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    Results: 17

    1.

    Molecular and clinical characterization of patients with a ring chromosome 11.

    Hansson KB, Gijsbers AC, Oostdijk W, Rehbock JJ, de Snoo F, Ruivenkamp CA, Kant SG.

    Eur J Med Genet. 2012 Dec;55(12):708-14. doi: 10.1016/j.ejmg.2012.08.004. Epub 2012 Aug 23.

    PMID:
    22975011
    [PubMed - indexed for MEDLINE]
    2.

    Replication timing in a single human chromosome 11 transferred into the Chinese hamster ovary (CHO) cell line.

    Watanabe Y, Kazuki Y, Oshimura M, Ikemura T, Maekawa M.

    Gene. 2012 Nov 15;510(1):1-6. doi: 10.1016/j.gene.2012.08.045. Epub 2012 Sep 3.

    PMID:
    22964274
    [PubMed - indexed for MEDLINE]
    3.

    Protective locus against renal scarring on chromosome 11 in affected sib pairs with familial vesicoureteral reflux identified by single nucleotide polymorphism linkage analysis.

    Onal B, Miao X, Ozonoff A, Bauer SB, Retik AB, Nguyen HT.

    J Urol. 2012 Oct;188(4 Suppl):1467-73. doi: 10.1016/j.juro.2012.02.018. Epub 2012 Aug 17.

    PMID:
    22906679
    [PubMed - indexed for MEDLINE]
    4.

    Hypomethylation of the KCNQ1OT1 imprinting center of chromosome 11 associated to Sotos-like features.

    Mayo S, Garin I, Monfort S, Roselló M, Orellana C, Oltra S, Zazo C, de Naclares GP, Martínez F.

    J Hum Genet. 2012 Feb;57(2):153-6. doi: 10.1038/jhg.2011.145. Epub 2012 Jan 5. No abstract available.

    PMID:
    22217647
    [PubMed - indexed for MEDLINE]
    5.

    Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11.

    Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, Capela de Matos RR, Pimenta G, Pulcheri W, Ribeiro RC, Abdelhay E, Silva ML.

    Int J Hematol. 2012 Jan;95(1):112-4. doi: 10.1007/s12185-011-0981-x. Epub 2012 Jan 5. No abstract available.

    PMID:
    22215484
    [PubMed - indexed for MEDLINE]
    6.

    Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver-Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11.

    Montenegro LR, Leal AC, Coutinho DC, Valassi HP, Nishi MY, Arnhold IJ, Mendonca BB, Jorge AA.

    Eur J Endocrinol. 2012 Mar;166(3):543-50. doi: 10.1530/EJE-11-0964. Epub 2011 Dec 14.

    PMID:
    22170793
    [PubMed - indexed for MEDLINE]
    Free Article
    7.

    Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.

    Rietschel M, Mattheisen M, Degenhardt F; Genetic Risk and Outcome in Psychosis (GROUP Investigators), Mühleisen TW, Kirsch P, Esslinger C, Herms S, Demontis D, Steffens M, Strohmaier J, Haenisch B, Breuer R, Czerski PM, Giegling I, Strengman E, Schmael C, Mors O, Mortensen PB, Hougaard DM, Ørntoft T, Kapelski P, Priebe L, Basmanav FF, Forstner AJ, Hoffman P, Meier S, Nikitopoulos J, Moebus S, Alexander M, Mössner R, Wichmann H-, Schreiber S, Rivandeneira F, Hofman A, Uitterlinden AG, Wienker TF, Schumacher J, Hauser J, Maier W, Cantor RM, Erk S, Schulze TG; SGENE-plus Consortium, Craddock N, Owen MJ, O'Donovan MC, Børglum AD, Rujescu D, Walter H, Meyer-Lindenberg A, Nöthen NM, Ophoff RA, Cichon S.

    Mol Psychiatry. 2012 Sep;17(9):906-17. doi: 10.1038/mp.2011.80. Epub 2011 Jul 12.

    PMID:
    21747397
    [PubMed - indexed for MEDLINE]
    8.

    Trisomy 6p and ring chromosome 11 in a melanotic schwannoma suggest relation to malignant melanoma rather than conventional schwannoma.

    Italiano A, Michalak S, Soulié P, Peyron AC, Pedeutour F.

    Acta Neuropathol. 2011 May;121(5):669-70. doi: 10.1007/s00401-011-0820-4. Epub 2011 Mar 22. No abstract available.

    PMID:
    21424748
    [PubMed - indexed for MEDLINE]
    9.

    Tissue-specific regulatory regions of the PTH gene localized by novel chromosome 11 rearrangement breakpoints in a parathyroid adenoma.

    Mallya SM, Wu HI, Saria EA, Corrado KR, Arnold A.

    J Bone Miner Res. 2010 Dec;25(12):2606-12. doi: 10.1002/jbmr.187. Epub 2010 Jul 16. Erratum in: J Bone Miner Res. 2011 Feb;26(2):439.

    PMID:
    20641034
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    10.

    Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies.

    Carella M, Spreafico F, Palumbo O, Storlazzi CT, Tabano S, Miozzo M, Miglionico L, Calvano S, Sindici G, Gamba B, Impera L, Collini P, Zelante L, Radice P, Perotti D.

    Am J Med Genet A. 2010 Jul;152A(7):1756-63. doi: 10.1002/ajmg.a.33420.

    PMID:
    20583153
    [PubMed - indexed for MEDLINE]
    11.

    Cytogenetic manifestation of chromosome 11 duplication/amplification in acute myeloid leukemia.

    Sárová I, Brezinová J, Zemanová Z, Izáková S, Lizcová L, Malinová E, Berková A, Cermák J, Maaloufová J, Nováková L, Michalová K.

    Cancer Genet Cytogenet. 2010 Jun;199(2):121-7. doi: 10.1016/j.cancergencyto.2010.02.012.

    PMID:
    20471515
    [PubMed - indexed for MEDLINE]
    12.

    Genome-wide association study of alcohol dependence implicates a region on chromosome 11.

    Edenberg HJ, Koller DL, Xuei X, Wetherill L, McClintick JN, Almasy L, Bierut LJ, Bucholz KK, Goate A, Aliev F, Dick D, Hesselbrock V, Hinrichs A, Kramer J, Kuperman S, Nurnberger JI Jr, Rice JP, Schuckit MA, Taylor R, Todd Webb B, Tischfield JA, Porjesz B, Foroud T.

    Alcohol Clin Exp Res. 2010 May;34(5):840-52. doi: 10.1111/j.1530-0277.2010.01156.x. Epub 2010 Mar 1.

    PMID:
    20201924
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    CD23 expression in plasma cell myeloma is specific for abnormalities of chromosome 11, and is associated with primary plasma cell leukaemia in this cytogenetic sub-group.

    Walters M, Olteanu H, Van Tuinen P, Kroft SH.

    Br J Haematol. 2010 Apr;149(2):292-3. doi: 10.1111/j.1365-2141.2009.08042.x. Epub 2010 Jan 8. No abstract available.

    PMID:
    20064156
    [PubMed - indexed for MEDLINE]
    14.

    Relations between cyclin D1 and chromosome 11 in thyroid carcinoma: analysis by dual stain using FISH and immunostaining method.

    Jikuzono T, Tenjin T, Shimizu K.

    J Nippon Med Sch. 2009 Apr;76(2):54-5.

    PMID:
    19443989
    [PubMed - indexed for MEDLINE]
    Free Article
    15.

    Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation.

    Shiura H, Nakamura K, Hikichi T, Hino T, Oda K, Suzuki-Migishima R, Kohda T, Kaneko-ishino T, Ishino F.

    Hum Mol Genet. 2009 Apr 15;18(8):1424-38. doi: 10.1093/hmg/ddp049. Epub 2009 Jan 27.

    PMID:
    19174477
    [PubMed - indexed for MEDLINE]
    Free Article
    16.

    Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae.

    Guo L, Choufani S, Ferreira J, Smith A, Chitayat D, Shuman C, Uxa R, Keating S, Kingdom J, Weksberg R.

    Dev Biol. 2008 Aug 1;320(1):79-91. doi: 10.1016/j.ydbio.2008.04.025. Epub 2008 Apr 27.

    PMID:
    18550048
    [PubMed - indexed for MEDLINE]
    17.

    Chromosome 11 genomic changes in parathyroid adenoma and hyperplasia: array CGH, FISH, and tissue microarrays.

    Yi Y, Nowak NJ, Pacchia AL, Morrison C.

    Genes Chromosomes Cancer. 2008 Aug;47(8):639-48. doi: 10.1002/gcc.20565.

    PMID:
    18398822
    [PubMed - indexed for MEDLINE]

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