Lahkim Bennani-Belhaj K, Buhagiar-Labarchede G, Jmari N, Onclercq-Delic R, Amor-Gueret M
J Nucleic Acids. 2010; 2010.
PMID: 20936166
PMC: 2945640.
DOI: 10.4061/2010/319754.
Bachrati C, Hickson I
Chromosoma. 2008; 117(3):219-33.
PMID: 18188578
DOI: 10.1007/s00412-007-0142-4.
Wang W, Seki M, Narita Y, Sonoda E, Takeda S, Yamada K
EMBO J. 2000; 19(13):3428-35.
PMID: 10880455
PMC: 313960.
DOI: 10.1093/emboj/19.13.3428.
Brosh Jr R, Karow J, White E, Shaw N, Hickson I, Bohr V
Nucleic Acids Res. 2000; 28(12):2420-30.
PMID: 10871376
PMC: 102731.
DOI: 10.1093/nar/28.12.2420.
Chester N, Kuo F, Kozak C, OHara C, Leder P
Genes Dev. 1998; 12(21):3382-93.
PMID: 9808625
PMC: 317228.
DOI: 10.1101/gad.12.21.3382.
Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance.
Murray J, Lindsay H, Munday C, Carr A
Mol Cell Biol. 1997; 17(12):6868-75.
PMID: 9372918
PMC: 232543.
DOI: 10.1128/MCB.17.12.6868.
DNA double-strand breaks caused by replication arrest.
Michel B, Ehrlich S, Uzest M
EMBO J. 1997; 16(2):430-8.
PMID: 9029161
PMC: 1169647.
DOI: 10.1093/emboj/16.2.430.
DNA ligase III is the major high molecular weight DNA joining activity in SV40-transformed human fibroblasts: normal levels of DNA ligase III activity in Bloom syndrome cells.
Tomkinson A, Starr R, Schultz R
Nucleic Acids Res. 1993; 21(23):5425-30.
PMID: 8265359
PMC: 310581.
DOI: 10.1093/nar/21.23.5425.
Effects of X-irradiation in G1 and G2 on Bloom's Syndrome and normal chromosomes.
Kuhn E
Hum Genet. 1980; 54(3):335-41.
PMID: 7399527
DOI: 10.1007/BF00291579.
Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts.
Rudiger H, Bartram C, Harder W, Passarge E
Am J Hum Genet. 1980; 32(2):150-7.
PMID: 7386453
PMC: 1685997.
Effect of incubation temperature on the frequency of sister chromatid exchanges in Bloom's syndrome lymphocytes.
West J, Lyttleton M, Giannelli F
Hum Genet. 1981; 59(3):204-7.
PMID: 7327581
DOI: 10.1007/BF00283664.
Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.
Bartram C, Rudiger H, Passarge E
Am J Hum Genet. 1981; 33(6):928-34.
PMID: 7325155
PMC: 1685170.
A clinical study of a family with Cockayne's syndrome.
Proops R, Taylor A, INSLEY J
J Med Genet. 1981; 18(4):288-93.
PMID: 7277423
PMC: 1048734.
DOI: 10.1136/jmg.18.4.288.
Sister chromatid exchange analysis.
LATT S, Schreck R
Am J Hum Genet. 1980; 32(3):297-313.
PMID: 6992563
PMC: 1686078.
12-O-tetradecanoylphorbol 13-acetate-inducible proteins are synthesized at an increased rate in Bloom syndrome fibroblasts.
Mallick U, Rahmsdorf H, Yamamoto N, Ponta H, Wegner R, Herrlich P
Proc Natl Acad Sci U S A. 1982; 79(24):7886-90.
PMID: 6961458
PMC: 347454.
DOI: 10.1073/pnas.79.24.7886.
Elevated spontaneous mutation rate in Bloom syndrome fibroblasts.
Warren S, Schultz R, Chang C, Wade M, Trosko J
Proc Natl Acad Sci U S A. 1981; 78(5):3133-7.
PMID: 6942420
PMC: 319514.
DOI: 10.1073/pnas.78.5.3133.
Clastogenic activity from Bloom syndrome fibroblast cultures.
Emerit I, Cerutti P
Proc Natl Acad Sci U S A. 1981; 78(3):1868-72.
PMID: 6940194
PMC: 319236.
DOI: 10.1073/pnas.78.3.1868.
Sister chromatid exchanges and chromosome aberrations in fibroblasts from patients with retinoblastoma.
Takabayashi T, Lin M, Wilson M
Hum Genet. 1983; 63(4):317-9.
PMID: 6862435
DOI: 10.1007/BF00274753.
Bloom's syndrome and EM9 cells in BrdU-containing medium exhibit similarly elevated frequencies of sister chromatid exchange but dissimilar amounts of cellular proliferation and chromosome disruption.
Ray J, German J
Chromosoma. 1984; 90(5):383-8.
PMID: 6510115
DOI: 10.1007/BF00294165.
Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage.
Helmerhorst F, Heaton D, Crossen P, von dem Borne A, Engelfriet C, Natarajan A
Hum Genet. 1984; 65(3):252-6.
PMID: 6421717
DOI: 10.1007/BF00286512.
