Dysregulation of fragile X mental retardation protein and metabotropic glutamate receptor 5 in superior frontal cortex of individuals with autism: a postmortem brain …

SH Fatemi, TD Folsom - Molecular autism, 2011 - Springer
Background Fragile X syndrome is caused by loss of function of the fragile X mental
retardation 1 (FMR1) gene and shares multiple phenotypes with autism. We have previously …

Metabotropic glutamate receptor 5 upregulation in children with autism is associated with underexpression of both Fragile X mental retardation protein and GABAA …

SH Fatemi, TD Folsom, RE Kneeland… - The Anatomical …, 2011 - Wiley Online Library
Recent work has demonstrated the impact of dysfunction of the GABAergic signaling system
in brain and the resultant behavioral pathologies in subjects with autism. In animal models …

Persistent astrocyte activation in the fragile X mouse cerebellum

LKK Pacey, S Guan, S Tharmalingam… - Brain and …, 2015 - Wiley Online Library
Background Fragile XS yndrome, the most common single gene cause of autism, results
from loss of the RNA‐binding protein FMRP. Although FMRP is highly expressed in neurons …

Expression of fragile X mental retardation protein in neurons and glia of the developing and adult mouse brain

S Gholizadeh, SK Halder, DR Hampson - Brain research, 2015 - Elsevier
Fragile X syndrome is the most common inherited form of mental retardation and autism. It is
caused by a reduction or elimination of the expression of fragile X mental retardation protein …

Impairment of fragile X mental retardation protein-metabotropic glutamate receptor 5 signaling and its downstream cognates ras-related C3 botulinum toxin substrate 1 …

SH Fatemi, TD Folsom, RE Kneeland, MK Yousefi… - Molecular autism, 2013 - Springer
Background Candidate genes associated with idiopathic forms of autism overlap with other
disorders including fragile X syndrome. Our laboratory has previously shown reduction in …

Fragile X mental retardation protein: from autism to neurodegenerative disease

H Wang - Frontiers in Cellular Neuroscience, 2015 - frontiersin.org
Fragile X mental retardation protein (FMRP) is a RNA binding protein, the absence of which
due to silencing of the FMR1 gene causes fragile X syndrome, an X-linked …

Protein expression of targets of the FMRP regulon is altered in brains of subjects with schizophrenia and mood disorders

TD Folsom, PD Thuras, SH Fatemi - Schizophrenia research, 2015 - Elsevier
Fragile X mental retardation protein (FMRP) is an RNA binding protein with 842 target
mRNAs in mammalian brain. Silencing of the fragile X mental retardation 1 (FMR1) gene …

Delayed myelination in a mouse model of fragile X syndrome

LKK Pacey, ICY Xuan, S Guan… - Human molecular …, 2013 - academic.oup.com
Fragile X Syndrome is the most common inherited cause of autism. Fragile X mental
retardation protein (FMRP), which is absent in fragile X, is an mRNA binding protein that …

[HTML][HTML] Fragile X mental retardation protein levels are decreased in major psychiatric disorders

SH Fatemi, RE Kneeland, SB Liesch… - Schizophrenia …, 2010 - ncbi.nlm.nih.gov
In individuals with fragile X syndrome (FXS), there is a silencing of the fragile X mental
retardation (FMR1) gene, usually due to an expansion of a CGG repeat in the 5'untranslated …

Deletion of Fmr1 in parvalbumin-expressing neurons results in dysregulated translation and selective behavioral deficits associated with fragile X syndrome

M Kalinowska, MB van der Lei, M Kitiashvili… - Molecular Autism, 2022 - Springer
Abstract Background Fragile X syndrome (FXS), the most common genetic cause of autism
spectrum disorder and intellectual disability, is caused by the lack of fragile X mental …