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Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels

PLoS genetics, 2011-12, Vol.7 (12), p.e1002399

2011

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Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d

The Journal of neuroscience, 2016-03, Vol.36 (11), p.3254-3267

2016

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Mutations in a P-type ATPase gene cause axonal degeneration

PLoS genetics, 2012-08, Vol.8 (8), p.e1002853-e1002853

2012

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An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model

Neuron (Cambridge, Mass.), 2006-09, Vol.51 (6), p.715-726

2006

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Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes

Cell reports (Cambridge), 2017-03, Vol.18 (13), p.3178-3191

2017

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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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A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy

Biology (Basel, Switzerland), 2023-07, Vol.12 (7), p.953

2023

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An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations

Molecular and cellular neuroscience, 2011-02, Vol.46 (2), p.432-443

2011

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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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Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease

Disease models & mechanisms, 2013-05, Vol.6 (3), p.780-792

2013

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Auditory brainstem responses in 10 inbred strains of mice

Brain research, 2006-05, Vol.1091 (1), p.16-26

2006

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Enhancing the versatility of wireless biopotential acquisition for myoelectric prosthetic control

Journal of neural engineering, 2016-08, Vol.13 (4), p.046012-046012

2016

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Altered terminal Schwann cell morphology precedes denervation in SOD1 mice

Experimental neurology, 2016-01, Vol.275 (1), p.172-181

2016

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A spontaneous mutation in contactin 1 in the mouse

PloS one, 2011-12, Vol.6 (12), p.e29538-e29538

2011

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An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

Disease models & mechanisms, 2009-07, Vol.2 (7-8), p.359-373

2009

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Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice

Genetics (Austin), 2004-10, Vol.168 (2), p.953-959

2004

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Nerve terminal degeneration is independent of muscle fiber genotype in SOD1 mice

PloS one, 2010-03, Vol.5 (3), p.e9802-e9802

2010

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Lack of Neuropathy-Related Phenotypes in Hint1 Knockout Mice

Journal of neuropathology and experimental neurology, 2014-07, Vol.73 (7), p.693-701

2014

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Motor terminal degeneration unaffected by activity changes in SOD1G93A mice; a possible role for glycolysis

Neurobiology of disease, 2012-10, Vol.48 (1), p.132-140

2012

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Genetic analysis of Pycr1 and Pycr2 in mice

Genetics (Austin), 2021-05, Vol.218 (1)

2021

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Metabolite profile of a mouse model of Charcot-Marie-Tooth type 2D neuropathy: implications for disease mechanisms and interventions

Biology open, 2016-07, Vol.5 (7), p.908-920

2016

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Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron disease

Experimental neurology, 2016-04, Vol.278, p.116-126

2016

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A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations

Human molecular genetics, 2012-02, Vol.21 (4), p.730-750

2012

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Neuromuscular Disease Models and Analysis

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1438, p.349

2016

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Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit

Mammalian genome, 2006-09, Vol.17 (9), p.950-955

2006

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Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels

Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d

Mutations in a P-type ATPase gene cause axonal degeneration

An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model

Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes

The harlequin mouse mutation downregulates apoptosis-inducing factor

A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy

An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations

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

Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease

Auditory brainstem responses in 10 inbred strains of mice

Enhancing the versatility of wireless biopotential acquisition for myoelectric prosthetic control

Altered terminal Schwann cell morphology precedes denervation in SOD1 mice

A spontaneous mutation in contactin 1 in the mouse

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice

Nerve terminal degeneration is independent of muscle fiber genotype in SOD1 mice

Lack of Neuropathy-Related Phenotypes in Hint1 Knockout Mice

Motor terminal degeneration unaffected by activity changes in SOD1G93A mice; a possible role for glycolysis

Genetic analysis of Pycr1 and Pycr2 in mice

Metabolite profile of a mouse model of Charcot-Marie-Tooth type 2D neuropathy: implications for disease mechanisms and interventions

Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron disease

A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations

Neuromuscular Disease Models and Analysis

Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit

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