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Journal Abstract Search

439 related items for PubMed ID: 24402520

  • 1. Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.
    Court F, Tayama C, Romanelli V, Martin-Trujillo A, Iglesias-Platas I, Okamura K, Sugahara N, Simón C, Moore H, Harness JV, Keirstead H, Sanchez-Mut JV, Kaneki E, Lapunzina P, Soejima H, Wake N, Esteller M, Ogata T, Hata K, Nakabayashi K, Monk D.
    Genome Res; 2014 Apr; 24(4):554-69. PubMed ID: 24402520
    [Abstract] [Full Text] [Related]

  • 2. Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting.
    Sanchez-Delgado M, Court F, Vidal E, Medrano J, Monteagudo-Sánchez A, Martin-Trujillo A, Tayama C, Iglesias-Platas I, Kondova I, Bontrop R, Poo-Llanillo ME, Marques-Bonet T, Nakabayashi K, Simón C, Monk D.
    PLoS Genet; 2016 Nov; 12(11):e1006427. PubMed ID: 27835649
    [Abstract] [Full Text] [Related]

  • 3. DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.
    Joshi RS, Garg P, Zaitlen N, Lappalainen T, Watson CT, Azam N, Ho D, Li X, Antonarakis SE, Brunner HG, Buiting K, Cheung SW, Coffee B, Eggermann T, Francis D, Geraedts JP, Gimelli G, Jacobson SG, Le Caignec C, de Leeuw N, Liehr T, Mackay DJ, Montgomery SB, Pagnamenta AT, Papenhausen P, Robinson DO, Ruivenkamp C, Schwartz C, Steiner B, Stevenson DA, Surti U, Wassink T, Sharp AJ.
    Am J Hum Genet; 2016 Sep 01; 99(3):555-566. PubMed ID: 27569549
    [Abstract] [Full Text] [Related]

  • 4. Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues.
    Pervjakova N, Kasela S, Morris AP, Kals M, Metspalu A, Lindgren CM, Salumets A, Mägi R.
    Epigenomics; 2016 Jun 01; 8(6):789-99. PubMed ID: 27004446
    [Abstract] [Full Text] [Related]

  • 5. Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes.
    Nakabayashi K, Trujillo AM, Tayama C, Camprubi C, Yoshida W, Lapunzina P, Sanchez A, Soejima H, Aburatani H, Nagae G, Ogata T, Hata K, Monk D.
    Hum Mol Genet; 2011 Aug 15; 20(16):3188-97. PubMed ID: 21593219
    [Abstract] [Full Text] [Related]

  • 6. Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytes.
    Tomizawa S, Kobayashi H, Watanabe T, Andrews S, Hata K, Kelsey G, Sasaki H.
    Development; 2011 Mar 15; 138(5):811-20. PubMed ID: 21247965
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  • 8. The loss of imprinted DNA methylation in mouse blastocysts is inflicted to a similar extent by in vitro follicle culture and ovulation induction.
    Saenz-de-Juano MD, Billooye K, Smitz J, Anckaert E.
    Mol Hum Reprod; 2016 Jun 15; 22(6):427-41. PubMed ID: 26908643
    [Abstract] [Full Text] [Related]

  • 9. DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation.
    Das R, Lee YK, Strogantsev R, Jin S, Lim YC, Ng PY, Lin XM, Chng K, Yeo GSh, Ferguson-Smith AC, Ding C.
    BMC Genomics; 2013 Oct 05; 14():685. PubMed ID: 24094292
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  • 11. A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes.
    Strichman-Almashanu LZ, Lee RS, Onyango PO, Perlman E, Flam F, Frieman MB, Feinberg AP.
    Genome Res; 2002 Apr 05; 12(4):543-54. PubMed ID: 11932239
    [Abstract] [Full Text] [Related]

  • 12. Germline-derived DNA methylation and early embryo epigenetic reprogramming: The selected survival of imprints.
    Monk D.
    Int J Biochem Cell Biol; 2015 Oct 05; 67():128-38. PubMed ID: 25966912
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  • 14. Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction.
    Monteagudo-Sánchez A, Sánchez-Delgado M, Mora JRH, Santamaría NT, Gratacós E, Esteller M, de Heredia ML, Nunes V, Choux C, Fauque P, de Nanclares GP, Anton L, Elovitz MA, Iglesias-Platas I, Monk D.
    Clin Epigenetics; 2019 Feb 26; 11(1):35. PubMed ID: 30808399
    [Abstract] [Full Text] [Related]

  • 15. Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes.
    Docherty LE, Rezwan FI, Poole RL, Jagoe H, Lake H, Lockett GA, Arshad H, Wilson DI, Holloway JW, Temple IK, Mackay DJ.
    J Med Genet; 2014 Apr 26; 51(4):229-38. PubMed ID: 24501229
    [Abstract] [Full Text] [Related]

  • 16. Genome-wide detection of imprinted differentially methylated regions using nanopore sequencing.
    Akbari V, Garant JM, O'Neill K, Pandoh P, Moore R, Marra MA, Hirst M, Jones SJM.
    Elife; 2022 Jul 05; 11():. PubMed ID: 35787786
    [Abstract] [Full Text] [Related]

  • 17. Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.
    Tabano S, Colapietro P, Cetin I, Grati FR, Zanutto S, Mandò C, Antonazzo P, Pileri P, Rossella F, Larizza L, Sirchia SM, Miozzo M.
    Epigenetics; 2010 May 16; 5(4):313-24. PubMed ID: 20418667
    [Abstract] [Full Text] [Related]

  • 18. Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta.
    Hamada H, Okae H, Toh H, Chiba H, Hiura H, Shirane K, Sato T, Suyama M, Yaegashi N, Sasaki H, Arima T.
    Am J Hum Genet; 2016 Nov 03; 99(5):1045-1058. PubMed ID: 27843122
    [Abstract] [Full Text] [Related]

  • 19. Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation.
    Paliwal A, Temkin AM, Kerkel K, Yale A, Yotova I, Drost N, Lax S, Nhan-Chang CL, Powell C, Borczuk A, Aviv A, Wapner R, Chen X, Nagy PL, Schork N, Do C, Torkamani A, Tycko B.
    PLoS Genet; 2013 Aug 03; 9(8):e1003622. PubMed ID: 24009515
    [Abstract] [Full Text] [Related]

  • 20. Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.
    Aoki S, Higashimoto K, Hidaka H, Ohtsuka Y, Aoki S, Mishima H, Yoshiura KI, Nakabayashi K, Hata K, Yatsuki H, Hara S, Ohba T, Katabuchi H, Soejima H.
    Clin Epigenetics; 2022 May 17; 14(1):64. PubMed ID: 35581658
    [Abstract] [Full Text] [Related]

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