Similar articles for PMID: 17184928

Year	Number of Results
1985	1
1986	2
1989	1
1991	1
1992	1
1993	2
1995	1
1996	3
1997	7
1998	1
1999	11
2000	10
2001	7
2002	5
2003	2
2004	1
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2006	6
2007	9
2008	10
2009	3
2010	2
2011	6
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2013	13
2014	7
2015	8
2016	9
2017	7
2018	10
2019	12
2020	6
2021	11
2022	18
2023	6
2024	0

1

The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum.

Brooks PJ. Brooks PJ. Neuroscience. 2007 Apr 14;145(4):1407-17. doi: 10.1016/j.neuroscience.2006.10.025. Epub 2006 Dec 19. Neuroscience. 2007. PMID: 17184928 Free PMC article. Review.

2

Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.

Kraemer KH, Patronas NJ, Schiffmann R, Brooks BP, Tamura D, DiGiovanna JJ. Kraemer KH, et al. Neuroscience. 2007 Apr 14;145(4):1388-96. doi: 10.1016/j.neuroscience.2006.12.020. Epub 2007 Feb 1. Neuroscience. 2007. PMID: 17276014 Free PMC article. Review.

3

Nucleotide Excision Repair: From Molecular Defects to Neurological Abnormalities.

Krasikova Y, Rechkunova N, Lavrik O. Krasikova Y, et al. Int J Mol Sci. 2021 Jun 9;22(12):6220. doi: 10.3390/ijms22126220. Int J Mol Sci. 2021. PMID: 34207557 Free PMC article. Review.

4

The cyclopurine deoxynucleosides: DNA repair, biological effects, mechanistic insights, and unanswered questions.

Brooks PJ. Brooks PJ. Free Radic Biol Med. 2017 Jun;107:90-100. doi: 10.1016/j.freeradbiomed.2016.12.028. Epub 2016 Dec 21. Free Radic Biol Med. 2017. PMID: 28011151 Review.

5

The 8,5'-cyclopurine-2'-deoxynucleosides: candidate neurodegenerative DNA lesions in xeroderma pigmentosum, and unique probes of transcription and nucleotide excision repair.

Brooks PJ. Brooks PJ. DNA Repair (Amst). 2008 Jul 1;7(7):1168-79. doi: 10.1016/j.dnarep.2008.03.016. Epub 2008 May 20. DNA Repair (Amst). 2008. PMID: 18495558 Free PMC article. Review.

6

Cancer in xeroderma pigmentosum and related disorders of DNA repair.

Cleaver JE. Cleaver JE. Nat Rev Cancer. 2005 Jul;5(7):564-73. doi: 10.1038/nrc1652. Nat Rev Cancer. 2005. PMID: 16069818 Review.

7

Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndrome.

Theron T, Fousteri MI, Volker M, Harries LW, Botta E, Stefanini M, Fujimoto M, Andressoo JO, Mitchell J, Jaspers NG, McDaniel LD, Mullenders LH, Lehmann AR. Theron T, et al. Mol Cell Biol. 2005 Sep;25(18):8368-78. doi: 10.1128/MCB.25.18.8368-8378.2005. Mol Cell Biol. 2005. PMID: 16135823 Free PMC article.

8

Clustered sites of DNA repair synthesis during early nucleotide excision repair in ultraviolet light-irradiated quiescent human fibroblasts.

Svetlova M, Solovjeva L, Pleskach N, Yartseva N, Yakovleva T, Tomilin N, Hanawalt P. Svetlova M, et al. Exp Cell Res. 2002 Jun 10;276(2):284-95. doi: 10.1006/excr.2002.5519. Exp Cell Res. 2002. PMID: 12027458

9

Cockayne syndrome and xeroderma pigmentosum.

Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH. Rapin I, et al. Neurology. 2000 Nov 28;55(10):1442-9. doi: 10.1212/wnl.55.10.1442. Neurology. 2000. PMID: 11185579 Free PMC article. Review.

10

DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.

Lehmann AR. Lehmann AR. Biochimie. 2003 Nov;85(11):1101-11. doi: 10.1016/j.biochi.2003.09.010. Biochimie. 2003. PMID: 14726016 Review.

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