These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 15516980)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives.
    Pattyn A; Morin X; Cremer H; Goridis C; Brunet JF
    Nature; 1999 May; 399(6734):366-70. PubMed ID: 10360575
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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 gene mutation in a patient with late-onset central hypoventilation.
    Trang H; Laudier B; Trochet D; Munnich A; Lyonnet S; Gaultier C; Amiel J
    Pediatr Pulmonol; 2004 Oct; 38(4):349-51. PubMed ID: 15334515
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Specification of the central noradrenergic phenotype by the homeobox gene Phox2b.
    Pattyn A; Goridis C; Brunet JF
    Mol Cell Neurosci; 2000 Mar; 15(3):235-43. PubMed ID: 10736201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cholinergic switch associated with morphological differentiation in neuroblastoma.
    Bourdeaut F; Janoueix-Lerosey I; Lucchesi C; Paris R; Ribeiro A; de Pontual L; Amiel J; Lyonnet S; Pierron G; Michon J; Peuchmaur M; Delattre O
    J Pathol; 2009 Dec; 219(4):463-72. PubMed ID: 19768740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence and functional consequence of PHOX2B mutations in neuroblastoma.
    Raabe EH; Laudenslager M; Winter C; Wasserman N; Cole K; LaQuaglia M; Maris DJ; Mosse YP; Maris JM
    Oncogene; 2008 Jan; 27(4):469-76. PubMed ID: 17637745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers.
    Jennings LJ; Yu M; Zhou L; Rand CM; Berry-Kravis EM; Weese-Mayer DE
    Diagn Mol Pathol; 2010 Dec; 19(4):224-31. PubMed ID: 21051998
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations.
    McConville C; Reid S; Baskcomb L; Douglas J; Rahman N
    Am J Med Genet A; 2006 Jun; 140(12):1297-301. PubMed ID: 16691592
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paired-like homeodomain proteins, Phox2a and Phox2b, are responsible for noradrenergic cell-specific transcription of the dopamine beta-hydroxylase gene.
    Yang C; Kim HS; Seo H; Kim CH; Brunet JF; Kim KS
    J Neurochem; 1998 Nov; 71(5):1813-26. PubMed ID: 9798905
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease.
    Lai D; Schroer B
    J Child Neurol; 2008 Mar; 23(3):341-3. PubMed ID: 18230845
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.