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Items: 1 to 20 of 42

1.

Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes.

Murai M, Enokido Y, Inamura N, Yoshino M, Nakatsu Y, van der Horst GT, Hoeijmakers JH, Tanaka K, Hatanaka H.

Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13379-84. Epub 2001 Oct 30.

2.

Xeroderma pigmentosum and molecular cloning of DNA repair genes.

Boulikas T.

Anticancer Res. 1996 Mar-Apr;16(2):693-708. Review.

PMID:
8687116
3.

Cockayne syndrome and xeroderma pigmentosum.

Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH.

Neurology. 2000 Nov 28;55(10):1442-9. Review.

4.

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 BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J, et al.

Am J Hum Genet. 1995 Jan;56(1):167-74. Review.

5.

DNA repair-deficient Xpa and Xpa/p53+/- knock-out mice: nature of the models.

van Steeg H, de Vries A, van Oostrom CTh, van Benthem J, Beems RB, van Kreijl CF.

Toxicol Pathol. 2001;29 Suppl:109-16. Review.

PMID:
11695546
6.

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

Kraemer KH, Patronas NJ, Schiffmann R, Brooks BP, Tamura D, DiGiovanna JJ.

Neuroscience. 2007 Apr 14;145(4):1388-96. Epub 2007 Feb 1. Review.

8.
9.

Cancer in xeroderma pigmentosum and related disorders of DNA repair.

Cleaver JE.

Nat Rev Cancer. 2005 Jul;5(7):564-73. Review.

PMID:
16069818
11.

Unraveling DNA repair in human: molecular mechanisms and consequences of repair defect.

Tuteja N, Tuteja R.

Crit Rev Biochem Mol Biol. 2001;36(3):261-90. Review.

PMID:
11450971
12.

Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases.

Lindenbaum Y, Dickson D, Rosenbaum P, Kraemer K, Robbins I, Rapin I.

Eur J Paediatr Neurol. 2001;5(6):225-42. Review.

PMID:
11764181
13.

Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription.

Berneburg M, Lehmann AR.

Adv Genet. 2001;43:71-102. Review.

PMID:
11037299
14.

[The metabolic and molecular bases of Cockayne syndrome].

Flores-Alvarado LJ, Ramirez-Garcia SA, Núñez-Reveles NY.

Rev Invest Clin. 2010 Sep-Oct;62(5):480-90. Review. Spanish.

PMID:
21416736
15.
16.

Bacterial DNA repair genes and their eukaryotic homologues: 4. The role of nucleotide excision DNA repair (NER) system in mammalian cells.

Maddukuri L, Dudzińska D, Tudek B.

Acta Biochim Pol. 2007;54(3):469-82. Epub 2007 Sep 23. Review.

17.

Nucleotide excision repair and human syndromes.

de Boer J, Hoeijmakers JH.

Carcinogenesis. 2000 Mar;21(3):453-60. Review.

PMID:
10688865
18.

Oxidative DNA damage and nucleotide excision repair.

Melis JP, van Steeg H, Luijten M.

Antioxid Redox Signal. 2013 Jun 20;18(18):2409-19. doi: 10.1089/ars.2012.5036. Epub 2012 Dec 7. Review.

19.

Xeroderma pigmentosum, Cockayne's syndrome, helicases, and DNA repair: what's the relationship?

Friedberg EC.

Cell. 1992 Dec 11;71(6):887-9. Review. No abstract available.

PMID:
1458537
20.

Cockayne syndrome group B (CSB) protein: at the crossroads of transcriptional networks.

Vélez-Cruz R, Egly JM.

Mech Ageing Dev. 2013 May-Jun;134(5-6):234-42. doi: 10.1016/j.mad.2013.03.004. Epub 2013 Apr 3. Review.

PMID:
23562425

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