About: PHOX2B mutations and genetic predisposition to neuroblastoma

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About: PHOX2B mutations and genetic predisposition to neuroblastoma Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 2005 (uk) im Februar 2005 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q58328232-BEA85B57-764B-4B0B-A305-F26F0139B9AA
publication date	2005-02-28 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58328232-A673ED14-50AD-4C99-969A-5BF135701DAD
language of work or name	English
exact match	wds:Q58328232-72A4756D-7E69-417C-B905-6AA045BEA10A
exact match	https://scigraph.springernature.com/pub.10.1038/sj.onc.1208532
cites work	wds:Q58328232-0846A692-95FF-4FEE-B53C-A04957C6B473 wds:Q58328232-0F76FEC3-6AB0-489D-A3B3-A8A08AB4A1A4 wds:Q58328232-19E8ED0B-2570-4720-A5A0-1556E8A3E5DA wds:Q58328232-3B57C18E-8E6B-400A-9A1C-22E7DE6525FE wds:Q58328232-4DEE4E04-C22E-404C-9C2D-FA03F8E7E9E2 wds:Q58328232-9CA136F8-BF68-4F68-9EEC-556B39F64381 wds:Q58328232-B736DBBE-041A-48A8-9AEA-2A2619CFCAE2 wds:Q58328232-B9FD8ADD-E6B0-4CA3-992E-1DFA171BF4B7 wds:Q58328232-EC859228-574E-4C79-AA6F-5871A4427689
cites work	Linkage analysis in families with recurrent neuroblastoma Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. Congenital central hypoventilation syndrome and Hirschsprung's disease PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma Multiple hits during early embryonic development: digenic diseases and holoprosencephaly Weak linkage at 4p16 to predisposition for human neuroblastoma The Phox2B homeobox gene is mutated in sporadic neuroblastomas
author name string	wds:Q58328232-8B878D4C-DFC3-42E6-AFE0-73010DEDC0A7 wds:Q58328232-8FAB422C-9F45-4C72-9DA7-3E5D9A5E5A5D
author name string	Ivana Matera Tiziana Bachetti
rdfs:label	PHOX2B mutations and genetic predisposition to neuroblastoma (en) PHOX2B mutations and genetic predisposition to neuroblastoma (nl)
skos:prefLabel	PHOX2B mutations and genetic predisposition to neuroblastoma (en) PHOX2B mutations and genetic predisposition to neuroblastoma (nl)
name	PHOX2B mutations and genetic predisposition to neuroblastoma (en) PHOX2B mutations and genetic predisposition to neuroblastoma (nl)
author	wds:Q58328232-5830395A-7AA5-4721-B689-332C8E6EE88A wds:Q58328232-663A0C50-7E28-4B63-88B9-AB3DF404C1AE wds:Q58328232-846DFC35-0142-484F-88E8-3282375DAA27 wds:Q58328232-8BC8F5B1-51A3-4C44-931B-5C9B653782C4 wds:Q58328232-E52AC011-1AD4-47A9-8B5E-6408BCCAA47D
author	Marco Seri Isabella Ceccherini Luca Longo Patrizia Perri Gian Paolo Tonini
title	wds:Q58328232-E2C2767B-3D33-462F-A682-211BD04981E6
title	PHOX2B mutations and genetic predisposition to neuroblastoma (en)
page(s)	wds:Q58328232-E5EA20AC-F35B-4E78-B45A-C2503A007E03
page(s)	3050-3053
instance of	wds:Q58328232-C05363FB-F119-40CB-9939-9A628EACB88F
instance of	scholarly article
main subject	wds:Q58328232-D5BEF141-7D42-4731-834C-0512E45BC420
main subject	neuroblastoma
PubMed ID	wds:Q58328232-F19078A8-13F0-4BCE-A06D-663D56F51B2F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15735672
PubMed ID	15735672
published in	wds:Q58328232-F2E6FB34-496C-4AF0-8796-2CEB1659741D
published in	Oncogene
issue	wds:Q58328232-B4B187DC-61EC-4684-ADF2-7246F28178D9
volume	wds:Q58328232-FAE79778-CB6C-45D0-A059-EF910D36A583
issue	18
volume	24
DOI	wds:Q58328232-69AE8518-DF4B-477E-A77F-DEE6C8649B2F
DOI	http://dx.doi.org/10.1038/SJ.ONC.1208532
DOI	10.1038/SJ.ONC.1208532
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58328232
is cites work of	Comprehensive analysis of animal TALE homeobox genes: new conserved motifs and cases of accelerated evolution. The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma Identification of GALNT14 as a novel neuroblastoma predisposition gene Autonomic neurocristopathy-associated mutations in PHOX2B dysregulate Sox10 expression PHOX2B-mediated regulation of ALK expression: in vitro identification of a functional relationship between two genes involved in neuroblastoma The role of genetic and epigenetic alterations in neuroblastoma disease pathogenesis Genetic basis of Hirschsprung's disease. CD114: A New Member of the Neural Crest-Derived Cancer Stem Cell Marker Family Knockout mouse models of Hirschsprung's disease Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non-Polyalanine Repeat Expansion Mutations. Additional data support the role of rs11655237 C>T in the development of neuroblastoma The zebrafish as a model for studying neuroblastoma Identification of novel pathways and molecules able to down-regulate PHOX2B gene expression by in vitro drug screening approaches in neuroblastoma cells Retinoblastoma and Neuroblastoma Predisposition and Surveillance PHOX2A and PHOX2B are differentially regulated during retinoic acid-driven differentiation of SK-N-BE(2)C neuroblastoma cell line Pleiotropic effect of common variants in Hirschsprung disease and neuroblastoma Neuroblastoma in children: Update on clinicopathologic and genetic prognostic factors.
is cites work of	wds:Q39412574-C81C06A2-E844-4984-999F-7F64E97DB727 wds:Q38900723-83307ABC-CB5E-4B33-8CBE-E715A640F3FF wds:Q34986444-E2D314E2-B493-4C15-8147-505D927AD0E7 wds:Q38791934-AAE6529E-3D61-4442-A794-70DCB4FF39E4 wds:Q47936860-6248967B-F18F-49F4-AAEA-481220715695 wds:Q47766225-4233EF6D-1028-43EA-8AB3-EA32BC4ECCD4 wds:Q64259100-6F23C647-FB87-4C76-B2EA-4D951075F590 wds:Q41450595-8136011E-2171-4F22-9EB5-0FAD504A35D5 wds:Q35604788-82876B32-944B-4570-A68C-F130DC3EBC03 wds:Q38702196-92F5AB73-CC9A-427F-B589-D1D08C82DE8E wds:Q33721880-74DBD737-9169-437C-BCA4-40C270339809 wds:Q38542132-85916805-589A-4BCE-8CC8-14EA783E6568 wds:Q40024162-61011415-298A-490D-AF12-DD5600E91767 wds:Q28070309-85153096-6CCA-489A-939B-D3A04CA26B1C

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