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Segregation of seizure traits in C57 black mouse substrains using the repeated-flurothyl model

PloS one, 2014-03, Vol.9 (3), p.e90506

2014

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Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus

G3 : genes - genomes - genetics, 2017-08, Vol.7 (8), p.2545-2558

2017

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Motor learning changes the axon initial segment of the spinal motoneuron

The Journal of physiology, 2024-05, Vol.602 (9), p.2107-2126

2024

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Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

Nature genetics, 2002-02, Vol.30 (2), p.185-189

2002

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A mutation in stratifin is responsible for the repeated epilation ( Er ) phenotype in mice

Nature genetics, 2005-11, Vol.37 (11), p.1210-1212

2005

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Prdm16 is required for normal palatogenesis in mice

Human molecular genetics, 2010-03, Vol.19 (5), p.774-789

2010

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THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia

Nature genetics, 2008-04, Vol.40 (4), p.403-410

2008

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Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission

The Journal of neuroscience, 2016-07, Vol.36 (28), p.7485-7496

2016

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Fog2 is required for normal diaphragm and lung development in mice and humans

PLoS genetics, 2005-07, Vol.1 (1), p.58-65

2005

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Divergence and inheritance of neocortical heterotopia in inbred and genetically-engineered mice

Neuroscience letters, 2017-01, Vol.638, p.175-180

2017

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Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: A dissociation of hippocampal Fos from seizure activity

Epilepsy research, 2015-01, Vol.109, p.183-196

2015

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Genetic heterogeneity of skin microvasculature

Developmental biology, 2010-04, Vol.340 (2), p.480-489

2010

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Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesis

Experimental neurology, 2009-01, Vol.215 (1), p.60-68

2009

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Angiogenesis QTL on Mouse Chromosome 8 Colocalizes with Differential β-Defensin Expression

Journal of biomolecular techniques, 2015-07, Vol.26 (2), p.45-53

2015

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Analysis of flurothyl-induced myoclonus in inbred strains of mice

Epilepsy research, 2009-12, Vol.87 (2), p.130-136

2009

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A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice

Human molecular genetics, 2005-03, Vol.14 (5), p.667-677

2005

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Genetic mapping and ENU mutagenesis

Genetica, 2004-09, Vol.122 (1), p.65-69

2004

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Scraggly, a new hair loss mutation on mouse chromosome 19

Mammalian genome, 1999-09, Vol.10 (9), p.864-869

1999

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Putative assignment of ESTs to the genetic map by use of the SSLP database

Mammalian genome, 1998-12, Vol.9 (12), p.1072-1074

1998

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Fog2 is required for normal diaphragm and lung development in mice and humans

PLoS genetics, 2005-07, Vol.1 (1), p.58-65

2005

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2001: a mouse genome odyssey

Genome biology, 2002, Vol.3 (2), p.REPORTS4005-reports4005.4

2002

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Three novel mutations of the ornithine aminotransferase ( OAT) gene in gyrate atrophy

Genomics (San Diego, Calif.), 1992-10, Vol.14 (2), p.553-554

1992

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Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3

Mammalian genome, 1992, Vol.3 (1), p.17-22

1992

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Genetic mapping and ENU mutagenesis

Mutagenesis of the Mouse Genome, p.65-69

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Factors influencing the latency of simple reaction time

Frontiers in human neuroscience, 2015-03, Vol.9, p.131-131

2015

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Segregation of seizure traits in C57 black mouse substrains using the repeated-flurothyl model

Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus

Motor learning changes the axon initial segment of the spinal motoneuron

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

A mutation in stratifin is responsible for the repeated epilation ( Er ) phenotype in mice

Prdm16 is required for normal palatogenesis in mice

THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia

Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission

Fog2 is required for normal diaphragm and lung development in mice and humans

Divergence and inheritance of neocortical heterotopia in inbred and genetically-engineered mice

Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: A dissociation of hippocampal Fos from seizure activity

Genetic heterogeneity of skin microvasculature

Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesis

Angiogenesis QTL on Mouse Chromosome 8 Colocalizes with Differential β-Defensin Expression

Analysis of flurothyl-induced myoclonus in inbred strains of mice

A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice

Genetic mapping and ENU mutagenesis

Scraggly, a new hair loss mutation on mouse chromosome 19

Putative assignment of ESTs to the genetic map by use of the SSLP database

Fog2 is required for normal diaphragm and lung development in mice and humans

2001: a mouse genome odyssey

Three novel mutations of the ornithine aminotransferase ( OAT) gene in gyrate atrophy

Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3

Genetic mapping and ENU mutagenesis

Factors influencing the latency of simple reaction time

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