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283 related items for PubMed ID: 12514746

  • 1. DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.
    Hitchins MP, Bentley L, Monk D, Beechey C, Peters J, Kelsey G, Ishino F, Preece MA, Stanier P, Moore GE.
    Mamm Genome; 2002 Dec; 13(12):686-91. PubMed ID: 12514746
    [Abstract] [Full Text] [Related]

  • 2. Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.
    Hitchins MP, Monk D, Bell GM, Ali Z, Preece MA, Stanier P, Moore GE.
    Eur J Hum Genet; 2001 Feb; 9(2):82-90. PubMed ID: 11313740
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  • 4. Evidence against GRB10 as the gene responsible for Silver-Russell syndrome.
    McCann JA, Zheng H, Islam A, Goodyer CG, Polychronakos C.
    Biochem Biophys Res Commun; 2001 Sep 07; 286(5):943-8. PubMed ID: 11527390
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  • 6. Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.
    Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, Preece MA, Moore GE.
    Am J Hum Genet; 2000 Jan 07; 66(1):36-46. PubMed ID: 10631135
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  • 7. Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.
    Wakeling EL, Abu-Amero SN, Stanier P, Preece MA, Moore GE.
    Eur J Hum Genet; 1998 Jan 07; 6(2):158-64. PubMed ID: 9781061
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  • 8. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome.
    Joyce CA, Sharp A, Walker JM, Bullman H, Temple IK.
    Hum Genet; 1999 Sep 07; 105(3):273-80. PubMed ID: 10987657
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  • 9. Monoallelic expression of nine imprinted genes in the sheep embryo occurs after the blastocyst stage.
    Thurston A, Taylor J, Gardner J, Sinclair KD, Young LE.
    Reproduction; 2008 Jan 07; 135(1):29-40. PubMed ID: 18159081
    [Abstract] [Full Text] [Related]

  • 10. Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion.
    Blagitko N, Mergenthaler S, Schulz U, Wollmann HA, Craigen W, Eggermann T, Ropers HH, Kalscheuer VM.
    Hum Mol Genet; 2000 Jul 01; 9(11):1587-95. PubMed ID: 10861285
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  • 11. (Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation?
    Schönherr N, Meyer E, Eggermann K, Ranke MB, Wollmann HA, Eggermann T.
    Eur J Med Genet; 2006 Jul 01; 49(5):414-8. PubMed ID: 16603426
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  • 12. [Expression of imprinted gene Grb10 in human oocytes and preimplantation embryos].
    Shen WJ, Kong LH, Chen SL, Li H, Xing FQ.
    Di Yi Jun Yi Da Xue Xue Bao; 2005 Mar 01; 25(3):305-7. PubMed ID: 15771999
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  • 14. Global survey of genomic imprinting by transcriptome sequencing.
    Babak T, Deveale B, Armour C, Raymond C, Cleary MA, van der Kooy D, Johnson JM, Lim LP.
    Curr Biol; 2008 Nov 25; 18(22):1735-41. PubMed ID: 19026546
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  • 15. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.
    Monk D, Smith R, Arnaud P, Preece MA, Stanier P, Beechey CV, Peters J, Kelsey G, Moore GE.
    Mamm Genome; 2003 Dec 25; 14(12):805-16. PubMed ID: 14724735
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  • 16. Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.
    Yoshihashi H, Maeyama K, Kosaki R, Ogata T, Tsukahara M, Goto Y, Hata J, Matsuo N, Smith RJ, Kosaki K.
    Am J Hum Genet; 2000 Aug 25; 67(2):476-82. PubMed ID: 10856193
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  • 17. Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10.
    Yamasaki-Ishizaki Y, Kayashima T, Mapendano CK, Soejima H, Ohta T, Masuzaki H, Kinoshita A, Urano T, Yoshiura K, Matsumoto N, Ishimaru T, Mukai T, Niikawa N, Kishino T.
    Mol Cell Biol; 2007 Jan 25; 27(2):732-42. PubMed ID: 17101788
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  • 18. Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.
    Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, Beechey CV, Peters J, Craigen W, Preece M, Stanier P, Moore GE, Kelsey G.
    Hum Mol Genet; 2003 May 01; 12(9):1005-19. PubMed ID: 12700169
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  • 19. Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13.
    Mergenthaler S, Sharp A, Ranke MB, Kalscheuer VM, Wollmann HA, Eggermann T.
    Genet Test; 2001 May 01; 5(3):261-6. PubMed ID: 11788094
    [Abstract] [Full Text] [Related]

  • 20. Genomic imprinting of Dopa decarboxylase in heart and reciprocal allelic expression with neighboring Grb10.
    Menheniott TR, Woodfine K, Schulz R, Wood AJ, Monk D, Giraud AS, Baldwin HS, Moore GE, Oakey RJ.
    Mol Cell Biol; 2008 Jan 01; 28(1):386-96. PubMed ID: 17967881
    [Abstract] [Full Text] [Related]


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