BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 22646060)

  • 1. IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance.
    Murphy R; Ibáñez L; Hattersley A; Tost J
    BMC Med Genet; 2012 May; 13():42. PubMed ID: 22646060
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Is ZFP57 binding to
    Sparago A; Cerrato F; Riccio A
    Clin Epigenetics; 2018; 10():23. PubMed ID: 29484033
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
    Abi Habib W; Brioude F; Azzi S; Salem J; Das Neves C; Personnier C; Chantot-Bastaraud S; Keren B; Le Bouc Y; Harbison MD; Netchine I
    Hum Mutat; 2017 Jan; 38(1):105-111. PubMed ID: 27701793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2.
    Yamaguchi Y; Tayama C; Tomikawa J; Akaishi R; Kamura H; Matsuoka K; Wake N; Minakami H; Kato K; Yamada T; Nakabayashi K; Hata K
    Clin Epigenetics; 2019 Aug; 11(1):113. PubMed ID: 31370882
    [TBL] [Abstract][Full Text] [Related]  

  • 5. IGF-I sensitivity in Silver-Russell syndrome with IGF2/H19 hypomethylation.
    Iliev DI; Kannenberg K; Weber K; Binder G
    Growth Horm IGF Res; 2014 Oct; 24(5):187-91. PubMed ID: 25066218
    [TBL] [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; 52(1):53-60. PubMed ID: 25395389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization.
    Cocchi G; Marsico C; Cosentino A; Spadoni C; Rocca A; De Crescenzo A; Riccio A
    Am J Med Genet A; 2013 Oct; 161A(10):2652-5. PubMed ID: 24038823
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation.
    Grønskov K; Poole RL; Hahnemann JM; Thomson J; Tümer Z; Brøndum-Nielsen K; Murphy R; Ravn K; Melchior L; Dedic A; Dolmer B; Temple IK; Boonen SE; Mackay DJ
    J Med Genet; 2011 May; 48(5):308-11. PubMed ID: 21278389
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.
    Yamazawa K; Kagami M; Nagai T; Kondoh T; Onigata K; Maeyama K; Hasegawa T; Hasegawa Y; Yamazaki T; Mizuno S; Miyoshi Y; Miyagawa S; Horikawa R; Matsuoka K; Ogata T
    J Mol Med (Berl); 2008 Oct; 86(10):1171-81. PubMed ID: 18607558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
    Jurkiewicz D; Kugaudo M; Skórka A; Śmigiel R; Smyk M; Ciara E; Chrzanowska K; Krajewska-Walasek M
    Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. IGF2 Mutations.
    Masunaga Y; Inoue T; Yamoto K; Fujisawa Y; Sato Y; Kawashima-Sonoyama Y; Morisada N; Iijima K; Ohata Y; Namba N; Suzumura H; Kuribayashi R; Yamaguchi Y; Yoshihashi H; Fukami M; Saitsu H; Kagami M; Ogata T
    J Clin Endocrinol Metab; 2020 Jan; 105(1):. PubMed ID: 31544945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.
    Hur SK; Freschi A; Ideraabdullah F; Thorvaldsen JL; Luense LJ; Weller AH; Berger SL; Cerrato F; Riccio A; Bartolomei MS
    Proc Natl Acad Sci U S A; 2016 Sep; 113(39):10938-43. PubMed ID: 27621468
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 46(3):192-7. PubMed ID: 19066168
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome.
    Kannenberg K; Urban C; Binder G
    Clin Genet; 2012 Apr; 81(4):366-77. PubMed ID: 22248018
    [TBL] [Abstract][Full Text] [Related]  

  • 15. No evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age.
    Murphy R; Thompson JM; Tost J; Mitchell EA;
    BMC Med Genet; 2014 Jun; 15():67. PubMed ID: 24934635
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide methylation analysis in Silver-Russell syndrome patients.
    Prickett AR; Ishida M; Böhm S; Frost JM; Puszyk W; Abu-Amero S; Stanier P; Schulz R; Moore GE; Oakey RJ
    Hum Genet; 2015 Mar; 134(3):317-332. PubMed ID: 25563730
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood.
    Lokulo-Sodipe O; Ballard L; Child J; Inskip HM; Byrne CD; Ishida M; Moore GE; Wakeling EL; Fenwick A; Mackay DJG; Davies JH; Temple IK
    J Med Genet; 2020 Oct; 57(10):683-691. PubMed ID: 32054688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dietary fat intake during early pregnancy is associated with cord blood DNA methylation at IGF2 and H19 genes in newborns.
    Chiu YH; Fadadu RP; Gaskins AJ; Rifas-Shiman SL; Laue HE; Moley KH; Hivert MF; Baccarelli A; Oken E; Chavarro JE; Cardenas A
    Environ Mol Mutagen; 2021 Aug; 62(7):388-398. PubMed ID: 34288135
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
    Kagami M; Mizuno S; Matsubara K; Nakabayashi K; Sano S; Fuke T; Fukami M; Ogata T
    Eur J Hum Genet; 2015 Aug; 23(8):1062-7. PubMed ID: 25351781
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.
    Murrell A; Ito Y; Verde G; Huddleston J; Woodfine K; Silengo MC; Spreafico F; Perotti D; De Crescenzo A; Sparago A; Cerrato F; Riccio A
    PLoS One; 2008 Mar; 3(3):e1849. PubMed ID: 18365005
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.