345 related articles for article (PubMed ID: 11950998)
1. Premature aging in mice deficient in DNA repair and transcription.
de Boer J; Andressoo JO; de Wit J; Huijmans J; Beems RB; van Steeg H; Weeda G; van der Horst GT; van Leeuwen W; Themmen AP; Meradji M; Hoeijmakers JH
Science; 2002 May; 296(5571):1276-9. PubMed ID: 11950998
[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. 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]
4. 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]
5. From a DNA helicase to brittle hair.
Winkler GS; Hoeijmakers JH
Nat Genet; 1998 Oct; 20(2):106-7. PubMed ID: 9771695
[No Abstract] [Full Text] [Related]
6. Recovery of normal DNA repair and mutagenesis in trichothiodystrophy cells after transduction of the XPD human gene.
Marionnet C; Quilliet X; Benoit A; Armier J; Sarasin A; Stary A
Cancer Res; 1996 Dec; 56(23):5450-6. PubMed ID: 8968100
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Aging. Genomic priorities in aging.
Hasty P; Vijg J
Science; 2002 May; 296(5571):1250-1. PubMed ID: 11951000
[No Abstract] [Full Text] [Related]
10. A temperature-sensitive disorder in basal transcription and DNA repair in humans.
Vermeulen W; Rademakers S; Jaspers NG; Appeldoorn E; Raams A; Klein B; Kleijer WJ; Hansen LK; Hoeijmakers JH
Nat Genet; 2001 Mar; 27(3):299-303. PubMed ID: 11242112
[TBL] [Abstract][Full Text] [Related]
11. Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder.
Vermeulen W; Bergmann E; Auriol J; Rademakers S; Frit P; Appeldoorn E; Hoeijmakers JH; Egly JM
Nat Genet; 2000 Nov; 26(3):307-13. PubMed ID: 11062469
[TBL] [Abstract][Full Text] [Related]
12. DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.
Takayama K; Danks DM; Salazar EP; Cleaver JE; Weber CA
Hum Mutat; 1997; 9(6):519-25. PubMed ID: 9195225
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Ageing: repair and transcription keep us from premature ageing.
Lehmann A
Curr Biol; 2002 Aug; 12(16):R550-1. PubMed ID: 12194834
[TBL] [Abstract][Full Text] [Related]
16. [Trichothiodystrophies: anomalies of the repair and transcription of genes].
Robert C; Sarasin A
Ann Dermatol Venereol; 1999 Oct; 126(10):669-71. PubMed ID: 10604001
[No Abstract] [Full Text] [Related]
17. 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]
18. A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy.
de Boer J; de Wit J; van Steeg H; Berg RJ; Morreau H; Visser P; Lehmann AR; Duran M; Hoeijmakers JH; Weeda G
Mol Cell; 1998 Jun; 1(7):981-90. PubMed ID: 9651581
[TBL] [Abstract][Full Text] [Related]
19. Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutation.
George JW; Salazar EP; Vreeswijk MP; Lamerdin JE; Reardon JT; Zdzienicka MZ; Sancar A; Kadkhodayan S; Tebbs RS; Mullenders LH; Thompson LH
Mol Cell Biol; 2001 Nov; 21(21):7355-65. PubMed ID: 11585917
[TBL] [Abstract][Full Text] [Related]
20. [DNA damage and aging].
Molenaar JC
Ned Tijdschr Geneeskd; 2003 Dec; 147(52):2578-81. PubMed ID: 14723025
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]