The Phox2B homeobox gene is mutated in sporadic neuroblastomas (Q40498073)

21 September 2017

title

The Phox2B homeobox gene is mutated in sporadic neuroblastomas (English)

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21 September 2017

Rogier Versteeg

10

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Frank Baas

object named as

Frank Baas

7

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Huib N. Caron

8

object named as

Huib Caron

1 reference

21 September 2017

Vera van Limpt

1

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21 September 2017

Alexander Schramm

2

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21 September 2017

Arjan van Lakeman

3

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21 September 2017

Peter Sluis

4

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21 September 2017

Alvin Chan

5

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21 September 2017

Max van Noesel

6

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21 September 2017

Angelika Eggert

9

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21 September 2017

language of work or name

English

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publication date

1 December 2004

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21 September 2017

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21 September 2017

volume

23

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21 September 2017

issue

57

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21 September 2017

page(s)

9280-9288

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1208157

21 September 2017

exact match

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cites work

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

1 reference

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Automated detection of point mutations using fluorescent sequence trace subtraction

21 January 2018

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N-myc enhances the expression of a large set of genes functioning in ribosome biogenesis and protein synthesis

21 January 2018

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Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage

21 January 2018

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Molecular dissection of TrkA signal transduction pathways mediating differentiation in human neuroblastoma cells

21 January 2018

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Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons

21 January 2018

1 reference

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Generation of neuroendocrine chromaffin cells from sympathoadrenal progenitors: beyond the glucocorticoid hypothesis

21 January 2018

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A transcriptional repressor obtained by alternative translation of a trinucleotide repeat

21 January 2018

1 reference

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Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains

21 January 2018

1 reference

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Defects in sensory and autonomic ganglia and absence of locus coeruleus in mice deficient for the homeobox gene Phox2a

21 January 2018

1 reference

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Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma

21 January 2018

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Expression and function of TRK-B and BDNF in human neuroblastomas

21 January 2018

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The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

21 January 2018

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Molecular analysis of congenital central hypoventilation syndrome

21 January 2018

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Enhanced expression of the human gene N-myc consequent to amplification of DNA may contribute to malignant progression of neuroblastoma

21 January 2018

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Three chromosomal rearrangements in neuroblastoma cluster within a 300-kb region on 1p36.1.

21 January 2018

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The MEIS1 oncogene is highly expressed in neuroblastoma and amplified in cell line IMR32

21 January 2018

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Interaction of Mash1 and Phox2b in sympathetic neuron development

21 January 2018

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Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

21 January 2018

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Molecular cytogenetic analysis of 1;17 translocations in neuroblastoma.

21 January 2018

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Weak linkage at 4p16 to predisposition for human neuroblastoma

21 January 2018

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Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavourable prognostic markers in neuroblastoma

21 January 2018

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7 January 2021

Rearrangements and increased expression of cyclin D1 (CCND1) in neuroblastoma

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7 January 2021

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

1 reference

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7 January 2021

Paired-like homeodomain proteins, Phox2a and Phox2b, are responsible for noradrenergic cell-specific transcription of the dopamine beta-hydroxylase gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208157

7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/SJ.ONC.1208157

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1038620394

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1 reference