153 related articles for article (PubMed ID: 16950814)
1. Methylation analysis of KvDMR1 in human oocytes.
Geuns E; Hilven P; Van Steirteghem A; Liebaers I; De Rycke M
J Med Genet; 2007 Feb; 44(2):144-7. PubMed ID: 16950814
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.
Chen CP; Su YN; Chen SU; Chang TY; Wu PC; Chern SR; Wu PS; Kuo YL; Wang W
Taiwan J Obstet Gynecol; 2014 Mar; 53(1):90-4. PubMed ID: 24767654
[TBL] [Abstract][Full Text] [Related]
3. Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.
Gomes MV; Huber J; Ferriani RA; Amaral Neto AM; Ramos ES
Mol Hum Reprod; 2009 Aug; 15(8):471-7. PubMed ID: 19494037
[TBL] [Abstract][Full Text] [Related]
4. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.
Rossignol S; Steunou V; Chalas C; Kerjean A; Rigolet M; Viegas-Pequignot E; Jouannet P; Le Bouc Y; Gicquel C
J Med Genet; 2006 Dec; 43(12):902-7. PubMed ID: 16825435
[TBL] [Abstract][Full Text] [Related]
5. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
[TBL] [Abstract][Full Text] [Related]
6. Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome.
Diaz-Meyer N; Day CD; Khatod K; Maher ER; Cooper W; Reik W; Junien C; Graham G; Algar E; Der Kaloustian VM; Higgins MJ
J Med Genet; 2003 Nov; 40(11):797-801. PubMed ID: 14627666
[TBL] [Abstract][Full Text] [Related]
7. Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human.
Tierling S; Souren NY; Gries J; Loporto C; Groth M; Lutsik P; Neitzel H; Utz-Billing I; Gillessen-Kaesbach G; Kentenich H; Griesinger G; Sperling K; Schwinger E; Walter J
J Med Genet; 2010 Jun; 47(6):371-6. PubMed ID: 19948534
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Beckwith-Weidemann syndrome with IC2 (KvDMR1) hypomethylation defect: a novel mutation.
Pandita A; Gupta S; Gupta G; Panghal A
BMJ Case Rep; 2018 Mar; 2018():. PubMed ID: 29602885
[TBL] [Abstract][Full Text] [Related]
11. The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation.
Senniappan S; Ismail D; Shipster C; Beesley C; Hussain K
J Pediatr Endocrinol Metab; 2015 Jan; 28(1-2):83-6. PubMed ID: 24468603
[TBL] [Abstract][Full Text] [Related]
12. Association of four imprinting disorders and ART.
Hattori H; Hiura H; Kitamura A; Miyauchi N; Kobayashi N; Takahashi S; Okae H; Kyono K; Kagami M; Ogata T; Arima T
Clin Epigenetics; 2019 Feb; 11(1):21. PubMed ID: 30732658
[TBL] [Abstract][Full Text] [Related]
13. Vitrification at the germinal vesicle stage does not affect the methylation profile of H19 and KCNQ1OT1 imprinting centers in human oocytes subsequently matured in vitro.
Al-Khtib M; Perret A; Khoueiry R; Ibala-Romdhane S; Blachère T; Greze C; Lornage J; Lefèvre A
Fertil Steril; 2011 May; 95(6):1955-60. PubMed ID: 21420679
[TBL] [Abstract][Full Text] [Related]
14. Aberrant DNA methylation of imprinted loci in human in vitro matured oocytes after long agonist stimulation.
Shi X; Chen S; Zheng H; Wang L; Wu Y
Eur J Obstet Gynecol Reprod Biol; 2013 Mar; 167(1):64-8. PubMed ID: 23164503
[TBL] [Abstract][Full Text] [Related]
15. Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos.
Geuns E; De Rycke M; Van Steirteghem A; Liebaers I
Hum Mol Genet; 2003 Nov; 12(22):2873-9. PubMed ID: 14500540
[TBL] [Abstract][Full Text] [Related]
16. Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11.
Beatty L; Weksberg R; Sadowski PD
Genomics; 2006 Jan; 87(1):46-56. PubMed ID: 16321503
[TBL] [Abstract][Full Text] [Related]
17. Dynamic CpG methylation of the KCNQ1OT1 gene during maturation of human oocytes.
Khoueiry R; Ibala-Rhomdane S; Méry L; Blachère T; Guérin JF; Lornage J; Lefèvre A
J Med Genet; 2008 Sep; 45(9):583-8. PubMed ID: 18762571
[TBL] [Abstract][Full Text] [Related]
18. DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith-Wiedemann syndrome.
Tierling S; Souren NY; Reither S; Zang KD; Meng-Hentschel J; Leitner D; Oehl-Jaschkowitz B; Walter J
Clin Genet; 2011 Jun; 79(6):546-53. PubMed ID: 20618351
[TBL] [Abstract][Full Text] [Related]
19. Abnormal methylation of KCNQ1OT1 and differential methylation of H19 imprinting control regions in human ICSI embryos.
Khoueiry R; Ibala-Romdhane S; Al-Khtib M; Blachère T; Lornage J; Guérin JF; Lefèvre A
Zygote; 2013 May; 21(2):129-38. PubMed ID: 22300968
[TBL] [Abstract][Full Text] [Related]
20. Expression of imprinted genes related to Beckwith-Wiedemann syndrome in human oocytes and preimplantation embryos.
Shen WJ; Xing FQ; Kong LH; Chen SL; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):265-7. PubMed ID: 15952111
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]