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Journal Abstract Search

202 related items for PubMed ID: 34039421

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  • 3. Molecular characterization of temple syndrome families with 14q32 epimutations.
    Brück J, Begemann M, Dey D, Elbracht M, Eggermann T.
    Eur J Med Genet; 2020 Dec; 63(12):104077. PubMed ID: 33010492
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  • 12. Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.
    Eggermann T, Yapici E, Bliek J, Pereda A, Begemann M, Russo S, Tannorella P, Calzari L, de Nanclares GP, Lombardi P, Temple IK, Mackay D, Riccio A, Kagami M, Ogata T, Lapunzina P, Monk D, Maher ER, Tümer Z.
    Clin Epigenetics; 2022 Mar 16; 14(1):41. PubMed ID: 35296332
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  • 14. The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndrome.
    Bens S, Kolarova J, Gillessen-Kaesbach G, Buiting K, Beygo J, Caliebe A, Ammerpohl O, Siebert R.
    Epigenomics; 2015 Oct 16; 7(7):1089-97. PubMed ID: 26541061
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  • 17. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
    Kagami M, Mizuno S, Matsubara K, Nakabayashi K, Sano S, Fuke T, Fukami M, Ogata T.
    Eur J Hum Genet; 2015 Aug 16; 23(8):1062-7. PubMed ID: 25351781
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  • 19. Meg3-DMR, not the Meg3 gene, regulates imprinting of the Dlk1-Dio3 locus.
    Zhu W, Botticelli EM, Kery RE, Mao Y, Wang X, Yang A, Wang X, Zhou J, Zhang X, Soberman RJ, Klibanski A, Zhou Y.
    Dev Biol; 2019 Nov 01; 455(1):10-18. PubMed ID: 31301299
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  • 20. The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances.
    Monteagudo-Sánchez A, Hernandez Mora JR, Simon C, Burton A, Tenorio J, Lapunzina P, Clark S, Esteller M, Kelsey G, López-Siguero JP, de Nanclares GP, Torres-Padilla ME, Monk D.
    Nucleic Acids Res; 2020 Nov 18; 48(20):11394-11407. PubMed ID: 33053156
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