124 related articles for article (PubMed ID: 7009681)
1. 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]
2. A case of xeroderma pigmentosum with clinical appearance of dyschromatosis symmetrica hereditaria.
Nishigori C; Miyachi Y; Takebe H; Imamura S
Pediatr Dermatol; 1986 Nov; 3(5):410-3. PubMed ID: 3809028
[TBL] [Abstract][Full Text] [Related]
3. Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum.
Ohtoshi E; Matsumura Y; Nishigori C; Toda KI; Horiguchi Y; Ikenaga M; Miyachi Y
Br J Dermatol; 2001 Jan; 144(1):162-8. PubMed ID: 11167700
[TBL] [Abstract][Full Text] [Related]
4. Genetical studies on skin diseases. I. Ephelides, dyschromatosis symmetrica hereditaria and xeroderma pigmentosum.
ITO M
Tohoku J Exp Med; 1950 Dec; 53(1/2):69-76. PubMed ID: 14828625
[No Abstract] [Full Text] [Related]
5. 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]
6. [Xeroderma pigmentosum. What may be expected from biological studies?].
Robert C; Sarasin A
Ann Dermatol Venereol; 1994; 121(5):434-9. PubMed ID: 7702274
[No Abstract] [Full Text] [Related]
7. 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]
8. Photobiological information obtained from XPA gene-deficient mice.
Horio T; Miyauchi-Hashimoto H; Kuwamoto K; Yamazaki F; Okamoto H
Photochem Photobiol; 2007; 83(1):218-24. PubMed ID: 16836470
[TBL] [Abstract][Full Text] [Related]
9. [Recent advances in the study of genophotodermatoses].
Ichihashi M
Nihon Hifuka Gakkai Zasshi; 1985 Oct; 95(12 Suppl):1262-6. PubMed ID: 3914564
[No Abstract] [Full Text] [Related]
10. 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]
11. [Xeroderma pigmentosum and pigmented xerodermoid. Clinical and molecular biological studies].
Jung EG; Schnyder UW
Schweiz Med Wochenschr; 1970 Oct; 100(41):1718-26. PubMed ID: 5480540
[No Abstract] [Full Text] [Related]
12. DNA repair in human diseases.
Giannelli F
Clin Exp Dermatol; 1980 Jun; 5(2):119-38. PubMed ID: 7002379
[No Abstract] [Full Text] [Related]
13. The red face: photogenodermatoses.
Jung EG
Clin Dermatol; 1993; 11(2):275-81. PubMed ID: 8348441
[No Abstract] [Full Text] [Related]
14. Human disorders showing increased sensitivity to the induction of genetic damage.
Arlett CF; Lehmann AR
Annu Rev Genet; 1978; 12():95-115. PubMed ID: 371535
[No Abstract] [Full Text] [Related]
15. 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]
16. Mutations not sufficient for carcinogenesis?
Bridges B
Science; 1995 Aug; 269(5226):909. PubMed ID: 7638608
[No Abstract] [Full Text] [Related]
17. DNA repair. Engagement with transcription.
Bootsma D; Hoeijmakers JH
Nature; 1993 May; 363(6425):114-5. PubMed ID: 8483493
[No Abstract] [Full Text] [Related]
18. Xeroderma pigmentosum group E and DDB2, a smaller subunit of damage-specific DNA binding protein: proposed classification of xeroderma pigmentosum, Cockayne syndrome, and ultraviolet-sensitive syndrome.
Itoh T
J Dermatol Sci; 2006 Feb; 41(2):87-96. PubMed ID: 16325378
[TBL] [Abstract][Full Text] [Related]
19. A young woman with xeroderma pigmentosum complementation group F and a morphoeic basal cell carcinoma.
Itoh T; Watanabe H; Yamaizumi M; Ono T
Br J Dermatol; 1995 Jan; 132(1):122-7. PubMed ID: 7756123
[TBL] [Abstract][Full Text] [Related]
20. A case of xeroderma pigmentosum group D determined by photobiological study.
Ishii N; Nakajima H; Kondo S; Satoh Y; Fujiwara Y; Shimoda N
J Dermatol; 1991 Jan; 18(1):31-5. PubMed ID: 2050904
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]