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Mouse models of fragile X-related disorders

Disease models & mechanisms, 2023-02, Vol.16 (2)

2023

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Exosome-mediated transmission of hepatitis C virus between human hepatoma Huh7.5 cells

Proceedings of the National Academy of Sciences - PNAS, 2013-08, Vol.110 (32), p.13109-13113

2013

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Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C)

Nature genetics, 2006-11, Vol.38 (11), p.1348-1354

2006

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Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice

Neuropharmacology, 2017-04, Vol.116, p.71-81

2017

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Proteomic profiling of exosomes leads to the identification of novel biomarkers for prostate cancer

PloS one, 2013-12, Vol.8 (12), p.e82589-e82589

2013

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Comparing Approaches to Normalize, Quantify, and Characterize Urinary Extracellular Vesicles

Journal of the American Society of Nephrology, 2021-05, Vol.32 (5), p.1210-1226

2021

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Perturbation of dendritic protrusions in intellectual disability

Progress in Brain Research, 2012, Vol.197, p.153-168

2012

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Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome

Cell reports (Cambridge), 2013-03, Vol.3 (3), p.869-880

2013

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The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.723-735

2012

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Microsatellite repeat instability and neurological disease

BioEssays, 2009, Vol.31 (1), p.71-83

2009

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Small molecule 1a reduces FMRpolyG-mediated toxicity in in vitro and in vivo models for FMR1 premutation

Human molecular genetics, 2021-08, Vol.30 (17), p.1632-1648

2021

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Inducible expression of human C9ORF72 36× G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice

Disease models & mechanisms, 2021-02, Vol.14 (2)

2021

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Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

Neurobiology of disease, 2008-07, Vol.31 (1), p.127-132

2008

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Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS

Human molecular genetics, 2015-09, Vol.24 (17), p.4948-4957

2015

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Post-GWAS screening of candidate genes for refractive error in mutant zebrafish models

Scientific reports, 2023-02, Vol.13 (1), p.2017-2017, Article 2017

2023

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Allopregnanolone Improves Locomotor Activity and Arousal in the Aged CGG Knock-in Mouse Model of Fragile X-Associated Tremor/Ataxia Syndrome

Frontiers in neuroscience, 2021-12, Vol.15, p.752973-752973

2021

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Binding of NUFIP2 to Roquin promotes recognition and regulation of ICOS mRNA

Nature communications, 2018-01, Vol.9 (1), p.299-15, Article 299

2018

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Locomotor activity assay in zebrafish larvae: Influence of age, strain and ethanol

Neurotoxicology and teratology, 2012-07, Vol.34 (4), p.425-433

2012

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Fragile X syndrome, the search for a targeted treatment

Journal of biomedicine and translational research (Semarang), 2019-07, Vol.5 (1), p.12

2019

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Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS)

Brain research, 2009-02, Vol.1253, p.176-183

2009

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Glut1/SLC2A1 is crucial for the development of the blood-brain barrier in vivo

Annals of neurology, 2010-12, Vol.68 (6), p.835-844

2010

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Reduction of oxidative stress suppresses poly-GR-mediated toxicity in zebrafish embryos

Disease models & mechanisms, 2021-11, Vol.14 (11)

2021

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Oxazolone-Induced Enterocolitis in Zebrafish Depends on the Composition of the Intestinal Microbiota

Gastroenterology (New York, N.Y. 1943), 2009-11, Vol.137 (5), p.1757-1767.e1

2009

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AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome

Neurobiology of disease, 2011-06, Vol.42 (3), p.311-317

2011

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CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation

Hippocampus, 2012-12, Vol.22 (12), p.2260-2275

2012

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Mouse models of fragile X-related disorders

Exosome-mediated transmission of hepatitis C virus between human hepatoma Huh7.5 cells

Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C)

Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice

Proteomic profiling of exosomes leads to the identification of novel biomarkers for prostate cancer

Comparing Approaches to Normalize, Quantify, and Characterize Urinary Extracellular Vesicles

Perturbation of dendritic protrusions in intellectual disability

Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

Microsatellite repeat instability and neurological disease

Small molecule 1a reduces FMRpolyG-mediated toxicity in in vitro and in vivo models for FMR1 premutation

Inducible expression of human C9ORF72 36× G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice

Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS

Post-GWAS screening of candidate genes for refractive error in mutant zebrafish models

Allopregnanolone Improves Locomotor Activity and Arousal in the Aged CGG Knock-in Mouse Model of Fragile X-Associated Tremor/Ataxia Syndrome

Binding of NUFIP2 to Roquin promotes recognition and regulation of ICOS mRNA

Locomotor activity assay in zebrafish larvae: Influence of age, strain and ethanol

Fragile X syndrome, the search for a targeted treatment

Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS)

Glut1/SLC2A1 is crucial for the development of the blood-brain barrier in vivo

Reduction of oxidative stress suppresses poly-GR-mediated toxicity in zebrafish embryos

Oxazolone-Induced Enterocolitis in Zebrafish Depends on the Composition of the Intestinal Microbiota

AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome

CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation

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