[PDF] Top 20 Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome
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Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome
... transgenic mouse was obtained by pronuclear injection of a construct containing the human FMR1 cDNA with 29 CGG repeats under control of a SV40/T7 ...(KO) mouse model of FXS that lacks FMRP, some of the ... See full document
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FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome
... novel mouse monoclonal antibodies against polyGlycine; 8FM and 9FM (for epitopes and specificity see Additional file 1: Figure S1), and performed immunostaining in CNS as well as in non-CNS organs of FXTAS patient ... See full document
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Neuropathology of RAN translation proteins in fragile X-associated tremor/ataxia syndrome
... repeat associated non- AUG (RAN) translation [3, ...and mouse models of the disease, expression of the 5′ UTR of FMR1 leads to RAN translation of a series of homo- polymeric proteins, with different ... See full document
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The multiple molecular facets of fragile X-associated tremor/ataxia syndrome
... In addition to hnRNP A2/B1, proteomic analyses performed by Jin and collaborators [61] also showed that purine-rich binding protein α (Purα) binds ro- bustly to RNA containing expanded CGG repeats. Purα is a ... See full document
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Genomic studies in fragile X premutation carriers
... FMR1: Fragile X mental retardation 1 gene; ADAM8: A disintegrin and metalloproteinase 8 gene; ADHD: Attention deficit hyperactivity disorder; ADI-R: Autism Diagnostic Interview-Revised; ADOS: Autism ... See full document
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Visual motion processing deficits in infants with the fragile X premutation
... be premutation carriers of FXS, a condition more commonly found in the general population, affecting approximately 1 in 130–250 women and 1 in 250–810 males ...the premutation range typically have normal ... See full document
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Altered Redox Mitochondrial Biology in the Neurodegenerative Disorder Fragile X-Tremor/Ataxia Syndrome: Use of Antioxidants in Precision Medicine
... Primary dermal fibroblasts from premutation carriers were analyzed for reactive oxygen species production by using electron paramagnetic spectros- copy (EPR). Direct detection of some free radicals (for example, ... See full document
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Fragile X Syndrome
... lems associated with the gene that re- sults in FXS as found in older individu- als in the family who have neurologic deficits such as tremor/ataxia or early ovarian failure in ... See full document
5
Targeted treatments for fragile X syndrome
... Abstract Fragile X syndrome (FXS) is the most common identifiable genetic cause of intellectual disability and autistic spectrum disorders (ASD), with up to 50% of males and some females with FXS ... See full document
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Fragile X syndrome: a pilot proton magnetic resonance spectroscopy study in premutation carriers
... that premutation carriers of FraX were unaffected, there is increasing evidence that they have a variety of cognitive deficits, differences in brain anatomy and that some develop Fragile X- ... See full document
9
Aging in fragile X syndrome
... the fragile X- associated tremor ataxia syndrome (FXTAS) (Hagerman et ...the premutation intensified the need for more detailed aging studies in ... See full document
7
Health Supervision for Children With Fragile X Syndrome
... tion tremor develops after 50 years of age and is typically followed by ...ataxia. Associated features include a periph- eral neuropathy; parkinsonian mani- festations; autonomic dysfunction such as ... See full document
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Intranuclear inclusions in a fragile X mosaic male
... neurological syndrome affecting older males and females over 50 years of age and presenting features such as action tremor and ataxia, cognitive decline, neuropathy, autonomic dysfunction and ... See full document
9
Public Health Literature Review of Fragile X Syndrome
... the premutation phenotype in older adults, specifically the impact of fragile X – associated tremor-ataxia syndrome and fragile X – associated primary ... See full document
21
Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X
... Fragile X syndrome, diagnosed by Fragile X Mental Retardation 1 (FMR1) DNA testing, is the most common single-gene cause of inherited intellectual ...to fragile X ... See full document
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X-inactivation in the clinical phenotype of fragile X premutation carrier sisters
... each associated with different lengths of the CGG tract. Fragile X syndrome (FXS), the most common inherited cause of intellectual disability in boys, results from a CGG expansion of ... See full document
7
Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)
... Fragile X-associated primary ovarian insufficiency (FXPOI) is among the family of disorders caused by the expansion of a CGG repeat sequence in the 5' untranslated region of the X-linked gene ... See full document
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Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome
... one fragile X syndrome (FXS), one amyotrophic lateral sclerosis (ALS), one Parkinson’s disease (PD), and three control brains were obtained from the FXTAS brain repository at the University of ... See full document
26
Advances in the Treatment of Fragile X Syndrome
... (fragile X syndrome) and distinct difficul- ties, including primary ovarian insufficiency, neuropathy and the fragile X-associated tremor/ataxia syndrome, in ... See full document
15
Instability of (CTG)n•(CAG)n trinucleotide repeats and DNA synthesis
... Murine models of several trinucleotide expansion diseases including Huntington disease, myotonic dystrophy type 1, Fragile X syndrome, and Friedrich ’ s ataxia have been gen- erated by ... See full document
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