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328 related items for PubMed ID: 18329128

  • 1. Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome.
    Eggermann T, Eggermann K, Schönherr N.
    Trends Genet; 2008 Apr; 24(4):195-204. PubMed ID: 18329128
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  • 2. Epigenetic regulation of growth: lessons from Silver-Russell syndrome.
    Eggermann T.
    Endocr Dev; 2009 Apr; 14():10-9. PubMed ID: 19293571
    [Abstract] [Full Text] [Related]

  • 3. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
    Eggermann T.
    Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
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  • 4. The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome.
    Schönherr N, Meyer E, Roos A, Schmidt A, Wollmann HA, Eggermann T.
    J Med Genet; 2007 Jan; 44(1):59-63. PubMed ID: 16963484
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  • 5. Epigenetic deregulation of imprinting in congenital diseases of aberrant growth.
    Delaval K, Wagschal A, Feil R.
    Bioessays; 2006 May; 28(5):453-9. PubMed ID: 16615080
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  • 6. (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 May; 49(5):414-8. PubMed ID: 16603426
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  • 7. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
    Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, Le Jule M, Heinrichs C, Cabrol S, Gicquel C, Le Bouc Y, Netchine I.
    Hum Mol Genet; 2009 Dec 15; 18(24):4724-33. PubMed ID: 19755383
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  • 8. Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes.
    Netchine I, Rossignol S, Azzi S, Brioude F, Le Bouc Y.
    Endocr Dev; 2012 Dec 15; 23():60-70. PubMed ID: 23182821
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  • 9. Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth.
    Jacob KJ, Robinson WP, Lefebvre L.
    Clin Genet; 2013 Oct 15; 84(4):326-34. PubMed ID: 23495910
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  • 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
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  • 12. Imprinted disorders and growth.
    Giabicani É, Brioude F, Le Bouc Y, Netchine I.
    Ann Endocrinol (Paris); 2017 Jun 15; 78(2):112-113. PubMed ID: 28478949
    [Abstract] [Full Text] [Related]

  • 13. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.
    Demars J, Gicquel C.
    Clin Genet; 2012 Apr 15; 81(4):350-61. PubMed ID: 22150955
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  • 14. Silver-Russell syndrome and its genetic origins.
    Rossignol S.
    J Endocrinol Invest; 2006 Apr 15; 29(1 Suppl):9-10. PubMed ID: 16615300
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  • 18. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
    Sun FL, Dean WL, Kelsey G, Allen ND, Reik W.
    Nature; 1997 Oct 23; 389(6653):809-15. PubMed ID: 9349812
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  • 19. Epigenetics in Silver-Russell syndrome.
    Rossignol S, Netchine I, Le Bouc Y, Gicquel C.
    Best Pract Res Clin Endocrinol Metab; 2008 Jun 23; 22(3):403-14. PubMed ID: 18538282
    [Abstract] [Full Text] [Related]

  • 20. Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation.
    Fisher AM, Thomas NS, Cockwell A, Stecko O, Kerr B, Temple IK, Clayton P.
    Hum Genet; 2002 Sep 23; 111(3):290-6. PubMed ID: 12215843
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