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    Results: 10

    1.

    Detection of numerical abnormalities of chromosome 9 and p16/CDKN2A gene alterations in ovarian cancer with fish analysis.

    Aravidis C, Panani AD, Kosmaidou Z, Thomakos N, Rodolakis A, Antsaklis A.

    Anticancer Res. 2012 Dec;32(12):5309-13.

    PMID:
    23225431
    [PubMed - indexed for MEDLINE]
    2.

    P53 mutation and LOH at chromosome 9 in urothelial carcinoma.

    Beothe T, Nagy A, Farkas L, Kovacs G.

    Anticancer Res. 2012 Feb;32(2):523-7.

    PMID:
    22287741
    [PubMed - indexed for MEDLINE]
    3.

    Chromosome 9 ALS and FTD locus is probably derived from a single founder.

    Mok K, Traynor BJ, Schymick J, Tienari PJ, Laaksovirta H, Peuralinna T, Myllykangas L, Chiò A, Shatunov A, Boeve BF, Boxer AL, DeJesus-Hernandez M, Mackenzie IR, Waite A, Williams N, Morris HR, Simón-Sánchez J, van Swieten JC, Heutink P, Restagno G, Mora G, Morrison KE, Shaw PJ, Rollinson PS, Al-Chalabi A, Rademakers R, Pickering-Brown S, Orrell RW, Nalls MA, Hardy J.

    Neurobiol Aging. 2012 Jan;33(1):209.e3-8. doi: 10.1016/j.neurobiolaging.2011.08.005. Epub 2011 Sep 16.

    PMID:
    21925771
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    Prognostic impact of deletions of derivative chromosome 9 in patients with chronic myelogenous leukemia treated with nilotinib or dasatinib.

    Quintás-Cardama A, Kantarjian H, Shan J, Jabbour E, Abruzzo LV, Verstovsek S, Garcia-Manero G, O'Brien S, Cortes J.

    Cancer. 2011 Nov 15;117(22):5085-93. doi: 10.1002/cncr.26147. Epub 2011 Apr 26.

    PMID:
    21523765
    [PubMed - indexed for MEDLINE]
    Free Article
    5.

    Molecular cytogenetic study of derivative chromosome 9 deletion in chronic myeloid leukemia patients.

    Bennour A, Ouahchi I, Ben Youssef Y, Zaier M, Laatiri MA, Harrabi I, Meddeb B, Elloumi M, Khelif A, Saad A, Sennana H.

    Med Oncol. 2012 Jun;29(2):1151-60. doi: 10.1007/s12032-011-9918-8. Epub 2011 Apr 3.

    PMID:
    21461967
    [PubMed - indexed for MEDLINE]
    6.

    Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1.

    Zambrano RM, Wohler E, Annerén G, Thuresson AC, Cutting GR, Batista DA.

    Eur J Med Genet. 2011 Mar-Apr;54(2):189-93. doi: 10.1016/j.ejmg.2010.11.008. Epub 2010 Dec 7.

    PMID:
    21144914
    [PubMed - indexed for MEDLINE]
    7.

    De novo pericentric inversion of chromosome 9 in congenital anomaly.

    Jeong SY, Kim BY, Yu JE.

    Yonsei Med J. 2010 Sep;51(5):775-80. doi: 10.3349/ymj.2010.51.5.775.

    PMID:
    20635455
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    Association of an allele on chromosome 9 and abdominal aortic aneurysm.

    Biros E, Cooper M, Palmer LJ, Walker PJ, Norman PE, Golledge J.

    Atherosclerosis. 2010 Oct;212(2):539-42. doi: 10.1016/j.atherosclerosis.2010.06.015. Epub 2010 Jun 15.

    PMID:
    20605023
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    9.

    Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism.

    Castanet M, Mallya U, Agostini M, Schoenmakers E, Mitchell C, Demuth S, Raymond FL, Schwabe J, Gurnell M, Chatterjee VK.

    J Clin Endocrinol Metab. 2010 Aug;95(8):4031-6. doi: 10.1210/jc.2010-0275. Epub 2010 May 19.

    PMID:
    20484477
    [PubMed - indexed for MEDLINE]
    Free Article
    10.

    Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene.

    Pointon JJ, Harvey D, Karaderi T, Appleton LH, Farrar C, Stone MA, Sturrock RD, Brown MA, Wordsworth BP.

    Genes Immun. 2010 Sep;11(6):490-6. doi: 10.1038/gene.2010.17. Epub 2010 May 13. Erratum in: Genes Immun. 2011 Jun;12(4):319-20.

    PMID:
    20463747
    [PubMed - indexed for MEDLINE]
    Free PMC Article

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