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.
Heart
,
Autoimmunity
,
Fluoxetine
,
rs6983267
,
TGFB1
,
calcium channel activity
)
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
fragile x mental retardation syndrome
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Neuroblastoma SH-SY5Y cells differentiated with retinoic acid and brain-derived neurotrophic factor
Myoblast C2C12 cells depleted of FXR1
FMRP associated mRNAs in HEK293 cells
Explore Curated Studies Results
Literature
Most Relevant Literature
Neocortical vasculature abnormalities in the Fragile X mental retardation syndrome.
Preparation and validation of the first WHO international genetic reference panel for Fragile X synd…
Molecular analysis of Fragile X syndrome.
Clinical utility gene card for: fragile X mental retardation syndrome, fragile X-associated tremor/a…
Fragile X syndrome: lifespan developmental implications for those without as well as with intellectu…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
A Trial of Metformin in Individuals With Fragile X Syndrome (Met)
A Trial of Metformin in Individuals With Fragile X Syndrome
A Study of RO4917523 in Patients With Fragile X Syndrome
Examining Physiology and Brain Function in People With the Fragile X Premutation
A Study of RO4917523 in Pediatric Patients With Fragile X Syndrome
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ