-
1
-
-
64749101619
-
-
Hebra F, Kaposi M. On diseases of the skin, including the exanthemata. New Sydenham Society 1874; 61:252-258 (Translated by W. Tay, London).
-
Hebra F, Kaposi M. On diseases of the skin, including the exanthemata. New Sydenham Society 1874; 61:252-258 (Translated by W. Tay, London).
-
-
-
-
2
-
-
0042264293
-
Xeroderma pigmentosum
-
Kaposi, M. Xeroderma pigmentosum. Ann Dermatol Venereol, 1883; 4:29-38.
-
(1883)
Ann Dermatol Venereol
, vol.4
, pp. 29-38
-
-
Kaposi, M.1
-
3
-
-
64749089951
-
Contribution to the pathogenesis of xeroderma pigmentosum
-
Ulicna-Zapletalova M. Contribution to the pathogenesis of xeroderma pigmentosum. Cesk Dermatol 1949; 24:330-334.
-
(1949)
Cesk Dermatol
, vol.24
, pp. 330-334
-
-
Ulicna-Zapletalova, M.1
-
4
-
-
0014421995
-
Defective repair replication of DNA in xeroderma pigmentosum
-
Cleaver, JE. Defective repair replication of DNA in xeroderma pigmentosum. Nature 1968; 218:652-656.
-
(1968)
Nature
, vol.218
, pp. 652-656
-
-
Cleaver, J.E.1
-
5
-
-
0014531281
-
Xeroderma pigmentosimi: A human disease in which an initial stage of DNA repair is defective
-
Cleaver, JE. Xeroderma pigmentosimi: a human disease in which an initial stage of DNA repair is defective. Proc Natl Acad Sci USA 1969; 63:428-435.
-
(1969)
Proc Natl Acad Sci USA
, vol.63
, pp. 428-435
-
-
Cleaver, J.E.1
-
7
-
-
34247219683
-
Xeroderma pigmentosum: Beyond skin cancer
-
Lichon V, Khachemoune A. Xeroderma pigmentosum: beyond skin cancer. J Drug Dermatol 2007; 6:281-288.
-
(2007)
J Drug Dermatol
, vol.6
, pp. 281-288
-
-
Lichon, V.1
Khachemoune, A.2
-
9
-
-
0023130695
-
-
Kraemer KH, Lee MM, Scotto J. Xeroderma pigmentosum. Cutaneous, ocular, and neurological abnormalities in 830 published case. Arch Dermatol 1987; 123:241-250.
-
Kraemer KH, Lee MM, Scotto J. Xeroderma pigmentosum. Cutaneous, ocular, and neurological abnormalities in 830 published case. Arch Dermatol 1987; 123:241-250.
-
-
-
-
10
-
-
34547916152
-
Polymorphism of DNA repair genes XPD and ERCCl and risk of cataract development
-
Unal M, Guven M, Batar B et al. Polymorphism of DNA repair genes XPD and ERCCl and risk of cataract development. Exp Eye Res 2007; 85(3):328-334.
-
(2007)
Exp Eye Res
, vol.85
, Issue.3
, pp. 328-334
-
-
Unal, M.1
Guven, M.2
Batar, B.3
-
11
-
-
33846923410
-
Genetic polymorphism in the nucleotide excision repair pathway and lung cancer risk: A meta analysis
-
Kiyohara C, Yoshimasu K. Genetic polymorphism in the nucleotide excision repair pathway and lung cancer risk: a meta analysis. Int J Med Sci 2007; 4:59-71.
-
(2007)
Int J Med Sci
, vol.4
, pp. 59-71
-
-
Kiyohara, C.1
Yoshimasu, K.2
-
12
-
-
34250183843
-
On the search of skin gene therapy strategies of xeroderma pigmentosum disease
-
Menck CF, Armelini MG, Lima-Bessa KM. On the search of skin gene therapy strategies of xeroderma pigmentosum disease. Curr Gene Ther 2007; 7:163-174.
-
(2007)
Curr Gene Ther
, vol.7
, pp. 163-174
-
-
Menck, C.F.1
Armelini, M.G.2
Lima-Bessa, K.M.3
-
13
-
-
33947279485
-
Sunlight, skin cancer and vitamin D: What are the conclusions of recent findings that protection against solar ultraviolet (UV) radiation causes 25-hydroxyvitamin D deficiency in solid organ transplant recipients, xeroderma pigmentosimi, and other risk groups?
-
Reichrath J. Sunlight, skin cancer and vitamin D: what are the conclusions of recent findings that protection against solar ultraviolet (UV) radiation causes 25-hydroxyvitamin D deficiency in solid organ transplant recipients, xeroderma pigmentosimi, and other risk groups? J Steroid Biochem Mol Biol 2007; 103:664-667.
-
(2007)
J Steroid Biochem Mol Biol
, vol.103
, pp. 664-667
-
-
Reichrath, J.1
-
14
-
-
0001007178
-
UV damage, DNA repair and skin carcinogenesis
-
Cleaver JE, Crowley E. UV damage, DNA repair and skin carcinogenesis. Front Biosci 2002; 7:dl024-1043.
-
(2002)
Front Biosci
, vol.7
-
-
Cleaver, J.E.1
Crowley, E.2
-
15
-
-
33748784343
-
Cyclobutane pyrimidine dimers are predominant DNA lesions in whole human skin exposed to UVA radiation
-
Mouret, S, Baudouin C, Charveron M et al. Cyclobutane pyrimidine dimers are predominant DNA lesions in whole human skin exposed to UVA radiation. Proc Natl Acad Sci USA 2006; 103:13765-13770.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 13765-13770
-
-
Mouret, S.1
Baudouin, C.2
Charveron, M.3
-
16
-
-
34548403117
-
The oxidatively induced DNA lesions 8,5'-cyclo-2'-deoxyadenosine and 8-hydroxy-2'-deoxyadenosine are strongly resistant to acid induced hydrolysis of glycosidic bond
-
Theruvatu JA, Jaruga P, Dizdaroglu M. The oxidatively induced DNA lesions 8,5'-cyclo-2'-deoxyadenosine and 8-hydroxy-2'-deoxyadenosine are strongly resistant to acid induced hydrolysis of glycosidic bond. Mech Ageing Dev 2007; 128(9):494-502.
-
(2007)
Mech Ageing Dev
, vol.128
, Issue.9
, pp. 494-502
-
-
Theruvatu, J.A.1
Jaruga, P.2
Dizdaroglu, M.3
-
17
-
-
0028021376
-
Synergistic action of near UV and phenylalanine, tyrosine or tryptophan on the inactivation of phage T7: Role of superoxide radicals and hydrogen peroxide
-
Craggs J, Kirk SH, Ahmad SL Synergistic action of near UV and phenylalanine, tyrosine or tryptophan on the inactivation of phage T7: role of superoxide radicals and hydrogen peroxide. J Photochem Photobiol 1994; 24:123-128.
-
(1994)
J Photochem Photobiol
, vol.24
, pp. 123-128
-
-
Craggs, J.1
Kirk, S.H.2
Ahmad, S.L.3
-
18
-
-
0032524674
-
Generation of reactive oxygen species from the photolysis of histidine by near-ultraviolet light: Effects on T7 as a model biological system
-
Paretzoglou C, Stockenhuber S, Kirk SH et al. Generation of reactive oxygen species from the photolysis of histidine by near-ultraviolet light: effects on T7 as a model biological system. J Photochem Photobiol 1998; 43:101-105.
-
(1998)
J Photochem Photobiol
, vol.43
, pp. 101-105
-
-
Paretzoglou, C.1
Stockenhuber, S.2
Kirk, S.H.3
-
19
-
-
8644276390
-
Near ultraviolet photolysis of L-mandelate, formation of reactive oxygen species, inactivation of phage T7 and implication on human health
-
Ahmad SI, Hargreaves A, Taiwo FA et al. Near ultraviolet photolysis of L-mandelate, formation of reactive oxygen species, inactivation of phage T7 and implication on human health. J Photochem Photobiol B 2004; 77:55-62.
-
(2004)
J Photochem Photobiol B
, vol.77
, pp. 55-62
-
-
Ahmad, S.I.1
Hargreaves, A.2
Taiwo, F.A.3
-
20
-
-
34247169028
-
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: A complex genotype-phenotype relationship
-
Kraemer KH, Patronas NJ, Schiffmann R. et al. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship. Neurosci 2007; 145:1388-1396.
-
(2007)
Neurosci
, vol.145
, pp. 1388-1396
-
-
Kraemer, K.H.1
Patronas, N.J.2
Schiffmann, R.3
-
21
-
-
34250182079
-
Preferential binding of hximan XPA to the mitomycin C-DNA interstrand crosslink and modulation by arsenic and cadmium
-
Mustra DJ, Warren AJ, Wilcox DE et al. Preferential binding of hximan XPA to the mitomycin C-DNA interstrand crosslink and modulation by arsenic and cadmium. Chem Biol Interact 2007; 168:159-168.
-
(2007)
Chem Biol Interact
, vol.168
, pp. 159-168
-
-
Mustra, D.J.1
Warren, A.J.2
Wilcox, D.E.3
-
22
-
-
34447115716
-
High mobility group Al proteins inhibit expression of nucleotide excision repair factor xeroderma pigmentosum group A
-
Adair JE, Maloney SC, Dement GA. High mobility group Al proteins inhibit expression of nucleotide excision repair factor xeroderma pigmentosum group A. Cancer Res 2007; 67:6044-6052.
-
(2007)
Cancer Res
, vol.67
, pp. 6044-6052
-
-
Adair, J.E.1
Maloney, S.C.2
Dement, G.A.3
-
23
-
-
3042781670
-
A new, tenth subunit of TFIIH is responsible for DNA repair syndrome Trichothiodystrophy group A
-
Giglia-Mari G, Coin F, Ranish JA et al. A new, tenth subunit of TFIIH is responsible for DNA repair syndrome Trichothiodystrophy group A. Nat Genet 2004; 36:714-719.
-
(2004)
Nat Genet
, vol.36
, pp. 714-719
-
-
Giglia-Mari, G.1
Coin, F.2
Ranish, J.A.3
-
24
-
-
34247513888
-
Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair
-
Coin F, Oksenych V, Egly JM. Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair. Mol Cell 2007; 26:245-256.
-
(2007)
Mol Cell
, vol.26
, pp. 245-256
-
-
Coin, F.1
Oksenych, V.2
Egly, J.M.3
-
25
-
-
34547669303
-
Polymorphism of the DNA gene XPD and risk of bladder cancer in a Southeastern Chinese population
-
Shao J, Gu M, Xu Z et al. Polymorphism of the DNA gene XPD and risk of bladder cancer in a Southeastern Chinese population. Cancer Genet Cytogenet 2007; 177:30-36.
-
(2007)
Cancer Genet Cytogenet
, vol.177
, pp. 30-36
-
-
Shao, J.1
Gu, M.2
Xu, Z.3
-
26
-
-
34250682202
-
Deficient base excision repair of oxidative DNA damage induced by methylene blue plus visible light in xeroderma pigmentosum group C fibroblasts
-
Kassam SN, Rainbow AJ. Deficient base excision repair of oxidative DNA damage induced by methylene blue plus visible light in xeroderma pigmentosum group C fibroblasts. Biochem Biophys Res Commun 2007; 359:1004-1009.
-
(2007)
Biochem Biophys Res Commun
, vol.359
, pp. 1004-1009
-
-
Kassam, S.N.1
Rainbow, A.J.2
-
27
-
-
34247118837
-
The INGlb tumor suppressor facilitates nucleotide excision repair by promoting chromatin accessibility to XPA
-
Kuo WH, Wang Y, Wong RP et al. The INGlb tumor suppressor facilitates nucleotide excision repair by promoting chromatin accessibility to XPA. Exp Cell Res 2007; 313:1628-1638.
-
(2007)
Exp Cell Res
, vol.313
, pp. 1628-1638
-
-
Kuo, W.H.1
Wang, Y.2
Wong, R.P.3
-
28
-
-
34250315639
-
Attenuated expression of xeroderma pigmentosum group C is associated with critical events in human bladder cancer carcinogenesis and progression
-
Chen Z, Yang J, Wang G et al. Attenuated expression of xeroderma pigmentosum group C is associated with critical events in human bladder cancer carcinogenesis and progression. Cancer Res 2007; 67:4578-4585.
-
(2007)
Cancer Res
, vol.67
, pp. 4578-4585
-
-
Chen, Z.1
Yang, J.2
Wang, G.3
-
29
-
-
0025122059
-
Electroporation of normal himaan DNA endonucleases into xeroderma pigmentosum cells corrects their DNA repair defect
-
Tsongalis GJ, Lambert WC, Lambert MW. Electroporation of normal himaan DNA endonucleases into xeroderma pigmentosum cells corrects their DNA repair defect. Carcinogenesis 1990; 11:499-503.
-
(1990)
Carcinogenesis
, vol.11
, pp. 499-503
-
-
Tsongalis, G.J.1
Lambert, W.C.2
Lambert, M.W.3
-
30
-
-
34247256517
-
XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: Implications for Cockayne syndrome in XP-G/CS patients
-
Ito S, Kuraoka I, Chymkowitch P et al. XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients. Mol Cell 2007; 26:231-243.
-
(2007)
Mol Cell
, vol.26
, pp. 231-243
-
-
Ito, S.1
Kuraoka, I.2
Chymkowitch, P.3
-
31
-
-
34247148895
-
The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum
-
Brooks PJ. The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum. Neuroscience 2007; 145:1407-1417.
-
(2007)
Neuroscience
, vol.145
, pp. 1407-1417
-
-
Brooks, P.J.1
-
32
-
-
27144512353
-
Development of a new mouse model (xeroderma pigmentosum A-deficient, stem cell factor-transgenic) of ultraviolet B-induced melanoma
-
Yamazaki F, Okamoto H, Matsxmiora Y. Development of a new mouse model (xeroderma pigmentosum A-deficient, stem cell factor-transgenic) of ultraviolet B-induced melanoma. J Invest Dermatol 2005; 125:521-525.
-
(2005)
J Invest Dermatol
, vol.125
, pp. 521-525
-
-
Yamazaki, F.1
Okamoto, H.2
Matsxmiora, Y.3
-
33
-
-
34250831624
-
Loss of xeroderma pigmentosum C (Xpc) enhances melanoma photocarcinogenesis in ink4a-Arf-deficient mice
-
Yang G, Curley D, Bosenberg MW et al. Loss of xeroderma pigmentosum C (Xpc) enhances melanoma photocarcinogenesis in ink4a-Arf-deficient mice. Cancer Res 2007; 67:5649-5657.
-
(2007)
Cancer Res
, vol.67
, pp. 5649-5657
-
-
Yang, G.1
Curley, D.2
Bosenberg, M.W.3
-
34
-
-
34250690390
-
Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as xeroderma pigmentosum variant type
-
Tanioka M, Masaki T, Ono R et al. Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as xeroderma pigmentosum variant type, J Invest Dermatol 2007; 127:1745-1751.
-
(2007)
J Invest Dermatol
, vol.127
, pp. 1745-1751
-
-
Tanioka, M.1
Masaki, T.2
Ono, R.3
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