These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

946 related items for PubMed ID: 20418667

  • 1. 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]

  • 2. Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia.
    Bourque DK, Avila L, Peñaherrera M, von Dadelszen P, Robinson WP.
    Placenta; 2010 Mar 16; 31(3):197-202. PubMed ID: 20060582
    [Abstract] [Full Text] [Related]

  • 3. 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 16; 214(5):625.e1-625.e11. PubMed ID: 26880735
    [Abstract] [Full Text] [Related]

  • 4. Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae.
    Guo L, Choufani S, Ferreira J, Smith A, Chitayat D, Shuman C, Uxa R, Keating S, Kingdom J, Weksberg R.
    Dev Biol; 2008 Aug 01; 320(1):79-91. PubMed ID: 18550048
    [Abstract] [Full Text] [Related]

  • 5. 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 Aug 01; 7(12):e51210. PubMed ID: 23227253
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 52(1):53-60. PubMed ID: 25395389
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Rapid detection of methylation change at H19 in human imprinting disorders using methylation-sensitive high-resolution melting.
    Wojdacz TK, Dobrovic A, Algar EM.
    Hum Mutat; 2008 Oct 05; 29(10):1255-60. PubMed ID: 18473334
    [Abstract] [Full Text] [Related]

  • 9. Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes.
    Cordeiro A, Neto AP, Carvalho F, Ramalho C, Dória S.
    J Assist Reprod Genet; 2014 Oct 05; 31(10):1361-8. PubMed ID: 24986528
    [Abstract] [Full Text] [Related]

  • 10. Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.
    Tost J, Jammes H, Dupont JM, Buffat C, Robert B, Mignot TM, Mondon F, Carbonne B, Siméoni U, Grangé G, Kerjean A, Ferré F, Gut IG, Vaiman D.
    Nucleic Acids Res; 2006 Oct 05; 34(19):5438-48. PubMed ID: 17012269
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.
    Bartholdi D, Krajewska-Walasek M, Ounap K, Gaspar H, Chrzanowska KH, Ilyana H, Kayserili H, Lurie IW, Schinzel A, Baumer A.
    J Med Genet; 2009 Mar 05; 46(3):192-7. PubMed ID: 19066168
    [Abstract] [Full Text] [Related]

  • 20. Role of epigenetic regulation of Igf2 and H19 in 2,3,7,8-Tetrachlorobenzo-p-dioxin (TCDD)-induced ovarian toxicity in offspring rats.
    Zhang X, Ji M, Tan X, Yu K, Xu L, Chen G, Yu Z.
    Toxicol Lett; 2019 Sep 01; 311():98-104. PubMed ID: 31063829
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 48.