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Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()

Induction of differentiation is a therapeutic strategy in neuroblastoma, a common pediatric cancer of the sympathetic nervous system. The homeobox protein HOXC9 is a key regulator of neuroblastoma differentiation. To gain a molecular understanding of the function of HOXC9 in promoting differentiatio...

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Detalles Bibliográficos
Autores principales: Wang, Xiangwei, Yang, Liqun, Choi, Jeong-Hyeon, Kitamura, Eiko, Chang, Chang-Sheng, Ding, Jane, Lee, Eun J., Cui, Hongjuan, Ding, Han-Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084856/
https://www.ncbi.nlm.nih.gov/pubmed/25013753
http://dx.doi.org/10.1016/j.gdata.2014.04.002
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author Wang, Xiangwei
Yang, Liqun
Choi, Jeong-Hyeon
Kitamura, Eiko
Chang, Chang-Sheng
Ding, Jane
Lee, Eun J.
Cui, Hongjuan
Ding, Han-Fei
author_facet Wang, Xiangwei
Yang, Liqun
Choi, Jeong-Hyeon
Kitamura, Eiko
Chang, Chang-Sheng
Ding, Jane
Lee, Eun J.
Cui, Hongjuan
Ding, Han-Fei
author_sort Wang, Xiangwei
collection PubMed
description Induction of differentiation is a therapeutic strategy in neuroblastoma, a common pediatric cancer of the sympathetic nervous system. The homeobox protein HOXC9 is a key regulator of neuroblastoma differentiation. To gain a molecular understanding of the function of HOXC9 in promoting differentiation of neuroblastoma cells, we conducted a genome-wide analysis of the HOXC9-induced differentiation program by microarray gene expression profiling and chromatin immunoprecipitation in combination with massively parallel sequencing (ChIP-seq). Here we describe in detail the experimental system, methods, and quality control for the generation of the microarray and ChIP-seq data associated with our recent publication [1].
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spelling pubmed-40848562015-10-19 Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells() Wang, Xiangwei Yang, Liqun Choi, Jeong-Hyeon Kitamura, Eiko Chang, Chang-Sheng Ding, Jane Lee, Eun J. Cui, Hongjuan Ding, Han-Fei Genom Data Data in Brief Induction of differentiation is a therapeutic strategy in neuroblastoma, a common pediatric cancer of the sympathetic nervous system. The homeobox protein HOXC9 is a key regulator of neuroblastoma differentiation. To gain a molecular understanding of the function of HOXC9 in promoting differentiation of neuroblastoma cells, we conducted a genome-wide analysis of the HOXC9-induced differentiation program by microarray gene expression profiling and chromatin immunoprecipitation in combination with massively parallel sequencing (ChIP-seq). Here we describe in detail the experimental system, methods, and quality control for the generation of the microarray and ChIP-seq data associated with our recent publication [1]. Elsevier 2014-04-18 /pmc/articles/PMC4084856/ /pubmed/25013753 http://dx.doi.org/10.1016/j.gdata.2014.04.002 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Data in Brief
Wang, Xiangwei
Yang, Liqun
Choi, Jeong-Hyeon
Kitamura, Eiko
Chang, Chang-Sheng
Ding, Jane
Lee, Eun J.
Cui, Hongjuan
Ding, Han-Fei
Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()
title Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()
title_full Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()
title_fullStr Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()
title_full_unstemmed Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()
title_short Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells()
title_sort genome-wide analysis of hoxc9-induced neuronal differentiation of neuroblastoma cells()
topic Data in Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084856/
https://www.ncbi.nlm.nih.gov/pubmed/25013753
http://dx.doi.org/10.1016/j.gdata.2014.04.002
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