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Jeffrey D Calhoun

Showing results (1-10 of 24) with videos related to

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Journal of Neurogenetics|September 25, 2018
Unravelling the genetic architecture of autosomal recessive epilepsy in the genomic eraJeffrey D Calhoun, Gemma L Carvill
Handbook of Experimental Pharmacology|April 17, 2014
The role of non-pore-forming β subunits in physiology and pathophysiology of voltage-gated sodium channelsJeffrey D Calhoun, Lori L Isom
STAR Protocols|May 26, 2025
Protocol to perform multiplexed assays of variant effect using curated loci prime editingCarina G Biar, Nicholas Bodkin, Gemma L Carvill, et al.
Arxiv|January 27, 2025
Curated loci prime editing (cliPE) for accessible multiplexed assays of variant effect (MAVEs)Carina G Biar, Nicholas Bodkin, Gemma L Carvill, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Multimodal framework to resolve variants of uncertain significance in <i>TSC2</i>Carina G Biar, Cole Pfeifer, Gemma L Carvill, et al.
Epilepsia|May 31, 2017
Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndromeJeffrey D Calhoun, Nicole A Hawkins, Nicole J Zachwieja, et al.
Experimental Neurology|October 23, 2018
Gene expression profiling in a mouse model of Dravet syndromeNicole A Hawkins, Jeffrey D Calhoun, Alexandra M Huffman, et al.
JCI Insight|February 13, 2025
Antisense oligonucleotides modulate aberrant inclusion of poison exons in SCN1A-related Dravet syndromeSheng Tang, Hannah Stamberger, Jeffrey D Calhoun, et al.
Epilepsia|April 27, 2016
Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2aJeffrey D Calhoun, Nicole A Hawkins, Nicole J Zachwieja, et al.
Neurology. Genetics|December 22, 2017
Characterization of a <i>KCNB1</i> variant associated with autism, intellectual disability, and epilepsyJeffrey D Calhoun, Carlos G Vanoye, Fernando Kok, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Journal of Neurogenetics|September 25, 2018
Unravelling the genetic architecture of autosomal recessive epilepsy in the genomic eraJeffrey D Calhoun, Gemma L Carvill
Handbook of Experimental Pharmacology|April 17, 2014
The role of non-pore-forming β subunits in physiology and pathophysiology of voltage-gated sodium channelsJeffrey D Calhoun, Lori L Isom
STAR Protocols|May 26, 2025
Protocol to perform multiplexed assays of variant effect using curated loci prime editingCarina G Biar, Nicholas Bodkin, Gemma L Carvill, et al.
Arxiv|January 27, 2025
Curated loci prime editing (cliPE) for accessible multiplexed assays of variant effect (MAVEs)Carina G Biar, Nicholas Bodkin, Gemma L Carvill, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Multimodal framework to resolve variants of uncertain significance in <i>TSC2</i>Carina G Biar, Cole Pfeifer, Gemma L Carvill, et al.
Epilepsia|May 31, 2017
Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndromeJeffrey D Calhoun, Nicole A Hawkins, Nicole J Zachwieja, et al.
Experimental Neurology|October 23, 2018
Gene expression profiling in a mouse model of Dravet syndromeNicole A Hawkins, Jeffrey D Calhoun, Alexandra M Huffman, et al.
JCI Insight|February 13, 2025
Antisense oligonucleotides modulate aberrant inclusion of poison exons in SCN1A-related Dravet syndromeSheng Tang, Hannah Stamberger, Jeffrey D Calhoun, et al.
Epilepsia|April 27, 2016
Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2aJeffrey D Calhoun, Nicole A Hawkins, Nicole J Zachwieja, et al.
Neurology. Genetics|December 22, 2017
Characterization of a <i>KCNB1</i> variant associated with autism, intellectual disability, and epilepsyJeffrey D Calhoun, Carlos G Vanoye, Fernando Kok, et al.
Pageof 3