BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 11286769)

  • 1. Homing in on Russell-Silver.
    Aldred M
    Trends Mol Med; 2001 Mar; 7(3):100. PubMed ID: 11286769
    [No Abstract]   [Full Text] [Related]  

  • 2. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.
    Hannula K; Lipsanen-Nyman M; Kontiokari T; Kere J
    Am J Hum Genet; 2001 Jan; 68(1):247-53. PubMed ID: 11112662
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Russell-Silver syndrome].
    Kosaki K; Izumi K; Hasegawa T
    Nihon Rinsho; 2006 Sep; Suppl 3():436-9. PubMed ID: 17022582
    [No Abstract]   [Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 105(3):273-80. PubMed ID: 10987657
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 66(1):36-46. PubMed ID: 10631135
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.
    Hitchins MP; Stanier P; Preece MA; Moore GE
    J Med Genet; 2001 Dec; 38(12):810-9. PubMed ID: 11748303
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays.
    Kim Y; Kim SS; Kim G; Park S; Park IS; Yoo HW
    Clin Genet; 2005 Mar; 67(3):267-9. PubMed ID: 15691366
    [No Abstract]   [Full Text] [Related]  

  • 9. 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; 67(2):476-82. PubMed ID: 10856193
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10.
    Eggermann T; Begemann M; Gogiel M; Palomares M; Vallespín E; Fernández L; Cazorla R; Spengler S; García-Miñaúr S
    Am J Med Genet A; 2012 Nov; 158A(11):2815-9. PubMed ID: 22987336
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Silver-Russell syndrome and ring chromosome 7.
    Wakeling EL; Hitchins M; Stanier P; Monk D; Moore GE; Preece MA
    J Med Genet; 2000 May; 37(5):380. PubMed ID: 10905891
    [No Abstract]   [Full Text] [Related]  

  • 12. Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases.
    Bernard LE; Peñaherrera MS; Van Allen MI; Wang MS; Yong SL; Gareis F; Langlois S; Robinson WP
    Am J Med Genet; 1999 Nov; 87(3):230-6. PubMed ID: 10564876
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 14(12):805-16. PubMed ID: 14724735
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 286(5):943-8. PubMed ID: 11527390
    [TBL] [Abstract][Full Text] [Related]  

  • 15. What is the evidence for causal epigenetic influences on the Silver-Russell syndrome phenotype?
    Moore GE
    Epigenomics; 2011 Oct; 3(5):529-31. PubMed ID: 22126241
    [No Abstract]   [Full Text] [Related]  

  • 16. Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome.
    Monk D; Bentley L; Beechey C; Hitchins M; Peters J; Preece MA; Stanier P; Moore GE
    J Med Genet; 2002 Aug; 39(8):575-81. PubMed ID: 12161597
    [No Abstract]   [Full Text] [Related]  

  • 17. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands.
    Preece MA; Abu-Amero SN; Ali Z; Abu-Amero KK; Wakeling EL; Stanier P; Moore GE
    J Med Genet; 1999 Jun; 36(6):457-60. PubMed ID: 10874633
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Silver-Russell syndrome and exclusion of uniparental disomy.
    Ayala-Madrigal ML; Shaffer LG; Ramírez-Dueñas ML
    Clin Genet; 1996 Dec; 50(6):494-7. PubMed ID: 9147881
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Quantification of GRB10 in 7p12-p14 by fluorogenic 5' nuclease chemistry and application for genetic diagnosis in Silver-Russell syndrome.
    Eggermann T; Meyer E; Wollmann HA
    Ann Genet; 2004; 47(1):99-102. PubMed ID: 15050880
    [No Abstract]   [Full Text] [Related]  

  • 20. Segmental maternal UPD(7q) in Silver-Russell syndrome.
    Eggermann T; Schönherr N; Jäger S; Spaich C; Ranke MB; Wollmann HA; Binder G
    Clin Genet; 2008 Nov; 74(5):486-9. PubMed ID: 18700897
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.