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2. Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan. Yamamura K, Ichihashi M, Hiramoto T, Ogoshi M, Nishioka K, Fujiwara Y. Br J Dermatol; 1989 Oct; 121(4):471-80. PubMed ID: 2696553 [Abstract] [Full Text] [Related]
4. [The determination of the complementation groups for the cells of patients with xeroderma pigmentosum and the Cockayne syndrome found in Russia]. Pleskach NM, Mikhel'son VM, Raams A, Bootsma D. Tsitologiia; 1996 Oct; 38(8):863-8. PubMed ID: 9027016 [Abstract] [Full Text] [Related]
6. Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiation. Itoh T, Linn S, Kamide R, Tokushige H, Katori N, Hosaka Y, Yamaizumi M. J Invest Dermatol; 2000 Dec; 115(6):981-5. PubMed ID: 11121129 [Abstract] [Full Text] [Related]
7. A case of xeroderma pigmentosum complementation group F with neurological abnormalities. Moriwaki S, Nishigori C, Imamura S, Yagi T, Takahashi C, Fujimoto N, Takebe H. Br J Dermatol; 1993 Jan; 128(1):91-4. PubMed ID: 8427828 [Abstract] [Full Text] [Related]
8. Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life. Slor H, Batko S, Khan SG, Sobe T, Emmert S, Khadavi A, Frumkin A, Busch DB, Albert RB, Kraemer KH. J Invest Dermatol; 2000 Dec; 115(6):974-80. PubMed ID: 11121128 [Abstract] [Full Text] [Related]
9. Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype. Itoh T, Cleaver JE, Yamaizumi M. Hum Genet; 1996 Feb; 97(2):176-9. PubMed ID: 8566949 [Abstract] [Full Text] [Related]
10. Assignment of a Chinese xeroderma pigmentosum patient from Taiwan to complementation group C. Wang Y, Kobayashi K, Chang HR, Zeng Y, Ishizaki K, Dai H, Kuan YZ, Ikenaga M. J Radiat Res; 1991 Jun; 32(2):181-90. PubMed ID: 1941768 [Abstract] [Full Text] [Related]
11. Xeroderma pigmentosum complementation group E: a case report. Kawada A, Satoh Y, Fujiwara Y. Photodermatol; 1986 Aug; 3(4):233-8. PubMed ID: 3774595 [Abstract] [Full Text] [Related]
15. A simple method for diagnosing xeroderma pigmentosum variant. Itoh T, Ono T, Yamaizumi M. J Invest Dermatol; 1996 Sep; 107(3):349-53. PubMed ID: 8751969 [Abstract] [Full Text] [Related]
16. A ninth complementation group in xeroderma pigmentosum, XP I. Fischer E, Keijzer W, Thielmann HW, Popanda O, Bohnert E, Edler L, Jung EG, Bootsma D. Mutat Res; 1985 May; 145(3):217-25. PubMed ID: 3982437 [Abstract] [Full Text] [Related]
17. Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates. Kraemer KH, Coon HG, Petinga RA, Barrett SF, Rahe AE, Robbins JH. Proc Natl Acad Sci U S A; 1975 Jan; 72(1):59-63. PubMed ID: 164028 [Abstract] [Full Text] [Related]
18. Late onset of skin cancers in 2 xeroderma pigmentosum group F siblings and a review of 30 Japanese xeroderma pigmentosum patients in groups D, E and F. Kondo S, Mamada A, Miyamoto C, Keong CH, Satoh Y, Fujiwara Y. Photodermatol; 1989 Apr; 6(2):89-95. PubMed ID: 2664729 [Abstract] [Full Text] [Related]
20. A rapid procedure for measurement of DNA repair in human fibroblasts and for complementation analysis of xeroderma pigmentosum cells. Lehmann AR, Stevens S. Mutat Res; 1980 Jan; 69(1):177-90. PubMed ID: 6987495 [Abstract] [Full Text] [Related] Page: [Next] [New Search]