BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 20179746)

  • 1. Paternal origin of the de novo constitutional t(11;22)(q23;q11).
    Ohye T; Inagaki H; Kogo H; Tsutsumi M; Kato T; Tong M; Macville MV; Medne L; Zackai EH; Emanuel BS; Kurahashi H
    Eur J Hum Genet; 2010 Jul; 18(7):783-7. PubMed ID: 20179746
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.
    Kurahashi H; Inagaki H; Ohye T; Kogo H; Tsutsumi M; Kato T; Tong M; Emanuel BS
    Clin Genet; 2010 Oct; 78(4):299-309. PubMed ID: 20507342
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.
    Tong M; Kato T; Yamada K; Inagaki H; Kogo H; Ohye T; Tsutsumi M; Wang J; Emanuel BS; Kurahashi H
    Hum Mol Genet; 2010 Jul; 19(13):2630-7. PubMed ID: 20392709
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).
    Kurahashi H; Shaikh TH; Hu P; Roe BA; Emanuel BS; Budarf ML
    Hum Mol Genet; 2000 Jul; 9(11):1665-70. PubMed ID: 10861293
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).
    Kurahashi H; Shaikh TH; Zackai EH; Celle L; Driscoll DA; Budarf ML; Emanuel BS
    Am J Hum Genet; 2000 Sep; 67(3):763-8. PubMed ID: 10903930
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Palindrome-mediated chromosomal translocations in humans.
    Kurahashi H; Inagaki H; Ohye T; Kogo H; Kato T; Emanuel BS
    DNA Repair (Amst); 2006 Sep; 5(9-10):1136-45. PubMed ID: 16829213
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic Event.
    Correll-Tash S; Conlin L; Mininger BA; Lilley B; Mennuti MT; Emanuel BS
    Cytogenet Genome Res; 2018; 156(4):185-190. PubMed ID: 30566958
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long AT-rich palindromes and the constitutional t(11;22) breakpoint.
    Kurahashi H; Emanuel BS
    Hum Mol Genet; 2001 Nov; 10(23):2605-17. PubMed ID: 11726547
    [TBL] [Abstract][Full Text] [Related]  

  • 9. AT-rich palindromes mediate the constitutional t(11;22) translocation.
    Edelmann L; Spiteri E; Koren K; Pulijaal V; Bialer MG; Shanske A; Goldberg R; Morrow BE
    Am J Hum Genet; 2001 Jan; 68(1):1-13. PubMed ID: 11095996
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosomal translocations and palindromic AT-rich repeats.
    Kato T; Kurahashi H; Emanuel BS
    Curr Opin Genet Dev; 2012 Jun; 22(3):221-8. PubMed ID: 22402448
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
    Sheridan MB; Kato T; Haldeman-Englert C; Jalali GR; Milunsky JM; Zou Y; Klaes R; Gimelli G; Gimelli S; Gemmill RM; Drabkin HA; Hacker AM; Brown J; Tomkins D; Shaikh TH; Kurahashi H; Zackai EH; Emanuel BS
    Am J Hum Genet; 2010 Aug; 87(2):209-18. PubMed ID: 20673865
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22).
    Ashley T; Gaeth AP; Inagaki H; Seftel A; Cohen MM; Anderson LK; Kurahashi H; Emanuel BS
    Am J Hum Genet; 2006 Sep; 79(3):524-38. PubMed ID: 16909390
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies.
    Gotter AL; Nimmakayalu MA; Jalali GR; Hacker AM; Vorstman J; Conforto Duffy D; Medne L; Emanuel BS
    Genome Res; 2007 Apr; 17(4):470-81. PubMed ID: 17351131
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint.
    Kurahashi H; Shaikh TH; Emanuel BS
    Hum Mol Genet; 2000 Nov; 9(18):2727-32. PubMed ID: 11063731
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal translocations mediated by palindromic DNA.
    Kurahashi H; Inagaki H; Ohye T; Kogo H; Kato T; Emanuel BS
    Cell Cycle; 2006 Jun; 5(12):1297-303. PubMed ID: 16760666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes.
    Spiteri E; Babcock M; Kashork CD; Wakui K; Gogineni S; Lewis DA; Williams KM; Minoshima S; Sasaki T; Shimizu N; Potocki L; Pulijaal V; Shanske A; Shaffer LG; Morrow BE
    Hum Mol Genet; 2003 Aug; 12(15):1823-37. PubMed ID: 12874103
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.
    Gotter AL; Shaikh TH; Budarf ML; Rhodes CH; Emanuel BS
    Hum Mol Genet; 2004 Jan; 13(1):103-15. PubMed ID: 14613967
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic variation affects de novo translocation frequency.
    Kato T; Inagaki H; Yamada K; Kogo H; Ohye T; Kowa H; Nagaoka K; Taniguchi M; Emanuel BS; Kurahashi H
    Science; 2006 Feb; 311(5763):971. PubMed ID: 16484486
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fine mapping of the constitutional translocation t(11;22)(q23;q11).
    Tapia-Páez I; O'Brien KP; Kost-Alimova M; Sahlén S; Kedra D; Bruder CE; Andersson B; Roe BA; Hu P; Imreh S; Blennow E; Dumanski JP
    Hum Genet; 2000 May; 106(5):506-16. PubMed ID: 10914680
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two different forms of palindrome resolution in the human genome: deletion or translocation.
    Kato T; Inagaki H; Kogo H; Ohye T; Yamada K; Emanuel BS; Kurahashi H
    Hum Mol Genet; 2008 Apr; 17(8):1184-91. PubMed ID: 18184694
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.