134 related articles for article (PubMed ID: 15900410)
1. Expression of p57KIP2 in infantile hemangioma.
Drut R; Drut RM
J Mol Histol; 2005 Mar; 36(3):195-7. PubMed ID: 15900410
[TBL] [Abstract][Full Text] [Related]
2. Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome.
John RM; Ainscough JF; Barton SC; Surani MA
Hum Mol Genet; 2001 Jul; 10(15):1601-9. PubMed ID: 11468278
[TBL] [Abstract][Full Text] [Related]
3. Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.
Gaston V; Le Bouc Y; Soupre V; Vazquez MP; Gicquel C
Horm Res; 2000; 54(1):1-5. PubMed ID: 11182628
[TBL] [Abstract][Full Text] [Related]
4. Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome.
Grandjean V; Smith J; Schofield PN; Ferguson-Smith AC
Proc Natl Acad Sci U S A; 2000 May; 97(10):5279-84. PubMed ID: 10779549
[TBL] [Abstract][Full Text] [Related]
5. p57(Kip2) knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome.
Duquesnes N; Callot C; Jeannot P; Daburon V; Nakayama KI; Manenti S; Davy A; Besson A
J Pathol; 2016 Jul; 239(3):250-61. PubMed ID: 27015986
[TBL] [Abstract][Full Text] [Related]
6. A Beckwith-Wiedemann-Associated
Stampone E; Bencivenga D; Barone C; Di Finizio M; Della Ragione F; Borriello A
Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299047
[TBL] [Abstract][Full Text] [Related]
7. CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms.
Romanelli V; Belinchón A; Benito-Sanz S; Martínez-Glez V; Gracia-Bouthelier R; Heath KE; Campos-Barros A; García-Miñaur S; Fernandez L; Meneses H; López-Siguero JP; Guillén-Navarro E; Gómez-Puertas P; Wesselink JJ; Mercado G; Esteban-Marfil V; Palomo R; Mena R; Sánchez A; Del Campo M; Lapunzina P
Am J Med Genet A; 2010 Jun; 152A(6):1390-7. PubMed ID: 20503313
[TBL] [Abstract][Full Text] [Related]
8. Extracutaneous infantile haemangioma is also Glut1 positive.
Drut RM; Drut R
J Clin Pathol; 2004 Nov; 57(11):1197-200. PubMed ID: 15509684
[TBL] [Abstract][Full Text] [Related]
9. ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.
Arima T; Kamikihara T; Hayashida T; Kato K; Inoue T; Shirayoshi Y; Oshimura M; Soejima H; Mukai T; Wake N
Nucleic Acids Res; 2005; 33(8):2650-60. PubMed ID: 15888726
[TBL] [Abstract][Full Text] [Related]
10. Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.
Lam WW; Hatada I; Ohishi S; Mukai T; Joyce JA; Cole TR; Donnai D; Reik W; Schofield PN; Maher ER
J Med Genet; 1999 Jul; 36(7):518-23. PubMed ID: 10424811
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia.
Armes JE; McGown I; Williams M; Broomfield A; Gough K; Lehane F; Lourie R
Pathology; 2012 Oct; 44(6):519-27. PubMed ID: 22772341
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Reduced expression of the cyclin-dependent kinase inhibitor gene p57KIP2 in Wilms' tumor.
Thompson JS; Reese KJ; DeBaun MR; Perlman EJ; Feinberg AP
Cancer Res; 1996 Dec; 56(24):5723-7. PubMed ID: 8971182
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization.
Brioude F; Netchine I; Praz F; Le Jule M; Calmel C; Lacombe D; Edery P; Catala M; Odent S; Isidor B; Lyonnet S; Sigaudy S; Leheup B; Audebert-Bellanger S; Burglen L; Giuliano F; Alessandri JL; Cormier-Daire V; Laffargue F; Blesson S; Coupier I; Lespinasse J; Blanchet P; Boute O; Baumann C; Polak M; Doray B; Verloes A; Viot G; Le Bouc Y; Rossignol S
Hum Mutat; 2015 Sep; 36(9):894-902. PubMed ID: 26077438
[TBL] [Abstract][Full Text] [Related]
20. Hepatic hemangioendotheliomas, placental chorioangiomas, and dysmorphic kidneys in Beckwith-Wiedemann syndrome.
Drut R; Drut RM; Toulouse JC
Pediatr Pathol; 1992; 12(2):197-203. PubMed ID: 1570237
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
