158 related articles for article (PubMed ID: 1458540)
1. A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene.
Mounkes LC; Jones RS; Liang BC; Gelbart W; Fuller MT
Cell; 1992 Dec; 71(6):925-37. PubMed ID: 1458540
[TBL] [Abstract][Full Text] [Related]
2. Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.
Koken MH; Vreeken C; Bol SA; Cheng NC; Jaspers-Dekker I; Hoeijmakers JH; Eeken JC; Weeda G; Pastink A
Nucleic Acids Res; 1992 Nov; 20(21):5541-8. PubMed ID: 1454518
[TBL] [Abstract][Full Text] [Related]
3. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.
Vermeulen W; Scott RJ; Rodgers S; Müller HJ; Cole J; Arlett CF; Kleijer WJ; Bootsma D; Hoeijmakers JH; Weeda G
Am J Hum Genet; 1994 Feb; 54(2):191-200. PubMed ID: 8304337
[TBL] [Abstract][Full Text] [Related]
4. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
Riou L; Zeng L; Chevallier-Lagente O; Stary A; Nikaido O; Taïeb A; Weeda G; Mezzina M; Sarasin A
Hum Mol Genet; 1999 Jun; 8(6):1125-33. PubMed ID: 10332046
[TBL] [Abstract][Full Text] [Related]
5. Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome.
Weeda G; Ma L; van Ham RC; Bootsma D; van der Eb AJ; Hoeijmakers JH
Carcinogenesis; 1991 Dec; 12(12):2361-8. PubMed ID: 1747940
[TBL] [Abstract][Full Text] [Related]
6. The COOH terminus of suppressor of stem loop (SSL2/RAD25) in yeast is essential for overall genomic excision repair and transcription-coupled repair.
Sweder KS; Hanawalt PC
J Biol Chem; 1994 Jan; 269(3):1852-7. PubMed ID: 8294433
[TBL] [Abstract][Full Text] [Related]
7. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome.
Weeda G; van Ham RC; Vermeulen W; Bootsma D; van der Eb AJ; Hoeijmakers JH
Cell; 1990 Aug; 62(4):777-91. PubMed ID: 2167179
[TBL] [Abstract][Full Text] [Related]
8. Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2.
Scherly D; Nouspikel T; Corlet J; Ucla C; Bairoch A; Clarkson SG
Nature; 1993 May; 363(6425):182-5. PubMed ID: 8483504
[TBL] [Abstract][Full Text] [Related]
9. Cockayne syndrome and xeroderma pigmentosum.
Rapin I; Lindenbaum Y; Dickson DW; Kraemer KH; Robbins JH
Neurology; 2000 Nov; 55(10):1442-9. PubMed ID: 11185579
[TBL] [Abstract][Full Text] [Related]
10. A mutation in repB, the dictyostelium homolog of the human xeroderma pigmentosum B gene, has increased sensitivity to UV-light but normal morphogenesis.
Lee SK; Yu SL; Alexander H; Alexander S
Biochim Biophys Acta; 1998 Aug; 1399(2-3):161-72. PubMed ID: 9765592
[TBL] [Abstract][Full Text] [Related]
11. Expression and functional analyses of the Dxpa gene, the Drosophila homolog of the human excision repair gene XPA.
Shimamoto T; Tanimura T; Yoneda Y; Kobayakawa Y; Sugasawa K; Hanaoka F; Oka M; Okada Y; Tanaka K; Kohno K
J Biol Chem; 1995 Sep; 270(38):22452-9. PubMed ID: 7673233
[TBL] [Abstract][Full Text] [Related]
12. Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy.
Norris PG; Limb GA; Hamblin AS; Lehmann AR; Arlett CF; Cole J; Waugh AP; Hawk JL
J Invest Dermatol; 1990 Jan; 94(1):94-100. PubMed ID: 2295840
[TBL] [Abstract][Full Text] [Related]
13. Transcriptional profiles of unirradiated or UV-irradiated human cells expressing either the cancer-prone XPB/CS allele or the noncancer-prone XPB/TTD allele.
da Costa RM; Riou L; Paquola A; Menck CF; Sarasin A
Oncogene; 2005 Feb; 24(8):1359-74. PubMed ID: 15608684
[TBL] [Abstract][Full Text] [Related]
14. The Drosophila melanogaster homologue of the Xeroderma pigmentosum D gene product is located in euchromatic regions and has a dynamic response to UV light-induced lesions in polytene chromosomes.
Reynaud E; Lomelí H; Vázquez M; Zurita M
Mol Biol Cell; 1999 Apr; 10(4):1191-203. PubMed ID: 10198066
[TBL] [Abstract][Full Text] [Related]
15. Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.
Weeda G; Ma LB; van Ham RC; van der Eb AJ; Hoeijmakers JH
Nucleic Acids Res; 1991 Nov; 19(22):6301-8. PubMed ID: 1956789
[TBL] [Abstract][Full Text] [Related]
16. Cancer in xeroderma pigmentosum and related disorders of DNA repair.
Cleaver JE
Nat Rev Cancer; 2005 Jul; 5(7):564-73. PubMed ID: 16069818
[TBL] [Abstract][Full Text] [Related]
17. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
Takayama K; Salazar EP; Lehmann A; Stefanini M; Thompson LH; Weber CA
Cancer Res; 1995 Dec; 55(23):5656-63. PubMed ID: 7585650
[TBL] [Abstract][Full Text] [Related]
18. Xeroderma pigmentosum, Cockayne's syndrome, helicases, and DNA repair: what's the relationship?
Friedberg EC
Cell; 1992 Dec; 71(6):887-9. PubMed ID: 1458537
[No Abstract] [Full Text] [Related]
19. Molecular characterization of mutant alleles of the DNA repair/basal transcription factor haywire/ERCC3 in Drosophila.
Mounkes LC; Fuller MT
Genetics; 1999 May; 152(1):291-7. PubMed ID: 10224261
[TBL] [Abstract][Full Text] [Related]
20. Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function.
Ma L; Westbroek A; Jochemsen AG; Weeda G; Bosch A; Bootsma D; Hoeijmakers JH; van der Eb AJ
Mol Cell Biol; 1994 Jun; 14(6):4126-34. PubMed ID: 8196650
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]