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163 related items for PubMed ID: 19948534

  • 1. Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human.
    Tierling S, Souren NY, Gries J, Loporto C, Groth M, Lutsik P, Neitzel H, Utz-Billing I, Gillessen-Kaesbach G, Kentenich H, Griesinger G, Sperling K, Schwinger E, Walter J.
    J Med Genet; 2010 Jun; 47(6):371-6. PubMed ID: 19948534
    [Abstract] [Full Text] [Related]

  • 2. 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; 28(4):1117-26. PubMed ID: 23343754
    [Abstract] [Full Text] [Related]

  • 3. A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously.
    Lazaraviciute G, Kauser M, Bhattacharya S, Haggarty P, Bhattacharya S.
    Hum Reprod Update; 2014 Apr; 20(6):840-52. PubMed ID: 24961233
    [Abstract] [Full Text] [Related]

  • 4. Aberrant DNA Methylation of IGF2-H19 Locus in Human Fetus and in Spermatozoa From Assisted Reproductive Technologies.
    Lou H, Le F, Hu M, Yang X, Li L, Wang L, Wang N, Gao H, Jin F.
    Reprod Sci; 2019 Jul; 26(7):997-1004. PubMed ID: 30270743
    [Abstract] [Full Text] [Related]

  • 5. Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.
    Gomes MV, Huber J, Ferriani RA, Amaral Neto AM, Ramos ES.
    Mol Hum Reprod; 2009 Aug; 15(8):471-7. PubMed ID: 19494037
    [Abstract] [Full Text] [Related]

  • 6. Profiling the DNA methylation patterns of imprinted genes in abnormal semen samples by next-generation bisulfite sequencing.
    He W, Sun Υ, Zhang S, Feng X, Xu M, Dai J, Ni X, Wang X, Wu Q.
    J Assist Reprod Genet; 2020 Sep; 37(9):2211-2221. PubMed ID: 32572674
    [Abstract] [Full Text] [Related]

  • 7. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.
    Rossignol S, Steunou V, Chalas C, Kerjean A, Rigolet M, Viegas-Pequignot E, Jouannet P, Le Bouc Y, Gicquel C.
    J Med Genet; 2006 Dec; 43(12):902-7. PubMed ID: 16825435
    [Abstract] [Full Text] [Related]

  • 8. Epigenetics, genomic imprinting and assisted reproductive technology.
    Le Bouc Y, Rossignol S, Azzi S, Steunou V, Netchine I, Gicquel C.
    Ann Endocrinol (Paris); 2010 May; 71(3):237-8. PubMed ID: 20362968
    [Abstract] [Full Text] [Related]

  • 9. Quantitative analysis of DNA methylation of imprinted genes in single human blastocysts by pyrosequencing.
    Huntriss J, Woodfine K, Huddleston JE, Murrell A, Rutherford AJ, Elder K, Khan AA, Hemmings K, Picton H.
    Fertil Steril; 2011 Jun 30; 95(8):2564-7.e1-8. PubMed ID: 21575943
    [Abstract] [Full Text] [Related]

  • 10. Aberrant DNA methylation of imprinted loci in human spontaneous abortions after assisted reproduction techniques and natural conception.
    Zheng HY, Tang Y, Niu J, Li P, Ye DS, Chen X, Shi XY, Li L, Chen SL.
    Hum Reprod; 2013 Jan 30; 28(1):265-73. PubMed ID: 23042795
    [Abstract] [Full Text] [Related]

  • 11. Imprinting alterations in sperm may not significantly influence ART outcomes and imprinting patterns in the cord blood of offspring.
    Tang L, Liu Z, Zhang R, Su C, Yang W, Yao Y, Zhao S.
    PLoS One; 2017 Jan 30; 12(11):e0187869. PubMed ID: 29136648
    [Abstract] [Full Text] [Related]

  • 12. Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib.
    Milioto A, Reyes M, Hanna P, Kiuchi Z, Turan S, Zeve D, Agarwal C, Grigelioniene G, Chen A, Mericq V, Frangos M, Ten S, Mantovani G, Salusky IB, Tebben P, Jüppner H.
    J Clin Endocrinol Metab; 2022 Mar 24; 107(4):e1610-e1619. PubMed ID: 34791361
    [Abstract] [Full Text] [Related]

  • 13. Study of DNA methylation patterns of imprinted genes in children born after assisted reproductive technologies reveals no imprinting errors: A pilot study.
    Zheng HY, Shi XY, Wang LL, Wu YQ, Chen SL, Zhang L.
    Exp Ther Med; 2011 Jul 24; 2(4):751-755. PubMed ID: 22977570
    [Abstract] [Full Text] [Related]

  • 14. Epigenetic status in the offspring of spontaneous and assisted conception.
    Whitelaw N, Bhattacharya S, Hoad G, Horgan GW, Hamilton M, Haggarty P.
    Hum Reprod; 2014 Jul 24; 29(7):1452-8. PubMed ID: 24812310
    [Abstract] [Full Text] [Related]

  • 15. Altered DNA methylation and expression of PLAGL1 in cord blood from assisted reproductive technology pregnancies compared with natural conceptions.
    Vincent RN, Gooding LD, Louie K, Chan Wong E, Ma S.
    Fertil Steril; 2016 Sep 01; 106(3):739-748.e3. PubMed ID: 27178226
    [Abstract] [Full Text] [Related]

  • 16. Methylation analysis of KvDMR1 in human oocytes.
    Geuns E, Hilven P, Van Steirteghem A, Liebaers I, De Rycke M.
    J Med Genet; 2007 Feb 01; 44(2):144-7. PubMed ID: 16950814
    [Abstract] [Full Text] [Related]

  • 17. Multifactorial analysis of the stochastic epigenetic variability in cord blood confirmed an impact of common behavioral and environmental factors but not of in vitro conception.
    Gentilini D, Somigliana E, Pagliardini L, Rabellotti E, Garagnani P, Bernardinelli L, Papaleo E, Candiani M, Di Blasio AM, Viganò P.
    Clin Epigenetics; 2018 Feb 01; 10():77. PubMed ID: 29930742
    [Abstract] [Full Text] [Related]

  • 18. Increased methylation at differentially methylated region of GNAS in infants born to gestational diabetes.
    Chen D, Zhang A, Fang M, Fang R, Ge J, Jiang Y, Zhang H, Han C, Ye X, Huang H, Liu Y, Dong M.
    BMC Med Genet; 2014 Oct 01; 15():108. PubMed ID: 25269528
    [Abstract] [Full Text] [Related]

  • 19. Abnormal DLK1/MEG3 imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis.
    Dimitriadou E, Noutsopoulos D, Markopoulos G, Vlaikou AM, Mantziou S, Traeger-Synodinos J, Kanavakis E, Chrousos GP, Tzavaras T, Syrrou M.
    Stress; 2013 Nov 01; 16(6):689-97. PubMed ID: 23786541
    [Abstract] [Full Text] [Related]

  • 20. 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]

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