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Journal Abstract Search

148 related items for PubMed ID: 9724321

  • 1. Masquerading repeats: paralogous pitfalls of the human genome.
    Eichler EE.
    Genome Res; 1998 Aug; 8(8):758-62. PubMed ID: 9724321
    [No Abstract] [Full Text] [Related]

  • 2. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.
    Chuzhanova N, Abeysinghe SS, Krawczak M, Cooper DN.
    Hum Mutat; 2003 Sep; 22(3):245-51. PubMed ID: 12938089
    [Abstract] [Full Text] [Related]

  • 3. Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.
    Eichler EE, Lu F, Shen Y, Antonacci R, Jurecic V, Doggett NA, Moyzis RK, Baldini A, Gibbs RA, Nelson DL.
    Hum Mol Genet; 1996 Jul; 5(7):899-912. PubMed ID: 8817324
    [Abstract] [Full Text] [Related]

  • 4. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.
    Abeysinghe SS, Chuzhanova N, Krawczak M, Ball EV, Cooper DN.
    Hum Mutat; 2003 Sep; 22(3):229-44. PubMed ID: 12938088
    [Abstract] [Full Text] [Related]

  • 5. Duplication and distribution of repetitive elements and non-unique regions in the human genome.
    Mazzarella R, Schlessinger D.
    Gene; 1997 Dec 31; 205(1-2):29-38. PubMed ID: 9461377
    [Abstract] [Full Text] [Related]

  • 6. [The MB1 family of repeats in clones from the genomes of mammals].
    Korotkov EV.
    Izv Akad Nauk SSSR Biol; 1992 Dec 31; (4):546-57. PubMed ID: 1452902
    [Abstract] [Full Text] [Related]

  • 7. De novo repeat classification and fragment assembly.
    Pevzner PA, Tang H, Tesler G.
    Genome Res; 2004 Sep 31; 14(9):1786-96. PubMed ID: 15342561
    [Abstract] [Full Text] [Related]

  • 8. Genome-wide detection and analysis of recent segmental duplications within mammalian organisms.
    Bailey JA, Eichler EE.
    Cold Spring Harb Symp Quant Biol; 2003 Sep 31; 68():115-24. PubMed ID: 15338609
    [No Abstract] [Full Text] [Related]

  • 9. Arabidopsis thaliana centromere regions: genetic map positions and repetitive DNA structure.
    Round EK, Flowers SK, Richards EJ.
    Genome Res; 1997 Nov 31; 7(11):1045-53. PubMed ID: 9371740
    [Abstract] [Full Text] [Related]

  • 10. DNA inverted repeats and human disease.
    Bissler JJ.
    Front Biosci; 1998 Mar 27; 3():d408-18. PubMed ID: 9516381
    [Abstract] [Full Text] [Related]

  • 11. The chAB4 and NF1-related long-range multisequence DNA families are contiguous in the centromeric heterochromatin of several human chromosomes.
    Cserpán I, Katona R, Praznovszky T, Novák E, Rózsavölgyi M, Csonka E, Mórocz M, Fodor K, Hadlaczky G.
    Nucleic Acids Res; 2002 Jul 01; 30(13):2899-905. PubMed ID: 12087175
    [Abstract] [Full Text] [Related]

  • 12. Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element.
    Dombroski BA, Scott AF, Kazazian HH.
    Proc Natl Acad Sci U S A; 1993 Jul 15; 90(14):6513-7. PubMed ID: 8393568
    [Abstract] [Full Text] [Related]

  • 13. Repetitive conundrums of centromere structure and function.
    Eichler EE.
    Hum Mol Genet; 1999 Feb 15; 8(2):151-5. PubMed ID: 9931322
    [Abstract] [Full Text] [Related]

  • 14. Automated de novo identification of repeat sequence families in sequenced genomes.
    Bao Z, Eddy SR.
    Genome Res; 2002 Aug 15; 12(8):1269-76. PubMed ID: 12176934
    [Abstract] [Full Text] [Related]

  • 15. Molecular-evolutionary mechanisms for genomic disorders.
    Stankiewicz P, Lupski JR.
    Curr Opin Genet Dev; 2002 Jun 15; 12(3):312-9. PubMed ID: 12076675
    [Abstract] [Full Text] [Related]

  • 16. The role of alphoid higher order repeats (HORs) in the centromere folding.
    Rosandić M, Gluncić M, Paar V, Basar I.
    J Theor Biol; 2008 Oct 07; 254(3):555-60. PubMed ID: 18625244
    [Abstract] [Full Text] [Related]

  • 17. 2002 Curt Stern Award Address. Genomic disorders recombination-based disease resulting from genomic architecture.
    Lupski JR.
    Am J Hum Genet; 2003 Feb 07; 72(2):246-52. PubMed ID: 12596790
    [No Abstract] [Full Text] [Related]

  • 18. Use of dinucleotide polymorphism analyses in physical mapping.
    Fairman J, Nagarajan L.
    Methods Mol Biol; 1997 Feb 07; 68():149-57. PubMed ID: 9055255
    [No Abstract] [Full Text] [Related]

  • 19. Two extended arrays of a satellite DNA sequence at the centromere and at the short-arm telomere of Chinese hamster chromosome 5.
    Faravelli M, Moralli D, Bertoni L, Attolini C, Chernova O, Raimondi E, Giulotto E.
    Cytogenet Cell Genet; 1998 Feb 07; 83(3-4):281-6. PubMed ID: 10072604
    [Abstract] [Full Text] [Related]

  • 20. α satellite DNA variation and function of the human centromere.
    Sullivan LL, Chew K, Sullivan BA.
    Nucleus; 2017 Jul 04; 8(4):331-339. PubMed ID: 28406740
    [Abstract] [Full Text] [Related]

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