Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma (Q33909753)

29 July 2017

0 references

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

1 reference

29 July 2017

1 reference

10

0 references

Stanislas Lyonnet

11

Isabelle Janoueix-Lerosey

Stanislas Lyonnet

0 references

3

Isabelle Janoueix-Lerosey

0 references

Delphine Trochet

Delphine Trochet

1

0 references

Jeanne Amiel

Jeanne Amiel

13

0 references

Olivier Delattre

Olivier Delattre

12

0 references

Franck Bourdeaut

2

Franck Bourdeaut

1 reference

PubMed ID

15024693

29 July 2017

Gudrun Schleiermacher

6

Gudrun Schleiermacher

1 reference

29 July 2017

7

Carole Coze

1 reference

29 July 2017

4

Anne Deville

1 reference

29 July 2017

5

Loïc de Pontual

1 reference

29 July 2017

8

Nicole Philip

1 reference

29 July 2017

Thierry Frébourg

9

1 reference

PubMed ID

15024693

29 July 2017

language of work or name

English

0 references

publication date

11 March 2004

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

74

1 reference

29 July 2017

761-764

1 reference

29 July 2017

4

1 reference

IN SITU NEUROBLASTOMAS: A CONTRIBUTION TO THE NATURAL HISTORY OF NEURAL CREST TUMORS

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

The role of the MEIS homeobox genes in neuroblastoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Advances in the diagnosis and treatment of neuroblastoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

The Homeodomain Resource: 2003 update

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Phox2 genes - from patterning to connectivity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Molecular biology of neuroblastoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Genomic structure and functional characterization of NBPhox (PMX2B), a homeodomain protein specific to catecholaminergic cells that is involved in second messenger-mediated transcriptional activation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Familial occurrence of neuroblastoma, von Recklinghausen's neurofibromatosis, Hirschsprung's agangliosis and jaw-winking syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Developmental Genetics of Neuroblastoma12

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Congenital central hypoventilation syndrome associated with Hirschsprung's disease and neuroblastoma: case of multiple neurocristopathies.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Specification of the central noradrenergic phenotype by the homeobox gene Phox2b.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

Weak linkage at 4p16 to predisposition for human neuroblastoma

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181953

The Phox2b transcription factor coordinately regulates neuronal cell cycle exit and identity

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15024693

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial neuroblastoma. Report of a kindred with multiple disorders, including neuroblastomas in four siblings

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15024693

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular genetic analysis of familial neuroblastoma

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15024693

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/383253

1 reference

29 July 2017

1 reference

29 July 2017

1 reference

PubMed ID

15024693