-
1
-
-
0025746675
-
Purification of an ultraviolet-inducible, damage-specific DNA-binding protein from primate cells
-
M Abramic A.S Levine M Protic Purification of an ultraviolet-inducible, damage-specific DNA-binding protein from primate cells J. Biol. Chem. 266 1991 22493 22500
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 22493-22500
-
-
Abramic, M1
Levine, A.S2
Protic, M3
-
2
-
-
12644305856
-
Photocarcinogenesis correlates with immunosuppression in DNA-repair-defective individuals
-
C Ahrens M Grewe M Berneburg S Grether-Beck S Quilliet M Mezzina A Sarasin A.R Lehmann C.E Arlett J Krutmann Photocarcinogenesis correlates with immunosuppression in DNA-repair-defective individuals Proc. Nail. Acad. Sci. (USA) 94 1997 6837 6841
-
(1997)
, pp. 6837-6841
-
-
Ahrens, C1
Grewe, M2
Berneburg, M3
Grether-Beck, S4
Quilliet, S5
Mezzina, M6
Sarasin, A7
Lehmann, A.R8
Arlett, C.E9
Krutmann, J10
-
3
-
-
0016727657
-
The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet light irradiation
-
C.E Arlett S.A Harcourt B.C Broughton The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet light irradiation Mutation Res. 33 1975 341 346
-
(1975)
Mutation Res.
, vol.33
, pp. 341-346
-
-
Arlett, C.E1
Harcourt, S.A2
Broughton, B.C3
-
4
-
-
0028089652
-
The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage
-
H Asahina I Kuraoka M Shirakawa E.H Morita N Miura I Miyamoto E Ohtsuka Y Okada K Tanaka The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage Mutation Res. 315 1994 229 237
-
(1994)
Mutation Res.
, vol.315
, pp. 229-237
-
-
Asahina, H1
Kuraoka, I2
Shirakawa, M3
Morita, E.H4
Miura, N5
Miyamoto, I6
Ohtsuka, E7
Okada, Y8
Tanaka, K9
-
5
-
-
0030902253
-
Reduced RNA polymerase 11 transcription in intact and permeabilized Cockayne syndrome group 13 cells
-
A.S Balajee A May G.L Dianov E.C Friedberg V.A Bohr Reduced RNA polymerase 11 transcription in intact and permeabilized Cockayne syndrome group 13 cells Proc. Natl. Acad. Set. (USA) 94 1997 4306 4311
-
(1997)
, pp. 4306-4311
-
-
Balajee, A.S1
May, A2
Dianov, G.L3
Friedberg, E.C4
Bohr, V.A5
-
6
-
-
0032504244
-
Nucleosome unfolding during DNA repair in normal and xeroderma Pigmentosum (group C) human cells
-
B.K Baxter M.J Smerdon Nucleosome unfolding during DNA repair in normal and xeroderma Pigmentosum (group C) human cells J. Biol. Chem 273 1998 17517 17524
-
(1998)
J. Biol. Chem
, vol.273
, pp. 17517-17524
-
-
Baxter, B.K1
Smerdon, M.J2
-
7
-
-
0031920594
-
Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema
-
R.J Berg H.J Ruven A.T Sands E.R de Gruijl L.H Mullenders Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema J. Invest. Dermatol. 110 1998 405 409
-
(1998)
J. Invest. Dermatol.
, vol.110
, pp. 405-409
-
-
Berg, R.J1
Ruven, H.J2
Sands, A.T3
de Gruijl, E.R4
Mullenders, L.H5
-
8
-
-
0034650773
-
The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect
-
M Berneburg P.H Clingen S.A Harcourt J.E Lowe E.M Taylor M.H.L Green J Krutmann C.E Arlett A.R Lehmann The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect Cancer Res. 60 2000 431 438
-
(2000)
Cancer Res.
, vol.60
, pp. 431-438
-
-
Berneburg, M1
Clingen, P.H2
Harcourt, S.A3
Lowe, J.E4
Taylor, E.M5
Green, M.H.L6
Krutmann, J7
Arlett, C.E8
Lehmann, A.R9
-
9
-
-
0034161270
-
DNA damage causes uncontrolled DNA breakage in cells from patients with combined features of XP-D and Cockayne syndrome
-
M Berneburg J.E Lowe T Nardo S Araujo M Fousteri M.H.L Green J Krutmann R.D Wood M Stefanini A.R Lehmann DNA damage causes uncontrolled DNA breakage in cells from patients with combined features of XP-D and Cockayne syndrome EMBO J. 19 2000 1157 1162
-
(2000)
EMBO J.
, vol.19
, pp. 1157-1162
-
-
Berneburg, M1
Lowe, J.E2
Nardo, T3
Araujo, S4
Fousteri, M5
Green, M.H.L6
Krutmann, J7
Wood, R.D8
Stefanini, M9
Lehmann, A.R10
-
10
-
-
0033557139
-
Nucleotide excision repair 3′ endonuclease XPG stimulates the activity of base excision repairenzyme thymine glycol DNA glycosylase
-
T Bessho Nucleotide excision repair 3′ endonuclease XPG stimulates the activity of base excision repairenzyme thymine glycol DNA glycosylase Nucleic Acids Res. 27 1999 979 983
-
(1999)
Nucleic Acids Res.
, vol.27
, pp. 979-983
-
-
Bessho, T1
-
11
-
-
0029793038
-
Molecular cloning; mid characterization of Saccharomyces cerevisiae RAD28, the yeast homolog of the human Cockayne syndrome A (CSA) gene
-
P.K Bhatia R.A Verhage J Brouwer E.C Friedberg Molecular cloning; mid characterization of Saccharomyces cerevisiae RAD28 , the yeast homolog of the human Cockayne syndrome A (CSA) gene J. Bacteriol.. 178 1996 5977 5988
-
(1996)
J. Bacteriol..
, vol.178
, pp. 5977-5988
-
-
Bhatia, P.K1
Verhage, R.A2
Brouwer, J3
Friedberg, E.C4
-
12
-
-
0027174179
-
Engagement with transcription
-
D Bootsma J.H.J Hoeijmakers Engagement with transcription Nature 363 1993 114 115
-
(1993)
Nature
, vol.363
, pp. 114-115
-
-
Bootsma, D1
Hoeijmakers, J.H.J2
-
13
-
-
0003095801
-
Nucleotide excision repair syndromes: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy
-
D Bootsma K.H Kraemer J.E Cleaver J.H.J Hoeijmakers Nucleotide excision repair syndromes: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy B Vogelstein K.W Kinzler The Genetic Basis of Human Cancer 1998 McGraw-Hill New York 245 274
-
(1998)
, pp. 245-274
-
-
Bootsma, D1
Kraemer, K.H2
Cleaver, J.E3
Hoeijmakers, J.H.J4
-
14
-
-
0032231836
-
Analysis Of mutations in the XPD gene in Italian patients with trichothiodystrophy: Site of mutation correlates with repair deficiency but gene dosage appears to determine clinical severity
-
E Botta T Nardo B.C Broughton S Marinoni A.R Lehmann M Stefanini Analysis Of mutations in the XPD gene in Italian patients with trichothiodystrophy: Site of mutation correlates with repair deficiency but gene dosage appears to determine clinical severity Am. J. Hum. Genet. 63 1998 190 196
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 190-196
-
-
Botta, E1
Nardo, T2
Broughton, B.C3
Marinoni, S4
Lehmann, A.R5
Stefanini, M6
-
15
-
-
0030814353
-
Sunlight and the onset of skin cancer
-
D.E Brash Sunlight and the onset of skin cancer Trends Genet. 13 1997 410 414
-
(1997)
Trends Genet.
, vol.13
, pp. 410-414
-
-
Brash, D.E1
-
16
-
-
0029859295
-
UV-induced ubiquitination of RNA polymerise II: A novel modification deficient in Cockayne syndrome cells
-
D.B Bregman R Halaban A.J van Gool K.A Henning E.C Friedberg S.L Warren UV-induced ubiquitination of RNA polymerise II: A novel modification deficient in Cockayne syndrome cells Proc. Natl. Acad. Sci. (USA) 93 1996 11586 11590
-
(1996)
, pp. 11586-11590
-
-
Bregman, D.B1
Halaban, R2
van Gool, A.J3
Henning, K.A4
Friedberg, E.C5
Warren, S.L6
-
17
-
-
0032501178
-
UV-induced mutations and skin cancer: I low important is the link?
-
B.A Bridges UV-induced mutations and skin cancer: I low important is the link? Mutation Res. 422 1998 23 30
-
(1998)
Mutation Res.
, vol.422
, pp. 23-30
-
-
Bridges, B.A1
-
18
-
-
0033534763
-
Extended X-ray absorption fine structure evidence for s single metal binding domain in Xenopus laevis nucleotide excision repair protein XPA
-
G.W Buchko L.M Iakoucheva M.A Kennedy E.J Ackerman N.J Hess Extended X-ray absorption fine structure evidence for s single metal binding domain in Xenopus laevis nucleotide excision repair protein XPA Biochem. Biophys. Res. Commun. 254 1999 109 113
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.254
, pp. 109-113
-
-
Buchko, G.W1
Iakoucheva, L.M2
Kennedy, M.A3
Ackerman, E.J4
Hess, N.J5
-
19
-
-
0034027382
-
Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein mid transcript levels
-
F Chavanne B.C Broughton D Pietra T Nardo A Browitt A.R Lehmann M Stefanini Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein mid transcript levels Cancer Res. 60 2000 1974 1982
-
(2000)
Cancer Res.
, vol.60
, pp. 1974-1982
-
-
Chavanne, F1
Broughton, B.C2
Pietra, D3
Nardo, T4
Browitt, A5
Lehmann, A.R6
Stefanini, M7
-
20
-
-
0030480945
-
Synergistic interactions between XPC and p53 mutations in double-mutant mice: Neural tube abnormalities mid accelerated UV radiation-induced skin cancer
-
D.L Cheo L.B Meira R.E Hammer D.K Burns A.T Doughty E.C Friedberg Synergistic interactions between XPC and p53 mutations in double-mutant mice: Neural tube abnormalities mid accelerated UV radiation-induced skin cancer Curr. Biol. 6 1996 1691 1694
-
(1996)
Curr. Biol.
, vol.6
, pp. 1691-1694
-
-
Cheo, D.L1
Meira, L.B2
Hammer, R.E3
Burns, D.K4
Doughty, A.T5
Friedberg, E.C6
-
21
-
-
0031049126
-
Characterization of defective nucleotide excision repair in XPC mutant mice
-
D.L Cheo H.J Ruven L.B Meira R.E Hammer D.K Burns N.J Tappe A.A van Zeeland L.H Mullenders E.C Friedberg Characterization of defective nucleotide excision repair in XPC mutant mice Mutat. Res. 374 1997 1 9
-
(1997)
Mutat. Res.
, vol.374
, pp. 1-9
-
-
Cheo, D.L1
Ruven, H.J2
Meira, L.B3
Hammer, R.E4
Burns, D.K5
Tappe, N.J6
van Zeeland, A.A7
Mullenders, L.H8
Friedberg, E.C9
-
22
-
-
0023803543
-
Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA
-
G Chu E Chang Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA Science 242 1988 564 567
-
(1988)
Science
, vol.242
, pp. 564-567
-
-
Chu, G1
Chang, E2
-
23
-
-
0032993689
-
A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, mid trichothiodystrophy
-
J.E Cleaver L.H Thompson A.S Richardson J.C States A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, mid trichothiodystrophy Hum. Mutat. 14 1999 9 22
-
(1999)
Hum. Mutat.
, vol.14
, pp. 9-22
-
-
Cleaver, J.E1
Thompson, L.H2
Richardson, A.S3
States, J.C4
-
24
-
-
0028983217
-
XPG protein has a structure-specific endonuclease activity
-
K.G Cloud B Shen G.E Strniste M.S Park XPG protein has a structure-specific endonuclease activity Mutat. Res. 347 1995 55 60
-
(1995)
Mutat. Res.
, vol.347
, pp. 55-60
-
-
Cloud, K.G1
Shen, B2
Strniste, G.E3
Park, M.S4
-
25
-
-
0033104514
-
Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH
-
F Coin E Bergmann A Tremeau-Bravard J.M Egly Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH EMBO. J. 18 1999 1357 1366
-
(1999)
EMBO. J.
, vol.18
, pp. 1357-1366
-
-
Coin, F1
Bergmann, E2
Tremeau-Bravard, A3
Egly, J.M4
-
26
-
-
0031025997
-
Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G
-
P.K Cooper T Nouspikel S.G Clarkson S.A Leaadon Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G Science 275 1997 990 993
-
(1997)
Science
, vol.275
, pp. 990-993
-
-
Cooper, P.K1
Nouspikel, T2
Clarkson, S.G3
Leaadon, S.A4
-
27
-
-
0030925436
-
Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis
-
M Coreiro-Stone L.S Zaritskaya L.K Price W.K Kaufmann Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis J. Biol. Chem. 272 1997 13945 13954
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 13945-13954
-
-
Coreiro-Stone, M1
Zaritskaya, L.S2
Price, L.K3
Kaufmann, W.K4
-
28
-
-
0033020150
-
Impaired translesion synthesis in xeroderma pigmentosum extracts
-
A.M Cordonnier A.R Lehmann R.P.P Fuchs Impaired translesion synthesis in xeroderma pigmentosum extracts Mol. Cell. Biol. 19 1999 2206 2211
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 2206-2211
-
-
Cordonnier, A.M1
Lehmann, A.R2
Fuchs, R.P.P3
-
29
-
-
0032085182
-
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy
-
J de Boer J de Wit H van Steeg R.J.W Berg H Morreau P Visser A.R Lehmann M Duran J.H.J Hoeijmakers G Weeda A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy Mol. Cell 1 1998 981 990
-
(1998)
Mol. Cell
, vol.1
, pp. 981-990
-
-
de Boer, J1
de Wit, J2
van Steeg, H3
Berg, R.J.W4
Morreau, H5
Visser, P6
Lehmann, A.R7
Duran, M8
Hoeijmakers, J.H.J9
Weeda, G10
-
30
-
-
0033565649
-
Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition
-
J de Boer H van Steeg R.J Berg J Garssen J de Wit C.T van Oostrum R.B Beems G.T van der Horst C.E van Kreijl E.R de Gruijl D Bootsma J.H Hoeijmakers G Weeda Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition Cancer Res. 59 1999 3489 3494
-
(1999)
Cancer Res.
, vol.59
, pp. 3489-3494
-
-
de Boer, J1
van Steeg, H2
Berg, R.J3
Garssen, J4
de Wit, J5
van Oostrum, C.T6
Beems, R.B7
van der Horst, G.T8
van Kreijl, C.E9
de Gruijl, E.R10
Bootsma, D11
Hoeijmakers, J.H12
Weeda, G13
-
32
-
-
0029083409
-
Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XFA
-
A de Vries C.T van Oostrom E.M Hofhuis P.M Dortant R.J Berg F.R de Gruijl P.W Wester C.F van Kreijl P.J Capel H van Steeg S.J Verbeck Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XFA Nature 377 1995 169 173
-
(1995)
Nature
, vol.377
, pp. 169-173
-
-
de Vries, A1
van Oostrom, C.T2
Hofhuis, E.M3
Dortant, P.M4
Berg, R.J5
de Gruijl, F.R6
Wester, P.W7
van Kreijl, C.F8
Capel, P.J9
van Steeg, H10
Verbeck, S.J11
-
33
-
-
0028360068
-
Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II
-
R Drapkin J.T Reardon A Ansari J.C Huang L Zawet K Ahn A Sancar D Reinherg Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II Nature 368 1994 769 772
-
(1994)
Nature
, vol.368
, pp. 769-772
-
-
Drapkin, R1
Reardon, J.T2
Ansari, A3
Huang, J.C4
Zawet, L5
Ahn, K6
Sancar, A7
Reinherg, D8
-
34
-
-
15844367100
-
Human cyclin-dependent kinase-activating kinase exists in three distinct complexes
-
R Drapkin G LeRoy H Cho S Akoulitchev D Reinberg Human cyclin-dependent kinase-activating kinase exists in three distinct complexes Proc. Natl. Acad. Sci. (USA) 93 1996 6488 6493
-
(1996)
, pp. 6488-6493
-
-
Drapkin, R1
LeRoy, G2
Cho, H3
Akoulitchev, S4
Reinberg, D5
-
35
-
-
0027379357
-
Specific UV-induced mutation spectrum in the p53 gene of skin rumors from DNA repair deficient xeroderma pigmentosum patients
-
N Dumaz C Drougar A Sarasin L Daya-Grosjean Specific UV-induced mutation spectrum in the p53 gene of skin rumors from DNA repair deficient xeroderma pigmentosum patients Proc. Natl. Acad. Sci. (USA) 90 1993 10529 10533
-
(1993)
, pp. 10529-10533
-
-
Dumaz, N1
Drougar, C2
Sarasin, A3
Daya-Grosjean, L4
-
36
-
-
0031426286
-
Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes
-
N Dumaz A Duthu J.C Ehrhart C Drougard E Appella C.W Anderson P May A Sarasin L Daya-Grosjean Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes Mol. Carcinog. 20 1997 340 347
-
(1997)
Mol. Carcinog.
, vol.20
, pp. 340-347
-
-
Dumaz, N1
Duthu, A2
Ehrhart, J.C3
Drougard, C4
Appella, E5
Anderson, C.W6
May, P7
Sarasin, A8
Daya-Grosjean, L9
-
37
-
-
0032992729
-
Polymorphisms in the DNA repair gene XPD: Correlations with risk and age at onset of basal cell carcinoma
-
M Dybdahl U Vogel G Frentz H Wallin B.A Nexo Polymorphisms in the DNA repair gene XPD: Correlations with risk and age at onset of basal cell carcinoma Cancer Epidemiol. Biomarkers Prev. 8 1999 77 81
-
(1999)
Cancer Epidemiol. Biomarkers Prev.
, vol.8
, pp. 77-81
-
-
Dybdahl, M1
Vogel, U2
Frentz, G3
Wallin, H4
Nexo, B.A5
-
38
-
-
0029157378
-
Evolution of the SNF2 family of proteins—Subfamilies with distinct sequences and functions
-
J.A Eisen K.S Sweder P.C Hanawalt 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.A1
Sweder, K.S2
Hanawalt, P.C3
-
39
-
-
0032474431
-
Bypass of a site-specific cis-Syn thymine dieter in an SV40 vector during in vitro replication by HeLa and XPV cell-free extracts
-
I Ensch-Simon P.M Burgers J.S Taylor Bypass of a site-specific cis-Syn thymine dieter in an SV40 vector during in vitro replication by HeLa and XPV cell-free extracts Biochemistry 37 1998 8218 8226
-
(1998)
Biochemistry
, vol.37
, pp. 8218-8226
-
-
Ensch-Simon, I1
Burgers, P.M2
Taylor, J.S3
-
40
-
-
0031013308
-
Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein
-
E Evans J Fellows A Coffer R.D Wood Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein EMBO J. 16 1997 625 638
-
(1997)
EMBO J.
, vol.16
, pp. 625-638
-
-
Evans, E1
Fellows, J2
Coffer, A3
Wood, R.D4
-
41
-
-
0030732132
-
Mechanism of open complex and dual incision formation by human nucleotide excision repair factors
-
E Evans J.G Moggs J.R Hwang J.M Egly R.D Wood Mechanism of open complex and dual incision formation by human nucleotide excision repair factors EMBO J. 16 1997 6559 6573
-
(1997)
EMBO J.
, vol.16
, pp. 6559-6573
-
-
Evans, E1
Moggs, J.G2
Hwang, J.R3
Egly, J.M4
Wood, R.D5
-
42
-
-
0027760994
-
Dual roles of a multiprotein complex from S. cevisiae in transcription and DNA repair
-
W.J Feaver J.Q Svejstrup L Bardwell A.J Bardwell S Buratowski K.D Gulyas T.F Donahue E.C Friedberg R.D Kornberg Dual roles of a multiprotein complex from S. cevisiae in transcription and DNA repair Cell 75 1993 1379 1387
-
(1993)
Cell
, vol.75
, pp. 1379-1387
-
-
Feaver, W.J1
Svejstrup, J.Q2
Bardwell, L3
Bardwell, A.J4
Buratowski, S5
Gulyas, K.D6
Donahue, T.F7
Friedberg, E.C8
Kornberg, R.D9
-
43
-
-
0026498944
-
Removal of nonhomologous DNA ends in double-strand break recombination: The role of the yeast ultraviolet repair gene RAD1
-
J Fishman-Lobell J.E Haber Removal of nonhomologous DNA ends in double-strand break recombination: The role of the yeast ultraviolet repair gene RAD1 Science 258 1992 480 484
-
(1992)
Science
, vol.258
, pp. 480-484
-
-
Fishman-Lobell, J1
Haber, J.E2
-
44
-
-
0029850732
-
Cockayne syndrome — a primary defect in DNA repair, transcription, both or neither?
-
E.C Friedberg Cockayne syndrome — a primary defect in DNA repair, transcription, both or neither? BioEssays 18 1996 731 738
-
(1996)
BioEssays
, vol.18
, pp. 731-738
-
-
Friedberg, E.C1
-
46
-
-
0027194332
-
Impaired interferon Production and natural killer cell activation in patients with the skin cancer prone disorder, xeroderma pigmentosum
-
A.A Gaspari T.A Fleisher K.H Kraemer Impaired interferon Production and natural killer cell activation in patients with the skin cancer prone disorder, xeroderma pigmentosum J. Clin. Invest. 92 1993 1135 1141
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 1135-1141
-
-
Gaspari, A.A1
Fleisher, T.A2
Kraemer, K.H3
-
47
-
-
0032188764
-
p53 Mutations in skin and internal tumors of xeroderma pigmentosum patients belonging to the complementation group C
-
G Giglia N Dumaz C Drougard M.E Avril L Daya-Grosjean A Sarasin p53 Mutations in skin and internal tumors of xeroderma pigmentosum patients belonging to the complementation group C Cancer Res. 58 1998 4402 4409
-
(1998)
Cancer Res.
, vol.58
, pp. 4402-4409
-
-
Giglia, G1
Dumaz, N2
Drougard, C3
Avril, M.E4
Daya-Grosjean, L5
Sarasin, A6
-
48
-
-
0028232284
-
Rad25 is a DNA helicase required for RNA repair and RNA-polymerase-II transcription
-
S.N Guzder P Sung V Bailly L Prakash S Prakash Rad25 is a DNA helicase required for RNA repair and RNA-polymerase-II transcription Nature 369 1994 578 581
-
(1994)
Nature
, vol.369
, pp. 578-581
-
-
Guzder, S.N1
Sung, P2
Bailly, V3
Prakash, L4
Prakash, S5
-
49
-
-
0032980573
-
Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene
-
Y.N Harada N Shiomi M Koike M Ikawa M Okabe S Hirota Y Kitamura M Kitagawa T Matsunaga 0 Nikaido T Shiomi Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene Mol. Cell. Biol. 19 1999 2366 2372
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 2366-2372
-
-
Harada, Y.N1
Shiomi, N2
Koike, M3
Ikawa, M4
Okabe, M5
Hirota, S6
Kitamura, Y7
Kitagawa, M8
Matsunaga, T9
Nikaido, 010
Shiomi, T11
-
50
-
-
0029088143
-
The Cockayne-syndrome group-A gene encodes a WD repeat protein that interact., with CSB protein and a subunit of RNA-polymerase-II TFIIH
-
K.A Henning L Li N Iyer L.D McDaniel M.S Reagan R Legerski R.A Schultz M Stefanini A.R Lehmann L.V Mayne E.C Friedberg The Cockayne-syndrome group-A gene encodes a WD repeat protein that interact., 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.A1
Li, L2
Iyer, N3
McDaniel, L.D4
Reagan, M.S5
Legerski, R6
Schultz, R.A7
Stefanini, M8
Lehmann, A.R9
Mayne, L.V10
Friedberg, E.C11
-
51
-
-
0031693584
-
Human nucleotide excision repair protein XPA: Extended X-ray absorption fine-structure evidence for a metal-binding domain
-
N.J Hess G.W Buchko S.D Conradson F.J Espinosa S Ni B.D Thrall M.A Kennedy Human nucleotide excision repair protein XPA: Extended X-ray absorption fine-structure evidence for a metal-binding domain Protein Sci. 7 1998 1970 1975
-
(1998)
Protein Sci.
, vol.7
, pp. 1970-1975
-
-
Hess, N.J1
Buchko, G.W2
Conradson, S.D3
Espinosa, F.J4
Ni, S5
Thrall, B.D6
Kennedy, M.A7
-
53
-
-
0032520894
-
Low catalase activity- in xeroderma pigmentosum fibroblasts and SV40-transformed human cell lines is directly related to decreased intracellular levels of the cofactor, NADPH
-
E Hoffschir L Daya-Grosjean P.X Petit S Nocentini B Dutrillaux A Sarasin M Vuillaume Low catalase activity- in xeroderma pigmentosum fibroblasts and SV40-transformed human cell lines is directly related to decreased intracellular levels of the cofactor, NADPH Free Radic. Biol. Med. 24 1998 809 816
-
(1998)
Free Radic. Biol. Med.
, vol.24
, pp. 809-816
-
-
Hoffschir, E1
Daya-Grosjean, L2
Petit, P.X3
Nocentini, S4
Dutrillaux, B5
Sarasin, A6
Vuillaume, M7
-
54
-
-
0001232093
-
p48 Activate, a UV-damaged DNA-binding factor and is detective in xeroderma pigmentosum group E cells that lack hireling activity
-
B.J Hwang S Toering U Francke G Chu p48 Activate, a UV-damaged DNA-binding factor and is detective in xeroderma pigmentosum group E cells that lack hireling activity Mol. Cell. Biol. 18 1998 4391 4399
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 4391-4399
-
-
Hwang, B.J1
Toering, S2
Francke, U3
Chu, G4
-
55
-
-
0000516293
-
Expression of the p48 xeroderma pigmentosum gene is p53-dependent mid is involved in global genomic repair
-
B.J Hwang J.M Ford P.C Hanawalt G Chu Expression of the p48 xeroderma pigmentosum gene is p53-dependent mid is involved in global genomic repair Proc. Natl. Acad. Sci. (USA) 96 1999 424 428
-
(1999)
, pp. 424-428
-
-
Hwang, B.J1
Ford, J.M2
Hanawalt, P.C3
Chu, G4
-
56
-
-
0025276699
-
Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
-
P.H Itin M.R Pittelkow Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias J. Am. Acid. Dermatol. 20 1990 705 717
-
(1990)
J. Am. Acid. Dermatol.
, vol.20
, pp. 705-717
-
-
Itin, P.H1
Pittelkow, M.R2
-
57
-
-
0030025947
-
Interactions involving the human RNA polymerise II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein
-
N Iyer M.S Reagan K.J Wu B Canagarajah E.C: Friedberg Interactions involving the human RNA polymerise II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein Biochemistry 35 1996 2157 2167
-
(1996)
Biochemistry
, vol.35
, pp. 2157-2167
-
-
Iyer, N1
Reagan, M.S2
Wu, K.J3
Canagarajah, B4
Friedberg, E.C:5
-
58
-
-
0033538470
-
hRAD30 Mutations in the variant form of xeroderma pigmentosum
-
R.E Johnson C.M Kondratick S Prakash L Prakash hRAD30 Mutations in the variant form of xeroderma pigmentosum Science 285 1999 263 265
-
(1999)
Science
, vol.285
, pp. 263-265
-
-
Johnson, R.E1
Kondratick, C.M2
Prakash, S3
Prakash, L4
-
59
-
-
0033548231
-
Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Polη
-
R.E Johnson S Prakash L Prakash Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Polη Science 283 1999 1001 1004
-
(1999)
Science
, vol.283
, pp. 1001-1004
-
-
Johnson, R.E1
Prakash, S2
Prakash, L3
-
60
-
-
0027483739
-
Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA
-
C.J Jones R.D Wood Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA Biochemistry 32 1993 12096 12104
-
(1993)
Biochemistry
, vol.32
, pp. 12096-12104
-
-
Jones, C.J1
Wood, R.D2
-
61
-
-
0026808227
-
Biochemical heterogeneity in xeroderma pigmentosum complementation group E
-
S Keeney H Wein S Linn Biochemical heterogeneity in xeroderma pigmentosum complementation group E Mutat. Res. 273 1992 49 56
-
(1992)
Mutat. Res.
, vol.273
, pp. 49-56
-
-
Keeney, S1
Wein, H2
Linn, S3
-
62
-
-
0027442869
-
Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum F
-
S Keeney G.J Chang S Linn Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum F J. Biol. Client. 268 1993 21293 21300
-
(1993)
J. Biol. Client.
, vol.268
, pp. 21293-21300
-
-
Keeney, S1
Chang, G.J2
Linn, S3
-
63
-
-
0032973211
-
Base excision repair of oxidative DNA damage activated by XPG protein
-
A Klungland M Hoss D Gunz A Constantinou S.G Clarkson P.W Doetsch P.H Bolton R.D Wood T Lindahl 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, A1
Hoss, M2
Gunz, D3
Constantinou, A4
Clarkson, S.G5
Doetsch, P.W6
Bolton, P.H7
Wood, R.D8
Lindahl, T9
-
64
-
-
0021282448
-
DNA repair protects against cutaneous and internal neoplasia: Evidence from xeroderma pigmentosum
-
K.H Kraemer M.M Lee K Scotto 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.H1
Lee, M.M2
Scotto, K3
-
65
-
-
0023130695
-
Xeroderma pigmentosum. Cutaneous, ocular and neurologic abnormalities in 830 published cases
-
K.H Kraemer M.M Lee J Scotto Xeroderma pigmentosum. Cutaneous, ocular and neurologic abnormalities in 830 published cases Arch. Dermatol. 123 1987 241 250
-
(1987)
Arch. Dermatol.
, vol.123
, pp. 241-250
-
-
Kraemer, K.H1
Lee, M.M2
Scotto, J3
-
66
-
-
0030443024
-
DNA polymerase zeta and the control of DNA damage induced mutagenesis in eukaryotes
-
C.W Lawrence D.C Hinkle DNA polymerase zeta and the control of DNA damage induced mutagenesis in eukaryotes Cancer Surv. 28 1996 21 31
-
(1996)
Cancer Surv.
, vol.28
, pp. 21-31
-
-
Lawrence, C.W1
Hinkle, D.C2
-
67
-
-
0034646516
-
Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome
-
F Le Page E.E Kwoh A Avrutskaya A Gentil S.A Leadon A Sarasin P.K Cooper Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome Cell 101 2000 159 171
-
(2000)
Cell
, vol.101
, pp. 159-171
-
-
Le Page, F1
Kwoh, E.E2
Avrutskaya, A3
Gentil, A4
Leadon, S.A5
Sarasin, A6
Cooper, P.K7
-
68
-
-
0027379353
-
Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome
-
S.A Leadon P.K Cooper 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. (USA) 90 1993 10499 10503
-
(1993)
, pp. 10499-10503
-
-
Leadon, S.A1
Cooper, P.K2
-
69
-
-
0023555206
-
Cockayne's syndrome and trichothiodystrophy: Defective repair without cancer
-
A.R Lehmann Cockayne's syndrome and trichothiodystrophy: Defective repair without cancer Cancer 7 1987 82 103
-
(1987)
Cancer
, vol.7
, pp. 82-103
-
-
Lehmann, A.R1
-
70
-
-
0028810356
-
Nucleotide excision repair and the link with transcription
-
A.R Lehmann Nucleotide excision repair and the link with transcription Trends Biochem. Sci. 20 1995 402 405
-
(1995)
Trends Biochem. Sci.
, vol.20
, pp. 402-405
-
-
Lehmann, A.R1
-
71
-
-
0032006182
-
Dual functions of DNA repair genes: Molecular, cellular, and clinical implications
-
A.R Lehmann Dual functions of DNA repair genes: Molecular, cellular, and clinical implications BioEssays 20 1998 146 155
-
(1998)
BioEssays
, vol.20
, pp. 146-155
-
-
Lehmann, A.R1
-
72
-
-
0000242262
-
Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation
-
A.R Lehmann S Kirk-Bell C.E Arlett M.C Paterson P.H.M Lohman E.A de Weerd-Kastetein D Bootsma Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation Proc. Natl. Acad. Sci. (USA) 72 1975 219 223
-
(1975)
, pp. 219-223
-
-
Lehmann, A.R1
Kirk-Bell, S2
Arlett, C.E3
Paterson, M.C4
Lohman, P.H.M5
de Weerd-Kastetein, E.A6
Bootsma, D7
-
73
-
-
0023763193
-
Trichothiodystrophy, a human DNA repair disorder with heterogeneity m the cellular response to ultraviolet light
-
A.R Lehmann C.F Arlett B.C Broughton S.A Harcourt H Steingrimsdottir M Stefanini A.M.R Taylor A.T Natarajan S Green M.D King R.M MacKie J.B.P Stephenson J.L Tolmie Trichothiodystrophy, a human DNA repair disorder with heterogeneity m the cellular response to ultraviolet light Cancer Res. 48 1988 6090 6096
-
(1988)
Cancer Res.
, vol.48
, pp. 6090-6096
-
-
Lehmann, A.R1
Arlett, C.F2
Broughton, B.C3
Harcourt, S.A4
Steingrimsdottir, H5
Stefanini, M6
Taylor, A.M.R7
Natarajan, A.T8
Green, S9
King, M.D10
MacKie, R.M11
Stephenson, J.B.P12
Tolmie, J.L13
-
74
-
-
0027370825
-
Characterization of molecular defects in xeroderma pigmentosum group C
-
L Li E.S Bales C.A Peterson R.J Legerski Characterization of molecular defects in xeroderma pigmentosum group C Nature Genet. 5 1993 413 417
-
(1993)
Nature Genet.
, vol.5
, pp. 413-417
-
-
Li, L1
Bales, E.S2
Peterson, C.A3
Legerski, R.J4
-
75
-
-
0032516786
-
Interactions of the transcription/DNA repair factor TFIIH and XP repair proteins with DNA lesions in a cell-free repair assay
-
R.Y Li P Calsou C.J Jones B Salles Interactions of the transcription/DNA repair factor TFIIH and XP repair proteins with DNA lesions in a cell-free repair assay J. Mol. Biol. 281 1998 211 218
-
(1998)
J. Mol. Biol.
, vol.281
, pp. 211-218
-
-
Li, R.Y1
Calsou, P2
Jones, C.J3
Salles, B4
-
76
-
-
0029785723
-
Blockage of RNA polymerase as a possible trigger for u.v. light-induced apoptosis
-
M Ljungman F Zhang Blockage of RNA polymerase as a possible trigger for u.v. light-induced apoptosis Oncogene 13 1996 823 831
-
(1996)
Oncogene
, vol.13
, pp. 823-831
-
-
Ljungman, M1
Zhang, F2
-
77
-
-
0028034048
-
The xeroderma pigmentosum group B protein ERCC3 produced in the baculovirus system exhibits DNA helicase activity
-
L Ma E.D Siemssen M Noteborn A.J Van der Eb The xeroderma pigmentosum group B protein ERCC3 produced in the baculovirus system exhibits DNA helicase activity Nucleic. Acids Res. 22 1994 4095 4102
-
(1994)
Nucleic. Acids Res.
, vol.22
, pp. 4095-4102
-
-
Ma, L1
Siemssen, E.D2
Noteborn, M3
Van der Eb, A.J4
-
78
-
-
0017309743
-
Frequency of ultraviolet light-induced mutations is higher in xeroderma pigmentosum variant cell, than in normal human cells
-
V.M Maher L.M Ouellette R.D Curren J.J McCormick Frequency of ultraviolet light-induced mutations is higher in xeroderma pigmentosum variant cell, than in normal human cells Nature 261 1976 593 595
-
(1976)
Nature
, vol.261
, pp. 593-595
-
-
Maher, V.M1
Ouellette, L.M2
Curren, R.D3
McCormick, J.J4
-
79
-
-
0031891880
-
Molecular analysis of mutations in the CSB(ERCC6) gene in patients with Cockayne syndrome
-
D.L Mallery B Tanganelli S Colella H Steingrimsdottir A.J Van Gool C Troelstra M Stefanini A.R Lehmann 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.L1
Tanganelli, B2
Colella, S3
Steingrimsdottir, H4
Van Gool, A.J5
Troelstra, C6
Stefanini, M7
Lehmann, A.R8
-
80
-
-
0029096805
-
Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells
-
C Marionnet A Benoit S Benhamou A Sarasin A Stary Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells J. Mol. Biol. 252 1995 550 562
-
(1995)
J. Mol. Biol.
, vol.252
, pp. 550-562
-
-
Marionnet, C1
Benoit, A2
Benhamou, S3
Sarasin, A4
Stary, A5
-
81
-
-
0028269240
-
Purification and cloning of a nucleotide excision-repair complex involving the xeroderma-pigmentosum group-C: protein and a human homolog of yeast RAD23
-
C Masutani K Sugasawa J Yanagisawa T Sonoyama M Ui T Enomoto K Takio K Tanaka P.J van der Spek D Bootsma J.H.J Hoeijmakers E Hanaoka Purification and cloning of a nucleotide excision-repair complex involving the xeroderma-pigmentosum group-C: protein and a human homolog of yeast RAD23 EMBO J. 13 1994 1831 1843
-
(1994)
EMBO J.
, vol.13
, pp. 1831-1843
-
-
Masutani, C1
Sugasawa, K2
Yanagisawa, J3
Sonoyama, T4
Ui, M5
Enomoto, T6
Takio, K7
Tanaka, K8
van der Spek, P.J9
Bootsma, D10
Hoeijmakers, J.H.J11
Hanaoka, E12
-
82
-
-
0033564917
-
Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerise activity
-
C Masutani M Araki A Yamada R Kusumoto T Nogimori T Maekawa S Iwai E Hanaoka Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerise activity EMBO J. 18 1999 3491 3501
-
(1999)
EMBO J.
, vol.18
, pp. 3491-3501
-
-
Masutani, C1
Araki, M2
Yamada, A3
Kusumoto, R4
Nogimori, T5
Maekawa, T6
Iwai, S7
Hanaoka, E8
-
83
-
-
0033578040
-
The human XPV (Xeroderma Pigmentosum Variant) gene encodes human polgmerase η
-
C Masutani R Kusumoto A Yamada N Dohmae M Yokoi M Yuasa M Araki S Iwai K Takio F Hanaoka The human XPV (Xeroderma Pigmentosum Variant) gene encodes human polgmerase η Nature 399 1999 700 704
-
(1999)
Nature
, vol.399
, pp. 700-704
-
-
Masutani, C1
Kusumoto, R2
Yamada, A3
Dohmae, N4
Yokoi, M5
Yuasa, M6
Araki, M7
Iwai, S8
Takio, K9
Hanaoka, F10
-
84
-
-
0029097197
-
High prevalence of narration, in the 1,5 3 gene in poorly differentiated squamous cell carcinomas in xeroderma pigmentosum patients
-
Y Matsumura M Sate C Nishigori M Zghal T Yagi S Imamura H Takebe High prevalence of narration, in the 1,5 3 gene in poorly differentiated squamous cell carcinomas in xeroderma pigmentosum patients J. Invest. Dermatol. 105 1995 399 401
-
(1995)
J. Invest. Dermatol.
, vol.105
, pp. 399-401
-
-
Matsumura, Y1
Sate, M2
Nishigori, C3
Zghal, M4
Yagi, T5
Imamura, S6
Takebe, H7
-
85
-
-
0020066520
-
Failure of RNA synthesis to recover after UV-irradiation: An early defect in cells from individuals with Cockayne syndrome and xeroderma pigmentosum
-
L.V Mayne A.R Lehmann Failure of RNA synthesis to recover after UV-irradiation: An early defect in cells from individuals with Cockayne syndrome and xeroderma pigmentosum Cancer Res. 42 1982 1473 1478
-
(1982)
Cancer Res.
, vol.42
, pp. 1473-1478
-
-
Mayne, L.V1
Lehmann, A.R2
-
86
-
-
0030735538
-
The Saccharomyces cerevisiae RAD30 gene, a homologue of Escherichia coli dinB and umuC, is DNA damage inducible an nd functions in a novel error-tree Postreplication repair mechanism
-
J.P McDonald A.S Levine R Woodgate The Saccharomyces cerevisiae RAD30 gene, a homologue of Escherichia coli dinB and umuC , is DNA damage inducible an nd functions in a novel error-tree Postreplication repair mechanism Genetics 147 1997 1557 1568
-
(1997)
Genetics
, vol.147
, pp. 1557-1568
-
-
McDonald, J.P1
Levine, A.S2
Woodgate, R3
-
87
-
-
0027378895
-
Mice with DNA repair gene (ERCC-1) deficiency- have elevated levels of p53, liver nuclear abnormalities, and die before weaning
-
J McWhir J Selfridge D.J Harrison S Squaires D.W Melton Mice with DNA repair gene ( ERCC-1 ) deficiency- have elevated levels of p53, liver nuclear abnormalities, and die before weaning Nature Genet 5 1993 217 223
-
(1993)
Nature Genet
, vol.5
, pp. 217-223
-
-
McWhir, J1
Selfridge, J2
Harrison, D.J3
Squaires, S4
Melton, D.W5
-
88
-
-
0030133842
-
Implications of the zinc-finger motif found in the DNA-binding domain of the human XPA protein
-
E.H Morita T Ohkubo I Kuraoka M Shirakawa K Tanaka K Morikawa Implications of the zinc-finger motif found in the DNA-binding domain of the human XPA protein Genes Cells 1 1996 437 442
-
(1996)
Genes Cells
, vol.1
, pp. 437-442
-
-
Morita, E.H1
Ohkubo, T2
Kuraoka, I3
Shirakawa, M4
Tanaka, K5
Morikawa, K6
-
89
-
-
0030944206
-
Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans
-
D Mu A Sancar Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans J. Biol. Chem. 272 1997 7570 7573
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 7570-7573
-
-
Mu, D1
Sancar, A2
-
90
-
-
0018290105
-
Ultraviolet mutagenesis of normal and xeroderma pigmentosum variant human fibroblast
-
B.C Myhr D Turnbull J.A di Paulo Ultraviolet mutagenesis of normal and xeroderma pigmentosum variant human fibroblast Mutat. Res. 62 1979 341 353
-
(1979)
Mutat. Res.
, vol.62
, pp. 341-353
-
-
Myhr, B.C1
Turnbull, D2
di Paulo, J.A3
-
91
-
-
0029147115
-
High incidence of ultraviolet-B or chemical-carcinogen-induced kin tumours in mice lacking the Xeroderma pigmentosum group A gene
-
H Nakane S Takeuchi S Yuba M Sijo Y Nakatsu H Murai Y Nakatsuru T Ishikawa S Hirota Y Kitamura Y Kato Y Tsunoda H Miyauchi T Horio T Tokunaga T Matsunaga O Nikaido Y Nishimune Y Okada K Tanaka High incidence of ultraviolet-B or chemical-carcinogen-induced kin tumours in mice lacking the Xeroderma pigmentosum group A gene Nature 377 1995 165 168
-
(1995)
Nature
, vol.377
, pp. 165-168
-
-
Nakane, H1
Takeuchi, S2
Yuba, S3
Sijo, M4
Nakatsu, Y5
Murai, H6
Nakatsuru, Y7
Ishikawa, T8
Hirota, S9
Kitamura, Y10
Kato, Y11
Tsunoda, Y12
Miyauchi, H13
Horio, T14
Tokunaga, T15
Matsunaga, T16
Nikaido, O17
Nishimune, Y18
Okada, Y19
Tanaka, K20
more..
-
92
-
-
0026508774
-
Cockayne syndrome: Review of 140 cases
-
M.A Nance C.A Berry 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.A1
Berry, C.A2
-
93
-
-
0029768095
-
Mutations specific to the xeroderma pigmentosum group E Ddb-phenotype
-
A.F Nichols P Ong S Linn Mutations specific to the xeroderma pigmentosum group E Ddb-phenotype J. Biol. Chem. 40 1996 24317 24320
-
(1996)
J. Biol. Chem.
, vol.40
, pp. 24317-24320
-
-
Nichols, A.F1
Ong, P2
Linn, S3
-
94
-
-
0027359248
-
High prevalence of the point mutation in eXon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients, in Tunisia
-
C Nishigori M Zghal T Yagi S Imamura M.R Komoun H Takebe High prevalence of the point mutation in eXon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients, in Tunisia Am. J. Hum. Genet. 53 1993 1001 1006
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 1001-1006
-
-
Nishigori, C1
Zghal, M2
Yagi, T3
Imamura, S4
Komoun, M.R5
Takebe, H6
-
95
-
-
0028047596
-
Gene alterations and clinical characteristics of xeroderma pigmentosum group A patients in Japan
-
C Nishigori S.I Moriwaki H Takebe T Tanaka S Imamura Gene alterations and clinical characteristics of xeroderma pigmentosum group A patients in Japan Arch. Dermatol. 130 1994 191 197
-
(1994)
Arch. Dermatol.
, vol.130
, pp. 191-197
-
-
Nishigori, C1
Moriwaki, S.I2
Takebe, H3
Tanaka, T4
Imamura, S5
-
96
-
-
0030817140
-
DNA damage recognition k XPA protein promote, efficient recruitment of transcription factor II H
-
S Nocentini F Coin M Saijo K Tanaka J.J Egly DNA damage recognition k XPA protein promote, efficient recruitment of transcription factor II H J. Biol. Chem. 272 1997 22991 22994
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 22991-22994
-
-
Nocentini, S1
Coin, F2
Saijo, M3
Tanaka, K4
Egly, J.J5
-
97
-
-
0025159160
-
Immune function, mutant frequency and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum Cockayne's syndrome and trichothiodystrophy
-
P.G Norris G.A Limb A.S Hamblin A.R Lehmann C.F Arlett J Cole A.P.W Waugh J.L.M Hawk Immune function, mutant frequency and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum Cockayne's syndrome and trichothiodystrophy J. Invest. Dermatol. 94 1990 94 100
-
(1990)
J. Invest. Dermatol.
, vol.94
, pp. 94-100
-
-
Norris, P.G1
Limb, G.A2
Hamblin, A.S3
Lehmann, A.R4
Arlett, C.F5
Cole, J6
Waugh, A.P.W7
Hawk, J.L.M8
-
98
-
-
0030990434
-
A common mutational pattern in Cockayne syndrome patient, from xeroderma pigmentosum, group G: Implications for a second XPG function
-
T Nouspikel P Lalle S.A Leadon P.K Cooper S.G Clarkson A common mutational pattern in Cockayne syndrome patient, from xeroderma pigmentosum, group G: Implications for a second XPG function Proc. Natl. Acad Sci (USA) 94 1997 3116 3121
-
(1997)
, pp. 3116-3121
-
-
Nouspikel, T1
Lalle, P2
Leadon, S.A3
Cooper, P.K4
Clarkson, S.G5
-
99
-
-
0028085556
-
XPG endonuclease makes the 3′ incision in human DNA nucleotide excision repair
-
A O'Donovan A.A Davies J.G Moggs S.C West R.D Wood XPG endonuclease makes the 3′ incision in human DNA nucleotide excision repair Nature 371 1994 432 435
-
(1994)
Nature
, vol.371
, pp. 432-435
-
-
O'Donovan, A1
Davies, A.A2
Moggs, J.G3
West, S.C4
Wood, R.D5
-
100
-
-
0026453401
-
RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential far viability
-
E Park S.N Guzder M.H.M Koken L Jaspers-Dekker G Weeda J.H.J Hoeijmakers S Prakash L Prakash RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential far viability Proc. Natl. Acad. Sci. (USA) 89 1992 11416 11420
-
(1992)
, pp. 11416-11420
-
-
Park, E1
Guzder, S.N2
Koken, M.H.M3
Jaspers-Dekker, L4
Weeda, G5
Hoeijmakers, J.H.J6
Prakash, S7
Prakash, L8
-
101
-
-
0030986934
-
SWI2/SNF2 and related proteins: ATP-driven motors that disrupt protein-DNA interactions
-
M.J Pazin J.T Kadonaga 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.J1
Kadonaga, J.T2
-
103
-
-
0031405766
-
Retroviral-mediated correction of DNA repair defect in xeroderma pigmentosum cells is associated with recovery of catalase activity
-
X Quilliet O Chevallier-Lagente L Zeng R Calvayrac M Mezzina A Sarasin M Vuillaume Retroviral-mediated correction of DNA repair defect in xeroderma pigmentosum cells is associated with recovery of catalase activity Mutat. Res. 385 1997 235 242
-
(1997)
Mutat. Res.
, vol.385
, pp. 235-242
-
-
Quilliet, X1
Chevallier-Lagente, O2
Zeng, L3
Calvayrac, R4
Mezzina, M5
Sarasin, A6
Vuillaume, M7
-
104
-
-
0031814129
-
Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A
-
V Rapic Otrin I Kuraoka T Nardo M McLenigan A.P Eker M Stefanini A.S Levine R.D Wood Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A Mol. Cell. Biol. 18 1998 3182 3190
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3182-3190
-
-
Rapic Otrin, V1
Kuraoka, I2
Nardo, T3
McLenigan, M4
Eker, A.P5
Stefanini, M6
Levine, A.S7
Wood, R.D8
-
105
-
-
85120146111
-
Isolation and characterisation of two human transcription factor 11H (TFIII I)-related complexes: ERCC2/CAK and TFIIH
-
J.T Reardon H Ge E Gibbs A Sancar J Hurwitz Z.Q Pan Isolation and characterisation of two human transcription factor 11H (TFIII I)-related complexes: ERCC2/CAK and TFIIH Proc. Natl. Acid. Sci. (USA) 93 1996 10538 published erratum appears in
-
(1996)
, pp. 10538
-
-
Reardon, J.T1
Ge, H2
Gibbs, E3
Sancar, A4
Hurwitz, J5
Pan, Z.Q6
-
107
-
-
0015982924
-
Xeroderma pigmentosum: An inherited disease with sun-sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair
-
J.H Robbins K.H Kraemer M.A Lutzner B.W Festoff H.G Coon Xeroderma pigmentosum: An inherited disease with sun-sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair Ann. Intern. Med. 80 1974 221 248
-
(1974)
Ann. Intern. Med.
, vol.80
, pp. 221-248
-
-
Robbins, J.H1
Kraemer, K.H2
Lutzner, M.A3
Festoff, B.W4
Coon, H.G5
-
108
-
-
0020632152
-
Evidence that lack of deoxyribonucleic acid repair causes death of neurons in xeroderma pigmentosum
-
J.H Robbins R.J Polinsky A.N Moshell Evidence that lack of deoxyribonucleic acid repair causes death of neurons in xeroderma pigmentosum Ann. Neurol. 13 1983 682 684
-
(1983)
Ann. Neurol.
, vol.13
, pp. 682-684
-
-
Robbins, J.H1
Polinsky, R.J2
Moshell, A.N3
-
109
-
-
0028978672
-
High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC
-
A.T Sands A Abuin A Sanchez C.J Conti A Bradley High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC Nature 377 1995 162 165
-
(1995)
Nature
, vol.377
, pp. 162-165
-
-
Sands, A.T1
Abuin, A2
Sanchez, A3
Conti, C.J4
Bradley, A5
-
110
-
-
0027905008
-
DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor
-
L Schaeffer R Roy S Humbert V Moncollin W Vermeulen J.H.J Hoeijmakers P Chambon J.-M Egly DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor Science 260 1993 58 63
-
(1993)
Science
, vol.260
, pp. 58-63
-
-
Schaeffer, L1
Roy, R2
Humbert, S3
Moncollin, V4
Vermeulen, W5
Hoeijmakers, J.H.J6
Chambon, P7
Egly, J.-M8
-
111
-
-
0028362248
-
The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor
-
L Schaeffer V Monocollin R Roy A Staub M Mezzina A Sarasin G Weeda J.H.J Hoeijmakers J.M Egly The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor EMBO J. 13 1994 2388 2392
-
(1994)
EMBO J.
, vol.13
, pp. 2388-2392
-
-
Schaeffer, L1
Monocollin, V2
Roy, R3
Staub, A4
Mezzina, M5
Sarasin, A6
Weeda, G7
Hoeijmakers, J.H.J8
Egly, J.M9
-
112
-
-
0028095381
-
Mechanisms of transcription-repair coupling and mutation frequency
-
C.P Selby A Sancar Mechanisms of transcription-repair coupling and mutation frequency Microbiol. Rev. 58 1994 317 329
-
(1994)
Microbiol. Rev.
, vol.58
, pp. 317-329
-
-
Selby, C.P1
Sancar, A2
-
113
-
-
0030822591
-
Cockayne syndrome group B protein enhances elongation by RNA polymerise II
-
C.P Selby A Sancar Cockayne syndrome group B protein enhances elongation by RNA polymerise II Proc. Natl. Acad. Sci. (USA) 95 1997 11205 11209
-
(1997)
, pp. 11205-11209
-
-
Selby, C.P1
Sancar, A2
-
114
-
-
0031020871
-
Human transcription-repair coupling factor CSB/ERCC6 is to DNA-stimulated ATPase hut is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerise II
-
C.P Selby A Sancar Human transcription-repair coupling factor CSB/ERCC6 is to DNA-stimulated ATPase hut is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerise II J. Biol. Chem. 272 1997 1885 1890
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 1885-1890
-
-
Selby, C.P1
Sancar, A2
-
115
-
-
16044373761
-
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease
-
A.M Sijbers W.L de Laat R.R Ariza M Biggersraft Y.-F Wei J.G Mogg K.C Carter B.K Shell E Evans M.C de Jong M Rademakers J de Rooij N.G.J Jaspers J.H.J Hoeijmakers R.D Wood 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.M1
de Laat, W.L2
Ariza, R.R3
Biggersraft, M4
Wei, Y.-F5
Mogg, J.G6
Carter, K.C7
Shell, B.K8
Evans, E9
de Jong, M.C10
Rademakers, M11
de Rooij, J12
Jaspers, N.G.J13
Hoeijmakers, J.H.J14
Wood, R.D15
-
116
-
-
0031802583
-
Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein
-
J.C States E.R McDuffie S.P Myrand M McDowell J.E Cleaver Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein Hum. Mutat. 12 1998 103 113
-
(1998)
Hum. Mutat.
, vol.12
, pp. 103-113
-
-
States, J.C1
McDuffie, E.R2
Myrand, S.P3
McDowell, M4
Cleaver, J.E5
-
117
-
-
0027262205
-
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy
-
M Stefanini P Lagomarsini S Giliani T Nardo E Botta A Peserico W.J Kleijer A.R Lehmann A Sarasin Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy Carcinogenesis 14 1993 1101 1105
-
(1993)
Carcinogenesis
, vol.14
, pp. 1101-1105
-
-
Stefanini, M1
Lagomarsini, P2
Giliani, S3
Nardo, T4
Botta, E5
Peserico, A6
Kleijer, W.J7
Lehmann, A.R8
Sarasin, A9
-
119
-
-
0032134423
-
Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair
-
K Sugasawa J.M Ng C Masutani S Iwai P.J van der Spek A.P Eker E Hanoaka D Bootsma J.H Hoeijmakers Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair Mol. Cell 2 1995 223 232
-
(1995)
Mol. Cell
, vol.2
, pp. 223-232
-
-
Sugasawa, K1
Ng, J.M2
Masutani, C3
Iwai, S4
van der Spek, P.J5
Eker, A.P6
Hanoaka, E7
Bootsma, D8
Hoeijmakers, J.H9
-
120
-
-
0024095589
-
Mutation Of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to find ATP
-
P Sung D Higgins L Prakash S Prakash Mutation Of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to find ATP EMBO J. 7 1998 3263 3269
-
(1998)
EMBO J.
, vol.7
, pp. 3263-3269
-
-
Sung, P1
Higgins, D2
Prakash, L3
Prakash, S4
-
121
-
-
0032101146
-
Defective bypass replication of a leading, strand cyclobutane thymine dimer in xeroderma pigmentosum variant cell extracts
-
D.L Svoboda L.P Briley J.M Vos Defective bypass replication of a leading, strand cyclobutane thymine dimer in xeroderma pigmentosum variant cell extracts Cancer Res. 58 1998 2445 2448
-
(1998)
Cancer Res.
, vol.58
, pp. 2445-2448
-
-
Svoboda, D.L1
Briley, L.P2
Vos, J.M3
-
122
-
-
0017360241
-
DNA repair characteristics and skin cancers of xeroderma pigmentosum patients in Japan
-
H Takebe Y Miki T Kozuka J.I Furuyama K Tanaka M.S Sasaki Y Fujiwara H Akiba DNA repair characteristics and skin cancers of xeroderma pigmentosum patients in Japan Cancer Res. 37 1977 490 495
-
(1977)
Cancer Res.
, vol.37
, pp. 490-495
-
-
Takebe, H1
Miki, Y2
Kozuka, T3
Furuyama, J.I4
Tanaka, K5
Sasaki, M.S6
Fujiwara, Y7
Akiba, H8
-
123
-
-
0025168640
-
Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain
-
K Tanaka M Naoyuki I Satokata I Miyamoto M.C Yoshida Y Satoh S Kondo A Yasui H Okayama Y Okada Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain Nature 348 1990 73 76
-
(1990)
Nature
, vol.348
, pp. 73-76
-
-
Tanaka, K1
Naoyuki, M2
Satokata, I3
Miyamoto, I4
Yoshida, M.C5
Satoh, Y6
Kondo, S7
Yasui, A8
Okayama, H9
Okada, Y10
-
124
-
-
0032561475
-
RNA polymerase II elongation complexes containing the Cockayne syndrome group, B protein interact with a molecular complex containing the transcription factor IIH component, xeroderma pigmentosum B aid p62
-
D Tantin RNA polymerase II elongation complexes containing the Cockayne syndrome group, B protein interact with a molecular complex containing the transcription factor IIH component, xeroderma pigmentosum B aid p62 J. Biol Chem. 273 1998 27794 27799
-
(1998)
J. Biol Chem.
, vol.273
, pp. 27794-27799
-
-
Tantin, D1
-
125
-
-
85120122475
-
Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase It elongation complexes
-
D Tantin A Kansal M Carey Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase It elongation complexes Mol. Cell. Biol. 17 1997 68013 68014
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 68013-68014
-
-
Tantin, D1
Kansal, A2
Carey, M3
-
126
-
-
0032160650
-
Conservation of eukaryotic DNA repair mechanisms
-
E.M Taylor A.R Lehmann Conservation of eukaryotic DNA repair mechanisms Int. Radiat. Biol. 74 1998 277 286
-
(1998)
Int. Radiat. Biol.
, vol.74
, pp. 277-286
-
-
Taylor, E.M1
Lehmann, A.R2
-
127
-
-
12644310290
-
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene
-
E Taylor B.C Broughton E Botta M Stefanini A Sarasin N.G.J Jaspers H Fawcett S.A Harcourt C.E Arlett A.R Lehmann Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the X PD ( ERCC2 ) repair/transcription gene Proc. Natl. Acad. Sci (USA) 94 1997 8658 8663
-
(1997)
, pp. 8658-8663
-
-
Taylor, E1
Broughton, B.C2
Botta, E3
Stefanini, M4
Sarasin, A5
Jaspers, N.G.J6
Fawcett, H7
Harcourt, S.A8
Arlett, C.E9
Lehmann, A.R10
-
128
-
-
0033010723
-
Reconstitution of the transcription factor TFIIH: Assignment Of functions for the three enzymatic subunit XPB, XPD, and cdk7
-
E Tirode D Busso F Coin J.M Egly Reconstitution of the transcription factor TFIIH: Assignment Of functions for the three enzymatic subunit XPB, XPD, and cdk7 Mol. Cell 3 1999 87 95
-
(1999)
Mol. Cell
, vol.3
, pp. 87-95
-
-
Tirode, E1
Busso, D2
Coin, F3
Egly, J.M4
-
129
-
-
0026465665
-
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's, syndrome and preferential repair of active genes
-
C Troelstra A van Cool J de Wit W Vermeulen D Bootsma J.H.J Hoeijmakers 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, C1
van Cool, A2
de Wit, J3
Vermeulen, W4
Bootsma, D5
Hoeijmakers, J.H.J6
-
130
-
-
0030916337
-
Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition
-
G.T.J van der Horst H van Steeg R.J.W Berg A.J van Gool J de Wit G Weeda H Morreau R.B Beems C.F van Kreijl E.R de Gruijl D Bootsma J.H.J Hoeijmakers 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.J1
van Steeg, H2
Berg, R.J.W3
van Gool, A.J4
de Wit, J5
Weeda, G6
Morreau, H7
Beems, R.B8
van Kreijl, C.F9
de Gruijl, E.R10
Bootsma, D11
Hoeijmakers, J.H.J12
-
131
-
-
0028109412
-
RAD26, the functional S. cerevisiae homolog of the cockayne syndrome B gene ERCC6
-
A.I van Gool R Verhage S.M.A Swagemakens P van de Putte J Brouwer C Troelstra D Bootsma J.H.J Hoeijmakers RAD26, the functional S. cerevisiae homolog of the cockayne syndrome B gene ERCC6 EMBO J. 13 1994 5361 5369
-
(1994)
EMBO J.
, vol.13
, pp. 5361-5369
-
-
van Gool, A.I1
Verhage, R2
Swagemakens, S.M.A3
van de Putte, P4
Brouwer, J5
Troelstra, C6
Bootsma, D7
Hoeijmakers, J.H.J8
-
132
-
-
0030826732
-
The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in a RNA polymerise II containing complex
-
A.J van Gool E Citterio S Rademaker R van Os W Vermeulen A Constantinou J.-M Egly D Bootsma H.J Hoeijmakers The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in a RNA polymerise II containing complex EMBO J. 16 1997 5955 5965
-
(1997)
EMBO J.
, vol.16
, pp. 5955-5965
-
-
van Gool, A.J1
Citterio, E2
Rademaker, S3
van Os, R4
Vermeulen, W5
Constantinou, A6
Egly, J.-M7
Bootsma, D8
Hoeijmakers, H.J9
-
135
-
-
0028985014
-
Transcription-coupled repair remove, both cyclobutane pyrimidine dimers and 6-4 photoproducts with equal efficiency and in a sequenctial way from transcribed DNA in xeroderma pigmentosum group C fibroblast
-
A van Hoffen J Venema R Meschini A.A van Zeeland L.H.E Mullenders Transcription-coupled repair remove, both cyclobutane pyrimidine dimers and 6-4 photoproducts with equal efficiency and in a sequenctial way from transcribed DNA in xeroderma pigmentosum group C fibroblast EMBO J. 14 1995 360 367
-
(1995)
EMBO J.
, vol.14
, pp. 360-367
-
-
van Hoffen, A1
Venema, J2
Meschini, R3
van Zeeland, A.A4
Mullenders, L.H.E5
-
136
-
-
0029941444
-
The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes
-
M.F van Oosterwijk A Versteeg R Filon A.A van Zeeland L.H.E Mullenders 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.F1
Versteeg, A2
Filon, R3
van Zeeland, A.A4
Mullenders, L.H.E5
-
137
-
-
0028085120
-
Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair mid transcription gene ERCC3
-
W Vermeulen R.J Scott S Potger H.J Muller J Cole C.E Arlett W.J Kleijer D Bootsma J.H.J Hoeijmakers G Weeda Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair mid transcription gene ERCC3 Am. J. Hum. Genet. 54 1994 191 200
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 191-200
-
-
Vermeulen, W1
Scott, R.J2
Potger, S3
Muller, H.J4
Cole, J5
Arlett, C.E6
Kleijer, W.J7
Bootsma, D8
Hoeijmakers, J.H.J9
Weeda, G10
-
138
-
-
0028673969
-
Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): Evidence for the existence of u transcription syndrome
-
W Vermeulen A.J van Vuuren M Chipoulet L Schaeffer E Appeldoorn G Weeda N.G.J Jaspers A Priestley C.E Arlert A.R Lehmann M Stefanini M Mezzina A Sarasin D Bootsma J.-M Egly J.H.J Hoeijmakers Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): Evidence for the existence of u transcription syndrome Cold Spring Harbor Symp. Quant. Biol. 59 1994 317 329
-
(1994)
, pp. 317-329
-
-
Vermeulen, W1
van Vuuren, A.J2
Chipoulet, M3
Schaeffer, L4
Appeldoorn, E5
Weeda, G6
Jaspers, N.G.J7
Priestley, A8
Arlert, C.E9
Lehmann, A.R10
Stefanini, M11
Mezzina, M12
Sarasin, A13
Bootsma, D14
Egly, J.-M15
Hoeijmakers, J.H.J16
-
139
-
-
0026510545
-
Striking differences in cellular catalase activity between two DNA repair-deficient diseases: Xeroderma pigmentosum and trichothiodystrophy
-
M Vuillaume L Daya-Grosjean P Vincens J.L Pennetier P Tarroux A Baret R Calvayrac A Taieb A Sarasin Striking differences in cellular catalase activity between two DNA repair-deficient diseases: Xeroderma pigmentosum and trichothiodystrophy Carcinogenesis 13 1992 321 328
-
(1992)
Carcinogenesis
, vol.13
, pp. 321-328
-
-
Vuillaume, M1
Daya-Grosjean, L2
Vincens, P3
Pennetier, J.L4
Tarroux, P5
Baret, A6
Calvayrac, R7
Taieb, A8
Sarasin, A9
-
141
-
-
0032499719
-
Assembly, subunit composition, mid footprint of human DNA repair excision nuclease
-
M Wakasugi A Sancar Assembly, subunit composition, mid footprint of human DNA repair excision nuclease Proc. Natl. Acad. Sci. (USA) 95 1998 6669 6674
-
(1998)
, pp. 6669-6674
-
-
Wakasugi, M1
Sancar, A2
-
142
-
-
0027159226
-
Evidence from mutation spectra that the UV hypermutability of xeroderma pigmentosum variant cells reflects abnormal, error-prone replication on a template containing photoproducts
-
Y.-C Wang V.M Maher D.L Mitchell J.J McCormick Evidence from mutation spectra that the UV hypermutability of xeroderma pigmentosum variant cells reflects abnormal, error-prone replication on a template containing photoproducts Mol. Cell Biol. 13 1993 4276 4283
-
(1993)
Mol. Cell Biol.
, vol.13
, pp. 4276-4283
-
-
Wang, Y.-C1
Maher, V.M2
Mitchell, D.L3
McCormick, J.J4
-
143
-
-
0025158110
-
A presumed DNA helicase encoded by ERCC-3 is involved in file human repair disorders xeroderma pigmentosum mid Cockayne's syndrome
-
G Weeda R.C.A van Ham W Vermeulen D Bootsma A.J van der Eb J.H.J Hoeijmakers A presumed DNA helicase encoded by ERCC-3 is involved in file human repair disorders xeroderma pigmentosum mid Cockayne's syndrome Cell 62 1990 777 791
-
(1990)
Cell
, vol.62
, pp. 777-791
-
-
Weeda, G1
van Ham, R.C.A2
Vermeulen, W3
Bootsma, D4
van der Eb, A.J5
Hoeijmakers, J.H.J6
-
144
-
-
12644266319
-
Disruption of arouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence
-
G Weeda I Donker J de Wit H Morreau R Janssen C.J Vissers A Nigg H van Steeg D Bootsma J.H.J Hoeijmakers Disruption of arouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence Curt. Biol. 7 1997 427 439
-
(1997)
Curt. Biol.
, vol.7
, pp. 427-439
-
-
Weeda, G1
Donker, I2
de Wit, J3
Morreau, H4
Janssen, R5
Vissers, C.J6
Nigg, A7
van Steeg, H8
Bootsma, D9
Hoeijmakers, J.H.J10
-
145
-
-
16944363270
-
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy
-
G Weeda F Eveno I Donker W Vermeulen O Chevallier-Lagente A Taieb A Stary J.H Hoeijmakers M Mezzina A Sarasin A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy Am. J. Hum. Genet. 60 1997 320 329
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 320-329
-
-
Weeda, G1
Eveno, F2
Donker, I3
Vermeulen, W4
Chevallier-Lagente, O5
Taieb, A6
Stary, A7
Hoeijmakers, J.H8
Mezzina, M9
Sarasin, A10
-
146
-
-
0029892791
-
DNA repair in eukaryotes
-
R.D Wood DNA repair in eukaryotes Annu. Rev. Biochem. 65 1996 135 167
-
(1996)
Annu. Rev. Biochem.
, vol.65
, pp. 135-167
-
-
Wood, R.D1
-
147
-
-
0030768038
-
Nucleotide excision repair in mammalian cells
-
R.D Wood Nucleotide excision repair in mammalian cells J. Biol. Chem. 272 1997 23465 23468
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 23465-23468
-
-
Wood, R.D1
-
148
-
-
0028030791
-
U.v.-induced nuclear accumulation of p53 is evoked through DNA damage of actively transcribed genes independent of the cell cycle
-
M Yamaizumi T Sugano U.v.-induced nuclear accumulation of p53 is evoked through DNA damage of actively transcribed genes independent of the cell cycle Oncogene 9 1994 2775 2784
-
(1994)
Oncogene
, vol.9
, pp. 2775-2784
-
-
Yamaizumi, M1
Sugano, T2
|