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Series GSE33133 Query DataSets for GSE33133
Status Public on Oct 01, 2012
Title Analysis of the early transcriptome signature of infection of primary endothelial cells by Nipah virus vs. Nipah virus deleted for the expression of non-structural C protein
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Nipah virus (NiV) is a highly pathogenic, negative strand RNA paramyxovirus that has recently emerged from flying foxes to cause serious human disease. To study the poorly-understood role of nonstructural NiV proteins in NiV pathogenesis, we generated recombinant viruse lacking the expression of accesory NiV C protein (NiV∆C).
 
Overall design To analyse the molecular basis of NiV∆C attenuation we have used the gene microarray approach to study early changes of gene expression in infected primary human endothelial cells, which is a major cellular target of human NiV infection.
We performed microarray gene expression profiling of NiV infected HUVEC cell (2 replicates), of uninfected HUVEC cell (2 replicates) and of NiV∆C infected HUVEC cell (2 replicates).
 
Contributor(s) MATHIEU C, GUILLAUME V, LEGRAS-LACHUER C, LACHUER J, HORVAT B
Citation(s) 22837207, 22393386
Mathieu Cyrille, Legras-Lachuer Catherine and Horvat Branka (2011). Transcriptome Signature of Nipah Virus Infected Endothelial Cells, Advances in the Etiology, Pathogenesis and Pathology of Vasculitis, Luis M. Amezcua-Guerra (Ed.), ISBN: 978-953-307-651-5, InTech; DOI: 10.5772/21512.
Submission date Oct 21, 2011
Last update date Oct 28, 2014
Contact name HORVAT Branka
E-mail(s) branka.horvat@inserm.fr
Phone 0437282392
Fax 0437282391
Organization name INSERM
Department human virology
Street address 21 avenue Tony Garnier
City LYON
ZIP/Postal code 69007
Country France
 
Platforms (1)
GPL2895 GE Healthcare/Amersham Biosciences CodeLink Human Whole Genome Bioarray
Samples (6)
GSM813064 MOCK_1
GSM813065 NiV_1
GSM813066 MOCK_2
Relations
BioProject PRJNA149403

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Supplementary data files not provided
Processed data included within Sample table

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