Xeroderma Pigmentosum and Related Disorders: Examining the Linkage Between Defective DNA Repair and Cancer
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XP patients have greater than a 1000-fold increased risk of developing skin cancer before age 20 compared to the general population.
“In fact, XP patients have greater than a 1000-fold increased risk of developing skin cancer before the age of 20 compared to the general population11.”
From Modulation of UVB-induced Carcinogenesis by Activation of Alternative DNA Repair Pathways (2018) · cites this paper as [11]
Cites
Kraemer, K. H. (1987) · Archives of Dermatology · doi:10.1001/archderm.123.2.241 · Cited by 1,205 · see citing works
Self-citationCockayne syndrome: Review of 140 cases
Nance, M. A., & Berry, S. A. (1992) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320420115 · Cited by 806 · see citing works
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., & Egly, J. (1993) · Science · doi:10.1126/science.8465201 · Cited by 794 · see citing works
Robbins, J. H., Kraemer, K. H., Lutzner, M. A., Festoff, B. W., & COON, H. G. (1974) · Annals of Internal Medicine · doi:10.7326/0003-4819-80-2-221 · Cited by 751 · see citing works
Self-citationTroelstra, C., van Gool, A., de Wit, J., Vermeulen, W., Bootsma, D., & Hoeijmakers, J. H. J. (1992) · Cell · doi:10.1016/0092-8674(92)90390-x · Cited by 729 · see citing works
Venema, J., Mullenders, L. H. F., Natarajan, A. T., van Zeeland, A. A., & Mayne, L. V. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4707 · Cited by 552 · see citing works
Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22
Cannon‐Albright, L., Goldgar, D. E., Meyer, L. J., Lewis, C. M., Anderson, D. E., Fountain, J. W., Hegi, M. E., Wiseman, R. W., Petty, E. M., Bale, A. E., et al. (1992) · Science · doi:10.1126/science.1439824 · Cited by 524 · see citing works
High Risk of Malignant Melanoma in Melanoma-Prone Families with Dysplastic Nevi
Greene, M. H., CLARK, W. H., TUCKER, M. A., KRAEMER, K. H., ELDER, D. E., & FRASER, M. C. (1985) · Annals of Internal Medicine · doi:10.7326/0003-4819-102-4-458 · Cited by 451 · see citing works
Self-citationWeeda, G., van Ham, R. C. A., Vermeulen, W., Bootsma, D., van der Eb, A. J., & Hoeijmakers, J. H. J. (1990) · Cell · doi:10.1016/0092-8674(90)90122-u · Cited by 435 · see citing works
Tanaka, K., Miura, N., Satokata, I., Miyamoto, I., Yoshida, M. C., Satoh, Y., Kondo, S., Yasui, A., Okayama, H., & Okada, Y. (1990) · Nature · doi:10.1038/348073a0 · Cited by 388 · see citing works
Acquired Precursors of Cutaneous Malignant Melanoma
Greene, M. H., Clark, W. H., Tucker, M. A., Elder, D. E., Kraemer, K. H., Guerry, D., Witmer, W. K., Thompson, J. C., Matozzo, I., & Fraser, M. C. (1985) · New England Journal of Medicine · doi:10.1056/nejm198501103120205 · Cited by 335 · see citing works
Self-citationMAHER, V. M., OUELLETTE, L. M., CURREN, R. D., & MCCORMICK, J. J. (1976) · Nature · doi:10.1038/261593a0 · Cited by 333 · see citing works
Mapping the Gene for Hereditary Cutaneous Malignant Melanoma–Dysplastic Nevus to Chromosome Lp
Bale, S. J., Dracopoli, N. C., Tucker, M. A., Clark, W. H., Fraser, M. C., Stanger, B. Z., Green, P., Donis-Keller, H., Housman, D. E., & Greene, M. H. (1989) · New England Journal of Medicine · doi:10.1056/nejm198905253202102 · Cited by 314 · see citing works
Nucleotide excision repair II: from yeast to mammals
Hoeijmakers, J. H. J. (1993) · Trends in Genetics · doi:10.1016/0168-9525(93)90121-w · Cited by 304 · see citing works
Weber, C. A., Salazar, E. P., Stewart, S. A., & Thompson, L. H. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb08260.x · Cited by 262 · see citing works
Sancar, A., & Tang, M. (1993) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1993.tb09233.x · Cited by 256 · see citing works
Andrews, A. D., Barrett, S. F., & Robbins, J. H. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.4.1984 · Cited by 250 · see citing works
Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C
Legerski, R. J., & Peterson, C. A. (1992) · Nature · doi:10.1038/359070a0 · Cited by 242 · see citing works
Bredberg, A. C. A., Kraemer, K. H., & Seidman, M. M. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.21.8273 · Cited by 214 · see citing works
Self-citationScherly, D., Nouspikel, T. P., Corlet, J., Ucla, C., Bairoch, A., & Clarkson, S. G. (1993) · Nature · doi:10.1038/363182a0 · Cited by 203 · see citing works
One pyrimidine dimer inactivates expression of a transfected gene in xeroderma pigmentosum cells.
Protić‐Sabljić, M., & Kraemer, K. H. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.19.6622 · Cited by 190 · see citing works
Self-citationThree complementation groups in Cockayne syndrome
Lehmann, A. R. (1982) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(82)90115-4 · Cited by 176 · see citing works
Flejter, W. L., McDaniel, L., Johns, D., Friedberg, E. C., & Schultz, R. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.1.261 · Cited by 170 · see citing works
Characterization of molecular defects in xeroderma pigmentosum group C
Li, L., Bales, E. S., Peterson, C. A., & Legerski, R. J. (1993) · Nature Genetics · doi:10.1038/ng1293-413 · Cited by 134 · see citing works
A signature element distinguishes sibling and independent mutations in a shuttle vector plasmid
Parris, C. N., & Seidman, M. M. (1992) · Gene · doi:10.1016/0378-1119(92)90482-5 · Cited by 131 · see citing works
Self-citationCharacterization of a splicing mutation in group A xeroderma pigmentosum.
Satokata, I., Tanaka, K., Miura, N., Miyamoto, I., Satoh, Y., Kondo, S., & Okada, Y. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.24.9908 · Cited by 126 · see citing works
Nucleotide excision repair I: from E. coli to yeast
Hoeijmakers, J. H. J. (1993) · Trends in Genetics · doi:10.1016/0168-9525(93)90164-d · Cited by 125 · see citing works
Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5
O’Donovan, A., & Wood, R. D. (1993) · Nature · doi:10.1038/363185a0 · Cited by 123 · see citing works
Norris, P. G., Limb, G. A., Hamblin, A. S., et al. (1990) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12873952 · Cited by 108 · see citing works
Lehmann, A. R., Arlett, C. F., Broughton, B. C., Harcourt, S. A., Steingrimsdottir, H., Stefanini, M., Malcolm, A. D. B., Taylor, R., Natarajan, A. T., & Green, S. A. (1988) · PubMed · Cited by 105 · see citing works
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
Vermeulen, W., Jaeken, J., Jaspers, N. G. J., Bootsma, D., & Hoeijmakers, J. H. J. (1993) · Europe PMC (PubMed Central) · Cited by 103 · see citing works
Genetic complementation groups in Cockayne syndrome
Tanaka, K., Kawai, K., Kumahara, Y., Ikenaga, M., & Okada, Y. (1981) · Somatic Cell and Molecular Genetics · doi:10.1007/bf01542989 · Cited by 103 · see citing works
Levy, D. D., Groopman, J. D., Lim, S. E., et al. (1992) · PubMed · Cited by 93 · see citing works
Self-citationGaspari, A. A., Fleisher, T. A., & Kraemer, K. H. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116682 · Cited by 80 · see citing works
Self-citationTroelstra, C., Hesen, W., Bootsma, D., & Hoeijmakers, J. H. J. (1993) · Nucleic Acids Research · doi:10.1093/nar/21.3.419 · Cited by 74 · see citing works
Perera, M. I., Um, K., Greene, M. H., et al. (1986) · PubMed · Cited by 69 · see citing works
The UvrABC endonuclease system of Escherichia coli — A view from Baltimore
Grossman, L. I., & Yeung, A. T. (1990) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(90)90006-q · Cited by 62 · see citing works
Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy
Mariani, E., Facchini, A., Honorati, M. C., et al. (1992) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.1992.tb06457.x · Cited by 61 · see citing works
Parris, C. N., & Kraemer, K. H. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.15.7260 · Cited by 58 · see citing works
Self-citationScott, R. J., Itin, P. H., Kleijer, W. J., Kolb, K., Arlett, C. F., & Muller, H. (1993) · Journal of the American Academy of Dermatology · doi:10.1016/0190-9622(93)70263-s · Cited by 54 · see citing works
Barrett, S. F., Robbins, J. H., Tarone, R. E., & Kraemer, K. H. (1991) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(91)90032-k · Cited by 52 · see citing works
Self-citationSeetharam, S., Kraemer, K. H., Waters, H. L., et al. (1991) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(91)90045-q · Cited by 37 · see citing works
Self-citationLocalization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11–q21
Troelstra, C., Landsvater, R. M., Wiegant, J. C. A. G., van der Ploeg, M., Viel, G. T., Buys, C. H. C. M., & Hoeijmakers, J. H. J. (1992) · Genomics · doi:10.1016/0888-7543(92)90304-b · Cited by 35 · see citing works
Seetharam, S., Waters, H. L., Seidman, M. M., & Kraemer, K. H. (1989) · PubMed · Cited by 29 · see citing works
Self-citationGözükara, E. M., Parris, C. N., Weber, C. A., Salazar, E. P., Seidman, M. M., Watkins, J. F., Prakash, L., & Kraemer, K. H. (1994) · PubMed · Cited by 28 · see citing works
Self-citationKore-eda, S. (1992) · Archives of Dermatology · doi:10.1001/archderm.128.7.971 · Cited by 23 · see citing works
Moriwaki, S., Tarone, R. E., & Kraemer, K. H. (1994) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12388847 · Cited by 21 · see citing works
Self-citationDay, R. S., Ziolkowski, C. H. J., & Dimattina, M. (1981) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1981.tb09049.x · Cited by 17 · see citing works
Co-recessive inheritance: A model for DNA repair and other surveillance genes in higher eukaryotes
Lambert, W. C., & Lambert, M. W. (1992) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(92)90079-i · Cited by 17 · see citing works
Nuzzo, F., Zei, G., Stefanini, M., et al. (1990) · Journal of Medical Genetics · doi:10.1136/jmg.27.1.21 · Cited by 16 · see citing works
Rinaldy, A., Bellew, T. M., Egli, E., et al. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.17.6818 · Cited by 15 · see citing works
Rare syndromes. I. Cockayne syndrome: a review of the 129 cases so far reported in the literature.
Cantani, A., Bamonte, G., Bellioni, P., et al. (1987) · PubMed · Cited by 10 · see citing works
Recent developments with the human repair genes ERCC2, ERCC4, and XRCC1
Thompson, L. H., Caldecott, K. W., Brookman, K. W., et al. (1992) · University of North Texas Digital Library (University of North Texas) · Cited by 2 · see citing works
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Sarasin, A. (1999) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/s1383-5742(99)00025-3 · Cited by 215 · see citing works
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Modulation of UVB-induced Carcinogenesis by Activation of Alternative DNA Repair Pathways
Sha, Y., Vartanian, V., Owen, N., Mengden Koon, S. J., Calkins, M. J., Thompson, C. S., Mirafzali, Z., Mir, S., Goldsmith, L. E., He, H., et al. (2018) · Scientific Reports · doi:10.1038/s41598-017-17940-8 · Cited by 12 · see citing works
- Authors
- Kraemer, K. H., Levy, D. D., Parris, C. N., Gozukara, E. M., Moriwaki, S., Adelberg, S., & Seidman, M. M.
- Affiliations
- National Cancer Institute (US)
- Otsuka (United States) (US)
- Venue
- Journal of Investigative Dermatology
- Publisher
- Elsevier BV
- Published
- 1994-11
- Volume
- 103
- Issue
- 5
- Pages
- S96-S101
- ISSN
- 0022-202X (ISSN-L)
- OpenAlex
- W1984191455
- Cited by
- 118
- References
- 53
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2020: 1 · 2019: 1 · 2018: 4 · 2017: 4 · 2016: 2 · 2015: 2 · 2014: 6 · 2013: 4 · 2012: 5
- FWCI
- 1.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Investigative Dermatology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (Z01BC004517)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and rare skin diseases.
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- xeroderma pigmentosum, Cockayne syndrome, trichothiodystrophy, DNA repair deficiency, UV mutagenesis, cyclobutane dimers, aflatoxins, complementation groups, carcinogenesis, cancer risk
- MeSH terms
- Cockayne Syndrome, DNA Repair, Dysplastic Nevus Syndrome, Hair, Humans, Genetic Linkage, Neoplasms, Xeroderma Pigmentosum
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