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.
Personalized medicine
,
Lovastatin
,
rs3825942
,
BRAF
,
calcium channel activity
,
Breast
)
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
uaa stop codons
(compound)
Summary
General Info
Genetic Markers
Most Correlated Genes
No genes found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
No biogroups found
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
No studies found
Explore Curated Studies Results
Literature
Most Relevant Literature
Nuclear genetic codes with a different meaning of the UAG and the UAA codon.
Multiplex base editing to convert TAG into TAA codons in the human genome.
Preparation of an ochre suppressor tRNA recognizing exclusively UAA codon by using the molecular sur…
Structural basis of translation termination, rescue, and recycling in mammalian mitochondria.
The complete mitochondrial genome of a satin moth: Leucoma chrysoscela (Lepidoptera: Erebidae, Lyman…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Azithromycin Treatment for Readthrough of APC Gene Stop Codon Mutations in Familial Adenomatous Poly…
Erythromycin Treatment for Readthrough of APC Gene Stop Codon Mutations in Familial Adenomatous Poly…
Erythromycin Treatment for Readthrough of APC Gene Stop Codon Mutation in Familial Adenomatous Polyp…
Six Month Study of Gentamicin in Duchenne Muscular Dystrophy With Stop Codons
Rare CFTR Mutation Cell Collection Protocol (RARE)
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ