154 related articles for article (PubMed ID: 1281671)
1. Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair.
Sarasin A; Blanchet-Bardon C; Renault G; Lehmann A; Arlett C; Dumez Y
Br J Dermatol; 1992 Nov; 127(5):485-91. PubMed ID: 1281671
[TBL] [Abstract][Full Text] [Related]
2. The comet assay as a repair test for prenatal diagnosis of Xeroderma pigmentosum and trichothiodystrophy.
Alapetite C; Benoit A; Moustacchi E; Sarasin A
J Invest Dermatol; 1997 Feb; 108(2):154-9. PubMed ID: 9008227
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of PIBIDS.
Savary JB; Vasseur F; Vinatier D; Manouvrier S; Thomas P; Deminatti MM
Prenat Diagn; 1991 Nov; 11(11):859-66. PubMed ID: 1754556
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Trichothiodystrophy: clinical spectrum, central nervous system imaging, and biochemical characterization of two siblings.
Chen E; Cleaver JE; Weber CA; Packman S; Barkovich AJ; Koch TK; Williams ML; Golabi M; Price VH
J Invest Dermatol; 1994 Nov; 103(5 Suppl):154S-158S. PubMed ID: 7963680
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.
Lehmann AR; Arlett CF; Broughton BC; Harcourt SA; Steingrimsdottir H; Stefanini M; Malcolm A; Taylor R; Natarajan AT; Green S
Cancer Res; 1988 Nov; 48(21):6090-6. PubMed ID: 2458832
[TBL] [Abstract][Full Text] [Related]
8. Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity.
Stefanini M; Lagomarsini P; Arlett CF; Marinoni S; Borrone C; Crovato F; Trevisan G; Cordone G; Nuzzo F
Hum Genet; 1986 Oct; 74(2):107-12. PubMed ID: 3770739
[TBL] [Abstract][Full Text] [Related]
9. Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.
Stefanini M; Lagomarsini P; Giorgi R; Nuzzo F
Mutat Res; 1987 Jun; 191(2):117-9. PubMed ID: 3600693
[TBL] [Abstract][Full Text] [Related]
10. Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
Mezzina M; Eveno E; Chevallier-Lagente O; Benoit A; Carreau M; Vermeulen W; Hoeijmakers JH; Stefanini M; Lehmann AR; Weber CA
Carcinogenesis; 1994 Aug; 15(8):1493-8. PubMed ID: 8055625
[TBL] [Abstract][Full Text] [Related]
11. [Trichothiodystrophy: progresssive manifestations].
Foulc P; Jumbou O; David A; Sarasin A; Stalder JF
Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
[TBL] [Abstract][Full Text] [Related]
12. DNA repair deficient photodermatoses.
Lehmann AR; Norris PG
Semin Dermatol; 1990 Mar; 9(1):55-62. PubMed ID: 2203444
[TBL] [Abstract][Full Text] [Related]
13. Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy.
Stefanini M; Lagomarsini P; Giliani S; Nardo T; Botta E; Peserico A; Kleijer WJ; Lehmann AR; Sarasin A
Carcinogenesis; 1993 Jun; 14(6):1101-5. PubMed ID: 8508495
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. DNA repair investigations in nine Italian patients affected by trichothiodystrophy.
Stefanini M; Giliani S; Nardo T; Marinoni S; Nazzaro V; Rizzo R; Trevisan G
Mutat Res; 1992 Mar; 273(2):119-25. PubMed ID: 1372095
[TBL] [Abstract][Full Text] [Related]
17. Characterization of tiger-tail banding and hair shaft abnormalities in trichothiodystrophy.
Liang C; Kraemer KH; Morris A; Schiffmann R; Price VH; Menefee E; DiGiovanna JJ
J Am Acad Dermatol; 2005 Feb; 52(2):224-32. PubMed ID: 15692466
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Differential behaviors toward ultraviolet A and B radiation of fibroblasts and keratinocytes from normal and DNA-repair-deficient patients.
Otto AI; Riou L; Marionnet C; Mori T; Sarasin A; Magnaldo T
Cancer Res; 1999 Mar; 59(6):1212-8. PubMed ID: 10096550
[TBL] [Abstract][Full Text] [Related]
20. PIBI(D)S syndrome--trichothiodystrophy with xeroderma pigmentosum (group D) mutation.
Rebora A; Crovato F
J Am Acad Dermatol; 1987 May; 16(5 Pt 1):940-7. PubMed ID: 3584577
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]