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Journal Abstract Search

174 related items for PubMed ID: 23249260

  • 1. Epigenetic analysis and suitability of amniotic fluid stem cells for research and therapeutic purposes.
    Phermthai T, Suksompong S, Tirawanchai N, Issaragrisil S, Julavijitphong S, Wichitwiengrat S, Silpsorn D, Pokathikorn P.
    Stem Cells Dev; 2013 May 01; 22(9):1319-28. PubMed ID: 23249260
    [Abstract] [Full Text] [Related]

  • 2. P53 Mutation and Epigenetic Imprinted IGF2/H19 Gene Analysis in Mesenchymal Stem Cells Derived from Amniotic Fluid, Amnion, Endometrium, and Wharton's Jelly.
    Phermthai T, Pokathikorn P, Wichitwiengrat S, Thongbopit S, Tungprasertpol K, Julavijitphong S.
    Stem Cells Dev; 2017 Sep 15; 26(18):1344-1354. PubMed ID: 28629288
    [Abstract] [Full Text] [Related]

  • 3. Analysis of imprinted IGF2/H19 gene methylation and expression in normal fertilized and parthenogenetic embryonic stem cells of pigs.
    Uh KJ, Park CH, Choi KH, Park JK, Jeong YW, Roh S, Hyun SH, Shin T, Lee CK, Hwang WS.
    Anim Reprod Sci; 2014 Jun 10; 147(1-2):47-55. PubMed ID: 24794444
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. DNA methylation patterns of imprinting centers for H19, SNRPN, and KCNQ1OT1 in single-cell clones of human amniotic fluid mesenchymal stem cell.
    Peng HH, Chang SD, Chao AS, Wang CN, Cheng PJ, Hwang SM, Wang TH.
    Taiwan J Obstet Gynecol; 2012 Sep 01; 51(3):342-9. PubMed ID: 23040914
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 01; 26(7):997-1004. PubMed ID: 30270743
    [Abstract] [Full Text] [Related]

  • 8. IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch.
    Li T, Vu TH, Ulaner GA, Littman E, Ling JQ, Chen HL, Hu JF, Behr B, Giudice L, Hoffman AR.
    Mol Hum Reprod; 2005 Sep 01; 11(9):631-40. PubMed ID: 16219628
    [Abstract] [Full Text] [Related]

  • 9. Methylation status of imprinting centers for H19/IGF2 and SNURF/SNRPN in primate embryonic stem cells.
    Mitalipov S, Clepper L, Sritanaudomchai H, Fujimoto A, Wolf D.
    Stem Cells; 2007 Mar 01; 25(3):581-8. PubMed ID: 17170068
    [Abstract] [Full Text] [Related]

  • 10. Epigenetic status of H19/IGF2 and SNRPN imprinted genes in aborted and successfully derived embryonic stem cell lines in non-human primates.
    Wianny F, Blachère T, Godet M, Guillermas R, Cortay V, Bourillot PY, Lefèvre A, Savatier P, Dehay C.
    Stem Cell Res; 2016 May 01; 16(3):557-67. PubMed ID: 26999759
    [Abstract] [Full Text] [Related]

  • 11. ART manipulation after controlled ovarian stimulation may not increase the risk of abnormal expression and DNA methylation at some CpG sites of H19,IGF2 and SNRPN in foetuses: a pilot study.
    Ji M, Wang X, Wu W, Guan Y, Liu J, Wang J, Liu W, Shen C.
    Reprod Biol Endocrinol; 2018 Jul 05; 16(1):63. PubMed ID: 29976200
    [Abstract] [Full Text] [Related]

  • 12. Alterations in expression of imprinted genes from the H19/IGF2 loci in a multigenerational model of intrauterine growth restriction (IUGR).
    Gonzalez-Rodriguez P, Cantu J, O'Neil D, Seferovic MD, Goodspeed DM, Suter MA, Aagaard KM.
    Am J Obstet Gynecol; 2016 May 05; 214(5):625.e1-625.e11. PubMed ID: 26880735
    [Abstract] [Full Text] [Related]

  • 13. Quantitative allele-specific expression and DNA methylation analysis of H19, IGF2 and IGF2R in the human placenta across gestation reveals H19 imprinting plasticity.
    Buckberry S, Bianco-Miotto T, Hiendleder S, Roberts CT.
    PLoS One; 2012 May 05; 7(12):e51210. PubMed ID: 23227253
    [Abstract] [Full Text] [Related]

  • 14. Hypomethylation trends in the intergenic region of the imprinted IGF2 and H19 genes in cloned cattle.
    Curchoe CL, Zhang S, Yang L, Page R, Tian XC.
    Anim Reprod Sci; 2009 Dec 05; 116(3-4):213-25. PubMed ID: 19282114
    [Abstract] [Full Text] [Related]

  • 15. De novo DNA methylation through the 5'-segment of the H19 ICR maintains its imprint during early embryogenesis.
    Matsuzaki H, Okamura E, Takahashi T, Ushiki A, Nakamura T, Nakano T, Hata K, Fukamizu A, Tanimoto K.
    Development; 2015 Nov 15; 142(22):3833-44. PubMed ID: 26417043
    [Abstract] [Full Text] [Related]

  • 16. In-utero stress and mode of conception: impact on regulation of imprinted genes, fetal development and future health.
    Argyraki M, Damdimopoulou P, Chatzimeletiou K, Grimbizis GF, Tarlatzis BC, Syrrou M, Lambropoulos A.
    Hum Reprod Update; 2019 Nov 05; 25(6):777-801. PubMed ID: 31633761
    [Abstract] [Full Text] [Related]

  • 17. TRIM28 regulates Igf2-H19 and Dlk1-Gtl2 imprinting by distinct mechanisms during sheep fibroblast proliferation.
    Luo J, Zhang Y, Guo Y, Tang H, Wei H, Liu S, Wang X, Wang L, Zhou P.
    Gene; 2017 Dec 30; 637():152-160. PubMed ID: 28947302
    [Abstract] [Full Text] [Related]

  • 18. The long non-coding RNA 91H increases aggressive phenotype of breast cancer cells and up-regulates H19/IGF2 expression through epigenetic modifications.
    Vennin C, Spruyt N, Robin YM, Chassat T, Le Bourhis X, Adriaenssens E.
    Cancer Lett; 2017 Jan 28; 385():198-206. PubMed ID: 27780718
    [Abstract] [Full Text] [Related]

  • 19. Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.
    Azzi S, Steunou V, Tost J, Rossignol S, Thibaud N, Das Neves C, Le Jule M, Habib WA, Blaise A, Koudou Y, Busato F, Le Bouc Y, Netchine I.
    J Med Genet; 2015 Jan 28; 52(1):53-60. PubMed ID: 25395389
    [Abstract] [Full Text] [Related]

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