-
1
-
-
0003866513
-
-
Fitzpatrick, T.B., Eisen, A.Z., Wolff, K. and Freedberg, I.M. (eds). McGraw-Hill, New York
-
Kripke, M.L. and Austen, K.F. (1993) In Fitzpatrick, T.B., Eisen, A.Z., Wolff, K. and Freedberg, I.M. (eds) Dermatology in General Medicine. 4th edn. McGraw-Hill, New York.
-
(1993)
Dermatology in General Medicine. 4th Edn.
-
-
Kripke, M.L.1
Austen, K.F.2
-
2
-
-
0029920370
-
Genetic analysis of ageing: Role of oxidative damage and environmental stresses
-
Martin, G.M., Austad, S.N. and Johnson, T.E. (1996) Genetic analysis of ageing: role of oxidative damage and environmental stresses. Nature Genet., 13, 25-34.
-
(1996)
Nature Genet.
, vol.13
, pp. 25-34
-
-
Martin, G.M.1
Austad, S.N.2
Johnson, T.E.3
-
3
-
-
0030989228
-
DNA excision repair pathways
-
Lindahl, T., Karran, P. and Wood, R.D. (1997) DNA excision repair pathways. Curr. Opin. Genet. Dev., 7, 158-169.
-
(1997)
Curr. Opin. Genet. Dev.
, vol.7
, pp. 158-169
-
-
Lindahl, T.1
Karran, P.2
Wood, R.D.3
-
4
-
-
0004228157
-
-
ASM Press, Washington, DC
-
Friedberg, E.C., Walker, G.C. and Siede, W. (1995) DNA Repair and Mutagenesis. ASM Press, Washington, DC
-
(1995)
DNA Repair and Mutagenesis.
-
-
Friedberg, E.C.1
Walker, G.C.2
Siede, W.3
-
5
-
-
0028948394
-
Mammalian DNA nucleotide excision repair reconstituted with purified components
-
Aboussekhra, A., Biggerstaff, M., Shivji, M.K.K., Vilpo, J.A., Moncollin, V., Podust, V.N., Protic, M., Hubscher, U., Egly, J.-M. and Wood, R.D. (1995) Mammalian DNA nucleotide excision repair reconstituted with purified components. Cell, 80, 859-868.
-
(1995)
Cell
, vol.80
, pp. 859-868
-
-
Aboussekhra, A.1
Biggerstaff, M.2
Shivji, M.K.K.3
Vilpo, J.A.4
Moncollin, V.5
Podust, V.N.6
Protic, M.7
Hubscher, U.8
Egly, J.-M.9
Wood, R.D.10
-
6
-
-
0033118354
-
Molecular mechanisms of nucleotide excision repair
-
de Laat, W.L., Jaspers, N.G.J. and Hoeijmakers, J.H.J. (1999) Molecular mechanisms of nucleotide excision repair. Genes Dev., 13, 768-785.
-
(1999)
Genes Dev.
, vol.13
, pp. 768-785
-
-
De Laat, W.L.1
Jaspers, N.G.J.2
Hoeijmakers, J.H.J.3
-
7
-
-
0029892790
-
Nucleotide excision repair
-
Sancar, A. (1996) Nucleotide excision repair. Annu. Rev. Biochem., 65, 43-81.
-
(1996)
Annu. Rev. Biochem.
, vol.65
, pp. 43-81
-
-
Sancar, A.1
-
8
-
-
0032742715
-
DNA damage recognition during nucleotide excision repair in mammalian cells
-
Wood, R.D. (1999) DNA damage recognition during nucleotide excision repair in mammalian cells. Biochimie, 81, 39-44.
-
(1999)
Biochimie
, vol.81
, pp. 39-44
-
-
Wood, R.D.1
-
9
-
-
0033065080
-
Recognition of nonhybridizing base pairs during nucleotide excision repair of DNA
-
Buschta-Hedayat, N., Buterin, T., Hess, M.T., Missura, M. and Naegeli, H. (1999) Recognition of nonhybridizing base pairs during nucleotide excision repair of DNA. Proc. Natl Acad. Sci. USA, 96, 6090-6095.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 6090-6095
-
-
Buschta-Hedayat, N.1
Buterin, T.2
Hess, M.T.3
Missura, M.4
Naegeli, H.5
-
10
-
-
0024675824
-
The biology of the (6-4) photoproduct
-
Mitchell, D.L. and Nairn, R.S. (1989) The biology of the (6-4) photoproduct. Photochem. Photobiol., 49, 805-819.
-
(1989)
Photochem. Photobiol.
, vol.49
, pp. 805-819
-
-
Mitchell, D.L.1
Nairn, R.S.2
-
11
-
-
0030038104
-
Replicative senescence: Implications for in vivo aging and tumor suppression
-
Smith, J.R. and Pereira-Smith, O.M. (1996) Replicative senescence: implications for in vivo aging and tumor suppression. Science, 273, 63-67.
-
(1996)
Science
, vol.273
, pp. 63-67
-
-
Smith, J.R.1
Pereira-Smith, O.M.2
-
12
-
-
0027318778
-
DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free radical-induced base lesions
-
Satoh, M.S., Jones, C.J., Wood, R.D. and Lindahl, T. (1993) DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free radical-induced base lesions. Proc. Natl Acad. Sci. USA, 90, 6335-6339.
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 6335-6339
-
-
Satoh, M.S.1
Jones, C.J.2
Wood, R.D.3
Lindahl, T.4
-
13
-
-
0028293319
-
Enzymatic repair of oxidative DNA damage
-
Satoh, M.S. and Lindahl, T. (1994) Enzymatic repair of oxidative DNA damage. Cancer Res., 54, 1899s-1901s.
-
(1994)
Cancer Res.
, vol.54
-
-
Satoh, M.S.1
Lindahl, T.2
-
14
-
-
0032134423
-
Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair
-
Sugasawa, K., Ng, J.M., Masutani, C., Iwai, S., van der Spek, P.J., Eker, A.P.M., Hanaoka, F., Bootsma, D. and Hoeijmakers, J.H.J. (1998) Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair. Mol. Cell, 2, 223-232.
-
(1998)
Mol. Cell
, vol.2
, pp. 223-232
-
-
Sugasawa, K.1
Ng, J.M.2
Masutani, C.3
Iwai, S.4
Van Der Spek, P.J.5
Eker, A.P.M.6
Hanaoka, F.7
Bootsma, D.8
Hoeijmakers, J.H.J.9
-
15
-
-
0030732132
-
Mechanism of open complex and dual incision formation by human nucleotide excision repair factors
-
Evans, E., Moggs, J.G., Hwang, J.R., Egly, J.-M. and Wood, R.D. (1997) Mechanism of open complex and dual incision formation by human nucleotide excision repair factors. EMBO J., 16, 6559-6573.
-
(1997)
EMBO J.
, vol.16
, pp. 6559-6573
-
-
Evans, E.1
Moggs, J.G.2
Hwang, J.R.3
Egly, J.-M.4
Wood, R.D.5
-
16
-
-
0032516786
-
Interactions of the transcription/DNA repair factor TFIIH and xp repair proteins with DNA lesions in a cell-free repair assay
-
Li, R.Y., Calsou, P., Jones, C.J. and Salles, B. (1998) 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, 211-218.
-
(1998)
J. Mol. Biol.
, vol.281
, pp. 211-218
-
-
Li, R.Y.1
Calsou, P.2
Jones, C.J.3
Salles, B.4
-
17
-
-
0030944206
-
Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans
-
Mu, D. and Sancar, A. (1997) ) Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans. J. Biol. Chem., 272, 7570-7573.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 7570-7573
-
-
Mu, D.1
Sancar, A.2
-
18
-
-
0027442869
-
Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum E
-
Keeney, S., Chang, G.J. and Linn, S. (1993) Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum E. J. Biol. Chem., 268, 21293-21300.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 21293-21300
-
-
Keeney, S.1
Chang, G.J.2
Linn, S.3
-
19
-
-
0027483739
-
Preferential binding of the xeroderma pigmentosum group a complementing protein to damaged DNA
-
Jones, C.J. and Wood, R.D. (1993) Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA. Biochemistry, 32, 12096-12104.
-
(1993)
Biochemistry
, vol.32
, pp. 12096-12104
-
-
Jones, C.J.1
Wood, R.D.2
-
20
-
-
0028929611
-
Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA
-
He, Z., Henricksen, L.A., Wold, M.S. and Ingles, C.J. (1995) Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA. Nature, 374, 566-569.
-
(1995)
Nature
, vol.374
, pp. 566-569
-
-
He, Z.1
Henricksen, L.A.2
Wold, M.S.3
Ingles, C.J.4
-
21
-
-
0028932889
-
The general transcription-repair factor TFIIH is recruited to the excision repair complex by the XPA protein independent of the TFIIE transcription factor
-
Park, C.-H., Mu, D., Reardon, J.T. and Sancar, A. (1995) The general transcription-repair factor TFIIH is recruited to the excision repair complex by the XPA protein independent of the TFIIE transcription factor. J. Biol. Chem., 270, 4896-4902.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 4896-4902
-
-
Park, C.-H.1
Mu, D.2
Reardon, J.T.3
Sancar, A.4
-
22
-
-
0028276805
-
Specific association between the human DNA repair proteins XPA and ERCC1
-
Li, L., Elledge, S.J., Peterson, C.A., Bales, E.S. and Legerski, R.J. (1994) Specific association between the human DNA repair proteins XPA and ERCC1. Proc. Natl Acad. Sci. USA, 91, 5012-5016.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 5012-5016
-
-
Li, L.1
Elledge, S.J.2
Peterson, C.A.3
Bales, E.S.4
Legerski, R.J.5
-
23
-
-
0030908093
-
Replication protein A: A heterotrimeric, single-stranded DNA-binding protein required for eukaryotic DNA metabolism
-
Wold, M.S. (1997) Replication protein A: a heterotrimeric, single-stranded DNA-binding protein required for eukaryotic DNA metabolism. Annu. Rev. Biochem., 66, 61-92.
-
(1997)
Annu. Rev. Biochem.
, vol.66
, pp. 61-92
-
-
Wold, M.S.1
-
24
-
-
0032529167
-
DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair
-
de Laat, W.L., Appeldoorn, E., Sugasawa, K., Weterings, E., Jaspers, N.G. and Hoeijmakers, J.H. (1998) DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair. Genes Dev., 12, 2598-2609.
-
(1998)
Genes Dev.
, vol.12
, pp. 2598-2609
-
-
De Laat, W.L.1
Appeldoorn, E.2
Sugasawa, K.3
Weterings, E.4
Jaspers, N.G.5
Hoeijmakers, J.H.6
-
25
-
-
0026772415
-
Binding properties of replication protein A from human and yeast cells
-
Kim, C., Snyder, R.O. and Wold, M.S. (1992) Binding properties of replication protein A from human and yeast cells. Mol. Cell. Biol., 12, 3050-3059.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 3050-3059
-
-
Kim, C.1
Snyder, R.O.2
Wold, M.S.3
-
26
-
-
0028242355
-
Determination of minimum substrate size for human excinuclease
-
Huang, J.C. and Sancar, A. (1994) Determination of minimum substrate size for human excinuclease. J. Biol. Chem., 269, 19034-19040.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 19034-19040
-
-
Huang, J.C.1
Sancar, A.2
-
27
-
-
0025787782
-
Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2
-
Gerard, M., Fischer, L., Moncollin, V., Chipoulet, J.M., Chambon, P. and Egly, J.M. (1991) Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2. J. Biol. Chem., 266, 20940-20945.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 20940-20945
-
-
Gerard, M.1
Fischer, L.2
Moncollin, V.3
Chipoulet, J.M.4
Chambon, P.5
Egly, J.M.6
-
28
-
-
0027905008
-
DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor
-
Schaeffer, L., Roy, R., Humbert, S., Moncollin, V., Vermeulen, W., Hoeijmakers, J.H.J., Chambon, P. and Egly, J. (1993) DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor. Science, 260, 58-63.
-
(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
-
29
-
-
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. (1994) The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor. EMBO J., 13, 2388-2392.
-
(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
-
30
-
-
0030007387
-
Opening of an RNA polymerase II promoter occurs in two distinct steps and requires the basal transcription factors TFIIE and TFIIH
-
Holstege, F.C.P., Van der Vliet, P.C. and Timmers, H.T.M. (1996) Opening of an RNA polymerase II promoter occurs in two distinct steps and requires the basal transcription factors TFIIE and TFIIH. EMBO J., 15, 1666-1677.
-
(1996)
EMBO J.
, vol.15
, pp. 1666-1677
-
-
Holstege, F.C.P.1
Van Der Vliet, P.C.2
Timmers, H.T.M.3
-
31
-
-
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. (1998) Disruption of the mouse xeroderma pigmentosum group D DNA repair/ basal transcription gene results in preimplantation lethality. Cancer Res., 58, 89-94.
-
(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
-
32
-
-
0029317904
-
Cyclin-dependent protein kinases: Key regulators of the eukaryotic cell cycle
-
Nigg, E.A. (1995) Cyclin-dependent protein kinases: key regulators of the eukaryotic cell cycle. BioEssays, 17, 471-480.
-
(1995)
BioEssays
, vol.17
, pp. 471-480
-
-
Nigg, E.A.1
-
33
-
-
0028885363
-
Different forms of TFIIH for transcription and DNA repair: Holo-TFIIH and a nucleotide excision repairosome
-
Svejstrup, J.Q., Wang, Z., Feaver, W.J., Wu, X., Bushnell, D.A., Donahue, T.F., Friedberg, E.C. and Kornberg, R.D. (1995) Different forms of TFIIH for transcription and DNA repair: holo-TFIIH and a nucleotide excision repairosome. Cell, 80, 21-28.
-
(1995)
Cell
, vol.80
, pp. 21-28
-
-
Svejstrup, J.Q.1
Wang, Z.2
Feaver, W.J.3
Wu, X.4
Bushnell, D.A.5
Donahue, T.F.6
Friedberg, E.C.7
Kornberg, R.D.8
-
34
-
-
0028085556
-
XPG endonuclease makes the 3′ incision in human DNA nucleotide excision repair
-
O'Donovan, A., Davies, A.A., Moggs, J.G., West, S.C. and Wood, R.D. (1994) XPG endonuclease makes the 3′ incision in human DNA nucleotide excision repair. Nature, 371, 432-435.
-
(1994)
Nature
, vol.371
, pp. 432-435
-
-
O'Donovan, A.1
Davies, A.A.2
Moggs, J.G.3
West, S.C.4
Wood, R.D.5
-
35
-
-
16044373761
-
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease
-
Sijbers, A.M., de Laat, W.L., Ariza, R.R., Biggerstaff, M., Wei, Y.F., Moggs, J.G., Carter, K.C., Shell, B.K., Evans, E., de Jong, M.C., Rademakers, S., de Rooij, J., Jaspers, N.G., Hoeijmakers, J.H. and Wood, R.D. (1996) Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease. Cell, 86, 811-822.
-
(1996)
Cell
, vol.86
, pp. 811-822
-
-
Sijbers, A.M.1
De Laat, W.L.2
Ariza, R.R.3
Biggerstaff, M.4
Wei, Y.F.5
Moggs, J.G.6
Carter, K.C.7
Shell, B.K.8
Evans, E.9
De Jong, M.C.10
Rademakers, S.11
De Rooij, J.12
Jaspers, N.G.13
Hoeijmakers, J.H.14
Wood, R.D.15
-
36
-
-
0030025947
-
Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG and Cockayne syndrome group B (CSB) protein
-
Iyer, N., Reagan, M.S., Wu, K.-J., Canagarajah, B. and Friedberg, E.C. (1996) Interactions involving the human RNA polymerase II transcription/ nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG and Cockayne syndrome group B (CSB) protein. Biochemistry, 35, 2157-2167.
-
(1996)
Biochemistry
, vol.35
, pp. 2157-2167
-
-
Iyer, N.1
Reagan, M.S.2
Wu, K.-J.3
Canagarajah, B.4
Friedberg, E.C.5
-
37
-
-
0028965151
-
Nucleotide excision repair DNA synthesis by DNA polymerase epsilon in the presence of PCNA, RFC and RPA
-
Shivji, M.K.K., Podust, V.N., Hubscher, U. and Wood, R.D. (1995) Nucleotide excision repair DNA synthesis by DNA polymerase epsilon in the presence of PCNA, RFC and RPA. Biochemistry, 34, 5011-5017.
-
(1995)
Biochemistry
, vol.34
, pp. 5011-5017
-
-
Shivji, M.K.K.1
Podust, V.N.2
Hubscher, U.3
Wood, R.D.4
-
38
-
-
0026680743
-
Mutations in the DNA ligase I gene of an individual with immunodeficienies and cellular hypersensitivity to DNA-damaging agents
-
Barnes, D.E., Tomkinson, A.E., Lehmann, A.R., Webster, A.D.B. and Lindahl, T. (1992) Mutations in the DNA ligase I gene of an individual with immunodeficienies and cellular hypersensitivity to DNA-damaging agents. Cell, 69, 495-503.
-
(1992)
Cell
, vol.69
, pp. 495-503
-
-
Barnes, D.E.1
Tomkinson, A.E.2
Lehmann, A.R.3
Webster, A.D.B.4
Lindahl, T.5
-
39
-
-
0021905437
-
DNA repair in an active gene: Removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall
-
Bohr, V.A., Smith, C.A., Okumoto, D.S. and Hanawalt, P.C. (1985) DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall. Cell. 40, 359-369.
-
(1985)
Cell.
, vol.40
, pp. 359-369
-
-
Bohr, V.A.1
Smith, C.A.2
Okumoto, D.S.3
Hanawalt, P.C.4
-
40
-
-
0023663101
-
Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene
-
Mellon, I., Spivak, G. and Hanawalt, P.C. (1987) Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene. Cell, 51, 241-249.
-
(1987)
Cell
, vol.51
, pp. 241-249
-
-
Mellon, I.1
Spivak, G.2
Hanawalt, P.C.3
-
41
-
-
0025775473
-
Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes
-
Venema, J., van Hoffen, A., Karcagi, V., Natarajan, A.T., van Zeeland, A.A. and Mullenders, L.H.F. (1991) Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes. Mol. Cell. Biol., 11, 4128-4134.
-
(1991)
Mol. Cell. Biol.
, vol.11
, pp. 4128-4134
-
-
Venema, J.1
Van Hoffen, A.2
Karcagi, V.3
Natarajan, A.T.4
Van Zeeland, A.A.5
Mullenders, L.H.F.6
-
42
-
-
0028106162
-
Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template
-
Donahue, B.A., Yin, S., Taylor, J.-S., Reines, D. and Hanawalt, P.C. (1994) Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template. Proc. Natl Acad. Sci. USA, 91, 8502-8506.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 8502-8506
-
-
Donahue, B.A.1
Yin, S.2
Taylor, J.-S.3
Reines, D.4
Hanawalt, P.C.5
-
43
-
-
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., Reagan, M.S., Legerski, R., Schultz, R.A., Stefanini, M., Lehmann, A.R., Mayne, L.V. and Friedberg, E.C. (1995) 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, 555-564.
-
(1995)
Cell
, vol.82
, pp. 555-564
-
-
Henning, K.A.1
Li, L.2
Iyer, N.3
McDaniel, L.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
-
44
-
-
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.J. (1992) ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell, 71, 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.J.6
-
45
-
-
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. (1997) The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex. EMBO J., 16, 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
-
46
-
-
0031025997
-
Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G
-
Cooper, P.K., Nouspikel, T., Clarkson, S.G. and Leadon, S.A. (1997) Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G. Science, 275, 990-993.
-
(1997)
Science
, vol.275
, pp. 990-993
-
-
Cooper, P.K.1
Nouspikel, T.2
Clarkson, S.G.3
Leadon, S.A.4
-
47
-
-
0003095801
-
Nucleotide excision repair syndromes: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. Vogelstein, b. And kinzler, k.W. (eds)
-
McGraw-Hill, New York
-
Bootsma, D., Kraemer, K.H., Cleaver, J.E. and Hoeijmakers, J.H.J. (1998) Nucleotide excision repair syndromes: xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. In Vogelstein, B. and Kinzler, K.W. (eds) The Genetic Basis of Human Cancer. McGraw-Hill, New York, pp. 245-274.
-
(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
-
48
-
-
0031022619
-
Sunlight and skin cancer: Another link revealed
-
Kraemer, K.H. (1997) Sunlight and skin cancer: another link revealed. Proc. Natl Acad. Sci. USA, 94, 11-14.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 11-14
-
-
Kraemer, K.H.1
-
49
-
-
0021282448
-
DNA repair protects against cutaneous and internal neoplasia: Evidence from xeroderma pigmentosum
-
Kraemer, K.H., Lee, M.M. and Scotto, J. (1984) DNA repair protects against cutaneous and internal neoplasia: evidence from xeroderma pigmentosum. Carcinogenesis, 5, 511-514.
-
(1984)
Carcinogenesis
, vol.5
, pp. 511-514
-
-
Kraemer, K.H.1
Lee, M.M.2
Scotto, J.3
-
51
-
-
0030745912
-
In vitro repair of oxidative DNA damage by human nucleotide excision repair system: Possible explanation for neurodegeneration in Xeroderma pigmentosum patients
-
Reardon, J.T., Bessho, T., Kung, H.C., Bolton, P.H. and Sancar, A. (1997) In vitro repair of oxidative DNA damage by human nucleotide excision repair system: possible explanation for neurodegeneration in Xeroderma pigmentosum patients. Proc. Natl Acad. Sci. USA, 94, 9463-9468.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 9463-9468
-
-
Reardon, J.T.1
Bessho, T.2
Kung, H.C.3
Bolton, P.H.4
Sancar, A.5
-
52
-
-
0028808098
-
Role of the Rad1 and Rad10 proteins in nucleotide excision repair and recombination
-
Davies, A.A., Friedberg, E.C., Tomkinson, A.E., Wood, R.D. and West, S.C. (1995) Role of the Rad1 and Rad10 proteins in nucleotide excision repair and recombination. J. Biol. Chem., 270, 24638-24641.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 24638-24641
-
-
Davies, A.A.1
Friedberg, E.C.2
Tomkinson, A.E.3
Wood, R.D.4
West, S.C.5
-
53
-
-
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., Ruven, H.J., Sands, A.T., de Gruijl, F.R. and Mullenders, L.H. (1998) 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)
J. Invest. Dermatol.
, vol.110
, pp. 405-409
-
-
Berg, R.J.1
Ruven, H.J.2
Sands, A.T.3
De Gruijl, F.R.4
Mullenders, L.H.5
-
54
-
-
0025341294
-
The genetic detect 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. (1990) The genetic detect 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)
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
-
55
-
-
0026508774
-
Cockayne syndrome: Review of 140 cases
-
Nance, M.A. and Berry, S.A. (1992) Cockayne syndrome: review of 140 cases. Am. J. Med. Genet., 42, 68-84.
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 68-84
-
-
Nance, M.A.1
Berry, S.A.2
-
56
-
-
0032739301
-
Cancer from the outside, aging from the inside: Mouse models to study the consequences of defective nucleotide excision repair
-
de Boer, J. and Hoeijmakers, J.H.J. (1999) Cancer from the outside, aging from the inside: mouse models to study the consequences of defective nucleotide excision repair. Biochimie, 81, 127-137.
-
(1999)
Biochimie
, vol.81
, pp. 127-137
-
-
De Boer, J.1
Hoeijmakers, J.H.J.2
-
57
-
-
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. (1993) 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, 10499-10503.
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 10499-10503
-
-
Leadon, S.A.1
Cooper, P.K.2
-
58
-
-
0019245621
-
Trichothiodystrophy: Sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex
-
Price, V.H., Odom, R.B., Ward, W.H. and Jones, F.T. (1980) Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex. Arch. Dermatol., 116, 1375-1384.
-
(1980)
Arch. Dermatol.
, vol.116
, pp. 1375-1384
-
-
Price, V.H.1
Odom, R.B.2
Ward, W.H.3
Jones, F.T.4
-
59
-
-
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. (1986) Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. Hum. Genet., 74, 107-112.
-
(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
-
60
-
-
0027262205
-
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy
-
Stefanini, M., Lagomarisini, P., Gilliani, S., Nardo, T., Botta, E., Peserico, A., Kleyer, W.J., Lehmann, A.R. and Sarasin, A. (1993) Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy. Carcinogenesis, 14, 1101-1105.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1101-1105
-
-
Stefanini, M.1
Lagomarisini, P.2
Gilliani, S.3
Nardo, T.4
Botta, E.5
Peserico, A.6
Kleyer, W.J.7
Lehmann, A.R.8
Sarasin, A.9
-
61
-
-
0027440658
-
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy
-
Stefanini, M., Vermeulen, W., Weeda, G., Giliani, S., Nardo, T., Mezzina, M., Sarasin, A., Harper, J.L., Arlett, C.F., Hoeijmakers, J.H.J. and Lehmann, A.R. (1993) A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy. Am. J. Hum. Genet., 53, 817-821.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 817-821
-
-
Stefanini, M.1
Vermeulen, W.2
Weeda, G.3
Giliani, S.4
Nardo, T.5
Mezzina, M.6
Sarasin, A.7
Harper, J.L.8
Arlett, C.F.9
Hoeijmakers, J.H.J.10
Lehmann, A.R.11
-
62
-
-
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. (1994) Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3. Am. J. Hum. Genet., 54, 191-200.
-
(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
-
63
-
-
0028353174
-
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2(TFIIH)
-
van Vuuren, A.J., Vermeulen, W., Ma, L., Weeda, G., Appeldoorn, E., Jaspers, N.G.J., van der Eb, A.J., Bootsma, D., Hoeijmakers, J.H.J., Humbert, S., Schaeffer, L. and Egly, J.-M. (1994) Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2(TFIIH). EMBO J., 13, 1645-1653.
-
(1994)
Embo J.
, vol.13
, pp. 1645-1653
-
-
Van Vuuren, A.J.1
Vermeulen, W.2
Ma, L.3
Weeda, G.4
Appeldoorn, E.5
Jaspers, N.G.J.6
Van Der Eb, A.J.7
Bootsma, D.8
Hoeijmakers, J.H.J.9
Humbert, S.10
Schaeffer, L.11
Egly, J.-M.12
-
64
-
-
0025276699
-
Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
-
Itin, P.H. and Pittelkow, M.R. (1990) Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias. J. Am. Acad. Dermatol., 22, 705-717.
-
(1990)
J. Am. Acad. Dermatol.
, vol.22
, pp. 705-717
-
-
Itin, P.H.1
Pittelkow, M.R.2
-
65
-
-
0032231836
-
Analysis of mutations in the XPD gene in 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. (1998) Analysis of mutations in the XPD gene in 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)
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
-
66
-
-
0000634906
-
Differentiation in hard keratin tissues: Hair and related structures
-
Leigh, I.M. and Lane, E.B. (eds). Cambridge University Press, Cambridge, UK
-
Powell, B.C. and Rogers, G.E. (1994) Differentiation in hard keratin tissues: hair and related structures. In Leigh, I.M. and Lane, E.B. (eds) The Keratinocyte Handbook. Cambridge University Press, Cambridge, UK, pp. 401-436.
-
(1994)
The Keratinocyte Handbook
, pp. 401-436
-
-
Powell, B.C.1
Rogers, G.E.2
-
67
-
-
0020692904
-
A comparison of the proteins of normal and trichothiodystrophic human hair
-
Gillespie, J. and Marshall, R. (1983) A comparison of the proteins of normal and trichothiodystrophic human hair. J. Invest. Dermatol., 80, 195-202.
-
(1983)
J. Invest. Dermatol.
, vol.80
, pp. 195-202
-
-
Gillespie, J.1
Marshall, R.2
-
68
-
-
0030064798
-
Central nervous system dysmyelination in PIBI(D)S syndrome: A further case
-
Battistella, P. and Peserico, A. (1996) Central nervous system dysmyelination in PIBI(D)S syndrome: a further case. Childs Nerv. Syst., 12, 110-113.
-
(1996)
Childs Nerv. Syst.
, vol.12
, pp. 110-113
-
-
Battistella, P.1
Peserico, A.2
-
69
-
-
0027315208
-
Trichothiodystrophy associated with photosensitivity, gonadal failure and striking osteosclerosis
-
McCuaig, C., Marcoux, D., Rasmussen, J.E., Werner, M.M. and Genter, N.E. (1993) Trichothiodystrophy associated with photosensitivity, gonadal failure and striking osteosclerosis. J. Am. Acad. Dermatol., 28, 820-826.
-
(1993)
J. Am. Acad. Dermatol.
, vol.28
, pp. 820-826
-
-
McCuaig, C.1
Marcoux, D.2
Rasmussen, J.E.3
Werner, M.M.4
Genter, N.E.5
-
70
-
-
0026462737
-
Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair
-
Sarasin, A., Blanchet-Bardon, C., Renault, G., Lehmann, A., Arlett, C. and Dumez, Y. (1992) Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair. Br. J. Dermatol., 127, 485-491.
-
(1992)
Br. J. Dermatol.
, vol.127
, pp. 485-491
-
-
Sarasin, A.1
Blanchet-Bardon, C.2
Renault, G.3
Lehmann, A.4
Arlett, C.5
Dumez, Y.6
-
71
-
-
0003840674
-
The Marinesco-Sjogren syndrome
-
Norwood, W.F. (1964) The Marinesco-Sjogren syndrome. J. Pediatric., 65, 431-437.
-
(1964)
J. Pediatric.
, vol.65
, pp. 431-437
-
-
Norwood, W.F.1
-
72
-
-
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. (1997) 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)
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
-
73
-
-
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. (1995) 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)
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
-
74
-
-
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. (1988) Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light. Cancer Res., 48, 6090-6096.
-
(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
-
75
-
-
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. (1992) DNA repair investigations in nine Italian patients affected by trichothiodystrophy. Mutat. Res., 273, 119-125.
-
(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
-
76
-
-
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. (1995) Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases. Cancer Res., 55, 4325-4332.
-
(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
-
77
-
-
0031974425
-
Cyclobutane pyrimidine dimers are the main mulagenic DNA photoproducts in DNA repair-deficient trichothiodystrophy cells
-
Marionnet, C., Armier, J., Sarasin, A. and Stary, A. (1998) Cyclobutane pyrimidine dimers are the main mulagenic DNA photoproducts in DNA repair-deficient trichothiodystrophy cells. Cancer Res., 58, 102-108.
-
(1998)
Cancer Res.
, vol.58
, pp. 102-108
-
-
Marionnet, C.1
Armier, J.2
Sarasin, A.3
Stary, A.4
-
78
-
-
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. (1995) 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)
J. Mol. Biol.
, vol.252
, pp. 550-562
-
-
Marionnet, C.1
Benoit, A.2
Benhamou, S.3
Sarasin, A.4
Stary, A.5
-
79
-
-
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. (1993) UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum. Carcinogenesis, 14, 1255-1260.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1255-1260
-
-
Madzak, C.1
Armier, J.2
Stary, A.3
Daya-Grosjean, L.4
Sarasin, A.5
-
80
-
-
12644305856
-
Photocarcinogenesis and inhibition of intercellular adhesion molecule I 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. (1997) Photocarcinogenesis and inhibition of intercellular adhesion molecule I expression in cells of DNA-repair-defective individuals. Proc. Natl Acad. Sci. USA, 94, 6837-6841.
-
(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
-
81
-
-
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. (1992) Striking differences in cellular catalase activity between two DNA repair-deficient diseases: xeroderma pigmentosum and trichothiodystrophy. Carcinogenesis, 13, 321-328.
-
(1992)
Carcinogenesis
, vol.13
, pp. 321-328
-
-
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
-
82
-
-
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. (1994) Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): Evidence for the existence of a transcription syndrome. Cold Spring Harbor Symp. Quant. Biol., 59, 317-329.
-
(1994)
Cold Spring Harbor 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
-
83
-
-
0027967644
-
Human nudeotide excision repair syndromes: Molecular clues to unexpected intricacies
-
Hoeijmakers, J.H.J. (1994) Human nudeotide excision repair syndromes: molecular clues to unexpected intricacies. Eur. J. Cancer, 30, 1912-1921.
-
(1994)
Eur. J. Cancer
, vol.30
, pp. 1912-1921
-
-
Hoeijmakers, J.H.J.1
-
84
-
-
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. (1998) A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy. Mol. Cell, 1, 981-990.
-
(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
-
85
-
-
0033565649
-
Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition
-
de Boer, J., van Steeg, H., Berg, R.J.W., Garssen, J., de Wit, J., van Oostrom, C.T.M., Beems, R.B., van der Horst, G.T.J., van Kreijl, C.F., de Gruijl, F.R., Bootsma, D., Hoeijmakers, J.H.J. and Weeda, G. (1999) Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition. Cancer Res., 59, 3489-3494.
-
(1999)
Cancer Res.
, vol.59
, pp. 3489-3494
-
-
De Boer, J.1
Van Steeg, H.2
Berg, R.J.W.3
Garssen, J.4
De Wit, J.5
Van Oostrom, C.T.M.6
Beems, R.B.7
Van Der Horst, G.T.J.8
Van Kreijl, C.F.9
De Gruijl, F.R.10
Bootsma, D.11
Hoeijmakers, J.H.J.12
Weeda, G.13
-
86
-
-
17344371392
-
From a DNA helicase to brittle hair
-
Winkler, G.S. and Hoeijmakers, J.H.J. (1998) From a DNA helicase to brittle hair. Nature Genet., 20, 106-107.
-
(1998)
Nature Genet.
, vol.20
, pp. 106-107
-
-
Winkler, G.S.1
Hoeijmakers, J.H.J.2
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