206 related articles for article (PubMed ID: 15949893)
1. 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]
2. 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]
3. Analysis of neuroblastoma tumour progression; loss of PHOX2B on 4p13 and 17q gain are early events in neuroblastoma tumourigenesis.
Krona C; Carén H; Sjöberg RM; Sandstedt B; Laureys G; Kogner P; Martinsson T
Int J Oncol; 2008 Mar; 32(3):575-83. PubMed ID: 18292934
[TBL] [Abstract][Full Text] [Related]
4. The Phox2B homeobox gene is mutated in sporadic neuroblastomas.
van Limpt V; Schramm A; van Lakeman A; Sluis P; Chan A; van Noesel M; Baas F; Caron H; Eggert A; Versteeg R
Oncogene; 2004 Dec; 23(57):9280-8. PubMed ID: 15516980
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Pediatric disorders with autonomic dysfunction: what role for PHOX2B?
Gaultier C; Trang H; Dauger S; Gallego J
Pediatr Res; 2005 Jul; 58(1):1-6. PubMed ID: 15901893
[TBL] [Abstract][Full Text] [Related]
7. Phox2B mutations and the Delta-Notch pathway in neuroblastoma.
van Limpt V; Chan A; Schramm A; Eggert A; Versteeg R
Cancer Lett; 2005 Oct; 228(1-2):59-63. PubMed ID: 16084642
[TBL] [Abstract][Full Text] [Related]
8. Concomitant existence of total bowel aganglionosis and congenital central hypoventilation syndrome in a neonate with PHOX2B gene mutation.
Ou-Yang MC; Yang SN; Hsu YM; Ou-Yang MH; Haung HC; Lee SY; Hsieh WS; Su YN; Liu CA
J Pediatr Surg; 2007 Feb; 42(2):e9-11. PubMed ID: 17270534
[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. Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE.
Hung CC; Su YN; Tsao PN; Chen PC; Lin SJ; Lin CH; Mu SC; Liu CA; Chang YC; Lin WL; Hsieh WS; Hsu SM
Electrophoresis; 2007 Mar; 28(6):894-9. PubMed ID: 17300129
[TBL] [Abstract][Full Text] [Related]
11. PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome.
Trochet D; de Pontual L; Straus C; Gozal D; Trang H; Landrieu P; Munnich A; Lyonnet S; Gaultier C; Amiel J
Am J Respir Crit Care Med; 2008 Apr; 177(8):906-11. PubMed ID: 18079495
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non-Polyalanine Repeat Expansion Mutations.
Heide S; Masliah-Planchon J; Isidor B; Guimier A; Bodet D; Coze C; Deville A; Thebault E; Pasquier CJ; Cassagnau E; Pierron G; Clément N; Schleiermacher G; Amiel J; Delattre O; Peuchmaur M; Bourdeaut F
Pediatr Blood Cancer; 2016 Jan; 63(1):71-7. PubMed ID: 26375764
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.
Cross SH; Morgan JE; Pattyn A; West K; McKie L; Hart A; Thaung C; Brunet JF; Jackson IJ
Hum Mol Genet; 2004 Jul; 13(14):1433-9. PubMed ID: 15150159
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A novel PHOX2B gene mutation in an extremely low birth weight infant with congenital central hypoventilation syndrome and variant Hirschsprung's disease.
Miura Y; Watanabe T; Uchida T; Nawa T; Endo N; Fukuzawa T; Ohkubo R; Takeyama J; Sasaki A; Hayasaka K
Eur J Med Genet; 2019 Sep; 62(9):103541. PubMed ID: 30227298
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Congenital central hypoventilation syndrome and Hirschsprung's disease in an extremely preterm infant.
Bajaj R; Smith J; Trochet D; Pitkin J; Ouvrier R; Graf N; Sillence D; Kluckow M
Pediatrics; 2005 Jun; 115(6):e737-8. PubMed ID: 15930201
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
