Opposing Phenotypes in Dravet Syndrome Patient-Derived Induced Pluripotent Stem Cell Neurons: Can Everyone Be Right? (Q47132023)

8 January 2018

title

Opposing Phenotypes in Dravet Syndrome Patient-Derived Induced Pluripotent Stem Cell Neurons: Can Everyone Be Right? (English)

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8 January 2018

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Lori L Isom

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8 January 2018

language of work or name

English

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publication date

1 July 2017

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8 January 2018

published in

Epilepsy Currents

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8 January 2018

volume

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8 January 2018

issue

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8 January 2018

page(s)

244-247

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8 January 2018

Genetic and activity-dependent mechanisms underlying interneuron diversity

cites work

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Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy

23 May 2018

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CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation

23 May 2018

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Using Patient-Derived Induced Pluripotent Stem Cells to Model and Treat Epilepsies

23 May 2018

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Reprogramming patient-derived cells to study the epilepsies

23 May 2018

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Revisiting enigmatic cortical calretinin-expressing interneurons

23 May 2018

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Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism

23 May 2018

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Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons

23 May 2018

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A human Dravet syndrome model from patient induced pluripotent stem cells

23 May 2018

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Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome

23 May 2018

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23 May 2018

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Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

23 May 2018

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10.5698/1535-7597.17.4.244

23 May 2018

Identifiers

DOI

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8 January 2018

PMC publication ID

5716123

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8 January 2018

PubMed publication ID

29225534

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8 January 2018