NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE129934 Query DataSets for GSE129934
Status Public on Apr 18, 2019
Title Lnc-ITSN1-2 promotes rheumatoid arthritis fibroblast-like synoviocytesproliferation and inflammation while represses apoptosis via positive regulation of IL-23R/JAK/STAT pathway, and correlates with increased disease risk and activity
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary This study aimed to investigate the effect of lnc-ITSN1-2 on cell proliferation, apoptosis and inflammation as well as its possible regulatory network and molecular mechanisms in rheumatoid arthritis (RA).
 
Overall design Lnc-ITSN1-2 overexpression and ShRNA were transfected into RA fibroblast-like synoviocytes (FLS) followed by measurement of cell proliferation, apoptosis, inflammatory cytokines and mRNA sequencing. 
 
Contributor(s) Yue T,  Xiao L
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Apr 17, 2019
Last update date Apr 18, 2019
Contact name Tao Yue
E-mail(s) taoye77403772@163.com
Phone +86-021-62803133
Organization name ShangHai GuangHua Hospital of Integrated Traditional Chinese and Western Medicine
Department Department of Rheumatology
Street address 540 Xinhua Road
City Shanghai
ZIP/Postal code 200052
Country China
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (4)
GSM3728308 Lnc-ITSN1-2 overexpression
GSM3728309 overexpression control
GSM3728310 Lnc-ITSN1-2 shRNA
Relations
BioProject PRJNA533228
SRA SRP192824

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE129934_rawcounts_matrix.txt.gz 482.7 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap