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Accession: PRJNA338783 ID: 338783

Expression profiling and occupancy after knockdown or over-expression of HFN1A or HNF4G in prostate cancer cells

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series
AccessionPRJNA338783; GEO: GSE85559
TypeUmbrella project
PublicationsShukla S et al., "Aberrant Activation of a Gastrointestinal Transcriptional Circuit in Prostate Cancer Mediates Castration Resistance.", Cancer Cell, 2017 Dec 11;32(6):792-806.e7
SubmissionRegistration date: 12-Aug-2016
MSKCC
RelevanceSuperseries
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments38
Publications
PubMed1
PMC1
Other datasets
BioSample38
GEO DataSets5
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes42
SRA Data Details
ParameterValue
Data volume, Gbases132
Data volume, Mbytes90748
Expression profiling and occupancy after knockdown or over-expression of HFN1A or HNF4G in prostate cancer cells encompasses the following 4 sub-projects:
Project TypeNumber of Projects
Epigenomics1
BioProject
accession
OrganismTitle
PRJNA338787Homo sapiensHNF4G, AR, FOXA1, H3K4me1, H3K27acetyl binding sites upon knockdown and overexpression of HNF4G in 22Rv1 and LNCaP prostate cancer cells respectively (MSKCC)
Transcriptome or Gene expression3
BioProject
accession
OrganismTitle
PRJNA338785Homo sapiensExpression profile of HNF1A knockdown and overexpression in 22RV1 and LNCaP cells respectively (MSKCC)
PRJNA338786Homo sapiensExpression profile of LNCaP/AR cells with or without HNF4G expression grown for long term in charcoal stripped-serum (CSS) media (MSKCC)
PRJNA342094Homo sapiensExpression profile of 22Rv1 cells upon DHT treatment (MSKCC)

Supplemental Content

Recent activity

  • Expression profiling and occupancy after knockdown or over-expression of HFN1A o...
    Expression profiling and occupancy after knockdown or over-expression of HFN1A or HNF4G in prostate cancer cells
    Expression profiling and occupancy after knockdown or over-expression of HFN1A or HNF4G in prostate cancer cells
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