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.
Ischemia
,
Breast
,
Personalized medicine
,
Vitamin E
,
rs2300478
,
DNMT1
)
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
proepithelin protein, human
(compound)
Summary
General Info
Genetic Markers
Most Correlated Genes
CXCL8
CXCL1
ID4
HMCN1
ALDH1A3
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
DACOSTA_UV_RESPONSE_VIA_ERCC3_DN
BLALOCK_ALZHEIMERS_DISEASE_DN
DIAZ_CHRONIC_MEYLOGENOUS_LEUKEMIA_UP
KINSEY_TARGETS_OF_EWSR1_FLII_FUSION_UP
WEI_MYCN_TARGETS_WITH_E_BOX
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
Mammary fibroblast gene expression following culture in the presence of granulin protein
Explore Curated Studies Results
Literature
Most Relevant Literature
Primary Progressive Aphasia Associated With GRN Mutations: New Insights Into the Nonamyloid Logopeni…
Rescue of a lysosomal storage disorder caused by Grn loss of function with a brain penetrant progran…
The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementi…
The progranulin (GRN) Cys157LysfsX97 mutation is associated with nonfluent variant of primary progre…
Structural brain signature of FTLD driven by Granulin mutation.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for proepithelin protein, human
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ