122 related articles for article (PubMed ID: 7464842)
1. Diphtheria toxin resistance in human fibroblast cell strains from normal and cancer-prone individuals.
Gupta RS; Goldstein S
Mutat Res; 1980 Dec; 73(2):331-8. PubMed ID: 7464842
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Isolation and characterization of mutants of human diploid fibroblasts resistant to diphtheria toxin.
Gupta RS; Siminovitch L
Proc Natl Acad Sci U S A; 1978 Jul; 75(7):3337-40. PubMed ID: 277932
[TBL] [Abstract][Full Text] [Related]
4. Diseases with DNA damage-processing defects.
Timme TL; Moses RE
Am J Med Sci; 1988 Jan; 295(1):40-8. PubMed ID: 3276189
[TBL] [Abstract][Full Text] [Related]
5. Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblasts.
Glover TW; Chang CC; Trosko JE; Li SS
Proc Natl Acad Sci U S A; 1979 Aug; 76(8):3982-6. PubMed ID: 291058
[TBL] [Abstract][Full Text] [Related]
6. Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens.
Auerbach AD; Wolman SR
Nature; 1976 Jun; 261(5560):494-6. PubMed ID: 934283
[No Abstract] [Full Text] [Related]
7. Defective reactivation of ultraviolet light-irradiated herpesvirus by a Bloom's syndrome fibroblast strain.
Selsky CA; Henson P; Weichselbaum RR; Little JB
Cancer Res; 1979 Sep; 39(9):3392-6. PubMed ID: 225021
[TBL] [Abstract][Full Text] [Related]
8. The Fritz-Lipmann lecture. DNA repair in human cells. Biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndrome.
Schweiger M; Auer B; Burtscher HJ; Hirsch-Kauffmann M; Klocker H; Schneider R
Eur J Biochem; 1987 Jun; 165(2):235-42. PubMed ID: 3109898
[No Abstract] [Full Text] [Related]
9. [Chromosome instability syndromes].
Germain D; Bernheim A
Pathol Biol (Paris); 1982 Nov; 30(9):802-16. PubMed ID: 6760085
[TBL] [Abstract][Full Text] [Related]
10. [Chromosome instability syndromes].
Germain D; Bernheim A
Sem Hop; 1983 Dec; 59(44):3065-79. PubMed ID: 6320395
[TBL] [Abstract][Full Text] [Related]
11. Autoradiographic detection of diphtheria toxin resistant mutants in human diploid fibroblasts.
Gupta RS; Singh B
Environ Mutagen; 1985; 7(5):611-24. PubMed ID: 2995027
[TBL] [Abstract][Full Text] [Related]
12. Characterization of the diphtheria toxin-resistance system in Chinese hamster ovary cells.
Moehring JM; Moehring TJ
Somatic Cell Genet; 1979 Jul; 5(4):453-68. PubMed ID: 494060
[TBL] [Abstract][Full Text] [Related]
13. Spontaneous chromosomal instability.
Passarge E
Humangenetik; 1972; 16(1):151-7. PubMed ID: 4647439
[No Abstract] [Full Text] [Related]
14. Selectivity of the excision of alkylation products in a xeroderma pigmentosum-derived lymphoblastoid line.
Altamirano-Dimas M; Sklar R; Strauss B
Mutat Res; 1979 Apr; 60(2):197-206. PubMed ID: 460288
[TBL] [Abstract][Full Text] [Related]
15. DNA repair defects in genetic diseases in man.
Bootsma D
Biochimie; 1978; 60(10):1173-4. PubMed ID: 737197
[No Abstract] [Full Text] [Related]
16. Deoxyribonucleoside triphosphate pool levels in three cell strains of human chromosome instability syndromes: ataxia telangiectasia (GM2052), Bloom's syndrome (GM1492), and Fanconi's anemia (GM368).
Kenne K; Akerblom L
Cancer Biochem Biophys; 1990 Jan; 11(1):69-77. PubMed ID: 2337882
[TBL] [Abstract][Full Text] [Related]
17. [Spontaneous chromosomal instability in the rare hereditary diseases: Fanconi's anemia and Bloom's syndrome].
Schroeder TM
Dtsch Med Wochenschr; 1973 Nov; 98(46):2213-5. PubMed ID: 4757391
[No Abstract] [Full Text] [Related]
18. [Mutagenic effects of N-methyl-N-nitro-N-nitrosoguanidine (MNNG) and ethyl methanesulfonate (EMS) on chloroquine resistance in Plasmodium berghei ANKA strain].
Yao SN; Guan WB
Zhongguo Yao Li Xue Bao; 1988 Jul; 9(4):356-60. PubMed ID: 3057812
[No Abstract] [Full Text] [Related]
19. Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome.
Heim RA; Lench NJ; Swift M
Mutat Res; 1992 Dec; 284(1):25-36. PubMed ID: 1279391
[No Abstract] [Full Text] [Related]
20. Chromosome-breakage syndromes: different genes, different treatments, different cancers.
German J
Basic Life Sci; 1980; 15():429-39. PubMed ID: 7011310
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]