392 related articles for article (PubMed ID: 16904611)
1. An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria.
Andressoo JO; Mitchell JR; de Wit J; Hoogstraten D; Volker M; Toussaint W; Speksnijder E; Beems RB; van Steeg H; Jans J; de Zeeuw CI; Jaspers NG; Raams A; Lehmann AR; Vermeulen W; Hoeijmakers JH; van der Horst GT
Cancer Cell; 2006 Aug; 10(2):121-32. PubMed ID: 16904611
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus.
Armelini MG; Muotri AR; Marchetto MC; de Lima-Bessa KM; Sarasin A; Menck CF
Cancer Gene Ther; 2005 Apr; 12(4):389-96. PubMed ID: 15650764
[TBL] [Abstract][Full Text] [Related]
5. The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
Berneburg M; Clingen PH; Harcourt SA; Lowe JE; Taylor EM; Green MH; Krutmann J; Arlett CF; Lehmann AR
Cancer Res; 2000 Jan; 60(2):431-8. PubMed ID: 10667598
[TBL] [Abstract][Full Text] [Related]
6. Tissue specific mutagenic and carcinogenic responses in NER defective mouse models.
Wijnhoven SW; Hoogervorst EM; de Waard H; van der Horst GT; van Steeg H
Mutat Res; 2007 Jan; 614(1-2):77-94. PubMed ID: 16769089
[TBL] [Abstract][Full Text] [Related]
7. Mutations in the XPD gene in xeroderma pigmentosum group D cell strains: confirmation of genotype-phenotype correlation.
Kobayashi T; Uchiyama M; Fukuro S; Tanaka K
Am J Med Genet; 2002 Jul; 110(3):248-52. PubMed ID: 12116233
[TBL] [Abstract][Full Text] [Related]
8. Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models.
van de Ven M; Andressoo JO; van der Horst GT; Hoeijmakers JH; Mitchell JR
DNA Repair (Amst); 2012 Nov; 11(11):874-83. PubMed ID: 23046824
[TBL] [Abstract][Full Text] [Related]
9. Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes.
Schäfer A; Gratchev A; Seebode C; Hofmann L; Schubert S; Laspe P; Apel A; Ohlenbusch A; Tzvetkov M; Weishaupt C; Oji V; Schön MP; Emmert S
Exp Dermatol; 2013 Jul; 22(7):486-9. PubMed ID: 23800062
[TBL] [Abstract][Full Text] [Related]
10. Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.
de Boer J; Donker I; de Wit J; Hoeijmakers JH; Weeda G
Cancer Res; 1998 Jan; 58(1):89-94. PubMed ID: 9426063
[TBL] [Abstract][Full Text] [Related]
11. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
Itin PH; Sarasin A; Pittelkow MR
J Am Acad Dermatol; 2001 Jun; 44(6):891-920; quiz 921-4. PubMed ID: 11369901
[TBL] [Abstract][Full Text] [Related]
12. Accelerated aging pathology in ad libitum fed Xpd(TTD) mice is accompanied by features suggestive of caloric restriction.
Wijnhoven SW; Beems RB; Roodbergen M; van den Berg J; Lohman PH; Diderich K; van der Horst GT; Vijg J; Hoeijmakers JH; van Steeg H
DNA Repair (Amst); 2005 Nov; 4(11):1314-24. PubMed ID: 16115803
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Age-related neuronal degeneration: complementary roles of nucleotide excision repair and transcription-coupled repair in preventing neuropathology.
Jaarsma D; van der Pluijm I; de Waard MC; Haasdijk ED; Brandt R; Vermeij M; Rijksen Y; Maas A; van Steeg H; Hoeijmakers JH; van der Horst GT
PLoS Genet; 2011 Dec; 7(12):e1002405. PubMed ID: 22174697
[TBL] [Abstract][Full Text] [Related]
15. Hot news: temperature-sensitive humans explain hereditary disease.
Friedberg EC
Bioessays; 2001 Aug; 23(8):671-3. PubMed ID: 11494313
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells.
Vélez-Cruz R; Zadorin AS; Coin F; Egly JM
Proc Natl Acad Sci U S A; 2013 Jan; 110(3):E212-20. PubMed ID: 23267107
[TBL] [Abstract][Full Text] [Related]
18. Nucleotide excision repair disorders and the balance between cancer and aging.
Andressoo JO; Hoeijmakers JH; Mitchell JR
Cell Cycle; 2006 Dec; 5(24):2886-8. PubMed ID: 17172862
[TBL] [Abstract][Full Text] [Related]
19. Xeroderma pigmentosum group E and DDB2, a smaller subunit of damage-specific DNA binding protein: proposed classification of xeroderma pigmentosum, Cockayne syndrome, and ultraviolet-sensitive syndrome.
Itoh T
J Dermatol Sci; 2006 Feb; 41(2):87-96. PubMed ID: 16325378
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
