222 related articles for article (PubMed ID: 21814739)
1. Bone fragility and decline in stem cells in prematurely aging DNA repair deficient trichothiodystrophy mice.
Diderich KE; Nicolaije C; Priemel M; Waarsing JH; Day JS; Brandt RM; Schilling AF; Botter SM; Weinans H; van der Horst GT; Hoeijmakers JH; van Leeuwen JP
Age (Dordr); 2012 Aug; 34(4):845-61. PubMed ID: 21814739
[TBL] [Abstract][Full Text] [Related]
2. Age-related skeletal dynamics and decrease in bone strength in DNA repair deficient male trichothiodystrophy mice.
Nicolaije C; Diderich KE; Botter SM; Priemel M; Waarsing JH; Day JS; Brandt RM; Schilling AF; Weinans H; Van der Eerden BC; van der Horst GT; Hoeijmakers JH; van Leeuwen JP
PLoS One; 2012; 7(4):e35246. PubMed ID: 22506075
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
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. Slowly progressing nucleotide excision repair in trichothiodystrophy group A patient fibroblasts.
Theil AF; Nonnekens J; Wijgers N; Vermeulen W; Giglia-Mari G
Mol Cell Biol; 2011 Sep; 31(17):3630-8. PubMed ID: 21730288
[TBL] [Abstract][Full Text] [Related]
7. Analysis of osteoarthritis in a mouse model of the progeroid human DNA repair syndrome trichothiodystrophy.
Botter SM; Zar M; van Osch GJ; van Steeg H; Dollé ME; Hoeijmakers JH; Weinans H; van Leeuwen JP
Age (Dordr); 2011 Sep; 33(3):247-60. PubMed ID: 20820927
[TBL] [Abstract][Full Text] [Related]
8. Defective transcription/repair factor IIH recruitment to specific UV lesions in trichothiodystrophy syndrome.
Chiganças V; Lima-Bessa KM; Stary A; Menck CF; Sarasin A
Cancer Res; 2008 Aug; 68(15):6074-83. PubMed ID: 18676829
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Trichothiodystrophy: from basic mechanisms to clinical implications.
Stefanini M; Botta E; Lanzafame M; Orioli D
DNA Repair (Amst); 2010 Jan; 9(1):2-10. PubMed ID: 19931493
[TBL] [Abstract][Full Text] [Related]
11. Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay syndrome.
Lambert WC; Gagna CE; Lambert MW
Adv Exp Med Biol; 2010; 685():106-10. PubMed ID: 20687499
[TBL] [Abstract][Full Text] [Related]
12. TTDA: big impact of a small protein.
Theil AF; Hoeijmakers JH; Vermeulen W
Exp Cell Res; 2014 Nov; 329(1):61-8. PubMed ID: 25016283
[TBL] [Abstract][Full Text] [Related]
13. Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH.
Hashimoto S; Egly JM
Hum Mol Genet; 2009 Oct; 18(R2):R224-30. PubMed ID: 19808800
[TBL] [Abstract][Full Text] [Related]
14. DNA damage and senescence in osteoprogenitors expressing Osx1 may cause their decrease with age.
Kim HN; Chang J; Shao L; Han L; Iyer S; Manolagas SC; O'Brien CA; Jilka RL; Zhou D; Almeida M
Aging Cell; 2017 Aug; 16(4):693-703. PubMed ID: 28401730
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum.
Zhou X; Khan SG; Tamura D; Ueda T; Boyle J; Compe E; Egly JM; DiGiovanna JJ; Kraemer KH
Eur J Hum Genet; 2013 Aug; 21(8):831-7. PubMed ID: 23232694
[TBL] [Abstract][Full Text] [Related]
20. Telomerase-deficient mice exhibit bone loss owing to defects in osteoblasts and increased osteoclastogenesis by inflammatory microenvironment.
Saeed H; Abdallah BM; Ditzel N; Catala-Lehnen P; Qiu W; Amling M; Kassem M
J Bone Miner Res; 2011 Jul; 26(7):1494-505. PubMed ID: 21308778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
