149 related articles for article (PubMed ID: 3338790)
1. Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome.
Rebora A; Crovato F
Hum Genet; 1988 Jan; 78(1):106-8. PubMed ID: 3338790
[No Abstract] [Full Text] [Related]
2. 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]
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. A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
Cleaver JE; Thompson LH; Richardson AS; States JC
Hum Mutat; 1999; 14(1):9-22. PubMed ID: 10447254
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The genetic basis of xeroderma pigmentosum and trichothiodystrophy syndromes.
Stary A; Sarasin A
Cancer Surv; 1996; 26():155-71. PubMed ID: 8783572
[No Abstract] [Full Text] [Related]
7. 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]
8. Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D.
Kleijer WJ; Beemer FA; Boom BW
Am J Med Genet; 1994 Aug; 52(2):227-30. PubMed ID: 7802014
[TBL] [Abstract][Full Text] [Related]
9. DNA repair and cancer: speculations based on studies with xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy.
Lehmann AR; Norris PG
Carcinogenesis; 1989 Aug; 10(8):1353-6. PubMed ID: 2752510
[No Abstract] [Full Text] [Related]
10. Chromosome and blood marker studies in families of patients affected by xeroderma pigmentosum and trichothiodystrophy.
Nuzzo F; Stefanini M; Rocchi M; Casati A; Colognola R; Lagomarsini P; Marinoni S; Scozzari R
Mutat Res; 1988 Jul; 208(3-4):159-61. PubMed ID: 3398868
[TBL] [Abstract][Full Text] [Related]
11. PIBI(D)S: clinical and molecular characterization of a new case.
Fortina AB; Alaibac M; Piaserico S; Peserico A
J Eur Acad Dermatol Venereol; 2001 Jan; 15(1):65-9. PubMed ID: 11451329
[TBL] [Abstract][Full Text] [Related]
12. [Xeroderma pigmentosum and related syndromes].
Berneburg M; Krutmann J
Hautarzt; 2003 Jan; 54(1):33-40. PubMed ID: 12567255
[TBL] [Abstract][Full Text] [Related]
13. Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure.
Lucky PA; Kirsch N; Lucky AW; Carter DM
J Am Acad Dermatol; 1984 Aug; 11(2 Pt 2):340-6. PubMed ID: 6480939
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [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]
16. The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases.
Lehmann AR
Genes Dev; 2001 Jan; 15(1):15-23. PubMed ID: 11156600
[No Abstract] [Full Text] [Related]
17. Ultraviolet light-induced sister chromatid exchanges in xeroderma pigmentosum and in Cockayne's syndrome lymphocyte cell lines.
Cheng WS; Tarone RE; Andrews AD; Whang-Peng JS; Robbins JH
Cancer Res; 1978 Jun; 38(6):1601-9. PubMed ID: 647673
[No Abstract] [Full Text] [Related]
18. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.
Broughton BC; Steingrimsdottir H; Weber CA; Lehmann AR
Nat Genet; 1994 Jun; 7(2):189-94. PubMed ID: 7920640
[TBL] [Abstract][Full Text] [Related]
19. Clinical and photobiological differences between dyschromatosis symmetrica hereditaria and xeroderma pigmentosum.
Satoh Y; Yoshida M
J Dermatol; 1980 Oct; 7(5):317-22. PubMed ID: 7009681
[No Abstract] [Full Text] [Related]
20. Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group D.
Mondello C; Nardo T; Giliani S; Arrand JE; Weber CA; Lehmann AR; Nuzzo F; Stefanini M
Mutat Res; 1994 Mar; 314(2):159-65. PubMed ID: 7510365
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]