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

154 related items for PubMed ID: 9192843

  • 1. Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses.
    Riesewijk AM, Hu L, Schulz U, Tariverdian G, Höglund P, Kere J, Ropers HH, Kalscheuer VM.
    Genomics; 1997 Jun 01; 42(2):236-44. PubMed ID: 9192843
    [Abstract] [Full Text] [Related]

  • 2. The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting.
    Yamasaki K, Hayashida S, Miura K, Masuzaki H, Ishimaru T, Niikawa N, Kishino T.
    Genomics; 2000 Sep 15; 68(3):330-5. PubMed ID: 10995575
    [Abstract] [Full Text] [Related]

  • 3. Imprinting of PEG1/MEST isoform 2 in human placenta.
    McMinn J, Wei M, Sadovsky Y, Thaker HM, Tycko B.
    Placenta; 2006 Sep 15; 27(2-3):119-26. PubMed ID: 16338457
    [Abstract] [Full Text] [Related]

  • 4. PEG1 expression in maternal uniparental disomy 7.
    Cuisset L, Le Stunff C, Dupont JM, Vasseur C, Cartigny M, Despert F, Delpech M, Bougnere P, Jeanpierre M.
    Ann Genet; 1997 Sep 15; 40(4):211-5. PubMed ID: 9526615
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7.
    Moore MW, Dietz LG, Tirtorahardjo B, Cotter PD.
    Hum Mutat; 2003 Jun 15; 21(6):645-8. PubMed ID: 12754712
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Genomic structure and parent-of-origin-specific methylation of Peg1.
    Lefebvre L, Viville S, Barton SC, Ishino F, Surani MA.
    Hum Mol Genet; 1997 Oct 15; 6(11):1907-15. PubMed ID: 9302270
    [Abstract] [Full Text] [Related]

  • 10. Evidence against a major role of PEG1/MEST in Silver-Russell syndrome.
    Riesewijk AM, Blagitko N, Schinzel AA, Hu L, Schulz U, Hamel BC, Ropers HH, Kalscheuer VM.
    Eur J Hum Genet; 1998 Oct 15; 6(2):114-20. PubMed ID: 9781054
    [Abstract] [Full Text] [Related]

  • 11. Loss of imprinting of PEG1/MEST in lung cancer cell lines.
    Nakanishi H, Suda T, Katoh M, Watanabe A, Igishi T, Kodani M, Matsumoto S, Nakamoto M, Shigeoka Y, Okabe T, Oshimura M, Shimizu E.
    Oncol Rep; 2004 Dec 15; 12(6):1273-8. PubMed ID: 15547750
    [Abstract] [Full Text] [Related]

  • 12. Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promoters.
    Valleley EM, Cordery SF, Bonthron DT.
    Hum Mol Genet; 2007 Apr 15; 16(8):972-81. PubMed ID: 17341487
    [Abstract] [Full Text] [Related]

  • 13. Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32.
    Hayashida S, Yamasaki K, Asada Y, Soeda E, Niikawa N, Kishino T.
    Genomics; 2000 Jun 01; 66(2):221-5. PubMed ID: 10860668
    [Abstract] [Full Text] [Related]

  • 14. Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription.
    Riesewijk AM, Schepens MT, Welch TR, van den Berg-Loonen EM, Mariman EM, Ropers HH, Kalscheuer VM.
    Genomics; 1996 Jan 15; 31(2):158-66. PubMed ID: 8824797
    [Abstract] [Full Text] [Related]

  • 15. Imprinting and expression status of isoforms 1 and 2 of PEG1/MEST gene in uterine leiomyoma.
    Moon YS, Park SK, Kim HT, Lee TS, Kim JH, Choi YS.
    Gynecol Obstet Invest; 2010 Jan 15; 70(2):120-5. PubMed ID: 20339302
    [Abstract] [Full Text] [Related]

  • 16. Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST.
    Kagami M, Nagai T, Fukami M, Yamazawa K, Ogata T.
    J Assist Reprod Genet; 2007 Apr 15; 24(4):131-6. PubMed ID: 17450433
    [Abstract] [Full Text] [Related]

  • 17. Frequent loss of imprinting of PEG1/MEST in invasive breast cancer.
    Pedersen IS, Dervan PA, Broderick D, Harrison M, Miller N, Delany E, O'Shea D, Costello P, McGoldrick A, Keating G, Tobin B, Gorey T, McCann A.
    Cancer Res; 1999 Nov 01; 59(21):5449-51. PubMed ID: 10554015
    [Abstract] [Full Text] [Related]

  • 18. Effect of CpG methylation on expression of the mouse imprinted gene Mest.
    Nishita Y, Sado T, Yoshida I, Takagi N.
    Gene; 1999 Jan 21; 226(2):199-209. PubMed ID: 9931489
    [Abstract] [Full Text] [Related]

  • 19. Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human.
    Ruf N, Bähring S, Galetzka D, Pliushch G, Luft FC, Nürnberg P, Haaf T, Kelsey G, Zechner U.
    Hum Mol Genet; 2007 Nov 01; 16(21):2591-9. PubMed ID: 17704508
    [Abstract] [Full Text] [Related]

  • 20. Oocyte growth-dependent progression of maternal imprinting in mice.
    Hiura H, Obata Y, Komiyama J, Shirai M, Kono T.
    Genes Cells; 2006 Apr 01; 11(4):353-61. PubMed ID: 16611239
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.