214 related articles for article (PubMed ID: 21176161)
1. Hydrogen peroxide induced genomic instability in nucleotide excision repair-deficient lymphoblastoid cells.
Gopalakrishnan K; Low GKM; Ting APL; Srikanth P; Slijepcevic P; Hande MP
Genome Integr; 2010 Dec; 1(1):16. PubMed ID: 21176161
[TBL] [Abstract][Full Text] [Related]
2. Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum.
Cleaver JE
J Dermatol Sci; 2000 May; 23(1):1-11. PubMed ID: 10699759
[TBL] [Abstract][Full Text] [Related]
3. Role of Xeroderma pigmentosum D (XPD) protein in genome maintenance in human cells under oxidative stress.
Low GKM; Ting APL; Fok EDZ; Gopalakrishnan K; Zeegers D; Khaw AK; Jayapal M; Martinez-Lopez W; Hande MP
Mutat Res Genet Toxicol Environ Mutagen; 2022; 876-877():503444. PubMed ID: 35483790
[TBL] [Abstract][Full Text] [Related]
4. An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair.
Andressoo JO; Weeda G; de Wit J; Mitchell JR; Beems RB; van Steeg H; van der Horst GT; Hoeijmakers JH
Mol Cell Biol; 2009 Mar; 29(5):1276-90. PubMed ID: 19114557
[TBL] [Abstract][Full Text] [Related]
5. Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.
Nishiwaki T; Kobayashi N; Iwamoto T; Yamamoto A; Sugiura S; Liu YC; Sarasin A; Okahashi Y; Hirano M; Ueno S; Mori T
DNA Repair (Amst); 2008 Dec; 7(12):1990-8. PubMed ID: 18817897
[TBL] [Abstract][Full Text] [Related]
6. Telomere attrition and genomic instability in xeroderma pigmentosum type-b deficient fibroblasts under oxidative stress.
Ting AP; Low GK; Gopalakrishnan K; Hande MP
J Cell Mol Med; 2010 Jan; 14(1-2):403-16. PubMed ID: 19840190
[TBL] [Abstract][Full Text] [Related]
7. A unified model for the molecular basis of Xeroderma pigmentosum-Cockayne Syndrome.
Moriel-Carretero M; Herrera-Moyano E; Aguilera A
Rare Dis; 2015; 3(1):e1079362. PubMed ID: 26460500
[TBL] [Abstract][Full Text] [Related]
8. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.
Lehmann AR
Biochimie; 2003 Nov; 85(11):1101-11. PubMed ID: 14726016
[TBL] [Abstract][Full Text] [Related]
9. Nucleotide excision repair activity on DNA damage induced by photoactivated methylene blue.
Berra CM; de Oliveira CS; Garcia CC; Rocha CR; Lerner LK; Lima LC; Baptista Mda S; Menck CF
Free Radic Biol Med; 2013 Aug; 61():343-56. PubMed ID: 23567189
[TBL] [Abstract][Full Text] [Related]
10. Competent transcription initiation by RNA polymerase II in cell-free extracts from xeroderma pigmentosum groups B and D in an optimized RNA transcription assay.
Satoh MS; Hanawalt PC
Biochim Biophys Acta; 1997 Nov; 1354(3):241-51. PubMed ID: 9427533
[TBL] [Abstract][Full Text] [Related]
11. XPD/ERCC2 mutations interfere in cellular responses to oxidative stress.
Lerner LK; Moreno NC; Rocha CRR; Munford V; Santos V; Soltys DT; Garcia CCM; Sarasin A; Menck CFM
Mutagenesis; 2019 Dec; 34(4):341-354. PubMed ID: 31348825
[TBL] [Abstract][Full Text] [Related]
12. Analysis of the conserved NER helicases (XPB and XPD) and UV-induced DNA damage in Hydra.
Galande AA; Perween N; Saijo M; Ghaskadbi SS; Ghaskadbi S
Biochim Biophys Acta Gen Subj; 2018 Sep; 1862(9):2031-2042. PubMed ID: 29959982
[TBL] [Abstract][Full Text] [Related]
13. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
Weeda G; Eveno E; Donker I; Vermeulen W; Chevallier-Lagente O; Taïeb A; Stary A; Hoeijmakers JH; Mezzina M; Sarasin A
Am J Hum Genet; 1997 Feb; 60(2):320-9. PubMed ID: 9012405
[TBL] [Abstract][Full Text] [Related]
14. A mutation in repB, the dictyostelium homolog of the human xeroderma pigmentosum B gene, has increased sensitivity to UV-light but normal morphogenesis.
Lee SK; Yu SL; Alexander H; Alexander S
Biochim Biophys Acta; 1998 Aug; 1399(2-3):161-72. PubMed ID: 9765592
[TBL] [Abstract][Full Text] [Related]
15. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
Graham JM; Anyane-Yeboa K; Raams A; Appeldoorn E; Kleijer WJ; Garritsen VH; Busch D; Edersheim TG; Jaspers NG
Am J Hum Genet; 2001 Aug; 69(2):291-300. PubMed ID: 11443545
[TBL] [Abstract][Full Text] [Related]
16. Effect of the anti-neoplastic drug doxorubicin on XPD-mutated DNA repair-deficient human cells.
Saffi J; Agnoletto MH; Guecheva TN; Batista LF; Carvalho H; Henriques JA; Stary A; Menck CF; Sarasin A
DNA Repair (Amst); 2010 Jan; 9(1):40-7. PubMed ID: 19926538
[TBL] [Abstract][Full Text] [Related]
17. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
Oh KS; Khan SG; Jaspers NG; Raams A; Ueda T; Lehmann A; Friedmann PS; Emmert S; Gratchev A; Lachlan K; Lucassan A; Baker CC; Kraemer KH
Hum Mutat; 2006 Nov; 27(11):1092-103. PubMed ID: 16947863
[TBL] [Abstract][Full Text] [Related]
18. Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression.
Garcia-Moreno H; Langbehn DR; Abiona A; Garrood I; Fleszar Z; Manes MA; Morley AMS; Craythorne E; Mohammed S; Henshaw T; Turner S; Naik H; Bodi I; Sarkany RPE; Fassihi H; Lehmann AR; Giunti P
Brain; 2023 Dec; 146(12):5044-5059. PubMed ID: 38040034
[TBL] [Abstract][Full Text] [Related]
19. Oxidative damage-induced PCNA complex formation is efficient in xeroderma pigmentosum group A but reduced in Cockayne syndrome group B cells.
Balajee AS; Dianova I; Bohr VA
Nucleic Acids Res; 1999 Nov; 27(22):4476-82. PubMed ID: 10536158
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
