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Journal Abstract Search

490 related items for PubMed ID: 28854270

  • 1. Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals.
    Haertle L, Maierhofer A, Böck J, Lehnen H, Böttcher Y, Blüher M, Schorsch M, Potabattula R, El Hajj N, Appenzeller S, Haaf T.
    PLoS One; 2017; 12(8):e0184030. PubMed ID: 28854270
    [Abstract] [Full Text] [Related]

  • 2. New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.
    Beygo J, Küchler A, Gillessen-Kaesbach G, Albrecht B, Eckle J, Eggermann T, Gellhaus A, Kanber D, Kordaß U, Lüdecke HJ, Purmann S, Rossier E, van de Nes J, van der Werf IM, Wenzel M, Wieczorek D, Horsthemke B, Buiting K.
    Eur J Hum Genet; 2017 Aug; 25(8):935-945. PubMed ID: 28635951
    [Abstract] [Full Text] [Related]

  • 3. DNA methylation defects in spermatozoa of male partners from couples experiencing recurrent pregnancy loss.
    Khambata K, Raut S, Deshpande S, Mohan S, Sonawane S, Gaonkar R, Ansari Z, Datar M, Bansal V, Patil A, Warke H, Balasinor NH.
    Hum Reprod; 2021 Jan 01; 36(1):48-60. PubMed ID: 33319906
    [Abstract] [Full Text] [Related]

  • 4. Male obesity effects on sperm and next-generation cord blood DNA methylation.
    Potabattula R, Dittrich M, Schorsch M, Hahn T, Haaf T, El Hajj N.
    PLoS One; 2019 Jan 01; 14(6):e0218615. PubMed ID: 31246962
    [Abstract] [Full Text] [Related]

  • 5. Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions.
    Nelissen EC, Dumoulin JC, Daunay A, Evers JL, Tost J, van Montfoort AP.
    Hum Reprod; 2013 Apr 01; 28(4):1117-26. PubMed ID: 23343754
    [Abstract] [Full Text] [Related]

  • 6. Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors.
    Potabattula R, Dittrich M, Böck J, Haertle L, Müller T, Hahn T, Schorsch M, Hajj NE, Haaf T.
    Epigenomics; 2018 Oct 01; 10(10):1315-1326. PubMed ID: 30238782
    [Abstract] [Full Text] [Related]

  • 7. Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.
    Kagami M, Yanagisawa A, Ota M, Matsuoka K, Nakamura A, Matsubara K, Nakabayashi K, Takada S, Fukami M, Ogata T.
    Clin Epigenetics; 2019 Mar 07; 11(1):42. PubMed ID: 30846001
    [Abstract] [Full Text] [Related]

  • 8. Epigenetic germline mosaicism in infertile men.
    Laurentino S, Beygo J, Nordhoff V, Kliesch S, Wistuba J, Borgmann J, Buiting K, Horsthemke B, Gromoll J.
    Hum Mol Genet; 2015 Mar 01; 24(5):1295-304. PubMed ID: 25336341
    [Abstract] [Full Text] [Related]

  • 9. Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlation.
    Corsello G, Salzano E, Vecchio D, Antona V, Grasso M, Malacarne M, Carella M, Palumbo P, Piro E, Giuffrè M.
    Am J Med Genet A; 2015 Dec 01; 167A(12):3130-8. PubMed ID: 26333487
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 23(8):1062-7. PubMed ID: 25351781
    [Abstract] [Full Text] [Related]

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  • 12. Newborns of obese parents have altered DNA methylation patterns at imprinted genes.
    Soubry A, Murphy SK, Wang F, Huang Z, Vidal AC, Fuemmeler BF, Kurtzberg J, Murtha A, Jirtle RL, Schildkraut JM, Hoyo C.
    Int J Obes (Lond); 2015 Apr 01; 39(4):650-7. PubMed ID: 24158121
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 7(7):1089-97. PubMed ID: 26541061
    [Abstract] [Full Text] [Related]

  • 14. Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
    Vu TH, Li T, Nguyen D, Nguyen BT, Yao XM, Hu JF, Hoffman AR.
    Genomics; 2000 Mar 01; 64(2):132-43. PubMed ID: 10729220
    [Abstract] [Full Text] [Related]

  • 15. Methylation dynamics of imprinted genes in mouse germ cells.
    Lucifero D, Mertineit C, Clarke HJ, Bestor TH, Trasler JM.
    Genomics; 2002 Apr 01; 79(4):530-8. PubMed ID: 11944985
    [Abstract] [Full Text] [Related]

  • 16. Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32.
    Rosa AL, Wu YQ, Kwabi-Addo B, Coveler KJ, Reid Sutton V, Shaffer LG.
    Chromosome Res; 2005 Apr 01; 13(8):809-18. PubMed ID: 16331412
    [Abstract] [Full Text] [Related]

  • 17. The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesis.
    Leitão E, Di Persio S, Laurentino S, Wöste M, Dugas M, Kliesch S, Neuhaus N, Horsthemke B.
    Clin Epigenetics; 2020 May 06; 12(1):61. PubMed ID: 32375885
    [Abstract] [Full Text] [Related]

  • 18. Allele-specific histone modifications regulate expression of the Dlk1-Gtl2 imprinted domain.
    Carr MS, Yevtodiyenko A, Schmidt CL, Schmidt JV.
    Genomics; 2007 Feb 06; 89(2):280-90. PubMed ID: 17126526
    [Abstract] [Full Text] [Related]

  • 19. Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour.
    Astuti D, Latif F, Wagner K, Gentle D, Cooper WN, Catchpoole D, Grundy R, Ferguson-Smith AC, Maher ER.
    Br J Cancer; 2005 Apr 25; 92(8):1574-80. PubMed ID: 15798773
    [Abstract] [Full Text] [Related]

  • 20. Two infants with mild, atypical clinical features of Kagami-Ogata syndrome caused by epimutation.
    Higashiyama H, Ohsone Y, Takatani R, Futatani T, Kosaki R, Kagami M.
    Eur J Med Genet; 2022 Oct 25; 65(10):104580. PubMed ID: 35953028
    [Abstract] [Full Text] [Related]

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