BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 28796236)

  • 1. Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction.
    Abi Habib W; Brioude F; Edouard T; Bennett JT; Lienhardt-Roussie A; Tixier F; Salem J; Yuen T; Azzi S; Le Bouc Y; Harbison MD; Netchine I
    Genet Med; 2018 Feb; 20(2):250-258. PubMed ID: 28796236
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement.
    Brereton RE; Nickerson SL; Woodward KJ; Edwards T; Sivamoorthy S; Ramos Vasques Walters F; Chabros V; Marchin V; Grumball T; Kennedy D; Uzaraga J; Peverall J; Arscott G; Beilby J; Choong CS; Townshend S; Azmanov DN
    Am J Med Genet A; 2021 Oct; 185(10):3136-3145. PubMed ID: 34223693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
    Inoue T; Nakamura A; Iwahashi-Odano M; Tanase-Nakao K; Matsubara K; Nishioka J; Maruo Y; Hasegawa Y; Suzumura H; Sato S; Kobayashi Y; Murakami N; Nakabayashi K; Yamazawa K; Fuke T; Narumi S; Oka A; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2020 Jun; 12(1):86. PubMed ID: 32546215
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel Variant in
    Vado Y; Pereda A; Llano-Rivas I; Gorria-Redondo N; Díez I; Perez de Nanclares G
    Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33291420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case report: Long term response to growth hormone in a child with Silver-Russell syndrome-like phenotype due to a novel paternally inherited IGF2 variant.
    Ventresca S; Lepri FR; Criscuolo S; Bottaro G; Novelli A; Loche S; Cappa M
    Front Endocrinol (Lausanne); 2024; 15():1364234. PubMed ID: 38596219
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case report and review of the literature indicate that HMGA2 should be added as a disease gene for Silver-Russell syndrome.
    Leszinski GS; Warncke K; Hoefele J; Wagner M
    Gene; 2018 Jul; 663():110-114. PubMed ID: 29655892
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome.
    Binder G; Ziegler J; Schweizer R; Habhab W; Haack TB; Heinrich T; Eggermann T
    Clin Epigenetics; 2020 Oct; 12(1):152. PubMed ID: 33076988
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.
    De Crescenzo A; Citro V; Freschi A; Sparago A; Palumbo O; Cubellis MV; Carella M; Castelluccio P; Cavaliere ML; Cerrato F; Riccio A
    J Hum Genet; 2015 Jun; 60(6):287-93. PubMed ID: 25809938
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence.
    Hübner CT; Meyer R; Kenawy A; Ambrozaityte L; Matuleviciene A; Kraft F; Begemann M; Elbracht M; Eggermann T
    J Clin Endocrinol Metab; 2020 Jul; 105(7):. PubMed ID: 32421827
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical characterization of PLAG1- related Silver-Russell syndrome:A clinical report.
    Dong P; Zhang N; Zhang Y; Liu CX; Li CL
    Eur J Med Genet; 2023 Oct; 66(10):104837. PubMed ID: 37673301
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.
    Demars J; Shmela ME; Rossignol S; Okabe J; Netchine I; Azzi S; Cabrol S; Le Caignec C; David A; Le Bouc Y; El-Osta A; Gicquel C
    Hum Mol Genet; 2010 Mar; 19(5):803-14. PubMed ID: 20007505
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature.
    Mercadante F; Busè M; Salzano E; Fragapane T; Palazzo D; Malacarne M; Piccione M
    Ital J Pediatr; 2020 Jul; 46(1):108. PubMed ID: 32723361
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Paternally Inherited IGF2 Mutation and Growth Restriction.
    Begemann M; Zirn B; Santen G; Wirthgen E; Soellner L; Büttel HM; Schweizer R; van Workum W; Binder G; Eggermann T
    N Engl J Med; 2015 Jul; 373(4):349-56. PubMed ID: 26154720
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal correction of IGF2 to rescue the growth phenotypes in mouse models of Beckwith-Wiedemann and Silver-Russell syndromes.
    Liao J; Zeng TB; Pierce N; Tran DA; Singh P; Mann JR; Szabó PE
    Cell Rep; 2021 Feb; 34(6):108729. PubMed ID: 33567274
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternally inherited autosomal dominant PLAG-1 related Silver Russell syndrome in a fetus with intra-uterine growth restriction.
    Tse WT; Bass C; Gurney L; Kinning E
    Prenat Diagn; 2023 Jun; 43(6):724-726. PubMed ID: 37165482
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.