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    Results: 1 to 20 of 99

    1.

    Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA.

    Yeshaya J, Amir I, Rimon A, Freedman J, Shohat M, Avivi L.

    Mol Cytogenet. 2009 Mar 14;2:11.

    PMID:
    19284877
    [PubMed]
    Free PMC Article
    2.

    Aberrant allele-specific replication, independent of parental origin, in blood cells of cancer patients.

    Dotan ZA, Dotan A, Ramon J, Avivi L.

    BMC Cancer. 2008 Dec 25;8:390.

    PMID:
    19109880
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    Asynchronous replication of alleles in genomes carrying a microdeletion.

    Amiel A, Reish O, Gaber E, Masterman R, Tohami T, Fejgin MD.

    Isr Med Assoc J. 2002 Sep;4(9):702-5.

    PMID:
    12440235
    [PubMed - indexed for MEDLINE]
    Free Article
    4.

    Allele-specific replication associated with aneuploidy in blood cells of patients with hematologic malignancies.

    Korenstein-Ilan A, Amiel A, Lalezari S, Lishner M, Avivi L.

    Cancer Genet Cytogenet. 2002 Dec;139(2):97-103.

    PMID:
    12550768
    [PubMed - indexed for MEDLINE]
    5.

    Modified allelic replication in lymphocytes of patients with neurofibromatosis type 1.

    Reish O, Orlovski A, Mashevitz M, Sher C, Libman V, Rosenblat M, Avivi L.

    Cancer Genet Cytogenet. 2003 Jun;143(2):133-9.

    PMID:
    12781447
    [PubMed - indexed for MEDLINE]
    6.

    Altered mode of allelic replication accompanied by aneuploidy in peripheral blood lymphocytes of prostate cancer patients.

    Dotan ZA, Dotan A, Ramon J, Avivi L.

    Int J Cancer. 2004 Aug 10;111(1):60-6.

    PMID:
    15185343
    [PubMed - indexed for MEDLINE]
    7.

    Asynchronous replication of biallelically expressed loci: a new phenomenon in Turner syndrome.

    Reish O, Gal R, Gaber E, Sher C, Bistritzer T, Amiel A.

    Genet Med. 2002 Nov-Dec;4(6):439-43.

    PMID:
    12509715
    [PubMed - indexed for MEDLINE]
    8.

    Epigenetic analyses in blood cells of men suspected of prostate cancer predict the outcome of biopsy better than serum PSA levels.

    Cytron S, Stepnov E, Bounkin I, Mashevich M, Dotan A, Avivi L.

    Clin Epigenetics. 2011 Aug;2(2):383-388. Epub 2011 Mar 29.

    PMID:
    21949550
    [PubMed]
    Free PMC Article
    9.

    Asynchronous replication of allelic loci in Down syndrome.

    Amiel A, Avivi L, Gaber E, Fejgin MD.

    Eur J Hum Genet. 1998 Jul-Aug;6(4):359-64.

    PMID:
    9781044
    [PubMed - indexed for MEDLINE]
    Free Article
    10.

    Granulocyte colony-stimulating factor generates epigenetic and genetic alterations in lymphocytes of normal volunteer donors of stem cells.

    Nagler A, Korenstein-Ilan A, Amiel A, Avivi L.

    Exp Hematol. 2004 Jan;32(1):122-30.

    PMID:
    14725909
    [PubMed - indexed for MEDLINE]
    11.

    Modification in the inherent mode of allelic replication in lymphocytes of patients suffering from renal cell carcinoma: a novel genetic alteration associated with malignancy.

    Dotan ZA, Dotan A, Litmanovitch T, Ravia Y, Oniashvili N, Leibovitch I, Ramon J, Avivi L.

    Genes Chromosomes Cancer. 2000 Mar;27(3):270-7.

    PMID:
    10679916
    [PubMed - indexed for MEDLINE]
    12.

    Asynchronous replication dynamics of imprinted and non-imprinted chromosome regions in early mouse embryos.

    May A, Reifenberg K, Zechner U, Haaf T.

    Exp Cell Res. 2008 Sep 10;314(15):2788-95. Epub 2008 Jul 22.

    PMID:
    18675801
    [PubMed - indexed for MEDLINE]
    13.

    The aberrant asynchronous replication - characterizing lymphocytes of cancer patients - is erased following stem cell transplantation.

    Nagler A, Cytron S, Mashevich M, Korenstein-Ilan A, Avivi L.

    BMC Cancer. 2010 May 24;10:230.

    PMID:
    20497575
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

    Eisenberg DP, Jabbi M, Berman KF.

    Neuroimage. 2010 Nov 15;53(3):857-69. Epub 2010 Mar 3. Review.

    PMID:
    20206275
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    [Clinical aspects and genetics of Williams-Beuren syndrome. Clinical and molecular genetic study of 44 patients with suspected Williams-Beuren syndrome].

    von Beust G, Laccone FA, del Pilar Andrino M, Wessel A.

    Klin Padiatr. 2000 Nov-Dec;212(6):299-307. German.

    PMID:
    11190824
    [PubMed - indexed for MEDLINE]
    16.

    Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion.

    Baumer A, Riegel M, Schinzel A.

    J Med Genet. 2004 Jun;41(6):413-20.

    PMID:
    15173225
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    Final Report on Carcinogens Background Document for Formaldehyde.

    National Toxicology Program.

    Rep Carcinog Backgr Doc. 2010 Jan;(10-5981):i-512.

    PMID:
    20737003
    [PubMed - as supplied by publisher]
    18.

    Prenatal detection of maternal UPD15 in a new case with i(15p) by Timing Replication Test (TRT) and methylation analysis.

    Constantinou M, KaƂuzewski B, Helszer Z, Zajac E, Nowacka J.

    J Appl Genet. 2003;44(2):209-18.

    PMID:
    12773799
    [PubMed - indexed for MEDLINE]
    Free Article
    19.

    Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients.

    Promkan M, Teingtat S, Stheinkijkarnchai A, Wasant P, Patmasiriwat P.

    Clin Chem Lab Med. 2007;45(8):972-80.

    PMID:
    17867985
    [PubMed - indexed for MEDLINE]
    20.

    Altered replication timing of the HIRA/Tuple1 locus in the DiGeorge and Velocardiofacial syndromes.

    D'Antoni S, Mattina T, Di Mare P, Federico C, Motta S, Saccone S.

    Gene. 2004 May 26;333:111-9.

    PMID:
    15177686
    [PubMed - indexed for MEDLINE]

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