436 related articles for article (PubMed ID: 23502140)
1. 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]
2. 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]
3. 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]
4. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.
Netchine I; Rossignol S; Dufourg MN; Azzi S; Rousseau A; Perin L; Houang M; Steunou V; Esteva B; Thibaud N; Demay MC; Danton F; Petriczko E; Bertrand AM; Heinrichs C; Carel JC; Loeuille GA; Pinto G; Jacquemont ML; Gicquel C; Cabrol S; Le Bouc Y
J Clin Endocrinol Metab; 2007 Aug; 92(8):3148-54. PubMed ID: 17504900
[TBL] [Abstract][Full Text] [Related]
5. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
Soejima H; Higashimoto K
J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome.
Brioude F; Oliver-Petit I; Blaise A; Praz F; Rossignol S; Le Jule M; Thibaud N; Faussat AM; Tauber M; Le Bouc Y; Netchine I
J Med Genet; 2013 Dec; 50(12):823-30. PubMed ID: 24065356
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. (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]
14. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER
J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
20. Epigenetics in Silver-Russell syndrome.
Rossignol S; Netchine I; Le Bouc Y; Gicquel C
Best Pract Res Clin Endocrinol Metab; 2008 Jun; 22(3):403-14. PubMed ID: 18538282
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
