124 related articles for article (PubMed ID: 1941768)
1. 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
[TBL] [Abstract][Full Text] [Related]
2. Xeroderma pigmentosum patients belonging to complementation group F and efficient liquid-holding recovery of ultraviolet damage.
Nishigori C; Fujisawa H; Uyeno K; Kawaguchi T; Takebe H
Photodermatol Photoimmunol Photomed; 1991 Aug; 8(4):146-50. PubMed ID: 1814424
[TBL] [Abstract][Full Text] [Related]
3. Sodium butyrate stimulates cellular recovery from UV damage in xeroderma pigmentosum cells belonging to complementation group F.
Nishigori C; Takebe H
Jpn J Cancer Res; 1987 Sep; 78(9):932-6. PubMed ID: 3117749
[TBL] [Abstract][Full Text] [Related]
4. Xeroderma pigmentosum and squamous cell carcinoma of the tongue. Identification of two black patients as members of complementation group C.
Wade MH; Plotnick H
J Am Acad Dermatol; 1985 Mar; 12(3):515-21. PubMed ID: 3989010
[TBL] [Abstract][Full Text] [Related]
5. Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany.
Thielmann HW; Popanda O; Edler L; Jung EG
Cancer Res; 1991 Jul; 51(13):3456-70. PubMed ID: 2054785
[TBL] [Abstract][Full Text] [Related]
6. Assignment of six patients with xeroderma pigmentosum in Hokkaido area to a variant form.
Fujikawa K; Ayaki H; Ishizaki K; Takatera H; Matsuo S; Iizuka H; Koizumi H; Ikenaga M
J Radiat Res; 1994 Sep; 35(3):168-78. PubMed ID: 7830260
[TBL] [Abstract][Full Text] [Related]
7. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
Moriwaki S; Stefanini M; Lehmann AR; Hoeijmakers JH; Robbins JH; Rapin I; Botta E; Tanganelli B; Vermeulen W; Broughton BC; Kraemer KH
J Invest Dermatol; 1996 Oct; 107(4):647-53. PubMed ID: 8823375
[TBL] [Abstract][Full Text] [Related]
8. Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells.
Stefanini M; Keijzer W; Westerveld A; Bootsma D
Exp Cell Res; 1985 Dec; 161(2):373-80. PubMed ID: 4065224
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
10. Defect in UV-induced unscheduled DNA synthesis in cultured epidermal keratinocytes from xeroderma pigmentosum.
Kondo S; Satoh Y; Kuroki T
Mutat Res; 1987 Jan; 183(1):95-101. PubMed ID: 2432425
[TBL] [Abstract][Full Text] [Related]
11. Assignment of two Japanese xeroderma pigmentosum patients to complementation group D and their characteristics.
Fujiwara Y; Satoh Y
Jpn J Cancer Res; 1985 Mar; 76(3):162-6. PubMed ID: 3922833
[TBL] [Abstract][Full Text] [Related]
12. Report of three sisters with XP-E, a rare xeroderma pigmentosum complementation group.
Fischer E; Schnyder UW; Jung EG
Photodermatol; 1984 Oct; 1(5):232-6. PubMed ID: 6531300
[TBL] [Abstract][Full Text] [Related]
13. Assignment of 2 patients with xeroderma pigmentosum to complementation group E.
Fujiwara Y; Uehara Y; Ichihashi M; Yamamoto Y; Nishioka K
Mutat Res; 1985; 145(1-2):55-61. PubMed ID: 3974603
[TBL] [Abstract][Full Text] [Related]
14. Xeroderma pigmentosum complementation group E: a case report.
Kawada A; Satoh Y; Fujiwara Y
Photodermatol; 1986 Aug; 3(4):233-8. PubMed ID: 3774595
[TBL] [Abstract][Full Text] [Related]
15. Assignment of three Chinese xeroderma pigmentosum patients to complementation group C and one to group E.
Han ZB; Hara R; Ayaki H; Wang JH; Sun LY; You Y; Zhang YP; Qiang KX; Ikenaga M
Br J Dermatol; 1998 Jan; 138(1):131-6. PubMed ID: 9536236
[TBL] [Abstract][Full Text] [Related]
16. Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1.
Keijzer W; Stefanini M; Bootsma D; Verkerk A; Geurts van Kessel AH; Jongkind JF; Westerveld A
Exp Cell Res; 1987 Apr; 169(2):490-501. PubMed ID: 3556430
[TBL] [Abstract][Full Text] [Related]
17. Analysis of point mutations in an ultraviolet-irradiated shuttle vector plasmid propagated in cells from Japanese xeroderma pigmentosum patients in complementation groups A and F.
Yagi T; Tatsumi-Miyajima J; Sato M; Kraemer KH; Takebe H
Cancer Res; 1991 Jun; 51(12):3177-82. PubMed ID: 2039995
[TBL] [Abstract][Full Text] [Related]
18. Somatic mosaicism for DNA repair capacity in fibroblasts derived from a group A xeroderma pigmentosum patient.
Chang HR; Ishizaki K; Sasaki MS; Toguchida J; Kato M; Nakamura Y; Kawamura S; Moriguchi T; Ikenaga M
J Invest Dermatol; 1989 Oct; 93(4):460-5. PubMed ID: 2570806
[TBL] [Abstract][Full Text] [Related]
19. UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.
Itoh T; Fujiwara Y; Ono T; Yamaizumi M
Am J Hum Genet; 1995 Jun; 56(6):1267-76. PubMed ID: 7539208
[TBL] [Abstract][Full Text] [Related]
20. 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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
