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Implementing Large-Scale ENU Mutagenesis Screens in North America

Genetica, 2004-09, Vol.122 (1), p.51-64

2004

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Overlaps, gaps, and complexities of mouse models of Developmental and Epileptic Encephalopathy

Neurobiology of disease, 2021-01, Vol.148, p.105220-105220, Article 105220

2021

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KICSTOR recruits GATOR1 to the lysosome and is necessary for nutrients to regulate mTORC1

Nature (London), 2017-03, Vol.543 (7645), p.438-442

2017

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Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures

The Journal of neuroscience, 2014-02, Vol.34 (7), p.2754-2763

2014

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The genomic landscape shaped by selection on transposable elements across 18 mouse strains

Genome Biology, 2012-06, Vol.13 (6), p.R45-R45, Article R45

2012

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PRAS: Predicting functional targets of RNA binding proteins based on CLIP-seq peaks

PLoS computational biology, 2019-08, Vol.15 (8), p.e1007227-e1007227

2019

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A new mode of corticothalamic transmission revealed in the Gria4 −/− model of absence epilepsy

Nature neuroscience, 2011-08, Vol.14 (9), p.1167-1173

2011

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Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats

Trends in genetics, 2009-08, Vol.25 (8), p.361-367

Frankel, Wayne N

2009

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Altered excitatory transmission onto hippocampal interneurons in the IQSEC2 mouse model of X-linked neurodevelopmental disease

Neurobiology of disease, 2020-04, Vol.137, p.104758-104758, Article 104758

2020

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CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function

PLoS genetics, 2012-11, Vol.8 (11), p.e1003067-e1003067

2012

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Dynamin 1 isoform roles in a mouse model of severe childhood epileptic encephalopathy

Neurobiology of disease, 2016-11, Vol.95, p.1-11

2016

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Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

PLoS genetics, 2023-10, Vol.19 (10), p.e1010952-e1010952

2023

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A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice

PLoS genetics, 2010-08, Vol.6 (8), p.e1001046

2010

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DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's disease

PloS one, 2015-05, Vol.10 (5), p.e0125897-e0125897

2015

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Arfgef1 haploinsufficiency in mice alters neuronal endosome composition and decreases membrane surface postsynaptic GABAA receptors

Neurobiology of disease, 2020-02, Vol.134, p.104632-104632, Article 104632

2020

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enzymatic cascade of Rab5 effectors regulates phosphoinositide turnover in the endocytic pathway

The Journal of cell biology, 2005-08, Vol.170 (4), p.607-618

2005

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Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus

Neurobiology of disease, 2011-03, Vol.41 (3), p.655-660

2011

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meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays

PLoS computational biology, 2018-10, Vol.14 (10), p.e1006506-e1006506

2018

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Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor

Frontiers in cellular neuroscience, 2023-05, Vol.17, p.1175895

2023

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Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy

PLoS genetics, 2014-07, Vol.10 (7), p.e1004454

2014

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The harlequin mouse mutation downregulates apoptosis-inducing factor

Nature (London), 2002-09, Vol.419 (6905), p.367-374

2002

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Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy

PLoS genetics, 2015-06, Vol.11 (6), p.e1005347

2015

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Sensory regulation of absence seizures in a mouse model of Gnb1 encephalopathy

iScience, 2022-11, Vol.25 (11), p.105488-105488, Article 105488

2022

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An early endothelial cell-specific requirement for Glut1 is revealed in Glut1 deficiency syndrome model mice

JCI insight, 2021-02, Vol.6 (3)

2021

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Gait analysis detects early changes in transgenic SOD1(G93A) mice

Muscle & nerve, 2005-07, Vol.32 (1), p.43-50

2005

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Implementing Large-Scale ENU Mutagenesis Screens in North America

Overlaps, gaps, and complexities of mouse models of Developmental and Epileptic Encephalopathy

KICSTOR recruits GATOR1 to the lysosome and is necessary for nutrients to regulate mTORC1

Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures

The genomic landscape shaped by selection on transposable elements across 18 mouse strains

PRAS: Predicting functional targets of RNA binding proteins based on CLIP-seq peaks

A new mode of corticothalamic transmission revealed in the Gria4 −/− model of absence epilepsy

Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats

Altered excitatory transmission onto hippocampal interneurons in the IQSEC2 mouse model of X-linked neurodevelopmental disease

CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function

Dynamin 1 isoform roles in a mouse model of severe childhood epileptic encephalopathy

Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice

DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's disease

Arfgef1 haploinsufficiency in mice alters neuronal endosome composition and decreases membrane surface postsynaptic GABAA receptors

enzymatic cascade of Rab5 effectors regulates phosphoinositide turnover in the endocytic pathway

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus

meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays

Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor

Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy

The harlequin mouse mutation downregulates apoptosis-inducing factor

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy

Sensory regulation of absence seizures in a mouse model of Gnb1 encephalopathy

An early endothelial cell-specific requirement for Glut1 is revealed in Glut1 deficiency syndrome model mice

Gait analysis detects early changes in transgenic SOD1(G93A) mice

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