Lista de obras - Maria Virginia Soldovieri

A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Activation of Kv7 Potassium Channels Inhibits Intracellular Ca2+ Increases Triggered By TRPV1-Mediated Pain-Inducing Stimuli in F11 Immortalized Sensory Neurons

scientific article published on 04 September 2019

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

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

Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin.

artículo científico publicado en 2015

Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features

scientific article published on 10 July 2019

Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia.

artículo científico publicado en 2014

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

Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists

artículo científico publicado en 2013

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

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

The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability.

artículo científico publicado en 2014

Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology

artículo científico publicado en 2012

Lista de obras de Maria Virginia Soldovieri

A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.

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

Activation of Kv7 Potassium Channels Inhibits Intracellular Ca2+ Increases Triggered By TRPV1-Mediated Pain-Inducing Stimuli in F11 Immortalized Sensory Neurons

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).

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.

Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin.

Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features

Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia.

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

Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists

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.

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

The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability.

Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology