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SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes

Neuron (Cambridge, Mass.), 2006-12, Vol.52 (5), p.767-774

2006

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Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits

PloS one, 2019-01, Vol.14 (1), p.e0211073

2019

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A Temporal Multifaceted Adaptation Approach to the Experiences of Employed Mothers

Marriage & family review, 2012-12, Vol.48 (8), p.732-768

Edwards, Michele Rees

2012

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An Examination of Employed Mothers' Work-Family Narratives and Perceptions of Husbands' Support

Marriage & family review, 2008-01, Vol.42 (3), p.59-89

Edwards, Michele Rees

2008

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The Role of Husbands' Supportive Communication Practices in the Lives of Employed Mothers

Marriage & family review, 2006-01, Vol.40 (4), p.23-46

Edwards, Michele Rees

2006

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Influence of Social Support on Gay Men Living with HIV

Marriage & family review, 2011-07, Vol.47 (5), p.265-288

Edwards, Michele Rees

2011

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Influence of Social Support on Gay Men Living with

Marriage & family review, 2011-07, Vol.47 (5), p.265

Edwards, Michele Rees

2011

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Molecular characterization of a neuronal low-voltage-activated T-type calcium channel

Nature (London), 1998-02, Vol.391 (6670), p.896-900

1998

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Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells

The Journal of neuroscience, 2001-08, Vol.21 (16), p.6095-6104

2001

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The ducky(2J) mutation in Cacna2d2 results in reduced spontaneous Purkinje cell activity and altered gene expression

The Journal of neuroscience, 2006-11, Vol.26 (48), p.12576-12586

2006

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The Ducky Mutation in Cacna2d2 Results in Altered Purkinje Cell Morphology and Is Associated with the Expression of a Truncated α2δ-2 Protein with Abnormal Function

The Journal of biological chemistry, 2002-03, Vol.277 (10), p.7684-7693

2002

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The ducky mutation in Cacna2d2 results in altered Purkinje cell morphology and is associated with the expression of a truncated alpha 2 delta-2 protein with abnormal function

The Journal of biological chemistry, 2002-03, Vol.277 (10), p.7684-7693

2002

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Genomic organization of the mouse and human α2δ2 voltage-dependent calcium channel subunit genes

Mammalian genome, 2000-12, Vol.11 (12), p.1142-1144

2000

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Genetic Mapping of a Major Susceptibility Locus for Juvenile Myoclonic Epilepsy on Chromosome 15q

Human molecular genetics, 1997-08, Vol.6 (8), p.1329-1334

1997

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Linkage and association analysis of CACNG3 in childhood absence epilepsy

European journal of human genetics : EJHG, 2007-04, Vol.15 (4), p.463-472

2007

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Genomic organization of the mouse and human [alpha]2[delta]2 voltage-dependent calcium channel subunit genes

Mammalian genome, 2000-12, Vol.11 (12), p.1142

2000

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Evaluation of CACNA1H in European patients with childhood absence epilepsy

Epilepsy research, 2006-05, Vol.69 (2), p.177-181

2006

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The ducky 2J Mutation in Cacna2d2 Results in Reduced Spontaneous Purkinje Cell Activity and Altered Gene Expression

The Journal of neuroscience, 2006-11, Vol.26 (48), p.12576-12586

2006

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The ducky super(2J) Mutation in Cacna2d2 Results in Reduced Spontaneous Purkinje Cell Activity and Altered Gene Expression

The Journal of neuroscience, 2006-11, Vol.26 (48), p.12576-12586

2006

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The ducky2J Mutation in Cacna2d2 Results in Reduced Spontaneous Purkinje Cell Activity and Altered Gene Expression

The Journal of neuroscience, 2006-11, Vol.26 (48), p.12576-12586

2006

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Mouse Models of Spike‐Wave Epilepsy

Epilepsia (Copenhagen), 1999-01, Vol.40 (s3), p.17-22

1999

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Linkage and association analysis of CACNG3 in childhood absence epilepsy

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.659-660

2008

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Linkage and association analysis of CACNG3 in childhood absence epilepsy

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.659

2008

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Erratum: Linkage and association analysis of CACNG3 in childhood absence epilepsy

European journal of human genetics : EJHG, 2008-04, Vol.16 (5), p.659-660

2008

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Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus ( EJM2) on chromosome 15q13–14

Epilepsy research, 2002-04, Vol.49 (2), p.157-172

2002

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SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes

Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits

A Temporal Multifaceted Adaptation Approach to the Experiences of Employed Mothers

An Examination of Employed Mothers' Work-Family Narratives and Perceptions of Husbands' Support

The Role of Husbands' Supportive Communication Practices in the Lives of Employed Mothers

Influence of Social Support on Gay Men Living with HIV

Influence of Social Support on Gay Men Living with

Molecular characterization of a neuronal low-voltage-activated T-type calcium channel

Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells

The ducky(2J) mutation in Cacna2d2 results in reduced spontaneous Purkinje cell activity and altered gene expression

The Ducky Mutation in Cacna2d2 Results in Altered Purkinje Cell Morphology and Is Associated with the Expression of a Truncated α2δ-2 Protein with Abnormal Function

The ducky mutation in Cacna2d2 results in altered Purkinje cell morphology and is associated with the expression of a truncated alpha 2 delta-2 protein with abnormal function

Genomic organization of the mouse and human α2δ2 voltage-dependent calcium channel subunit genes

Genetic Mapping of a Major Susceptibility Locus for Juvenile Myoclonic Epilepsy on Chromosome 15q

Linkage and association analysis of CACNG3 in childhood absence epilepsy

Genomic organization of the mouse and human [alpha]2[delta]2 voltage-dependent calcium channel subunit genes

Evaluation of CACNA1H in European patients with childhood absence epilepsy

The ducky 2J Mutation in Cacna2d2 Results in Reduced Spontaneous Purkinje Cell Activity and Altered Gene Expression

The ducky super(2J) Mutation in Cacna2d2 Results in Reduced Spontaneous Purkinje Cell Activity and Altered Gene Expression

The ducky2J Mutation in Cacna2d2 Results in Reduced Spontaneous Purkinje Cell Activity and Altered Gene Expression

Mouse Models of Spike‐Wave Epilepsy

Linkage and association analysis of CACNG3 in childhood absence epilepsy

Linkage and association analysis of CACNG3 in childhood absence epilepsy

Erratum: Linkage and association analysis of CACNG3 in childhood absence epilepsy

Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus ( EJM2) on chromosome 15q13–14

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