-
2
-
-
0029892791
-
DNA in eukaryotes
-
Wood, R. D. DNA in eukaryotes. Ann. Rev. Biochem., 65: 135-167, 1996.
-
(1996)
Ann. Rev. Biochem.
, vol.65
, pp. 135-167
-
-
Wood, R.D.1
-
3
-
-
0003095801
-
Nucleotide excision repair syndromes: Xeroderma Pigmentosum, Cockayne syndrome and Trichothiodystrophy
-
B. Vogelstein, and K. W. Kinzler (eds.), New York: McGraw-Hill
-
Bootsma, D., Kraemer, K. H., Cleaver, J. E., and Hoeijmakers, J. H. J. Nucleotide excision repair syndromes: Xeroderma Pigmentosum, Cockayne syndrome and Trichothiodystrophy. In: B. Vogelstein, and K. W. Kinzler (eds.), The Genetic Basis of Human Cancer, pp. 245-274. New York: McGraw-Hill, 1998.
-
(1998)
The Genetic Basis of Human Cancer
, pp. 245-274
-
-
Bootsma, D.1
Kraemer, K.H.2
Cleaver, J.E.3
Hoeijmakers, J.H.J.4
-
4
-
-
0031022619
-
Sunlight and skin cancer: Another link revealed
-
Kraemer, K. H. Sunlight and skin cancer: another link revealed. Proc. Nail. Acad. Sci. USA, 94: 11-14, 1997.
-
(1997)
Proc. Nail. Acad. Sci. USA
, vol.94
, pp. 11-14
-
-
Kraemer, K.H.1
-
5
-
-
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. F., 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. USA, 87: 4707-4711, 1990.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 4707-4711
-
-
Venema, J.1
Mullenders, L.H.F.2
Natarajan, A.T.3
Van Zeeland, A.A.4
Mayne, L.V.5
-
6
-
-
0025158110
-
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
-
Weeda, G., Van Ham, R. C. A., Vermeulen, W., Bootsma, D., Van der Eb, A. J., and Hoeijmakers, J. H. J. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome. Cell, 62:777-791, 1990.
-
(1990)
Cell
, vol.62
, pp. 777-791
-
-
Weeda, G.1
Van Ham, R.C.A.2
Vermeulen, W.3
Bootsma, D.4
Van Der Eb, A.J.5
Hoeijmakers, J.H.J.6
-
7
-
-
0028868125
-
Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome
-
Broughton, B. C., Thompson, A. F., Harcourt, S. A., Vermeulen, W., Hoeijmakers, J. H. J., Botta, E., Stefanini, M., King, M. D., Weber, C. A., Cole, J., Arlett, C. F., and Lehmann, A. R. Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome. Am. J. Hum. Genet., 56: 167-174, 1995.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 167-174
-
-
Broughton, B.C.1
Thompson, A.F.2
Harcourt, S.A.3
Vermeulen, W.4
Hoeijmakers, J.H.J.5
Botta, E.6
Stefanini, M.7
King, M.D.8
Weber, C.A.9
Cole, J.10
Arlett, C.F.11
Lehmann, A.R.12
-
8
-
-
0027360041
-
Xeroderma pigmentosum complementation group G associated with Cockayne's syndrome
-
Vermeulen, W., Jaeken, J., Jaspers, N. G. J., Bootsma, D., and Hoeijmakers, J. H. J. Xeroderma pigmentosum complementation group G associated with Cockayne's syndrome. Am. J. Hum. Genet., 53: 185-192, 1993.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 185-192
-
-
Vermeulen, W.1
Jaeken, J.2
Jaspers, N.G.J.3
Bootsma, D.4
Hoeijmakers, J.H.J.5
-
9
-
-
0022868911
-
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity
-
Stefanini, M., Lagomarsini, P., Arlett, C. F., Marinoni, S., Borrone, C., Crovato, F., Trevisan, G., Cordone, G., and Nuzzo, F. Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. Hum. Genet., 74: 107-112, 1986.
-
(1986)
Hum. Genet.
, vol.74
, pp. 107-112
-
-
Stefanini, M.1
Lagomarsini, P.2
Arlett, C.F.3
Marinoni, S.4
Borrone, C.5
Crovato, F.6
Trevisan, G.7
Cordone, G.8
Nuzzo, F.9
-
10
-
-
16944363270
-
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy
-
Weeda, G., Eveno, E., Donker, I., Vermeulen, W., Chevallier-Lagente, O., Taïeb, A., Stary, A., Hoeijmakers, J. H. J., Mezzina, M., and Sarasin, A. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy. Am. J. Hum. Genet., 60: 320-329, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 320-329
-
-
Weeda, G.1
Eveno, E.2
Donker, I.3
Vermeulen, W.4
Chevallier-Lagente, O.5
Taïeb, A.6
Stary, A.7
Hoeijmakers, J.H.J.8
Mezzina, M.9
Sarasin, A.10
-
11
-
-
0020692904
-
A comparison of the proteins of normal and trichothiodystrophic human hair
-
Gillespie, J., and Marshall, R. A comparison of the proteins of normal and trichothiodystrophic human hair. J. Invest. Dermatol., 80: 195-202, 1983.
-
(1983)
J. Invest. Dermatol.
, vol.80
, pp. 195-202
-
-
Gillespie, J.1
Marshall, R.2
-
12
-
-
0026543076
-
DNA repair investigations in nine Italian patients affected by trichothiodystrophy
-
Stefanini, M., Giliani, S., Nardo, T., Marinoni, S., Nazzaro, V., Rizzo, R., and Trevisan, G. DNA repair investigations in nine Italian patients affected by trichothiodystrophy. Mutat. Res., 273: 119-125, 1992.
-
(1992)
Mutat. Res.
, vol.273
, pp. 119-125
-
-
Stefanini, M.1
Giliani, S.2
Nardo, T.3
Marinoni, S.4
Nazzaro, V.5
Rizzo, R.6
Trevisan, G.7
-
13
-
-
0023763193
-
Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light
-
Lehmann, A. R., Arlett, C. F., Broughton, B. C., Harcourt, S. A., Steingrimsdottir, H., Stefanini, M., Malcolm, A., Taylor, R., Natarajan, A. T., Green, S., King, M. D., MacKie, R. M., Stephenson, J. B. P., and Tolmie, J. L. Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light. Cancer Res., 48: 6090-6096, 1988.
-
(1988)
Cancer Res.
, vol.48
, pp. 6090-6096
-
-
Lehmann, A.R.1
Arlett, C.F.2
Broughton, B.C.3
Harcourt, S.A.4
Steingrimsdottir, H.5
Stefanini, M.6
Malcolm, A.7
Taylor, R.8
Natarajan, A.T.9
Green, S.10
King, M.D.11
Mackie, R.M.12
Stephenson, J.B.P.13
Tolmie, J.L.14
-
14
-
-
0028362248
-
The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor
-
Schaeffer, L., Moncollin, V., Roy, R., Staub, A., Mezzina, M., Sarasin, A., Weeda, G., Hoeijmakers, J. H. J., and Egly, J. M. The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor. EMBO J., 13: 2388-2392, 1994.
-
(1994)
EMBO J.
, vol.13
, pp. 2388-2392
-
-
Schaeffer, L.1
Moncollin, V.2
Roy, R.3
Staub, A.4
Mezzina, M.5
Sarasin, A.6
Weeda, G.7
Hoeijmakers, J.H.J.8
Egly, J.M.9
-
15
-
-
0027905008
-
DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor
-
Washington DC
-
Schaeffer, L., Roy, R., Humbert, S., Moncollin, V., Vermeulen, W., Hoeijmakers, J. H. J., Chambon, P., and Egly, J. DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor. Science (Washington DC), 260: 58-63, 1993.
-
(1993)
Science
, vol.260
, pp. 58-63
-
-
Schaeffer, L.1
Roy, R.2
Humbert, S.3
Moncollin, V.4
Vermeulen, W.5
Hoeijmakers, J.H.J.6
Chambon, P.7
Egly, J.8
-
16
-
-
0027364921
-
Human xeroderma pigmentosum group D gene encodes a DNA helicase
-
Sung, P., Bailly, V., Weber, C., Thompson, L. H., Prakash, L., and Prakash, S. Human xeroderma pigmentosum group D gene encodes a DNA helicase. Nature (Lond.), 365: 852-855, 1993.
-
(1993)
Nature (Lond.)
, vol.365
, pp. 852-855
-
-
Sung, P.1
Bailly, V.2
Weber, C.3
Thompson, L.H.4
Prakash, L.5
Prakash, S.6
-
17
-
-
0027489079
-
The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II
-
Qiu, H., Park, E., Prakash, L., and Prakash, S. The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II. Genes Dev., 7: 2161-2171, 1993.
-
(1993)
Genes Dev.
, vol.7
, pp. 2161-2171
-
-
Qiu, H.1
Park, E.2
Prakash, L.3
Prakash, S.4
-
18
-
-
0028140494
-
DNA repair gene RAD3 of S. Cerevisiae is essential for transcription by RNA polymerase II
-
Guzder, S. N., Qiu, H., Sommers, C. H., Sung, P., Prakash, L., and Prakash, S. DNA repair gene RAD3 of S. cerevisiae is essential for transcription by RNA polymerase II. Nature (Lond.), 367: 91-94, 1994.
-
(1994)
Nature (Lond.)
, vol.367
, pp. 91-94
-
-
Guzder, S.N.1
Qiu, H.2
Sommers, C.H.3
Sung, P.4
Prakash, L.5
Prakash, S.6
-
19
-
-
0027967644
-
Human nucleotide excision repair syndromes: Molecular clues to unexpected intricacies
-
Hoeijmakers, J. H. J. Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies. Eur. J. Cancer, 30A: 1912-1921, 1994.
-
(1994)
Eur. J. Cancer
, vol.30 A
, pp. 1912-1921
-
-
Hoeijmakers, J.H.J.1
-
20
-
-
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. J., Priestley, A., Arlett, C. F., Lehmann, A. R., Stefanini, M., Mezzina, M., Sarasin, A., Bootsma, D., Egly, J-M., and Hoeijmakers, J. H. J. 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: 317-329, 1994.
-
(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.J.7
Priestley, A.8
Arlett, C.F.9
Lehmann, A.R.10
Stefanini, M.11
Mezzina, M.12
Sarasin, A.13
Bootsma, D.14
Egly, J.-M.15
Hoeijmakers, J.H.J.16
-
21
-
-
0028358988
-
Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy
-
Broughton, B. C., Steingrimsdottir, H., Weber, C. A., and Lehmann, A. R. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy. Nat. Genet., 7: 189-194, 1994.
-
(1994)
Nat. Genet.
, vol.7
, pp. 189-194
-
-
Broughton, B.C.1
Steingrimsdottir, H.2
Weber, C.A.3
Lehmann, A.R.4
-
22
-
-
0028832388
-
Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D
-
Takayama, K., Salazar, E. P., Lehmann, A. R., Stefanini, M., Thompson, L. H., and Weber, C. A. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D. Cancer Res., 55: 5656-5663, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 5656-5663
-
-
Takayama, K.1
Salazar, E.P.2
Lehmann, A.R.3
Stefanini, M.4
Thompson, L.H.5
Weber, C.A.6
-
23
-
-
0030051768
-
Defects in the DNA repair and transcription gene ERCC2 (XPD) in trichthiodystrophy
-
Takayama, K., Salazar, E. P., Broughton, B. C., Lehmann, A. R., Sarasin, A., Thompson, L. H., and Weber, C. A. Defects in the DNA repair and transcription gene ERCC2 (XPD) in trichthiodystrophy. Am. J. Hum. Genet., 58: 263-270, 1996.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 263-270
-
-
Takayama, K.1
Salazar, E.P.2
Broughton, B.C.3
Lehmann, A.R.4
Sarasin, A.5
Thompson, L.H.6
Weber, C.A.7
-
24
-
-
12644310290
-
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/ transcription gene
-
Taylor, E., Broughton, B., Botta, E., Stefanini, M., Sarasin, A., Jaspers, N., Fawcett, H., Harcourt, S., Arlett, C., and Lehmann, A. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/ transcription gene. Proc. Natl. Acad. Sci. USA, 94: 8658-8663, 1997.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 8658-8663
-
-
Taylor, E.1
Broughton, B.2
Botta, E.3
Stefanini, M.4
Sarasin, A.5
Jaspers, N.6
Fawcett, H.7
Harcourt, S.8
Arlett, C.9
Lehmann, A.10
-
25
-
-
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
-
Botta, E., Nardo, T., Broughton, B. C., Marinoni, S., Lehmann, A. R., and Stefanini, M. 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: 1036-1048, 1998.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1036-1048
-
-
Botta, E.1
Nardo, T.2
Broughton, B.C.3
Marinoni, S.4
Lehmann, A.R.5
Stefanini, M.6
-
26
-
-
0031964151
-
Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality
-
de Boer, J., Donker, I., de Wit, J., Hoeijmakers, J. H. J., and Weeda, G. Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality. Cancer Res., 58: 89-94, 1998.
-
(1998)
Cancer Res.
, vol.58
, pp. 89-94
-
-
De Boer, J.1
Donker, I.2
De Wit, J.3
Hoeijmakers, J.H.J.4
Weeda, G.5
-
27
-
-
0032085182
-
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy
-
de Boer, J., de Wit, J., van Steeg, H., Berg, R. J. W., Morreau, M., Visser, P., Lehmann, A. R., Duran, M., Hoeijmakers, J. H. J., and Weeda, G. A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy. Mol. Cell, 1: 981-990, 1998.
-
(1998)
Mol. Cell
, vol.1
, pp. 981-990
-
-
De Boer, J.1
De Wit, J.2
Van Steeg, H.3
Berg, R.J.W.4
Morreau, M.5
Visser, P.6
Lehmann, A.R.7
Duran, M.8
Hoeijmakers, J.H.J.9
Weeda, G.10
-
28
-
-
0030916337
-
Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition
-
van der Horst, G. T. J., van Steeg, H., Berg, R. J. W., van Gool, A., de Wit, J., Weeda, G., Morreau, H., Beems, R. B., van Kreijl, C. F., de Gruijl, F. R., Bootsma, D., and Hoeijmakers, J. H. J. Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition. Cell, 89: 425-435, 1997.
-
(1997)
Cell
, vol.89
, pp. 425-435
-
-
Van Der Horst, G.T.J.1
Van Steeg, H.2
Berg, R.J.W.3
Van Gool, A.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.J.12
-
29
-
-
0028978672
-
High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC
-
Sands, A. T., Abuin, A., Sanchez, A., Conti, C. J., and Bradley, A. High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC. Nature (Lond.), 377: 162-165, 1995.
-
(1995)
Nature (Lond.)
, vol.377
, pp. 162-165
-
-
Sands, A.T.1
Abuin, A.2
Sanchez, A.3
Conti, C.J.4
Bradley, A.5
-
30
-
-
0029083409
-
Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA
-
de Vries, A., van Oostrom, C. T. M., Hofhuis, F. M. A., Dortant, P. M., Berg, R. J. W., de Gruijl, F. R., Wester, P. W., van Kreijl, C. F., Capel, P. J. A., van Steeg, H., and Verbeek, S. J. Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA. Nature (Lond.), 377: 169-173, 1995.
-
(1995)
Nature (Lond.)
, vol.377
, pp. 169-173
-
-
De Vries, A.1
Van Oostrom, C.T.M.2
Hofhuis, F.M.A.3
Dortant, P.M.4
Berg, R.J.W.5
De Gruijl, F.R.6
Wester, P.W.7
Van Kreijl, C.F.8
Capel, P.J.A.9
Van Steeg, H.10
Verbeek, S.J.11
-
31
-
-
0028085120
-
Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3
-
Vermeulen, W., Scott, R. J., Potger, S., Muller, H. J., Cole, J., Arlett, C. F., Kleijer, W. J., Bootsma, D., Hoeijmakers, J. H. J., and Weeda, G. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3. Am. J. Hum. Genet., 54: 191-200, 1994.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 191-200
-
-
Vermeulen, W.1
Scott, R.J.2
Potger, S.3
Muller, H.J.4
Cole, J.5
Arlett, C.F.6
Kleijer, W.J.7
Bootsma, D.8
Hoeijmakers, J.H.J.9
Weeda, G.10
-
32
-
-
0020066520
-
Failure of RNA synthesis to recover after UV irradiation: An early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum
-
Mayne, L. V., and Lehmann, A. R. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum. Cancer Res., 42: 1473-1478, 1982.
-
(1982)
Cancer Res.
, vol.42
, pp. 1473-1478
-
-
Mayne, L.V.1
Lehmann, A.R.2
-
33
-
-
0028289952
-
Ultraviolet radiation-induced impairment of the early initiating and the late effector phases of contact hypersensitivity to picrylchloride: Regulation by different mechanisms
-
Sontag, Y., Garssen, J., de Gruijl, F. R., van der Leun, J. C., van Vloten, W. A., and van Loveren, H. Ultraviolet radiation-induced impairment of the early initiating and the late effector phases of contact hypersensitivity to picrylchloride: regulation by different mechanisms. J. Invest. Dermatol., 102: 923-927, 1994.
-
(1994)
J. Invest. Dermatol.
, vol.102
, pp. 923-927
-
-
Sontag, Y.1
Garssen, J.2
De Gruijl, F.R.3
Van Der Leun, J.C.4
Van Vloten, W.A.5
Van Loveren, H.6
-
34
-
-
0031920594
-
Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema
-
Berg, R. J. W., Ruven, H. J., Sands, A. T., de Gruijl, F. R., and Mullenders, L. H. 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: 405-409, 1998.
-
(1998)
J. Invest. Dermatol.
, vol.110
, pp. 405-409
-
-
Berg, R.J.W.1
Ruven, H.J.2
Sands, A.T.3
De Gruijl, F.R.A.4
Mullenders, L.H.5
-
35
-
-
0029096805
-
Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells
-
Marionnet, C., Benoit, A., Benhamou, S., Sarasin, A., and Stary, A. Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells. J. Mol. Biol., 252: 550-562, 1995.
-
(1995)
J. Mol. Biol.
, vol.252
, pp. 550-562
-
-
Marionnet, C.1
Benoit, A.2
Benhamou, S.3
Sarasin, A.4
Stary, A.5
-
36
-
-
0025276699
-
Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
-
Itin, P. H., and Pittelkow, M. R. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias. J. Am. Acad. Dermatol., 22: 705-717, 1990.
-
(1990)
J. Am. Acad. Dermatol.
, vol.22
, pp. 705-717
-
-
Itin, P.H.1
Pittelkow, M.R.2
-
37
-
-
0032128389
-
Ultraviolet-B induced hyperplasia and squamous cell carcinomas in the cornea of XPA-deficient mice
-
de Vries, A., Gorgels, T. G., Berg, R. J. W., Jansen, G. H., and van Steeg, H. Ultraviolet-B induced hyperplasia and squamous cell carcinomas in the cornea of XPA-deficient mice. Exp. Eye Res., 67: 53-59, 1998.
-
(1998)
Exp. Eye Res.
, vol.67
, pp. 53-59
-
-
De Vries, A.1
Gorgels, T.G.2
Berg, R.J.W.3
Jansen, G.H.4
Van Steeg, H.5
-
38
-
-
0027317209
-
UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum
-
Madzak, C., Armier, J., Stary, A., Daya-Grosjean, L., and Sarasin, A. UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum. Carcinogenesis (Lond.), 14: 1255-1260, 1993.
-
(1993)
Carcinogenesis (Lond.)
, vol.14
, pp. 1255-1260
-
-
Madzak, C.1
Armier, J.2
Stary, A.3
Daya-Grosjean, L.4
Sarasin, A.5
-
39
-
-
12644305856
-
Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals
-
Ahrens, C., Grewe, M., Berneburg, M., Grether-Beck, S., Quilliet, X., Mezzina, M., Sarasin, A., Lehmann, A. R., Arlett, C. F., and Krutmann, J. Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals. Proc. Natl. Acad. Sci. USA, 94: 6837-6841, 1997.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 6837-6841
-
-
Ahrens, C.1
Grewe, M.2
Berneburg, M.3
Grether-Beck, S.4
Quilliet, X.5
Mezzina, M.6
Sarasin, A.7
Lehmann, A.R.8
Arlett, C.F.9
Krutmann, J.10
-
40
-
-
0029066259
-
Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases
-
Eveno, E., Bourre, F., Quilliet, X., Chevallier-Lagente, O., Roza, L., Eker, A., Kleijer, W., Nikaido, O., Stefanini, M., Hoeijmakers, J. H. J., Bootsma, D., Cleaver, J. E., Sarasin, A., and Mezzina, M. Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases. Cancer Res., 55: 4325-4332, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 4325-4332
-
-
Eveno, E.1
Bourre, F.2
Quilliet, X.3
Chevallier-Lagente, O.4
Roza, L.5
Eker, A.6
Kleijer, W.7
Nikaido, O.8
Stefanini, M.9
Hoeijmakers, J.H.J.10
Bootsma, D.11
Cleaver, J.E.12
Sarasin, A.13
Mezzina, M.14
-
41
-
-
0031974425
-
Cyclobutane pyrimidine dimers are the main mutagenic DNA photoproducts in DNA repair-deficient trichothiodystrophy cells
-
Marionnet, C., Armier, J., Sarasin, A., and Stary, A. Cyclobutane pyrimidine dimers are the main mutagenic DNA photoproducts in DNA repair-deficient trichothiodystrophy cells. Cancer Res., 58: 102-108, 1998.
-
(1998)
Cancer Res.
, vol.58
, pp. 102-108
-
-
Marionnet, C.1
Armier, J.2
Sarasin, A.3
Stary, A.4
-
42
-
-
0026510545
-
Striking differences in cellular catalase activity between two DNA repair-deficient diseases: Xeroderma pigmentosum and trichothiodystrophy
-
Vuillaume, M., Daya-Grosjean, L., Vincens, P., Pennetier, J., Tarroux, P., Baret, A., Calvayrac, R., Taieb, A., and Sarasin, A. Striking differences in cellular catalase activity between two DNA repair-deficient diseases: xeroderma pigmentosum and trichothiodystrophy. Carcinogenesis (Lond.), 13: 321-325, 1992.
-
(1992)
Carcinogenesis (Lond.)
, vol.13
, pp. 321-325
-
-
Vuillaume, M.1
Daya-Grosjean, L.2
Vincens, P.3
Pennetier, J.4
Tarroux, P.5
Baret, A.6
Calvayrac, R.7
Taieb, A.8
Sarasin, A.9
-
43
-
-
0026752690
-
Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy
-
Mariani, E., Facchini, A., Honorati, M. C., Lalli, E., Berardesca, E., Ghetti, P., Marinoni, S., Nuzzo, F., Astaldi Ricotti, G. C. B., and Stefanini, M. Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy. Clin. Exp. Immunol., 88: 376-382, 1992.
-
(1992)
Clin. Exp. Immunol.
, vol.88
, pp. 376-382
-
-
Mariani, E.1
Facchini, A.2
Honorati, M.C.3
Lalli, E.4
Berardesca, E.5
Ghetti, P.6
Marinoni, S.7
Nuzzo, F.8
Astaldi Ricotti, G.C.B.9
Stefanini, M.10
-
44
-
-
0001166257
-
The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway
-
Wang, X. W., Vermeulen, W., Coursen, J. D., Gibson, M., Lupold, S. E., Forrester, K., Xu, G., Elmore, L., Yen, H., Hoeijmakers, J. H. J., and Harris, C. C. The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway. Genes Dev., 10: 1219-1232, 1996.
-
(1996)
Genes Dev.
, vol.10
, pp. 1219-1232
-
-
Wang, X.W.1
Vermeulen, W.2
Coursen, J.D.3
Gibson, M.4
Lupold, S.E.5
Forrester, K.6
Xu, G.7
Elmore, L.8
Yen, H.9
Hoeijmakers, J.H.J.10
Harris, C.C.11
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