List of works - Francesco Miceli

A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability

scientific article published on 19 December 2014

A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists.

scientific article published on 5 April 2004

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

scientific article published on May 2007

Cardiotoxic effects of antihistamines: from basics to clinics (...and back).

scientific article published on 29 April 2008

Coupling between the voltage-sensing and phosphatase domains of Ci-VSP.

scientific article published on July 2009

Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons.

scientific article

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels

scientific article

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.

scientific article

Expression and function of Kv7.4 channels in rat cardiac mitochondria: possible targets for cardioprotection.

scientific article published on 29 December 2015

Gating currents from Kv7 channels carrying neuronal hyperexcitability mutations in the voltage-sensing domain.

scientific article published on 20 March 2012

Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits

scientific article published on 25 February 2013

Hyperekplexia caused by dominant-negative suppression of glyra1 function

scientific article published on 01 May 2007

IKs channels open slowly because KCNE1 accessory subunits slow the movement of S4 voltage sensors in KCNQ1 pore-forming subunits

scientific article

Involvement of KCNQ2 subunits in [3H]dopamine release triggered by depolarization and pre-synaptic muscarinic receptor activation from rat striatal synaptosomes.

scientific article published on 16 April 2007

Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels

scientific article

Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine.

scientific article published on 7 December 2010

Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures

scientific article published on April 2009

Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.

scientific article published on 13 January 2014

Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous-Heterozygous Mosaicism of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome

scientific article published on 5 May 2016

Subtype-selective activation of K(v)7 channels by AaTXKβ₂₋₆₄, a novel toxin variant from the Androctonus australis scorpion venom

scientific article

The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.

scientific article published on February 2011

Vasorelaxation by hydrogen sulphide involves activation of Kv7 potassium channels.

scientific article

List of works by Francesco Miceli

A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability

A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists.

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

Cardiotoxic effects of antihistamines: from basics to clinics (...and back).

Coupling between the voltage-sensing and phosphatase domains of Ci-VSP.

Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons.

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.

Expression and function of Kv7.4 channels in rat cardiac mitochondria: possible targets for cardioprotection.

Gating currents from Kv7 channels carrying neuronal hyperexcitability mutations in the voltage-sensing domain.

Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits

Hyperekplexia caused by dominant-negative suppression of glyra1 function

IKs channels open slowly because KCNE1 accessory subunits slow the movement of S4 voltage sensors in KCNQ1 pore-forming subunits

Involvement of KCNQ2 subunits in [3H]dopamine release triggered by depolarization and pre-synaptic muscarinic receptor activation from rat striatal synaptosomes.

Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels

Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine.

Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures

Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.

Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous-Heterozygous Mosaicism of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome

Subtype-selective activation of K(v)7 channels by AaTXKβ₂₋₆₄, a novel toxin variant from the Androctonus australis scorpion venom

The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.

Vasorelaxation by hydrogen sulphide involves activation of Kv7 potassium channels.