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    Results: 8

    1.

    Cohesin acetyltransferase Esco2 is a cell viability factor and is required for cohesion in pericentric heterochromatin.

    Whelan G, Kreidl E, Wutz G, Egner A, Peters JM, Eichele G.

    EMBO J. 2012 Jan 4;31(1):71-82. doi: 10.1038/emboj.2011.381. Epub 2011 Nov 18.

    PMID:
    22101327
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle.

    Mönnich M, Kuriger Z, Print CG, Horsfield JA.

    PLoS One. 2011;6(5):e20051. doi: 10.1371/journal.pone.0020051. Epub 2011 May 26.

    PMID:
    21637801
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    Identification and expression of potential regulators of the mammalian mitotic-to-meiotic transition.

    Hogarth CA, Mitchell D, Evanoff R, Small C, Griswold M.

    Biol Reprod. 2011 Jan;84(1):34-42. doi: 10.1095/biolreprod.110.086215. Epub 2010 Sep 8.

    PMID:
    20826732
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    Transcriptional regulation of the human establishment of cohesion 1 homolog 2 gene.

    Nishihara M, Yamada M, Nozaki M, Nakahira K, Yanagihara I.

    Biochem Biophys Res Commun. 2010 Feb 26;393(1):111-7. doi: 10.1016/j.bbrc.2010.01.094. Epub 2010 Jan 29.

    PMID:
    20116366
    [PubMed - indexed for MEDLINE]
    5.

    The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature.

    Goh ES, Li C, Horsburgh S, Kasai Y, Kolomietz E, Morel CF.

    Am J Med Genet A. 2010 Feb;152A(2):472-8. doi: 10.1002/ajmg.a.33261.

    PMID:
    20101700
    [PubMed - indexed for MEDLINE]
    6.

    Cohesin acetylation speeds the replication fork.

    Terret ME, Sherwood R, Rahman S, Qin J, Jallepalli PV.

    Nature. 2009 Nov 12;462(7270):231-4. doi: 10.1038/nature08550.

    PMID:
    19907496
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2.

    van der Lelij P, Godthelp BC, van Zon W, van Gosliga D, Oostra AB, Steltenpool J, de Groot J, Scheper RJ, Wolthuis RM, Waisfisz Q, Darroudi F, Joenje H, de Winter JP.

    PLoS One. 2009 Sep 7;4(9):e6936. doi: 10.1371/journal.pone.0006936.

    PMID:
    19738907
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome.

    Vega H, Trainer AH, Gordillo M, Crosier M, Kayserili H, Skovby F, Uzielli ML, Schnur RE, Manouvrier S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Hennekam RC, Jabs EW.

    J Med Genet. 2010 Jan;47(1):30-7. doi: 10.1136/jmg.2009.068395. Epub 2009 Jul 1.

    PMID:
    19574259
    [PubMed - indexed for MEDLINE]

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