These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 21466477)

  • 1. Epigenetic and genetic mechanisms of abnormal 11p15 genomic imprinting in Silver-Russell and Beckwith-Wiedemann syndromes.
    Demars J; Le Bouc Y; El-Osta A; Gicquel C
    Curr Med Chem; 2011; 18(12):1740-50. PubMed ID: 21466477
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.
    Demars J; Gicquel C
    Clin Genet; 2012 Apr; 81(4):350-61. PubMed ID: 22150955
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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; 84(4):326-34. PubMed ID: 23495910
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Beckwith-Wiedemann and Russell-Silver Syndromes: from new molecular insights to the comprehension of imprinting regulation.
    Azzi S; Abi Habib W; Netchine I
    Curr Opin Endocrinol Diabetes Obes; 2014 Feb; 21(1):30-8. PubMed ID: 24322424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Imprinted disorders and growth.
    Giabicani É; Brioude F; Le Bouc Y; Netchine I
    Ann Endocrinol (Paris); 2017 Jun; 78(2):112-113. PubMed ID: 28478949
    [TBL] [Abstract][Full Text] [Related]  

  • 7. No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.
    Müller A; Soellner L; Binder G; Begemann M; Eggermann T
    Am J Med Genet A; 2016 Jan; 170A(1):283-4. PubMed ID: 26447000
    [No Abstract]   [Full Text] [Related]  

  • 8. 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; 18(24):4724-33. PubMed ID: 19755383
    [TBL] [Abstract][Full Text] [Related]  

  • 9. New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects.
    Demars J; Rossignol S; Netchine I; Lee KS; Shmela M; Faivre L; Weill J; Odent S; Azzi S; Callier P; Lucas J; Dubourg C; Andrieux J; Le Bouc Y; El-Osta A; Gicquel C
    Hum Mutat; 2011 Oct; 32(10):1171-82. PubMed ID: 21780245
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.
    Heide S; Chantot-Bastaraud S; Keren B; Harbison MD; Azzi S; Rossignol S; Michot C; Lackmy-Port Lys M; Demeer B; Heinrichs C; Newfield RS; Sarda P; Van Maldergem L; Trifard V; Giabicani E; Siffroi JP; Le Bouc Y; Netchine I; Brioude F
    J Med Genet; 2018 Mar; 55(3):205-213. PubMed ID: 29223973
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.
    Rovina D; La Vecchia M; Cortesi A; Fontana L; Pesant M; Maitz S; Tabano S; Bodega B; Miozzo M; Sirchia SM
    Sci Rep; 2020 May; 10(1):8275. PubMed ID: 32427849
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains.
    Eggermann T; Begemann M; Pfeiffer L
    Clin Epigenetics; 2021 Feb; 13(1):30. PubMed ID: 33541417
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterogeneous phenotypes in families with duplications of the paternal allele within the imprinting center 1 (H19/IGF2:TSS-DMR) in 11p15.5.
    Eggermann T; Kraft F; Kloth K; Klopocki E; Hüning I; Hempel M; Kunstmann E
    Clin Genet; 2020 Oct; 98(4):418-419. PubMed ID: 33294970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
    Sperandeo MP; Ungaro P; Vernucci M; Pedone PV; Cerrato F; Perone L; Casola S; Cubellis MV; Bruni CB; Andria G; Sebastio G; Riccio A
    Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single family.
    Cardarelli L; Sparago A; De Crescenzo A; Nalesso E; Zavan B; Cubellis MV; Selicorni A; Cavicchioli P; Pozzan GB; Petrella M; Riccio A
    Pediatr Dev Pathol; 2010; 13(4):326-30. PubMed ID: 20028213
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 23():60-70. PubMed ID: 23182821
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epigenetics, genomic imprinting and assisted reproductive technology.
    Le Bouc Y; Rossignol S; Azzi S; Steunou V; Netchine I; Gicquel C
    Ann Endocrinol (Paris); 2010 May; 71(3):237-8. PubMed ID: 20362968
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Chang S; Bartolomei MS
    Dis Model Mech; 2020 May; 13(5):. PubMed ID: 32424032
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
    Higashimoto K; Jozaki K; Kosho T; Matsubara K; Fuke T; Yamada D; Yatsuki H; Maeda T; Ohtsuka Y; Nishioka K; Joh K; Koseki H; Ogata T; Soejima H
    Clin Genet; 2014 Dec; 86(6):539-44. PubMed ID: 24299031
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epigenetic anomalies in childhood growth disorders.
    Netchine I; Rossignol S; Azzi S; Le Bouc Y
    Nestle Nutr Inst Workshop Ser; 2013; 71():65-73. PubMed ID: 23502140
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.