These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 24926858

  • 1. An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.
    Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL.
    PLoS One; 2014; 9(6):e99560. PubMed ID: 24926858
    [Abstract] [Full Text] [Related]

  • 2. The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.
    Pal U, Halder P, Ray A, Sarkar S, Datta S, Ghosh P, Ghosh S.
    PLoS Genet; 2021 Mar; 17(3):e1009462. PubMed ID: 33750944
    [Abstract] [Full Text] [Related]

  • 3. Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.
    Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SL.
    Hum Genet; 2012 Jul; 131(7):1039-46. PubMed ID: 22160426
    [Abstract] [Full Text] [Related]

  • 4. New insights into human nondisjunction of chromosome 21 in oocytes.
    Oliver TR, Feingold E, Yu K, Cheung V, Tinker S, Yadav-Shah M, Masse N, Sherman SL.
    PLoS Genet; 2008 Mar 14; 4(3):e1000033. PubMed ID: 18369452
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Risk of Down syndrome birth: Consanguineous marriage is associated with maternal meiosis-II nondisjunction at younger age and without any detectable recombination error.
    Ray A, Oliver TR, Halder P, Pal U, Sarkar S, Dutta S, Ghosh S.
    Am J Med Genet A; 2018 Nov 14; 176(11):2342-2349. PubMed ID: 30240118
    [Abstract] [Full Text] [Related]

  • 8. Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.
    Middlebrooks CD, Mukhopadhyay N, Tinker SW, Allen EG, Bean LJ, Begum F, Chowdhury R, Cheung V, Doheny K, Adams M, Feingold E, Sherman SL.
    Hum Mol Genet; 2014 Jan 15; 23(2):408-17. PubMed ID: 24014426
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. The association between maternal occupation and down syndrome: A report from the national Down syndrome project.
    Keen C, Hunter JE, Allen EG, Rocheleau C, Waters M, Sherman SL.
    Int J Hyg Environ Health; 2020 Jan 15; 223(1):207-213. PubMed ID: 31519426
    [Abstract] [Full Text] [Related]

  • 13. Nondisjunction in trisomy 21: origin and mechanisms.
    Petersen MB, Mikkelsen M.
    Cytogenet Cell Genet; 2000 Jan 15; 91(1-4):199-203. PubMed ID: 11173856
    [Abstract] [Full Text] [Related]

  • 14. Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.
    Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL, Watkins PC, Metaxotou C, Antonarakis SE.
    Science; 1987 Aug 07; 237(4815):652-4. PubMed ID: 2955519
    [Abstract] [Full Text] [Related]

  • 15. Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome.
    Shen JJ, Sherman SL, Hassold TJ.
    Chromosoma; 1998 Jun 07; 107(3):166-72. PubMed ID: 9639654
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomies.
    Brahe C, Tassone F, Moscetti A, Millington-Ward A, Bova R, Serra A.
    Am J Med Genet Suppl; 1990 Jun 07; 7():125-8. PubMed ID: 2149938
    [Abstract] [Full Text] [Related]

  • 18. 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 07; 14(4):400-5. PubMed ID: 8944019
    [Abstract] [Full Text] [Related]

  • 19. Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations.
    Ghosh S, Feingold E, Dey SK.
    Am J Med Genet A; 2009 Jul 07; 149A(7):1415-20. PubMed ID: 19533770
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.