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Similar articles for PubMed (Select 16084642)

1.

Phox2B mutations and the Delta-Notch pathway in neuroblastoma.

van Limpt V, Chan A, Schramm A, Eggert A, Versteeg R.

Cancer Lett. 2005 Oct 18;228(1-2):59-63. Review.

PMID:
16084642
2.

The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma.

Revet I, Huizenga G, Chan A, Koster J, Volckmann R, van Sluis P, Øra I, Versteeg R, Geerts D.

Exp Cell Res. 2008 Feb 15;314(4):707-19. doi: 10.1016/j.yexcr.2007.12.008. Epub 2008 Jan 16.

PMID:
18201699
3.

High delta-like 1 expression in a subset of neuroblastoma cell lines corresponds to a differentiated chromaffin cell type.

Van Limpt VA, Chan AJ, Van Sluis PG, Caron HN, Van Noesel CJ, Versteeg R.

Int J Cancer. 2003 May 20;105(1):61-9.

PMID:
12672031
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 9;23(57):9280-8.

PMID:
15516980
5.

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 17;27(4):469-76. Epub 2007 Jul 16.

PMID:
17637745
6.

Neuroblastoma phox2b variants stimulate proliferation and dedifferentiation of immature sympathetic neurons.

Reiff T, Tsarovina K, Majdazari A, Schmidt M, del Pino I, Rohrer H.

J Neurosci. 2010 Jan 20;30(3):905-15. doi: 10.1523/JNEUROSCI.5368-09.2010.

7.

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 18;228(1-2):51-8. Review.

PMID:
15949893
8.

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. Epub 2007 Aug 31.

PMID:
17765533
9.

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.

PMID:
18949361
10.

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. Epub 2004 Mar 11.

11.

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 15;140(12):1297-301.

PMID:
16691592
12.

PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome.

Trochet D, O'Brien LM, Gozal D, Trang H, Nordenskjöld A, Laudier B, Svensson PJ, Uhrig S, Cole T, Niemann S, Munnich A, Gaultier C, Lyonnet S, Amiel J.

Am J Hum Genet. 2005 Mar;76(3):421-6. Epub 2005 Jan 18. Erratum in: Am J Hum Genet. 2005 Apr;76(4):715. Niemann, Stephan [added].

13.

Identification of Phox2b-regulated genes by expression profiling of cranial motoneuron precursors.

Pla P, Hirsch MR, Le Crom S, Reiprich S, Harley VR, Goridis C.

Neural Dev. 2008 Jun 19;3:14. doi: 10.1186/1749-8104-3-14.

14.

Mutations that disrupt PHOXB interaction with the neuronal calcium sensor HPCAL1 impede cellular differentiation in neuroblastoma.

Wang W, Zhong Q, Teng L, Bhatnagar N, Sharma B, Zhang X, Luther W 2nd, Haynes LP, Burgoyne RD, Vidal M, Volchenboum S, Hill DE, George RE.

Oncogene. 2014 Jun 19;33(25):3316-24. doi: 10.1038/onc.2013.290. Epub 2013 Jul 22.

15.

The role of Phox2B in chromaffin cell development.

Huber K, Karch N, Ernsberger U, Goridis C, Unsicker K.

Dev Biol. 2005 Mar 15;279(2):501-8.

16.

PHOX2B mutations and genetic predisposition to neuroblastoma.

Perri P, Bachetti T, Longo L, Matera I, Seri M, Tonini GP, Ceccherini I.

Oncogene. 2005 Apr 21;24(18):3050-3.

PMID:
15735672
17.

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. doi: 10.1097/MPH.0b013e3181772141.

PMID:
19011468
18.

Distinct neuroblastoma-associated alterations of PHOX2B impair sympathetic neuronal differentiation in zebrafish models.

Pei D, Luther W, Wang W, Paw BH, Stewart RA, George RE.

PLoS Genet. 2013 Jun;9(6):e1003533. doi: 10.1371/journal.pgen.1003533. Epub 2013 Jun 6.

19.

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.

PMID:
18292934
20.

Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis.

Pattyn A, Morin X, Cremer H, Goridis C, Brunet JF.

Development. 1997 Oct;124(20):4065-75.

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