148 related articles for article (PubMed ID: 3396600)
1. Trichothiodystrophy without photosensitivity. Biochemical, ultrastructural and DNA repair studies.
Fois A; Balestri P; Calvieri S; Zampetti M; Giustini S; Stefanini M; Lagomarsini P
Eur J Pediatr; 1988 May; 147(4):439-41. PubMed ID: 3396600
[TBL] [Abstract][Full Text] [Related]
2. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias.
Itin PH; Pittelkow MR
J Am Acad Dermatol; 1990 May; 22(5 Pt 1):705-17. PubMed ID: 2189905
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Trichothiodystrophy: ultrastructural studies of two patients.
Calvieri S; Rossi A; Amorosi B; Giustini S; Innocenzi D; Micali G; Rizzo R
Pediatr Dermatol; 1993 Jun; 10(2):111-6. PubMed ID: 8346099
[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. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. [Trichothiodystrophy: PIBIDS syndrome].
Jiménez-Puya R; Moreno-Giménez JC; Camacho-Martínez F; Ferrando-Barbera J; Grimalt R
Actas Dermosifiliogr; 2007 Apr; 98(3):183-7. PubMed ID: 17504703
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes.
Dumaz N; Duthu A; Ehrhart JC; Drougard C; Appella E; Anderson CW; May P; Sarasin A; Daya-Grosjean L
Mol Carcinog; 1997 Dec; 20(4):340-7. PubMed ID: 9433478
[TBL] [Abstract][Full Text] [Related]
15. Human hair production by scalp samples grafted onto nude mice. Biochemical data on normal human hair and the genetic defect trichothiodystrophy.
de Brouwer B; Föhles J; Van Neste DJ
J Dermatol Sci; 1994 Jul; 7 Suppl():S39-46. PubMed ID: 7528049
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. Trichothiodystrophy with chronic neutropenia and mild mental retardation.
Itin PH; Pittelkow MR
J Am Acad Dermatol; 1991 Feb; 24(2 Pt 2):356-8. PubMed ID: 1999547
[TBL] [Abstract][Full Text] [Related]
19. Structural and molecular hair abnormalities in trichothiodystrophy.
Liang C; Morris A; Schlücker S; Imoto K; Price VH; Menefee E; Wincovitch SM; Levin IW; Tamura D; Strehle KR; Kraemer KH; DiGiovanna JJ
J Invest Dermatol; 2006 Oct; 126(10):2210-6. PubMed ID: 16728971
[TBL] [Abstract][Full Text] [Related]
20. Trichothiodystrophy fibroblasts are deficient in the repair of ultraviolet-induced cyclobutane pyrimidine dimers and (6-4)photoproducts.
Nishiwaki Y; Kobayashi N; Imoto K; Iwamoto TA; Yamamoto A; Katsumi S; Shirai T; Sugiura S; Nakamura Y; Sarasin A; Miyagawa S; Mori T
J Invest Dermatol; 2004 Feb; 122(2):526-32. PubMed ID: 15009740
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]