365 related articles for article (PubMed ID: 11063728)
1. Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
Engemann S; Strödicke M; Paulsen M; Franck O; Reinhardt R; Lane N; Reik W; Walter J
Hum Mol Genet; 2000 Nov; 9(18):2691-706. PubMed ID: 11063728
[TBL] [Abstract][Full Text] [Related]
2. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J
Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
Cerrato F; Sparago A; Di Matteo I; Zou X; Dean W; Sasaki H; Smith P; Genesio R; Bruggemann M; Reik W; Riccio A
Hum Mol Genet; 2005 Feb; 14(4):503-11. PubMed ID: 15640248
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
Lee MP; DeBaun M; Randhawa G; Reichard BA; Elledge SJ; Feinberg AP
Am J Hum Genet; 1997 Aug; 61(2):304-9. PubMed ID: 9311734
[TBL] [Abstract][Full Text] [Related]
7. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.
Mitsuya K; Meguro M; Lee MP; Katoh M; Schulz TC; Kugoh H; Yoshida MA; Niikawa N; Feinberg AP; Oshimura M
Hum Mol Genet; 1999 Jul; 8(7):1209-17. PubMed ID: 10369866
[TBL] [Abstract][Full Text] [Related]
8. Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.
Yatsuki H; Watanabe H; Hattori M; Joh K; Soejima H; Komoda H; Xin Z; Zhu X; Higashimoto K; Nishimura M; Kuratomi S; Sasaki H; Sakaki Y; Mukai T
DNA Res; 2000 Jun; 7(3):195-206. PubMed ID: 10907850
[TBL] [Abstract][Full Text] [Related]
9. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
Weksberg R; Nishikawa J; Caluseriu O; Fei YL; Shuman C; Wei C; Steele L; Cameron J; Smith A; Ambus I; Li M; Ray PN; Sadowski P; Squire J
Hum Mol Genet; 2001 Dec; 10(26):2989-3000. PubMed ID: 11751681
[TBL] [Abstract][Full Text] [Related]
10. Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.
Higashimoto K; Soejima H; Saito T; Okumura K; Mukai T
Cytogenet Genome Res; 2006; 113(1-4):306-12. PubMed ID: 16575194
[TBL] [Abstract][Full Text] [Related]
11. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
Lee MP; Hu RJ; Johnson LA; Feinberg AP
Nat Genet; 1997 Feb; 15(2):181-5. PubMed ID: 9020845
[TBL] [Abstract][Full Text] [Related]
12. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome.
Smilinich NJ; Day CD; Fitzpatrick GV; Caldwell GM; Lossie AC; Cooper PR; Smallwood AC; Joyce JA; Schofield PN; Reik W; Nicholls RD; Weksberg R; Driscoll DJ; Maher ER; Shows TB; Higgins MJ
Proc Natl Acad Sci U S A; 1999 Jul; 96(14):8064-9. PubMed ID: 10393948
[TBL] [Abstract][Full Text] [Related]
13. Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse.
Paulsen M; El-Maarri O; Engemann S; Strödicke M; Franck O; Davies K; Reinhardt R; Reik W; Walter J
Hum Mol Genet; 2000 Jul; 9(12):1829-41. PubMed ID: 10915772
[TBL] [Abstract][Full Text] [Related]
14. An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C.
Algar E; Dagar V; Sebaj M; Pachter N
PLoS One; 2011; 6(12):e29034. PubMed ID: 22205991
[TBL] [Abstract][Full Text] [Related]
15. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.
Lee MP; DeBaun MR; Mitsuya K; Galonek HL; Brandenburg S; Oshimura M; Feinberg AP
Proc Natl Acad Sci U S A; 1999 Apr; 96(9):5203-8. PubMed ID: 10220444
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus.
Valente FM; Sparago A; Freschi A; Hill-Harfe K; Maas SM; Frints SGM; Alders M; Pignata L; Franzese M; Angelini C; Carli D; Mussa A; Gazzin A; Gabbarini F; Acurzio B; Ferrero GB; Bliek J; Williams CA; Riccio A; Cerrato F
Genet Med; 2019 Aug; 21(8):1808-1820. PubMed ID: 30635621
[TBL] [Abstract][Full Text] [Related]
18. Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.
Li M; Squire J; Shuman C; Fei YL; Atkin J; Pauli R; Smith A; Nishikawa J; Chitayat D; Weksberg R
Genomics; 2001 Jun; 74(3):370-6. PubMed ID: 11414765
[TBL] [Abstract][Full Text] [Related]
19. [Beckwith-Wiedemann syndrome].
Yoshiura K; Niikawa N
Nihon Rinsho; 2000 Jul; 58(7):1511-4. PubMed ID: 10921333
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
