171 related articles for article (PubMed ID: 37932266)
1. Preneoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma.
Pilet J; Hirsch TZ; Gupta B; Roehrig A; Morcrette G; Pire A; Letouzé E; Fresneau B; Taque S; Brugières L; Branchereau S; Chardot C; Aerts I; Sarnacki S; Fabre M; Guettier C; Rebouissou S; Zucman-Rossi J
Nat Commun; 2023 Nov; 14(1):7122. PubMed ID: 37932266
[TBL] [Abstract][Full Text] [Related]
2. 11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood.
Fiala EM; Ortiz MV; Kennedy JA; Glodzik D; Fleischut MH; Duffy KA; Hathaway ER; Heaton T; Gerstle JT; Steinherz P; Shukla N; McNeer N; Tkachuk K; Bouvier N; Cadoo K; Carlo MI; Latham A; Dubard Gault M; Joseph V; Kemel Y; Kentsis A; Stadler Z; La Quaglia M; Papaemmanuil E; Friedman D; Ganguly A; Kung A; Offit K; Kalish JM; Walsh MF
Cancer; 2020 Jul; 126(13):3114-3121. PubMed ID: 32320050
[TBL] [Abstract][Full Text] [Related]
3. Concurrent Hepatoblastoma and Wilms Tumor Leading to Diagnosis of Beckwith-Wiedemann Syndrome.
Wolfe DM; Webster Carrion A; Masukhani MM; Oberg JA; Pavisic J; El-Ali A; Gupta M; Weng K; Glasser CL
J Pediatr Hematol Oncol; 2023 May; 45(4):e525-e529. PubMed ID: 36730589
[TBL] [Abstract][Full Text] [Related]
4. Improved molecular detection of mosaicism in Beckwith-Wiedemann Syndrome.
Baker SW; Duffy KA; Richards-Yutz J; Deardorff MA; Kalish JM; Ganguly A
J Med Genet; 2021 Mar; 58(3):178-184. PubMed ID: 32430359
[TBL] [Abstract][Full Text] [Related]
5. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
[TBL] [Abstract][Full Text] [Related]
6. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
Jurkiewicz D; Kugaudo M; Skórka A; Śmigiel R; Smyk M; Ciara E; Chrzanowska K; Krajewska-Walasek M
Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Calcifying nested stromal-epithelial tumor (CNSET) of the liver in Beckwith-Wiedemann syndrome.
Khoshnam N; Robinson H; Clay MR; Schaffer LR; Gillespie SE; Shehata BM
Eur J Med Genet; 2017 Feb; 60(2):136-139. PubMed ID: 27965001
[TBL] [Abstract][Full Text] [Related]
9. SNP arrays in Beckwith-Wiedemann syndrome: an improved diagnostic strategy.
Keren B; Chantot-Bastaraud S; Brioude F; Mach C; Fonteneau E; Azzi S; Depienne C; Brice A; Netchine I; Le Bouc Y; Siffroi JP; Rossignol S
Eur J Med Genet; 2013 Oct; 56(10):546-50. PubMed ID: 23892181
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetic mosaicism at the insulin locus in liver associated with childhood hepatoblastoma.
Simms LA; Reeve AE; Smith PJ
Genes Chromosomes Cancer; 1995 May; 13(1):72-3. PubMed ID: 7541647
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
Catchpoole D; Lam WW; Valler D; Temple IK; Joyce JA; Reik W; Schofield PN; Maher ER
J Med Genet; 1997 May; 34(5):353-9. PubMed ID: 9152830
[TBL] [Abstract][Full Text] [Related]
14. Diffuse infantile hepatic hemangiomas in a patient with Beckwith-Wiedemann syndrome: A new association?
Macchiaiolo M; Markowich AH; Diociaiuti A; Gonfiantini MV; Buonuomo PS; Rana I; Monti L; El Hachem M; Bartuli A
Am J Med Genet A; 2020 Aug; 182(8):1972-1976. PubMed ID: 32573107
[TBL] [Abstract][Full Text] [Related]
15. Mosaic paternal genome-wide uniparental isodisomy with down syndrome.
Darcy D; Atwal PS; Angell C; Gadi I; Wallerstein R
Am J Med Genet A; 2015 Oct; 167A(10):2463-9. PubMed ID: 26219535
[TBL] [Abstract][Full Text] [Related]
16. Beckwith-Wiedemann syndrome-associated hepatoblastoma: wnt signal activation occurs later in tumorigenesis in patients with 11p15.5 uniparental disomy.
Fukuzawa R; Hata J; Hayashi Y; Ikeda H; Reeve AE
Pediatr Dev Pathol; 2003; 6(4):299-306. PubMed ID: 14692643
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour.
Gogiel M; Begemann M; Spengler S; Soellner L; Göretzlehner U; Eggermann T; Strobl-Wildemann G
Eur J Hum Genet; 2013 Jul; 21(7):788-91. PubMed ID: 23188046
[TBL] [Abstract][Full Text] [Related]
19. Genomic profiles of a hepatoblastoma from a patient with Beckwith-Wiedemann syndrome with uniparental disomy on chromosome 11p15 and germline mutation of APC and PALB2.
Kim SY; Jung SH; Kim MS; Han MR; Park HC; Jung ES; Lee SH; Lee SH; Chung YJ
Oncotarget; 2017 Nov; 8(54):91950-91957. PubMed ID: 29190888
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
