116 related articles for article (PubMed ID: 1283322)
1. Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13.
Flejter WL; McDaniel LD; Askari M; Friedberg EC; Schultz RA
Genes Chromosomes Cancer; 1992 Nov; 5(4):335-42. PubMed ID: 1283322
[TBL] [Abstract][Full Text] [Related]
2. Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.
Flejter WL; McDaniel LD; Johns D; Friedberg EC; Schultz RA
Proc Natl Acad Sci U S A; 1992 Jan; 89(1):261-5. PubMed ID: 1729695
[TBL] [Abstract][Full Text] [Related]
3. Gene complementing xeroderma pigmentosum group A cells maps to distal human chromosome 9q.
Henning KA; Schultz RA; Sekhon GS; Friedberg EC
Somat Cell Mol Genet; 1990 Jul; 16(4):395-400. PubMed ID: 2218726
[TBL] [Abstract][Full Text] [Related]
4. Human chromosome 15 confers partial complementation of phenotypes to xeroderma pigmentosum group F cells.
Saxon PJ; Schultz RA; Stanbridge EJ; Friedberg EC
Am J Hum Genet; 1989 Apr; 44(4):474-85. PubMed ID: 2929593
[TBL] [Abstract][Full Text] [Related]
5. Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes.
Lamerdin JE; Stilwagen SA; Ramirez MH; Stubbs L; Carrano AV
Genomics; 1996 Jun; 34(3):399-409. PubMed ID: 8786141
[TBL] [Abstract][Full Text] [Related]
6. Complementation of DNA repair defect in xeroderma pigmentosum cells of group C by the transfer of human chromosome 5.
Kaur GP; Athwal RS
Somat Cell Mol Genet; 1993 Jan; 19(1):83-93. PubMed ID: 8460401
[TBL] [Abstract][Full Text] [Related]
7. Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblasts.
Schultz RA; Saxon PJ; Glover TW; Friedberg EC
Proc Natl Acad Sci U S A; 1987 Jun; 84(12):4176-9. PubMed ID: 3035572
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Chromosomal localization of three repair genes: the xeroderma pigmentosum group C gene and two human homologs of yeast RAD23.
van der Spek PJ; Smit EM; Beverloo HB; Sugasawa K; Masutani C; Hanaoka F; Hoeijmakers JH; Hagemeijer A
Genomics; 1994 Oct; 23(3):651-8. PubMed ID: 7851894
[TBL] [Abstract][Full Text] [Related]
10. Assignment of xeroderma pigmentosum group C (XPC) gene to chromosome 3p25.
Legerski RJ; Liu P; Li L; Peterson CA; Zhao Y; Leach RJ; Naylor SL; Siciliano MJ
Genomics; 1994 May; 21(1):266-9. PubMed ID: 8088800
[TBL] [Abstract][Full Text] [Related]
11. Human chromosome 9 can complement UV sensitivity of xeroderma pigmentosum group A cells.
Ishizaki K; Oshimura M; Sasaki MS; Nakamura Y; Ikenaga M
Mutat Res; 1990 May; 235(3):209-15. PubMed ID: 2342508
[TBL] [Abstract][Full Text] [Related]
12. Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
Mezzina M; Eveno E; Chevallier-Lagente O; Benoit A; Carreau M; Vermeulen W; Hoeijmakers JH; Stefanini M; Lehmann AR; Weber CA
Carcinogenesis; 1994 Aug; 15(8):1493-8. PubMed ID: 8055625
[TBL] [Abstract][Full Text] [Related]
13. Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21.
Weeda G; Wiegant J; van der Ploeg M; Geurts van Kessel AH; van der Eb AJ; Hoeijmakers JH
Genomics; 1991 Aug; 10(4):1035-40. PubMed ID: 1916809
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridization.
Samec S; Jones TA; Corlet J; Scherly D; Sheer D; Wood RD; Clarkson SG
Genomics; 1994 May; 21(1):283-5. PubMed ID: 8088806
[No Abstract] [Full Text] [Related]
16. Molecular cloning and characterization of a mammalian excision repair gene that partially restores UV resistance to xeroderma pigmentosum complementation group D cells.
Arrand JE; Bone NM; Johnson RT
Proc Natl Acad Sci U S A; 1989 Sep; 86(18):6997-7001. PubMed ID: 2780557
[TBL] [Abstract][Full Text] [Related]
17. Complementation of a DNA repair defect in xeroderma pigmentosum cells by transfer of human chromosome 9.
Kaur GP; Athwal RS
Proc Natl Acad Sci U S A; 1989 Nov; 86(22):8872-6. PubMed ID: 2813428
[TBL] [Abstract][Full Text] [Related]
18. Clonal chromosome rearrangements in a fibroblast strain from a patient affected by xeroderma pigmentosum (complementation group C).
Nuzzo F; Lagomarsini P; Casati A; Giorgi R; Berardesca E; Stefanini M
Mutat Res; 1989 Jul; 219(4):209-15. PubMed ID: 2770768
[TBL] [Abstract][Full Text] [Related]
19. Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene.
Frederick GD; Amirkhan RH; Schultz RA; Friedberg EC
Hum Mol Genet; 1994 Oct; 3(10):1783-8. PubMed ID: 7849702
[TBL] [Abstract][Full Text] [Related]
20. Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.
Liu P; Siciliano J; White B; Legerski R; Callen D; Reeders S; Siciliano MJ; Thompson LH
Mutagenesis; 1993 May; 8(3):199-205. PubMed ID: 8332082
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]