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 *

367 related articles for article (PubMed ID: 16963484)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. (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; 49(5):414-8. PubMed ID: 16603426
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
    Bullman H; Lever M; Robinson DO; Mackay DJ; Holder SE; Wakeling EL
    J Med Genet; 2008 Jun; 45(6):396-9. PubMed ID: 18474587
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain.
    Eggermann T; Schönherr N; Meyer E; Obermann C; Mavany M; Eggermann K; Ranke MB; Wollmann HA
    J Med Genet; 2006 Jul; 43(7):615-6. PubMed ID: 16236811
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
    Eggermann T; Meyer E; Obermann C; Heil I; Schüler H; Ranke MB; Eggermann K; Wollmann HA
    J Med Genet; 2005 May; 42(5):e26. PubMed ID: 15863658
    [TBL] [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. 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]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.
    Gicquel C; Rossignol S; Cabrol S; Houang M; Steunou V; Barbu V; Danton F; Thibaud N; Le Merrer M; Burglen L; Bertrand AM; Netchine I; Le Bouc Y
    Nat Genet; 2005 Sep; 37(9):1003-7. PubMed ID: 16086014
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation.
    Schönherr N; Meyer E; Binder G; Wollmann HA; Eggermann T
    J Pediatr Endocrinol Metab; 2007 Dec; 20(12):1329-31. PubMed ID: 18341093
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epigenetic regulation of growth: lessons from Silver-Russell syndrome.
    Eggermann T
    Endocr Dev; 2009; 14():10-9. PubMed ID: 19293571
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Epigenetics, genomic imprinting and developmental disorders].
    Le Bouc Y; Rossignol S; Azzi S; Brioude F; Cabrol S; Gicquel C; Netchine I
    Bull Acad Natl Med; 2010 Feb; 194(2):287-97; discussion 297-300. PubMed ID: 21166119
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues.
    Begemann M; Spengler S; Kanber D; Haake A; Baudis M; Leisten I; Binder G; Markus S; Rupprecht T; Segerer H; Fricke-Otto S; Mühlenberg R; Siebert R; Buiting K; Eggermann T
    Clin Genet; 2011 Jul; 80(1):83-8. PubMed ID: 20738330
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Silver-Russell syndrome and its genetic origins.
    Rossignol S
    J Endocrinol Invest; 2006; 29(1 Suppl):9-10. PubMed ID: 16615300
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.