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2. Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F. van Vuuren AJ; Appeldoorn E; Odijk H; Yasui A; Jaspers NG; Bootsma D; Hoeijmakers JH EMBO J; 1993 Sep; 12(9):3693-701. PubMed ID: 8253091 [TBL] [Abstract][Full Text] [Related]
3. Nucleotide excision repair syndromes: molecular basis and clinical symptoms. Bootsma D; Weeda G; Vermeulen W; van Vuuren H; Troelstra C; van der Spek P; Hoeijmakers J Philos Trans R Soc Lond B Biol Sci; 1995 Jan; 347(1319):75-81. PubMed ID: 7746858 [TBL] [Abstract][Full Text] [Related]
4. DNA repair in mammalian cells : Nucleotide excision repair: variations on versatility. Nouspikel T Cell Mol Life Sci; 2009 Mar; 66(6):994-1009. PubMed ID: 19153657 [TBL] [Abstract][Full Text] [Related]
5. Nucleotide excision repair and human syndromes. de Boer J; Hoeijmakers JH Carcinogenesis; 2000 Mar; 21(3):453-60. PubMed ID: 10688865 [TBL] [Abstract][Full Text] [Related]
6. Multiple involvement of nucleotide excision repair enzymes: clinical manifestations of molecular intricacies. Jaspers NG Cytokines Mol Ther; 1996 Jun; 2(2):115-9. PubMed ID: 9384696 [TBL] [Abstract][Full Text] [Related]
7. Human cancer and DNA repair-deficient diseases. Sarasin A; Stary A Cancer Detect Prev; 1997; 21(5):406-11. PubMed ID: 9307843 [TBL] [Abstract][Full Text] [Related]
9. Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2. Scherly D; Nouspikel T; Corlet J; Ucla C; Bairoch A; Clarkson SG Nature; 1993 May; 363(6425):182-5. PubMed ID: 8483504 [TBL] [Abstract][Full Text] [Related]
10. Mutations in Cockayne Syndrome-Associated Genes (Csa and Csb) Predispose to Cisplatin-Induced Hearing Loss in Mice. Rainey RN; Ng SY; Llamas J; van der Horst GT; Segil N J Neurosci; 2016 Apr; 36(17):4758-70. PubMed ID: 27122034 [TBL] [Abstract][Full Text] [Related]
11. Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes. Carreau M; Eveno E; Quilliet X; Chevalier-Lagente O; Benoit A; Tanganelli B; Stefanini M; Vermeulen W; Hoeijmakers JH; Sarasin A Carcinogenesis; 1995 May; 16(5):1003-9. PubMed ID: 7767957 [TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 17893751 [TBL] [Abstract][Full Text] [Related]
13. Oxidative and energy metabolism as potential clues for clinical heterogeneity in nucleotide excision repair disorders. Hosseini M; Ezzedine K; Taieb A; Rezvani HR J Invest Dermatol; 2015 Feb; 135(2):341-351. PubMed ID: 25296907 [TBL] [Abstract][Full Text] [Related]
14. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes. Riou L; Zeng L; Chevallier-Lagente O; Stary A; Nikaido O; Taïeb A; Weeda G; Mezzina M; Sarasin A Hum Mol Genet; 1999 Jun; 8(6):1125-33. PubMed ID: 10332046 [TBL] [Abstract][Full Text] [Related]
15. A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. Cleaver JE; Thompson LH; Richardson AS; States JC Hum Mutat; 1999; 14(1):9-22. PubMed ID: 10447254 [TBL] [Abstract][Full Text] [Related]
16. Actual state of knowledge in the field of diseases related with defective nucleotide excision repair. Bukowska B; Karwowski BT Life Sci; 2018 Feb; 195():6-18. PubMed ID: 29305302 [TBL] [Abstract][Full Text] [Related]
17. [Repair of DNA damage using nucleotide excision repair (NER)--relationship with cancer risk]. Butkiewicz D; Rusin M; Pawlas M; Czarny M; Chorazy M Postepy Hig Med Dosw; 2002; 56(4):485-98. PubMed ID: 12418414 [TBL] [Abstract][Full Text] [Related]
18. The COOH terminus of suppressor of stem loop (SSL2/RAD25) in yeast is essential for overall genomic excision repair and transcription-coupled repair. Sweder KS; Hanawalt PC J Biol Chem; 1994 Jan; 269(3):1852-7. PubMed ID: 8294433 [TBL] [Abstract][Full Text] [Related]
19. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition. de Boer J; van Steeg H; Berg RJ; Garssen J; de Wit J; van Oostrum CT; Beems RB; van der Horst GT; van Kreijl CF; de Gruijl FR; Bootsma D; Hoeijmakers JH; Weeda G Cancer Res; 1999 Jul; 59(14):3489-94. PubMed ID: 10416615 [TBL] [Abstract][Full Text] [Related]
20. Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy. Norris PG; Limb GA; Hamblin AS; Lehmann AR; Arlett CF; Cole J; Waugh AP; Hawk JL J Invest Dermatol; 1990 Jan; 94(1):94-100. PubMed ID: 2295840 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]