270 related articles for article (PubMed ID: 31144574)
21. 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]
22. Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome.
Chang S; Hur SK; Naveh NSS; Thorvaldsen JL; French DL; Gagne AL; Jobaliya CD; Anguera MC; Bartolomei MS; Kalish JM
Epigenetics; 2021 Dec; 16(12):1295-1305. PubMed ID: 33300436
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies.
Hiura H; Okae H; Miyauchi N; Sato F; Sato A; Van De Pette M; John RM; Kagami M; Nakai K; Soejima H; Ogata T; Arima T
Hum Reprod; 2012 Aug; 27(8):2541-8. PubMed ID: 22674207
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome.
Sobel Naveh NS; Traxler EM; Duffy KA; Kalish JM
Hepatol Commun; 2022 Aug; 6(8):2132-2146. PubMed ID: 35507738
[TBL] [Abstract][Full Text] [Related]
28. The Upregulation of Genomic Imprinted DLK1-Dio3 miRNAs in Murine Lupus Is Associated with Global DNA Hypomethylation.
Dai R; Lu R; Ahmed SA
PLoS One; 2016; 11(4):e0153509. PubMed ID: 27070142
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
Weksberg R; Smith AC; Squire J; Sadowski P
Hum Mol Genet; 2003 Apr; 12 Spec No 1():R61-8. PubMed ID: 12668598
[TBL] [Abstract][Full Text] [Related]
31. Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood.
Alders M; Maas SM; Kadouch DJ; van der Lip K; Bliek J; van der Horst CM; Mannens MM
Eur J Med Genet; 2014; 57(6):293-7. PubMed ID: 24704790
[TBL] [Abstract][Full Text] [Related]
32. Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome.
Mussa A; Molinatto C; Cerrato F; Palumbo O; Carella M; Baldassarre G; Carli D; Peris C; Riccio A; Ferrero GB
Pediatrics; 2017 Jul; 140(1):. PubMed ID: 28634246
[TBL] [Abstract][Full Text] [Related]
33. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
Bachmann N; Crazzolara R; Bohne F; Kotzot D; Maurer K; Enklaar T; Prawitt D; Bergmann C
Pediatr Blood Cancer; 2017 Mar; 64(3):. PubMed ID: 27650505
[TBL] [Abstract][Full Text] [Related]
34. A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).
Janchevska A; Tasic V; Laban N; Polenakovic M; Gucev Z; Bachmann N; Bergmann C
Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2018 Dec; 39(2-3):131-135. PubMed ID: 30864369
[TBL] [Abstract][Full Text] [Related]
35. Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome.
Diaz-Meyer N; Yang Y; Sait SN; Maher ER; Higgins MJ
J Med Genet; 2005 Aug; 42(8):648-55. PubMed ID: 16061564
[TBL] [Abstract][Full Text] [Related]
36. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome.
Horike S; Mitsuya K; Meguro M; Kotobuki N; Kashiwagi A; Notsu T; Schulz TC; Shirayoshi Y; Oshimura M
Hum Mol Genet; 2000 Sep; 9(14):2075-83. PubMed ID: 10958646
[TBL] [Abstract][Full Text] [Related]
37. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.
Caspary T; Cleary MA; Perlman EJ; Zhang P; Elledge SJ; Tilghman SM
Genes Dev; 1999 Dec; 13(23):3115-24. PubMed ID: 10601037
[TBL] [Abstract][Full Text] [Related]
38. Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.
Weksberg R; Shuman C; Caluseriu O; Smith AC; Fei YL; Nishikawa J; Stockley TL; Best L; Chitayat D; Olney A; Ives E; Schneider A; Bestor TH; Li M; Sadowski P; Squire J
Hum Mol Genet; 2002 May; 11(11):1317-25. PubMed ID: 12019213
[TBL] [Abstract][Full Text] [Related]
39. Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome.
Reik W; Maher ER
Trends Genet; 1997 Aug; 13(8):330-4. PubMed ID: 9260520
[TBL] [Abstract][Full Text] [Related]
40. Molecular biology of Beckwith-Wiedemann syndrome.
Weksberg R; Squire JA
Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]