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Steven Petrou

Showing results (141-150 of 182) with videos related to

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Biorxiv : the Preprint Server for Biology|September 16, 2024
Brain-wide circuitry underlying altered auditory habituation in zebrafish models of autismMaya Wilde, Anahita Ghanbari, Tessa Mancienne, et al.
Nature Genetics|October 23, 2012
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsySarah E Heron, Katherine R Smith, Melanie Bahlo, et al.
EMBO Reports|March 27, 2014
A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formationMartin Puskarjov, Patricia Seja, Sarah E Heron, et al.
Neurology|March 8, 2013
Hippocampal volume and cell density changes in a mouse model of human genetic epilepsyKay L Richards, Nyoman D Kurniawan, Zhengyi Yang, et al.
Brain : a Journal of Neurology|April 8, 2010
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsyYunxiang Liao, Liesbet Deprez, Snezana Maljevic, et al.
Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
The Journal of Biological Chemistry|November 3, 2005
A Thr357 to Ser polymorphism in homozygous and compound heterozygous subjects causes absent or reduced P2X7 function and impairs ATP-induced mycobacterial killing by macrophagesAnne N Shemon, Ronald Sluyter, Suran L Fernando, et al.
Neuroimage|September 25, 2013
Visualization of mouse barrel cortex using ex-vivo track density imagingNyoman D Kurniawan, Kay L Richards, Zhengyi Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 2018
Selective Na<sub>V</sub>1.1 activation rescues Dravet syndrome mice from seizures and premature deathKay L Richards, Carol J Milligan, Robert J Richardson, et al.
Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.
Pageof 19

Showing results (141-150 of 182) with videos related to

Sort By:
Pageof 19
Biorxiv : the Preprint Server for Biology|September 16, 2024
Brain-wide circuitry underlying altered auditory habituation in zebrafish models of autismMaya Wilde, Anahita Ghanbari, Tessa Mancienne, et al.
Nature Genetics|October 23, 2012
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsySarah E Heron, Katherine R Smith, Melanie Bahlo, et al.
EMBO Reports|March 27, 2014
A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formationMartin Puskarjov, Patricia Seja, Sarah E Heron, et al.
Neurology|March 8, 2013
Hippocampal volume and cell density changes in a mouse model of human genetic epilepsyKay L Richards, Nyoman D Kurniawan, Zhengyi Yang, et al.
Brain : a Journal of Neurology|April 8, 2010
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsyYunxiang Liao, Liesbet Deprez, Snezana Maljevic, et al.
Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
The Journal of Biological Chemistry|November 3, 2005
A Thr357 to Ser polymorphism in homozygous and compound heterozygous subjects causes absent or reduced P2X7 function and impairs ATP-induced mycobacterial killing by macrophagesAnne N Shemon, Ronald Sluyter, Suran L Fernando, et al.
Neuroimage|September 25, 2013
Visualization of mouse barrel cortex using ex-vivo track density imagingNyoman D Kurniawan, Kay L Richards, Zhengyi Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 2018
Selective Na<sub>V</sub>1.1 activation rescues Dravet syndrome mice from seizures and premature deathKay L Richards, Carol J Milligan, Robert J Richardson, et al.
Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.
Pageof 19