BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
Lung cancer
,
Lung
,
Holistic medicine
,
Rosiglitazone
,
rs2230926
,
LEP
,
Angiogenesis
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
HDAC2;jsessionid=056E890387A2938369DEA124BD9B3F45
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Endometrium
Testes
Fallopian tube
Conjunctiva
Myometrium
Explore Body Atlas Results
Disease Atlas
Most Correlated Diseases
Loading...
Explore Disease Atlas Results
Pharmaco Atlas
Most Correlated Compounds
Loading...
Explore Pharmaco Atlas Results
Knockdown Atlas
Most Correlated Gene Perturbations
Loading...
Explore Knockdown Atlas Results
Curated Studies
Most Correlated Studies
No studies found
Explore Curated Studies Results
Literature
Most Relevant Literature
HDAC2 counteracts vascular calcification by activating autophagy in chronic kidney disease.
Differential expression of Hdac2 in male and female mice of differing social status.
Pb inhibited C2C12 myoblast differentiation by regulating HDAC2.
Discovery of novel and potent dual-targeting AXL/HDAC2 inhibitors for colorectal cancer treatment vi…
Novel dual-targeting inhibitors of NSD2 and HDAC2 for the treatment of liver cancer: structure-based…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for HDAC2;jsessionid=056E890387A2938369DEA124BD9B3F45
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ