BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1546 related articles for article (PubMed ID: 11283700)

  • 1. To err (meiotically) is human: the genesis of human aneuploidy.
    Hassold T; Hunt P
    Nat Rev Genet; 2001 Apr; 2(4):280-91. PubMed ID: 11283700
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular basis of maternal age-related increase in oocyte aneuploidy.
    Kurahashi H; Tsutsumi M; Nishiyama S; Kogo H; Inagaki H; Ohye T
    Congenit Anom (Kyoto); 2012 Mar; 52(1):8-15. PubMed ID: 22348779
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Female germ cell aneuploidy and embryo death in mice lacking the meiosis-specific protein SCP3.
    Yuan L; Liu JG; Hoja MR; Wilbertz J; Nordqvist K; Höög C
    Science; 2002 May; 296(5570):1115-8. PubMed ID: 12004129
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The origin of human aneuploidy: where we have been, where we are going.
    Hassold T; Hall H; Hunt P
    Hum Mol Genet; 2007 Oct; 16 Spec No. 2():R203-8. PubMed ID: 17911163
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nondisjunction in trisomy 21: origin and mechanisms.
    Petersen MB; Mikkelsen M
    Cytogenet Cell Genet; 2000; 91(1-4):199-203. PubMed ID: 11173856
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
    Lamb NE; Freeman SB; Savage-Austin A; Pettay D; Taft L; Hersey J; Gu Y; Shen J; Saker D; May KM; Avramopoulos D; Petersen MB; Hallberg A; Mikkelsen M; Hassold TJ; Sherman SL
    Nat Genet; 1996 Dec; 14(4):400-5. PubMed ID: 8944019
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
    Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effect of meiotic recombination on the production of aneuploid gametes in humans.
    Lamb NE; Sherman SL; Hassold TJ
    Cytogenet Genome Res; 2005; 111(3-4):250-5. PubMed ID: 16192701
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The origin of trisomy in humans.
    Hassold T; Sherman S; Hunt PA
    Prog Clin Biol Res; 1995; 393():1-12. PubMed ID: 8545442
    [No Abstract]   [Full Text] [Related]  

  • 10. Etiology of nondisjunction in humans.
    Abruzzo MA; Hassold TJ
    Environ Mol Mutagen; 1995; 25 Suppl 26():38-47. PubMed ID: 7789361
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The origin of sex chromosome aneuploidy.
    Jacobs P; Hassold T; Harvey J; May K
    Prog Clin Biol Res; 1989; 311():135-51. PubMed ID: 2528150
    [No Abstract]   [Full Text] [Related]  

  • 12. Etiology and mechanisms of aneuploidy: A synopsis.
    Hoffman GR
    Basic Life Sci; 1985; 36():539-48. PubMed ID: 2937400
    [No Abstract]   [Full Text] [Related]  

  • 13. [Trisomy 21: fifty years between medicine and science].
    Turleau C; Vekemans M
    Med Sci (Paris); 2010 Mar; 26(3):267-72. PubMed ID: 20346276
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age.
    Antonarakis SE; Avramopoulos D; Blouin JL; Talbot CC; Schinzel AA
    Nat Genet; 1993 Feb; 3(2):146-50. PubMed ID: 8499948
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.
    Ramírez NJ; Belalcázar HM; Yunis JJ; Quintero LN; Arboleda GH; Arboleda H
    Biomedica; 2007 Mar; 27(1):141-8. PubMed ID: 17546231
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nondisjunction--a view from ringside.
    Lamb NE; Hassold TJ
    N Engl J Med; 2004 Nov; 351(19):1931-4. PubMed ID: 15525719
    [No Abstract]   [Full Text] [Related]  

  • 17. A molecular model for sporadic human aneuploidy.
    Warren WD; Gorringe KL
    Trends Genet; 2006 Apr; 22(4):218-24. PubMed ID: 16497408
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Issues pertaining to the impact and etiology of trisomy 21 and other aneuploidy in humans; a consideration of evolutionary implications, maternal age mechanisms, and other matters.
    Hook EB
    Prog Clin Biol Res; 1989; 311():1-27. PubMed ID: 2528149
    [No Abstract]   [Full Text] [Related]  

  • 19. Human aneuploidy: lessons from achiasmate segregation in Drosophila melanogaster.
    Koehler KE; Hassold TJ
    Ann Hum Genet; 1998 Nov; 62(Pt 6):467-79. PubMed ID: 10363125
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Polymorphism of C-heterochromatin chromosome regions in the etiology of human aneuploidy].
    Kovaleva NV; Butomo IV; Pavlova MN; Khitrikova LE
    Genetika; 1993 Sep; 29(9):1536-43. PubMed ID: 8276221
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 78.