.1
Kwon, K.2
Coin, F.3
Egly, J.M.4
Klungland, A.5
-
40
-
-
39749184830
-
Deletion of 5′ sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome
-
Laugel V., Dalloz C., Stary A., Cormier-Daire V., Desguerre I., Renouil M., Fourmaintraux A., Velez-Cruz R., Egly J.M., Sarasin A., and Dollfus H. Deletion of 5′ sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome. Eur. J. Hum. Genet. 16 (2008) 320-327
-
(2008)
Eur. J. Hum. Genet.
, vol.16
, pp. 320-327
-
-
Laugel, V.1
Dalloz, C.2
Stary, A.3
Cormier-Daire, V.4
Desguerre, I.5
Renouil, M.6
Fourmaintraux, A.7
Velez-Cruz, R.8
Egly, J.M.9
Sarasin, A.10
Dollfus, H.11
-
41
-
-
0027379353
-
Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome
-
Leadon S.A., and Cooper P.K. Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome. Proc. Natl. Acad. Sci. U.S.A. 90 (1993) 10499-10503
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, pp. 10499-10503
-
-
Leadon, S.A.1
Cooper, P.K.2
-
42
-
-
0346101496
-
Cockayne syndrome group B cellular and biochemical functions
-
Licht C.L., Stevnsner T., and Bohr V.A. Cockayne syndrome group B cellular and biochemical functions. Am. J. Hum. Genet. 73 (2003) 1217-1239
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1217-1239
-
-
Licht, C.L.1
Stevnsner, T.2
Bohr, V.A.3
-
43
-
-
38149140159
-
A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer
-
Lin Z., Zhang X., Tuo J., Guo Y., Green B., Chan C.C., Tan W., Huang Y., Ling W., Kadlubar F.F., Lin D., and Ning B. A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer. Hum. Mutat. 29 (2008) 113-122
-
(2008)
Hum. Mutat.
, vol.29
, pp. 113-122
-
-
Lin, Z.1
Zhang, X.2
Tuo, J.3
Guo, Y.4
Green, B.5
Chan, C.C.6
Tan, W.7
Huang, Y.8
Ling, W.9
Kadlubar, F.F.10
Lin, D.11
Ning, B.12
-
44
-
-
33744467061
-
siRNA-mediated silencing of Cockayne Cyndrome group B gene potentiates radiation-induced apoptosis and antiproliferative effect in HeLa cells
-
Liu F., Yu Z.J., Sui J.L., Bai B., and Zhou P.K. siRNA-mediated silencing of Cockayne Cyndrome group B gene potentiates radiation-induced apoptosis and antiproliferative effect in HeLa cells. Chin. Med. J. (Engl) 119 (2006) 731-739
-
(2006)
Chin. Med. J. (Engl)
, vol.119
, pp. 731-739
-
-
Liu, F.1
Yu, Z.J.2
Sui, J.L.3
Bai, B.4
Zhou, P.K.5
-
45
-
-
0035137181
-
Disruption of the Cockayne syndrome B gene impairs spontaneous tumorigenesis in cancer-predisposed Ink4a/ARF knockout mice
-
Lu Y., Lian H., Sharma P., Schreiber-Agus N., Russell R.G., Chin L., van der Horst G.T., and Bregman D.B. Disruption of the Cockayne syndrome B gene impairs spontaneous tumorigenesis in cancer-predisposed Ink4a/ARF knockout mice. Mol. Cell Biol. 21 (2001) 1810-1818
-
(2001)
Mol. Cell Biol.
, vol.21
, pp. 1810-1818
-
-
Lu, Y.1
Lian, H.2
Sharma, P.3
Schreiber-Agus, N.4
Russell, R.G.5
Chin, L.6
van der Horst, G.T.7
Bregman, D.B.8
-
46
-
-
0031891880
-
Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome
-
Mallery D.L., Tanganelli B., Colella S., Steingrimsdottir H., van Gool A.J., Troelstra C., Stefanini M., and Lehmann A.R. Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome. Am. J. Hum. Genet. 62 (1998) 77-85
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 77-85
-
-
Mallery, D.L.1
Tanganelli, B.2
Colella, S.3
Steingrimsdottir, H.4
van Gool, A.J.5
Troelstra, C.6
Stefanini, M.7
Lehmann, A.R.8
-
47
-
-
0017840139
-
Genetic syndromes in man with potential relevance to the pathobiology of aging
-
Martin G.M. Genetic syndromes in man with potential relevance to the pathobiology of aging. Birth Defects Orig. Artic. Ser. 14 (1978) 5-39
-
(1978)
Birth Defects Orig. Artic. Ser.
, vol.14
, pp. 5-39
-
-
Martin, G.M.1
-
48
-
-
34548239142
-
ATP-dependent chromatin remodeling is required for base excision repair in conventional but not in variant H2A. Bbd nucleosomes
-
Menoni H., Gasparutto D., Hamiche A., Cadet J., Dimitrov S., Bouvet P., and Angelov D. ATP-dependent chromatin remodeling is required for base excision repair in conventional but not in variant H2A. Bbd nucleosomes. Mol. Cell Biol. 27 (2007) 5949-5956
-
(2007)
Mol. Cell Biol.
, vol.27
, pp. 5949-5956
-
-
Menoni, H.1
Gasparutto, D.2
Hamiche, A.3
Cadet, J.4
Dimitrov, S.5
Bouvet, P.6
Angelov, D.7
-
49
-
-
2642572541
-
Potassium bromate but not X-rays cause unexpectedly elevated levels of DNA breakage similar to those induced by ultraviolet light in Cockayne syndrome (CS-B) fibroblasts
-
Mosesso P., Penna S., Pepe G., Lorenti-Garcia C., and Palitti F. Potassium bromate but not X-rays cause unexpectedly elevated levels of DNA breakage similar to those induced by ultraviolet light in Cockayne syndrome (CS-B) fibroblasts. Cytogenet. Genome Res. 104 (2004) 178-181
-
(2004)
Cytogenet. Genome Res.
, vol.104
, pp. 178-181
-
-
Mosesso, P.1
Penna, S.2
Pepe, G.3
Lorenti-Garcia, C.4
Palitti, F.5
-
50
-
-
0037160513
-
Phenotypic consequences of mutations in the conserved motifs of the putative helicase domain of the human Cockayne syndrome group B gene
-
Muftuoglu M., Selzer R., Tuo J., Brosh Jr. R.M., and Bohr V.A. Phenotypic consequences of mutations in the conserved motifs of the putative helicase domain of the human Cockayne syndrome group B gene. Gene 283 (2002) 27-40
-
(2002)
Gene
, vol.283
, pp. 27-40
-
-
Muftuoglu, M.1
Selzer, R.2
Tuo, J.3
Brosh Jr., R.M.4
Bohr, V.A.5
-
51
-
-
31544432337
-
Cockayne syndrome group B protein has novel strand annealing and exchange activities
-
Muftuoglu M., Sharma S., Thorslund T., Stevnsner T., Soerensen M.M., Brosh Jr. R.M., and Bohr V.A. Cockayne syndrome group B protein has novel strand annealing and exchange activities. Nucleic Acids Res. 34 (2006) 295-304
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. 295-304
-
-
Muftuoglu, M.1
Sharma, S.2
Thorslund, T.3
Stevnsner, T.4
Soerensen, M.M.5
Brosh Jr., R.M.6
Bohr, V.A.7
-
52
-
-
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
-
53
-
-
33745460647
-
Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodelling
-
Newman J.C., Bailey A.D., and Weiner A.M. Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodelling. Proc. Natl. Acad. Sci. U.S.A. 103 (2006) 9613-9618
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 9613-9618
-
-
Newman, J.C.1
Bailey, A.D.2
Weiner, A.M.3
-
54
-
-
34147162118
-
ATP-dependent chromatin remodeling factors and DNA damage repair
-
Osley M.A., Tsukuda T., and Nickoloff J.A. ATP-dependent chromatin remodeling factors and DNA damage repair. Mutat. Res. 618 (2007) 65-80
-
(2007)
Mutat. Res.
, vol.618
, pp. 65-80
-
-
Osley, M.A.1
Tsukuda, T.2
Nickoloff, J.A.3
-
55
-
-
18744368449
-
A global DNA repair mechanism involving the Cockayne syndrome B (CSB) gene product can prevent the in vivo accumulation of endogenous oxidative DNA base damage
-
Osterod M., Larsen E., Le Page F., Hengstler J.G., Van Der Horst G.T., Boiteux S., Klungland A., and Epe B. A global DNA repair mechanism involving the Cockayne syndrome B (CSB) gene product can prevent the in vivo accumulation of endogenous oxidative DNA base damage. Oncogene 21 (2002) 8232-8239
-
(2002)
Oncogene
, vol.21
, pp. 8232-8239
-
-
Osterod, M.1
Larsen, E.2
Le Page, F.3
Hengstler, J.G.4
Van Der Horst, G.T.5
Boiteux, S.6
Klungland, A.7
Epe, B.8
-
56
-
-
34548461604
-
Transcription through 8-oxoguanine in DNA repair-proficient and Csb(-)/Ogg1(-) DNA repair-deficient mouse embryonic fibroblasts is dependent upon promoter strength and sequence context
-
Pastoriza-Gallego M., Armier J., and Sarasin A. Transcription through 8-oxoguanine in DNA repair-proficient and Csb(-)/Ogg1(-) DNA repair-deficient mouse embryonic fibroblasts is dependent upon promoter strength and sequence context. Mutagenesis 22 (2007) 343-351
-
(2007)
Mutagenesis
, vol.22
, pp. 343-351
-
-
Pastoriza-Gallego, M.1
Armier, J.2
Sarasin, A.3
-
57
-
-
0030986934
-
SWI2/SNF2 and related proteins: ATP-driven motors that disrupt protein-DNA interactions?
-
Pazin M.J., and Kadonaga J.T. SWI2/SNF2 and related proteins: ATP-driven motors that disrupt protein-DNA interactions?. Cell 88 (1997) 737-740
-
(1997)
Cell
, vol.88
, pp. 737-740
-
-
Pazin, M.J.1
Kadonaga, J.T.2
-
58
-
-
33646589650
-
Cockayne syndrome B protein regulates the transcriptional program after UV irradiation
-
Proietti-De-Santis L., Drane P., and Egly J.M. Cockayne syndrome B protein regulates the transcriptional program after UV irradiation. EMBO J. 25 (2006) 1915-1923
-
(2006)
EMBO J.
, vol.25
, pp. 1915-1923
-
-
Proietti-De-Santis, L.1
Drane, P.2
Egly, J.M.3
-
59
-
-
34248525265
-
Complementation of the oxidatively damaged DNA repair defect in Cockayne syndrome A and B cells by Escherichia coli formamidopyrimidine DNA glycosylase
-
Ropolo M., Degan P., Foresta M., D'Errico M., Lasiglie D., Dogliotti E., Casartelli G., Zupo S., Poggi A., and Frosina G. Complementation of the oxidatively damaged DNA repair defect in Cockayne syndrome A and B cells by Escherichia coli formamidopyrimidine DNA glycosylase. Free Radic. Biol. Med. 42 (2007) 1807-1817
-
(2007)
Free Radic. Biol. Med.
, vol.42
, pp. 1807-1817
-
-
Ropolo, M.1
Degan, P.2
Foresta, M.3
D'Errico, M.4
Lasiglie, D.5
Dogliotti, E.6
Casartelli, G.7
Zupo, S.8
Poggi, A.9
Frosina, G.10
-
60
-
-
0030804783
-
RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair
-
Selby C.P., Drapkin R., Reinberg D., and Sancar A. RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair. Nucleic Acids Res. 25 (1997) 787-793
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 787-793
-
-
Selby, C.P.1
Drapkin, R.2
Reinberg, D.3
Sancar, A.4
-
61
-
-
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
-
62
-
-
0031020871
-
Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II
-
Selby C.P., and Sancar A. Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II. J. Biol. Chem. 272 (1997) 1885-1890
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 1885-1890
-
-
Selby, C.P.1
Sancar, A.2
-
63
-
-
0037069933
-
Mitochondrial repair of 8-oxoguanine is deficient in Cockayne syndrome group B
-
Stevnsner T., Nyaga S., de Souza-Pinto N.C., van der Horst G.T., Gorgels T.G., Hogue B.A., Thorslund T., and Bohr V.A. Mitochondrial repair of 8-oxoguanine is deficient in Cockayne syndrome group B. Oncogene 21 (2002) 8675-8682
-
(2002)
Oncogene
, vol.21
, pp. 8675-8682
-
-
Stevnsner, T.1
Nyaga, S.2
de Souza-Pinto, N.C.3
van der Horst, G.T.4
Gorgels, T.G.5
Hogue, B.A.6
Thorslund, T.7
Bohr, V.A.8
-
64
-
-
0034663737
-
Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein
-
Sunesen M., Selzer R.R., Brosh Jr. R.M., Balajee A.S., Stevnsner T., and Bohr V.A. Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein. Nucleic Acids Res. 28 (2000) 3151-3159
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 3151-3159
-
-
Sunesen, M.1
Selzer, R.R.2
Brosh Jr., R.M.3
Balajee, A.S.4
Stevnsner, T.5
Bohr, V.A.6
-
65
-
-
0030667078
-
Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes
-
Tantin D., Kansal A., and Carey M. Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes. Mol. Cell Biol. 17 (1997) 6803-6814
-
(1997)
Mol. Cell Biol.
, vol.17
, pp. 6803-6814
-
-
Tantin, D.1
Kansal, A.2
Carey, M.3
-
66
-
-
23844483200
-
Cooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress
-
Thorslund T., von Kobbe C., Harrigan J.A., Indig F.E., Christiansen M., Stevnsner T., and Bohr V.A. Cooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress. Mol. Cell Biol. 25 (2005) 7625-7636
-
(2005)
Mol. Cell Biol.
, vol.25
, pp. 7625-7636
-
-
Thorslund, T.1
von Kobbe, C.2
Harrigan, J.A.3
Indig, F.E.4
Christiansen, M.5
Stevnsner, T.6
Bohr, V.A.7
-
67
-
-
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
-
68
-
-
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
-
70
-
-
0026604950
-
Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21
-
Troelstra C., Landsvater R.M., Wiegant J., van der Ploeg M., Viel G., Buys C.H., and Hoeijmakers J.H. Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21. Genomics 12 (1992) 745-749
-
(1992)
Genomics
, vol.12
, pp. 745-749
-
-
Troelstra, C.1
Landsvater, R.M.2
Wiegant, J.3
van der Ploeg, M.4
Viel, G.5
Buys, C.H.6
Hoeijmakers, J.H.7
-
71
-
-
0026465665
-
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes
-
Troelstra C., van Gool A., de Wit J., Vermeulen W., Bootsma D., and Hoeijmakers J.H. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell 71 (1992) 939-953
-
(1992)
Cell
, vol.71
, pp. 939-953
-
-
Troelstra, C.1
van Gool, A.2
de Wit, J.3
Vermeulen, W.4
Bootsma, D.5
Hoeijmakers, J.H.6
-
72
-
-
0036837549
-
Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein
-
Tuo J., Chen C., Zeng X., Christiansen M., and Bohr V.A. Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein. DNA Repair (Amst) 1 (2002) 913-927
-
(2002)
DNA Repair (Amst)
, vol.1
, pp. 913-927
-
-
Tuo, J.1
Chen, C.2
Zeng, X.3
Christiansen, M.4
Bohr, V.A.5
-
73
-
-
0141869885
-
Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress
-
Tuo J., Jaruga P., Rodriguez H., Bohr V.A., and Dizdaroglu M. Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress. FASEB J. 17 (2003) 668-674
-
(2003)
FASEB J.
, vol.17
, pp. 668-674
-
-
Tuo, J.1
Jaruga, P.2
Rodriguez, H.3
Bohr, V.A.4
Dizdaroglu, M.5
-
74
-
-
0037163123
-
The cockayne syndrome group B gene product is involved in cellular repair of 8-hydroxyadenine in DNA
-
Tuo J., Jaruga P., Rodriguez H., Dizdaroglu M., and Bohr V.A. The cockayne syndrome group B gene product is involved in cellular repair of 8-hydroxyadenine in DNA. J. Biol. Chem. 277 (2002) 30832-30837
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 30832-30837
-
-
Tuo, J.1
Jaruga, P.2
Rodriguez, H.3
Dizdaroglu, M.4
Bohr, V.A.5
-
75
-
-
0035824601
-
The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA
-
Tuo J., Muftuoglu M., Chen C., Jaruga P., Selzer R.R., Brosh Jr. R.M., Rodriguez H., Dizdaroglu M., and Bohr V.A. The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA. J. Biol. Chem. 276 (2001) 45772-45779
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 45772-45779
-
-
Tuo, J.1
Muftuoglu, M.2
Chen, C.3
Jaruga, P.4
Selzer, R.R.5
Brosh Jr., R.M.6
Rodriguez, H.7
Dizdaroglu, M.8
Bohr, V.A.9
-
76
-
-
0030916337
-
Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition
-
van der Horst G.T., van Steeg H., Berg R.J., van Gool A.J., de Wit J., Weeda G., Morreau H., Beems R.B., van Kreijl C.F., de Gruijl F.R., Bootsma D., and Hoeijmakers J.H. Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition. Cell 89 (1997) 425-435
-
(1997)
Cell
, vol.89
, pp. 425-435
-
-
van der Horst, G.T.1
van Steeg, H.2
Berg, R.J.3
van Gool, A.J.4
de Wit, J.5
Weeda, G.6
Morreau, H.7
Beems, R.B.8
van Kreijl, C.F.9
de Gruijl, F.R.10
Bootsma, D.11
Hoeijmakers, J.H.12
-
77
-
-
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
-
78
-
-
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
-
79
-
-
0028673969
-
Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome
-
Vermeulen W., van Vuuren A.J., Chipoulet M., Schaeffer L., Appeldoorn E., Weeda G., Jaspers N.G., Priestley A., Arlett C.F., Lehmann A.R., et al. Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome. Cold Spring Harb. Symp. Quant. Biol. 59 (1994) 317-329
-
(1994)
Cold Spring Harb. Symp. Quant. Biol.
, vol.59
, pp. 317-329
-
-
Vermeulen, W.1
van Vuuren, A.J.2
Chipoulet, M.3
Schaeffer, L.4
Appeldoorn, E.5
Weeda, G.6
Jaspers, N.G.7
Priestley, A.8
Arlett, C.F.9
Lehmann, A.R.10
-
80
-
-
0032516880
-
Effects of nonbulky DNA base damages on Escherichia coli RNA polymerase-mediated elongation and promoter clearance
-
Viswanathan A., and Doetsch P.W. Effects of nonbulky DNA base damages on Escherichia coli RNA polymerase-mediated elongation and promoter clearance. J. Biol. Chem. 273 (1998) 21276-21281
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 21276-21281
-
-
Viswanathan, A.1
Doetsch, P.W.2
-
81
-
-
0018328670
-
Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome
-
Wade M.H., and Chu E.H. Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome. Mutat. Res. 59 (1979) 49-60
-
(1979)
Mutat. Res.
, vol.59
, pp. 49-60
-
-
Wade, M.H.1
Chu, E.H.2
-
82
-
-
0031921725
-
Mitochondrial biology, degenerative diseases and aging
-
Wallace D.C., Brown M.D., Melov S., Graham B., and Lott M. Mitochondrial biology, degenerative diseases and aging. Biofactors 7 (1998) 187-190
-
(1998)
Biofactors
, vol.7
, pp. 187-190
-
-
Wallace, D.C.1
Brown, M.D.2
Melov, S.3
Graham, B.4
Lott, M.5
-
83
-
-
34547627642
-
Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediates
-
Wong H.K., Muftuoglu M., Beck G., Imam S.Z., Bohr V.A., and Wilson III D.M. Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediates. Nucleic Acids Res. 35 (2007) 4103-4113
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. 4103-4113
-
-
Wong, H.K.1
Muftuoglu, M.2
Beck, G.3
Imam, S.Z.4
Bohr, V.A.5
Wilson III, D.M.6
-
84
-
-
33845726097
-
Methylating agents and DNA repair responses: methylated bases and sources of strand breaks
-
Wyatt M.D., and Pittman D.L. Methylating agents and DNA repair responses: methylated bases and sources of strand breaks. Chem. Res. Toxicol. 19 (2006) 1580-1594
-
(2006)
Chem. Res. Toxicol.
, vol.19
, pp. 1580-1594
-
-
Wyatt, M.D.1
Pittman, D.L.2
-
85
-
-
34547743163
-
Activation of RNA polymerase I transcription by cockayne syndrome group B protein and histone methyltransferase G9a
-
Yuan X., Feng W., Imhof A., Grummt I., and Zhou Y. Activation of RNA polymerase I transcription by cockayne syndrome group B protein and histone methyltransferase G9a. Mol. Cell. 27 (2007) 585-595
-
(2007)
Mol. Cell.
, vol.27
, pp. 585-595
-
-
Yuan, X.1
Feng, W.2
Imhof, A.3
Grummt, I.4
Zhou, Y.5
|