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High cortical spreading depression susceptibility and migraine-associated symptoms in Cav2.1 S218L mice

Annals of neurology, 2010-01, Vol.67 (1), p.85-98

2010

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Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine

Molecular neurobiology, 2017-05, Vol.54 (4), p.2986-2996

2017

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The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulation

Acta neuropathologica communications, 2015-12, Vol.3 (89), p.89-89, Article 89

2015

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Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice

Journal of neurophysiology, 2010-09, Vol.104 (3), p.1445-1455

2010

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Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated CaV2.1 calcium channels

Proteomics (Weinheim), 2010, Vol.10 (13), p.2531-2535

2010

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RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice

Cephalalgia, 2014-03, Vol.34 (3), p.174-182

2014

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High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice

Annals of neurology, 2010-01, Vol.67 (1), p.85-98

2010

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A Cacna1a Knockin Migraine Mouse Model with Increased Susceptibility to Cortical Spreading Depression

Neuron (Cambridge, Mass.), 2004-03, Vol.41 (5), p.701-710

2004

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Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine

Molecular neurobiology, 2017-05, Vol.54 (4), p.2986-2996

2017

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Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channels

Proteomics (Weinheim), 2010-07, Vol.10 (13), p.2531-2535

2010

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Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine

European journal of human genetics : EJHG, 2006-05, Vol.14 (5), p.555-560

2006

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Conditional inactivation of the Cacna1a gene in transgenic mice

Genesis (New York, N.Y. : 2000), 2006-12, Vol.44 (12), p.589-594

2006

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Neuropathophysiological potential of Guillain-Barré syndrome anti-ganglioside-complex antibodies at mouse motor nerve terminals

Clinical & experimental neuroimmunology, 2011-09, Vol.2 (3), p.59-67

2011

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Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca V 2.1 calcium channels

Proteomics (Weinheim), 2010-07, Vol.10 (13), p.2531-2535

2010

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High cortical spreading depression susceptibility and migraine‐associated symptoms in Ca v 2.1 S218L mice

Annals of neurology, 2010-01, Vol.67 (1), p.85-98

2010

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Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

The Journal of biological chemistry, 2004-12, Vol.279 (50), p.51844

2004

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Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Cav2.1 Ca2+ Channel Gating

The Journal of biological chemistry, 2004-12, Vol.279 (50), p.51844-51850

2004

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Neuropathophysiological potential of Guillain-Barré syndrome anti-ganglioside-complex antibodies at mouse motor nerve terminals: Anti-ganglioside-complex antibody effects

Clinical & experimental neuroimmunology, 2011-09, Vol.2 (3), p.59-67

2011

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Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Ca sub(v)2.1 Ca super(2+) Channel Gating: Evidence for beta-Subunit Isoform-Specific Effects

The Journal of biological chemistry, 2004-12, Vol.279 (50), p.51844-51850

2004

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The POU Factor Oct-6 and Schwann Cell Differentiation

Science (American Association for the Advancement of Science), 1996-07, Vol.273 (5274), p.507-510

1996

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Cell autonomy of the mouse claw paw mutation

Developmental biology, 2004-08, Vol.272 (2), p.470-482

2004

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The chimpanzee major histocompatibility complex class II DR subregion contains an unexpectedly high number of beta-chain genes

Immunogenetics (New York), 1990-10, Vol.32 (4), p.272-280

1990

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High cortical spreading depression susceptibility and migraine-associated symptoms in Cav2.1 S218L mice

Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine

The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulation

Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice

Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated CaV2.1 calcium channels

RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice

A Cacna1a Knockin Migraine Mouse Model with Increased Susceptibility to Cortical Spreading Depression

Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine

Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channels

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine

Conditional inactivation of the Cacna1a gene in transgenic mice

Neuropathophysiological potential of Guillain-Barré syndrome anti-ganglioside-complex antibodies at mouse motor nerve terminals

Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca V 2.1 calcium channels

High cortical spreading depression susceptibility and migraine‐associated symptoms in Ca v 2.1 S218L mice

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Cav2.1 Ca2+ Channel Gating

Neuropathophysiological potential of Guillain-Barré syndrome anti-ganglioside-complex antibodies at mouse motor nerve terminals: Anti-ganglioside-complex antibody effects

Familial Hemiplegic Migraine Type 1 Mutations K1336E, W1684R, and V1696I Alter Ca sub(v)2.1 Ca super(2+) Channel Gating: Evidence for beta-Subunit Isoform-Specific Effects

The POU Factor Oct-6 and Schwann Cell Differentiation

Cell autonomy of the mouse claw paw mutation

The chimpanzee major histocompatibility complex class II DR subregion contains an unexpectedly high number of beta-chain genes

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