126 related articles for article (PubMed ID: 15923081)
1. Oligogenic inheritance in neuroblastoma.
Longo L; Tonini GP; Ceccherini I; Perri P
Cancer Lett; 2005 Oct; 228(1-2):65-9. PubMed ID: 15923081
[TBL] [Abstract][Full Text] [Related]
2. Genetic predisposition to familial neuroblastoma: identification of two novel genomic regions at 2p and 12p.
Longo L; Panza E; Schena F; Seri M; Devoto M; Romeo G; Bini C; Pappalardo G; Tonini GP; Perri P
Hum Hered; 2007; 63(3-4):205-11. PubMed ID: 17317969
[TBL] [Abstract][Full Text] [Related]
3. Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.
de Pontual L; Trochet D; Bourdeaut F; Thomas S; Etchevers H; Chompret A; Minard V; Valteau D; Brugieres L; Munnich A; Delattre O; Lyonnet S; Janoueix-Lerosey I; Amiel J
Eur J Cancer; 2007 Nov; 43(16):2366-72. PubMed ID: 17765533
[TBL] [Abstract][Full Text] [Related]
4. Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.
Bourdeaut F; Trochet D; Janoueix-Lerosey I; Ribeiro A; Deville A; Coz C; Michiels JF; Lyonnet S; Amiel J; Delattre O
Cancer Lett; 2005 Oct; 228(1-2):51-8. PubMed ID: 15949893
[TBL] [Abstract][Full Text] [Related]
5. PHOX2B mutations and genetic predisposition to neuroblastoma.
Perri P; Bachetti T; Longo L; Matera I; Seri M; Tonini GP; Ceccherini I
Oncogene; 2005 Apr; 24(18):3050-3. PubMed ID: 15735672
[TBL] [Abstract][Full Text] [Related]
6. Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.
Trochet D; Bourdeaut F; Janoueix-Lerosey I; Deville A; de Pontual L; Schleiermacher G; Coze C; Philip N; Frébourg T; Munnich A; Lyonnet S; Delattre O; Amiel J
Am J Hum Genet; 2004 Apr; 74(4):761-4. PubMed ID: 15024693
[TBL] [Abstract][Full Text] [Related]
7. PHOX2A and PHOX2B genes are highly co-expressed in human neuroblastoma.
Longo L; Borghini S; Schena F; Parodi S; Albino D; Bachetti T; Da Prato L; Truini M; Gambini C; Tonini GP; Ceccherini I; Perri P
Int J Oncol; 2008 Nov; 33(5):985-91. PubMed ID: 18949361
[TBL] [Abstract][Full Text] [Related]
8. Familial predisposition to neuroblastoma does not map to chromosome band 1p36.
Maris JM; Kyemba SM; Rebbeck TR; White PS; Sulman EP; Jensen SJ; Allen C; Biegel JA; Yanofsky RA; Feldman GL; Brodeur GM
Cancer Res; 1996 Aug; 56(15):3421-5. PubMed ID: 8758905
[TBL] [Abstract][Full Text] [Related]
9. Rare occurrence of PHOX2b mutations in sporadic neuroblastomas.
Serra A; Häberle B; König IR; Kappler R; Suttorp M; Schackert HK; Roesner D; Fitze G
J Pediatr Hematol Oncol; 2008 Oct; 30(10):728-32. PubMed ID: 19011468
[TBL] [Abstract][Full Text] [Related]
10. Weak linkage at 4p16 to predisposition for human neuroblastoma.
Perri P; Longo L; Cusano R; McConville CM; Rees SA; Devoto M; Conte M; Ferrara GB; Seri M; Romeo G; Tonini GP
Oncogene; 2002 Nov; 21(54):8356-60. PubMed ID: 12447700
[TBL] [Abstract][Full Text] [Related]
11. Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma.
Janoueix-Lerosey I; Lequin D; Brugières L; Ribeiro A; de Pontual L; Combaret V; Raynal V; Puisieux A; Schleiermacher G; Pierron G; Valteau-Couanet D; Frebourg T; Michon J; Lyonnet S; Amiel J; Delattre O
Nature; 2008 Oct; 455(7215):967-70. PubMed ID: 18923523
[TBL] [Abstract][Full Text] [Related]
12. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.
Maris JM; Weiss MJ; Mosse Y; Hii G; Guo C; White PS; Hogarty MD; Mirensky T; Brodeur GM; Rebbeck TR; Urbanek M; Shusterman S
Cancer Res; 2002 Nov; 62(22):6651-8. PubMed ID: 12438263
[TBL] [Abstract][Full Text] [Related]
13. Familial neuroblastoma: a complex heritable disease.
Tonini GP; Longo L; Coco S; Perri P
Cancer Lett; 2003 Jul; 197(1-2):41-5. PubMed ID: 12880958
[TBL] [Abstract][Full Text] [Related]
14. Molecular pathogenesis of peripheral neuroblastic tumors.
Janoueix-Lerosey I; Schleiermacher G; Delattre O
Oncogene; 2010 Mar; 29(11):1566-79. PubMed ID: 20101209
[TBL] [Abstract][Full Text] [Related]
15. The oligogenic properties of Bardet-Biedl syndrome.
Katsanis N
Hum Mol Genet; 2004 Apr; 13 Spec No 1():R65-71. PubMed ID: 14976158
[TBL] [Abstract][Full Text] [Related]
16. Genetic heterogeneity and clonal evolution in neuroblastoma.
Mora J; Cheung NK; Gerald WL
Br J Cancer; 2001 Jul; 85(2):182-9. PubMed ID: 11461074
[TBL] [Abstract][Full Text] [Related]
17. Familial Wilms tumor.
Ruteshouser EC; Huff V
Am J Med Genet C Semin Med Genet; 2004 Aug; 129C(1):29-34. PubMed ID: 15264270
[TBL] [Abstract][Full Text] [Related]
18. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
[TBL] [Abstract][Full Text] [Related]
19. Germline gain-of-function mutations of ALK disrupt central nervous system development.
de Pontual L; Kettaneh D; Gordon CT; Oufadem M; Boddaert N; Lees M; Balu L; Lachassinne E; Petros A; Mollet J; Wilson LC; Munnich A; Brugière L; Delattre O; Vekemans M; Etchevers H; Lyonnet S; Janoueix-Lerosey I; Amiel J
Hum Mutat; 2011 Mar; 32(3):272-6. PubMed ID: 21972109
[TBL] [Abstract][Full Text] [Related]
20. Outcomes in multifocal neuroblastoma as part of the neurocristopathy syndrome.
Williams P; Wegner E; Ziegler DS
Pediatrics; 2014 Aug; 134(2):e611-6. PubMed ID: 25070313
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
