List of works - Steven Petrou

A Novel Ultra-Stable, Monomeric Green Fluorescent Protein For Direct Volumetric Imaging of Whole Organs Using CLARITY.

scientific article published on 12 January 2018

A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel

scientific article published on 13 March 2007

A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formation

scientific journal article

An epilepsy-related region in the GABA(A) receptor mediates long-distance effects on GABA and benzodiazepine binding sites

scientific article

Antisense oligonucleotide therapy reduces seizures and extends life span in an SCN2A gain-of-function epilepsy model

scientific article published in 2021

Axon initial segment structural plasticity in animal models of genetic and acquired epilepsy

scientific article published on 17 April 2013

Gain-of-function HCN2 variants in genetic epilepsy.

scientific article published on 24 October 2017

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies

scientific article published in January 2018

Loss of synaptic Zn2+ transporter function increases risk of febrile seizures

scientific journal article

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

article

Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures

scientific article

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties

scientific article published on 5 April 2017

P2X7 purinoceptor expression in Xenopus oocytes is not sufficient to produce a pore‐forming P2Z‐like phenotype ⬇️

scientific article published on July 14, 1997

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

scientific article

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain ⬇️

scientific article published on October 19, 2010

Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizures

scientific article

State transitions through inhibitory interneurons in a cortical network model

scientific article published on 15 October 2021

Stretch activation of a toad smooth muscle K+ channel may be mediated by fatty acids ⬇️

scientific article published on April 15, 1995

The hyperpolarization-activated cyclic nucleotide-gated 4 channel as a potential anti-seizure drug target

scientific article published on 04 May 2020

Toluene inhalation in adolescent rats reduces flexible behaviour in adulthood and alters glutamatergic and GABAergic signalling

scientific article

Using a Multiplex Nucleic Acid in situ Hybridization Technique to Determine HCN4 mRNA Expression in the Adult Rodent Brain

scientific article published on 28 August 2019

List of works by Steven Petrou

A Novel Ultra-Stable, Monomeric Green Fluorescent Protein For Direct Volumetric Imaging of Whole Organs Using CLARITY.

A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel

A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formation

An epilepsy-related region in the GABA(A) receptor mediates long-distance effects on GABA and benzodiazepine binding sites

Antisense oligonucleotide therapy reduces seizures and extends life span in an SCN2A gain-of-function epilepsy model

Axon initial segment structural plasticity in animal models of genetic and acquired epilepsy

Gain-of-function HCN2 variants in genetic epilepsy.

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies

Loss of synaptic Zn2+ transporter function increases risk of febrile seizures

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties

P2X7 purinoceptor expression in Xenopus oocytes is not sufficient to produce a pore‐forming P2Z‐like phenotype ⬇️

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain ⬇️

Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizures

State transitions through inhibitory interneurons in a cortical network model

Stretch activation of a toad smooth muscle K+ channel may be mediated by fatty acids ⬇️

The hyperpolarization-activated cyclic nucleotide-gated 4 channel as a potential anti-seizure drug target

Toluene inhalation in adolescent rats reduces flexible behaviour in adulthood and alters glutamatergic and GABAergic signalling

Using a Multiplex Nucleic Acid in situ Hybridization Technique to Determine HCN4 mRNA Expression in the Adult Rodent Brain