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.
Fatty acid metabolic process
,
Allergy to pollen
,
Kidney
,
Pharmacogenetics
,
FGF21
)
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
LOR gene
Summary
General Info
Curated Studies
Most Correlated Studies
Expression changes in organotypic epidermis upon depletion of TINCR ncRNA or STAU1 protein
ZNF750 Drives Terminal Epidermal Differentiation via Induction of Klf4
Skin biopsies from lesional/non-lesional skin of atopic dermatitis patients treated with dupilumab
Explore Curated Studies Results
Literature
Most Relevant Literature
Genome-wide investigation and expression profiling of LOR gene family in rapeseed under salinity and…
Mutation analysis for GJB2 and LOR genes in two patients with Vohwinkel syndrome].
No exonic mutations at GJB2, GJB3, GJB4, GJB6, ARS (Component B), and LOR genes responsible for a Ch…
Two novel mutations in the LOR gene in three families with loricrin keratoderma.
Identification of a novel mutation in the LOR gene in an Iraqi patient with loricrin keratoderma res…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Personalising Anti-TNF Therapy in Crohns Disease (PANTS)
Huntsman Biopsy Study
Pharmacogenomics Validation for Imatinib in Chronic Myeloid Leukemia
Iran- Premature Coronary Artery Disease
Response of Children With Atopic Dermatitis (Eczema) to Eucrisa
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ