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Journal Abstract Search

184 related items for PubMed ID: 9833069

  • 1.
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  • 2. Human (Homo sapiens) and chimpanzee (Pan troglodytes) share similar ancestral centromeric alpha satellite DNA sequences but other fractions of heterochromatin differ considerably.
    Luke S, Verma RS.
    Am J Phys Anthropol; 1995 Jan; 96(1):63-71. PubMed ID: 7726296
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  • 3. Structural rearrangements and insertions of dispersed elements in pericentromeric alpha satellites occur preferably at kinkable DNA sites.
    Mashkova TD, Oparina NY, Lacroix MH, Fedorova LI, G Tumeneva I, Zinovieva OL, Kisselev LL.
    J Mol Biol; 2001 Jan 05; 305(1):33-48. PubMed ID: 11114245
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  • 4. Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1.
    Verma RS, Ramesh KH, Mathews T, Kleyman SM, Conte RA.
    Ann Genet; 1996 Jan 05; 39(4):205-8. PubMed ID: 9037348
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  • 6. Heteromorphism of human chromosome 18 detected by fluorescent in situ hybridization.
    Bonfatti A, Giunta C, Sensi A, Gruppioni R, Rubini M, Fontana F.
    Eur J Histochem; 1993 Jan 05; 37(2):149-54. PubMed ID: 7688600
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  • 8. Contiguous arrays of satellites 1, 3, and beta form a 1.5-Mb domain on chromosome 22p.
    Shiels C, Coutelle C, Huxley C.
    Genomics; 1997 Aug 15; 44(1):35-44. PubMed ID: 9286698
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  • 10. Interstitial telomeric sequence blocks in constitutive pericentromeric heterochromatin from Pyrgomorpha conica (Orthoptera) are enriched in constitutive alkali-labile sites.
    López-Fernández C, Arroyo F, Fernández JL, Gosálvez J.
    Mutat Res; 2006 Jul 25; 599(1-2):36-44. PubMed ID: 16481011
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  • 13. A 37-kb fragment common to the pericentromeric region of human chromosomes 13 and 21 and to the ancestral inactive centromere of chromosome 2.
    Charlieu JP, Laurent AM, Orti R, Viegas-Péquignot E, Bellis M, Roizès G.
    Genomics; 1993 Mar 25; 15(3):576-81. PubMed ID: 8468052
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  • 14. Large-scale dissociation and sequential reassembly of pericentric heterochromatin in dedifferentiated Arabidopsis cells.
    Tessadori F, Chupeau MC, Chupeau Y, Knip M, Germann S, van Driel R, Fransz P, Gaudin V.
    J Cell Sci; 2007 Apr 01; 120(Pt 7):1200-8. PubMed ID: 17376962
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  • 15. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
    Iourov IY, Soloviev IV, Vorsanova SG, Monakhov VV, Yurov YB.
    J Histochem Cytochem; 2005 Mar 01; 53(3):401-8. PubMed ID: 15750029
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  • 18. Genetic and physical analyses of the centromeric and pericentromeric regions of human chromosome 5: recombination across 5cen.
    Puechberty J, Laurent AM, Gimenez S, Billault A, Brun-Laurent ME, Calenda A, Marçais B, Prades C, Ioannou P, Yurov Y, Roizès G.
    Genomics; 1999 Mar 15; 56(3):274-87. PubMed ID: 10087194
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  • 19. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
    Wei S, Siu VM, Decker A, Quigg MH, Roberson J, Xu J, Adeyinka A.
    Prenat Diagn; 2007 Nov 15; 27(11):1064-6. PubMed ID: 17654752
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  • 20. Nonrandom degradation of DNA in human leukemic cells during radiation-induced apoptosis.
    Dullea RG, Robinson JF, Bedford JS.
    Cancer Res; 1999 Aug 01; 59(15):3712-8. PubMed ID: 10446986
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