345 related articles for article (PubMed ID: 8841187)
1. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
Hatada I; Ohashi H; Fukushima Y; Kaneko Y; Inoue M; Komoto Y; Okada A; Ohishi S; Nabetani A; Morisaki H; Nakayama M; Niikawa N; Mukai T
Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
[TBL] [Abstract][Full Text] [Related]
2. Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse.
Hatada I; Mukai T
Nat Genet; 1995 Oct; 11(2):204-6. PubMed ID: 7550351
[TBL] [Abstract][Full Text] [Related]
3. p57K1P2 is expressed in Wilms' tumor with LOH of 11p15.5.
Overall ML; Spencer J; Bakker M; Dziadek M; Smith PJ
Genes Chromosomes Cancer; 1996 Sep; 17(1):56-9. PubMed ID: 8889507
[TBL] [Abstract][Full Text] [Related]
4. Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome.
Bhuiyan ZA; Yatsuki H; Sasaguri T; Joh K; Soejima H; Zhu X; Hatada I; Morisaki H; Morisaki T; Mukai T
Hum Genet; 1999 Mar; 104(3):205-10. PubMed ID: 10323243
[TBL] [Abstract][Full Text] [Related]
5. Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.
Hatada I; Inazawa J; Abe T; Nakayama M; Kaneko Y; Jinno Y; Niikawa N; Ohashi H; Fukushima Y; Iida K; Yutani C; Takahashi S; Chiba Y; Ohishi S; Mukai T
Hum Mol Genet; 1996 Jun; 5(6):783-8. PubMed ID: 8776593
[TBL] [Abstract][Full Text] [Related]
6. Selective maternal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5.
Kondo M; Matsuoka S; Uchida K; Osada H; Nagatake M; Takagi K; Harper JW; Takahashi T; Elledge SJ; Takahashi T
Oncogene; 1996 Mar; 12(6):1365-8. PubMed ID: 8649840
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
Enklaar T; Zabel BU; Prawitt D
Expert Rev Mol Med; 2006 Jul; 8(17):1-19. PubMed ID: 16842655
[TBL] [Abstract][Full Text] [Related]
10. Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour.
Taniguchi T; Okamoto K; Reeve AE
Oncogene; 1997 Mar; 14(10):1201-6. PubMed ID: 9121769
[TBL] [Abstract][Full Text] [Related]
11. CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance.
Algar EM; Deeble GJ; Smith PJ
J Med Genet; 1999 Jul; 36(7):524-31. PubMed ID: 10424812
[TBL] [Abstract][Full Text] [Related]
12. Cyclin-dependent kinase inhibitor p57KIP2 in soft tissue sarcomas and Wilms'tumors.
Orlow I; Iavarone A; Crider-Miller SJ; Bonilla F; Latres E; Lee MH; Gerald WL; Massagué J; Weissman BE; Cordón-Cardó C
Cancer Res; 1996 Mar; 56(6):1219-21. PubMed ID: 8640801
[TBL] [Abstract][Full Text] [Related]
13. Overgrowth syndromes and genomic imprinting: from mouse to man.
Li M; Squire JA; Weksberg R
Clin Genet; 1998 Mar; 53(3):165-70. PubMed ID: 9630066
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. New p57KIP2 mutations in Beckwith-Wiedemann syndrome.
Hatada I; Nabetani A; Morisaki H; Xin Z; Ohishi S; Tonoki H; Niikawa N; Inoue M; Komoto Y; Okada A; Steichen E; Ohashi H; Fukushima Y; Nakayama M; Mukai T
Hum Genet; 1997 Oct; 100(5-6):681-3. PubMed ID: 9341892
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Analysis of CDKN1C in Beckwith Wiedemann syndrome.
Algar E; Brickell S; Deeble G; Amor D; Smith P
Hum Mutat; 2000; 15(6):497-508. PubMed ID: 10862080
[TBL] [Abstract][Full Text] [Related]
18. Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation.
Abadie C; Bernard F; Netchine I; Sanlaville D; Roque A; Rossignol S; Coupier I
Eur J Med Genet; 2010; 53(6):400-3. PubMed ID: 20826236
[TBL] [Abstract][Full Text] [Related]
19. p57KIP2 targeted disruption and Beckwith-Wiedemann syndrome: is the inhibitor just a contributor?
Swanger WJ; Roberts JM
Bioessays; 1997 Oct; 19(10):839-42. PubMed ID: 9363677
[TBL] [Abstract][Full Text] [Related]
20. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
Cooper WN; Luharia A; Evans GA; Raza H; Haire AC; Grundy R; Bowdin SC; Riccio A; Sebastio G; Bliek J; Schofield PN; Reik W; Macdonald F; Maher ER
Eur J Hum Genet; 2005 Sep; 13(9):1025-32. PubMed ID: 15999116
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
