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PUBMED FOR HANDHELDS

Journal Abstract Search


143 related items for PubMed ID: 6984382

  • 41. Segregation of DNA polynucleotide strands into sister chromatids and the use of endoreduplicated cells to track sister chromatid exchanges induced by crosslinks, alkylations, or x-ray damage.
    Wolff S, Afzal V.
    Proc Natl Acad Sci U S A; 1996 Jun 11; 93(12):5765-9. PubMed ID: 8650167
    [Abstract] [Full Text] [Related]

  • 42. Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridisation (FISH) technique.
    Sakamoto Hojo ET, van Diemen PC, Darroudi F, Natarajan AT.
    Mutat Res; 1995 Feb 11; 334(1):59-69. PubMed ID: 7799980
    [Abstract] [Full Text] [Related]

  • 43. Effect of incubation temperature on the frequency of sister chromatid exchanges in Bloom's syndrome lymphocytes.
    West J, Lyttleton MJ, Giannelli F.
    Hum Genet; 1981 Feb 11; 59(3):204-7. PubMed ID: 7327581
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  • 44. Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.
    Bartram CR, Rüdiger HW, Schmidt-Preuss U, Passarge E.
    Am J Hum Genet; 1981 Nov 11; 33(6):928-34. PubMed ID: 7325155
    [Abstract] [Full Text] [Related]

  • 45. Spontaneous and cyclophosphamide-induced sister-chromatid exchanges in diploid and endoreduplicated tetraploid metaphases of preimplantation mouse embryos.
    Vogel R, Spielmann H.
    Mutat Res; 1987 Oct 11; 192(2):137-40. PubMed ID: 3657842
    [Abstract] [Full Text] [Related]

  • 46. Increased sister-chromatid exchanges (SCEs) and chromosomal fragilities by BrdU in a human mutant B-lymphoblastoid cell line.
    Taguchi T, Shiraishi Y.
    Mutat Res; 1989 Mar 11; 211(1):43-9. PubMed ID: 2784189
    [Abstract] [Full Text] [Related]

  • 47. Strand breaks arising from the repair of the 5-bromodeoxyuridine-substituted template and methyl methanesulphonate-induced lesions can explain the formation of sister chromatid exchanges.
    Saffhill R, Ockey CH.
    Chromosoma; 1985 Mar 11; 92(3):218-24. PubMed ID: 4017746
    [Abstract] [Full Text] [Related]

  • 48. Complementation studies in murine/human hybrids suggest multiple etiology for increased rate of sister chromatid exchange in mammalian cells.
    Alhadeff B, Siniscalco M.
    Basic Life Sci; 1984 Mar 11; 29 Pt B():741-63. PubMed ID: 6529423
    [Abstract] [Full Text] [Related]

  • 49. Different mutations are responsible for the elevated sister-chromatid exchange frequencies characteristic of Bloom's syndrome and hamster EM9 cells.
    Ray JH, Louie E, German J.
    Proc Natl Acad Sci U S A; 1987 Apr 11; 84(8):2368-71. PubMed ID: 3470802
    [Abstract] [Full Text] [Related]

  • 50. Uncorrected SCE levels of Bloom syndrome cells by cell hybridization with malignant cells with 14q32 structural abnormalities.
    Shiraishi Y, Li MJ.
    Cancer Genet Cytogenet; 1993 Aug 11; 69(1):45-50. PubMed ID: 8374900
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  • 53. iPSC line derived from a Bloom syndrome patient retains an increased disease-specific sister-chromatid exchange activity.
    Gatinois V, Desprat R, Becker F, Pichard L, Bernex F, Isidor B, Pellestor F, Lemaitre JM.
    Stem Cell Res; 2020 Mar 11; 43():101696. PubMed ID: 31918214
    [Abstract] [Full Text] [Related]

  • 54. Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15.
    McDaniel LD, Schultz RA.
    Proc Natl Acad Sci U S A; 1992 Sep 01; 89(17):7968-72. PubMed ID: 1518822
    [Abstract] [Full Text] [Related]

  • 55. A path probability model for sister-chromatid exchanges induced by alkylating agents.
    Conner MK, Cheng M, Biegel JA.
    Mutat Res; 1984 Mar 01; 126(1):35-46. PubMed ID: 6700613
    [Abstract] [Full Text] [Related]

  • 56. Bloom's syndrome. XIII. DNA-polymerase activity of cultured lymphoblastoid cells.
    Spanos A, Holliday R, German J.
    Hum Genet; 1986 Jun 01; 73(2):119-22. PubMed ID: 3013755
    [Abstract] [Full Text] [Related]

  • 57. Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM.
    Owen N, Hejna J, Rennie S, Mitchell A, Newell AH, Ziaie N, Moses RE, Olson SB.
    Cytogenet Genome Res; 2014 Jun 01; 144(4):255-263. PubMed ID: 25766002
    [Abstract] [Full Text] [Related]

  • 58. Incidence and origin of symmetric and asymmetric dicentrics in Bloom's syndrome.
    Therman E, Kuhn EM.
    Cancer Genet Cytogenet; 1985 Feb 15; 15(3-4):293-301. PubMed ID: 3971321
    [Abstract] [Full Text] [Related]

  • 59. Cytogenetic study in a mentally retarded child with Bloom syndrome and acute lymphoblastic leukemia.
    Werner-Favre C, Wyss M, Cabrol C, Félix F, Guenin R, Laufer D, Engel E.
    Am J Med Genet; 1984 Jun 15; 18(2):215-21. PubMed ID: 6589956
    [Abstract] [Full Text] [Related]

  • 60. The effects of beta-radiation on sister-chromatid exchanges in cultured human lymphocytes.
    Crossen PE, Morgan WF.
    Mutat Res; 1979 Aug 15; 62(1):125-9. PubMed ID: 492193
    [Abstract] [Full Text] [Related]


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