343 related articles for article (PubMed ID: 9020845)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.
Jiang S; Hemann MA; Lee MP; Feinberg AP
Genomics; 1998 Nov; 53(3):395-9. PubMed ID: 9799609
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. KVLQT1, the rhythm of imprinting.
Mannens M; Wilde A
Nat Genet; 1997 Feb; 15(2):113-5. PubMed ID: 9020829
[No Abstract] [Full Text] [Related]
14. Imprinting of mouse Kvlqt1 is developmentally regulated.
Gould TD; Pfeifer K
Hum Mol Genet; 1998 Mar; 7(3):483-7. PubMed ID: 9467008
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Beckwith-Wiedemann syndrome].
Yoshiura K; Niikawa N
Nihon Rinsho; 2000 Jul; 58(7):1511-4. PubMed ID: 10921333
[TBL] [Abstract][Full Text] [Related]
17. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.
O'Keefe D; Dao D; Zhao L; Sanderson R; Warburton D; Weiss L; Anyane-Yeboa K; Tycko B
Am J Hum Genet; 1997 Aug; 61(2):295-303. PubMed ID: 9311733
[TBL] [Abstract][Full Text] [Related]
18. A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues.
Hu RJ; Lee MP; Johnson LA; Feinberg AP
Hum Mol Genet; 1996 Nov; 5(11):1743-8. PubMed ID: 8923002
[TBL] [Abstract][Full Text] [Related]
19. Role of genomic imprinting in Wilms' tumour and overgrowth disorders.
Reeve AE
Med Pediatr Oncol; 1996 Nov; 27(5):470-5. PubMed ID: 8827076
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]