Lista de obras - Francesco Miceli - Dominio Público Uruguay

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

artículo científico publicado en 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.

artículo científico publicado en 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.

artículo científico publicado en 2007

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

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

artículo científico publicado en 2014

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2013

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

artículo científico publicado en 2007

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 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.

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Specification of skeletal muscle differentiation by repressor element-1 silencing transcription factor (REST)-regulated Kv7.4 potassium channels ⬇️

artículo científico publicado el 14 de diciembre de 2012

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

artículo científico publicado en 2013

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

artículo científico publicado en 2011

Vasorelaxation by hydrogen sulphide involves activation of Kv7 potassium channels.

artículo científico publicado en 2013

Lista de obras de 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

Specification of skeletal muscle differentiation by repressor element-1 silencing transcription factor (REST)-regulated Kv7.4 potassium channels ⬇️

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.