Lista de obras - Mauro Pessia - Dominio Público Uruguay

5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates.

artículo científico

A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia

artículo científico publicado en 2015

A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release

artículo científico publicado en 2016

A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

artículo científico publicado en 2017

A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time: the case of sensory ganglia.

artículo científico publicado en 2014

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1

artículo científico publicado en 2008

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions

artículo científico publicado en 2017

Actions of 5-hydroxytryptamine on ventral tegmental area neurons of the rat in vitro

artículo científico publicado en 1994

Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability

scientific article published on 12 May 2020

An episodic ataxia type-1 mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+.

artículo científico publicado en 2004

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia

artículo científico publicado en 2020

Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.

artículo científico publicado en 2011

Chronic treatment with DAU 6215, a new 5-HT3 receptor antagonist, causes a selective decrease in the number of spontaneously active dopaminergic neurons in the rat ventral tegmental area

artículo científico publicado el 7 de abril de 1992

ClC-1 chloride channels: state-of-the-art research and future challenges.

artículo científico publicado en 2015

Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.

artículo científico publicado en 2018

Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties

artículo científico publicado en 2009

Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels

artículo científico publicado en 1995

De novo point mutations in patients diagnosed with ataxic cerebral palsy.

artículo científico publicado en 2015

Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies

scientific article published on 29 March 2019

ERG voltage-gated K+ channels regulate excitability and discharge dynamics of the medial vestibular nucleus neurones.

artículo científico publicado en 2008

Episodic ataxia results from voltage-dependent potassium channels with altered functions

artículo científico publicado en 1995

Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1.

artículo científico publicado en 2006

Episodic ataxia type 1 mutations affect fast inactivation of K+ channels by a reduction in either subunit surface expression or affinity for inactivation domain.

artículo científico publicado en 2011

Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.

artículo científico publicado en 2006

Episodic ataxia type-1 mutations in the hKv1.1 cytoplasmic pore region alter the gating properties of the channel ⬇️

artículo científico publicado el 2 de marzo de 1998

Expression and function of a CP339,818-sensitive K⁺ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia.

artículo científico publicado en 2015

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.

artículo científico publicado en 2016

Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity ⬇️

artículo científico publicado el 3 de noviembre de 2010

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.

artículo científico publicado en 2014

Heteromeric channel formation and Ca(2+)-free media reduce the toxic effect of the weaver Kir 3.2 allele.

artículo científico publicado en 1996

High dose of 8-OH-DPAT decreases maximal dentate gyrus activation and facilitates granular cell plasticity in vivo

article by Gergely Orban et al published 19 June 2013 in Experimental Brain Research

Hypoxia Modulates the Swelling-Activated Cl Current in Human Glioblastoma Cells: Role in Volume Regulation and Cell Survival

artículo científico publicado en 2016

Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I

artículo científico publicado en 2018

K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy

artículo científico publicado en 2013

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

artículo científico publicado en 2016

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches

scientific article published on 22 April 2020

Lethal digenic mutations in the K+ channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay

artículo científico publicado en 2017

Megalencephalic leukoencephalopathy with subcortical cysts protein-1 regulates epidermal growth factor receptor signaling in astrocytes

artículo científico publicado en 2016

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene

artículo científico publicado en 2014

Overexpression of Large-Conductance Calcium-Activated Potassium Channels in Human Glioblastoma Stem-Like Cells and Their Role in Cell Migration

artículo científico publicado en 2016

Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration

artículo científico

Role of receptor protein tyrosine phosphatase alpha (RPTPalpha) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels

artículo científico publicado en 2000

Role(s) of the 5-HT2C receptor in the development of maximal dentate activation in the hippocampus of anesthetized rats

artículo científico publicado en 2014

Seasonal and circadian variations of behavioural response to antidepressants in the forced swimming test in rats

article

Structure, gating and basic functions of the Ca2+-activated K channel of intermediate conductance

artículo científico publicado en 2017

The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma.

artículo científico publicado en 2014

The role of the serotonergic system at the interface of aggression and suicide

artículo científico publicado en 2013

Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis

artículo científico publicado en 2017

Trace amines depress D(2)-autoreceptor-mediated responses on midbrain dopaminergic cells.

artículo científico publicado en 2010

Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder

artículo científico

Lista de obras de Mauro Pessia

5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates.

A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia

A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release

A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time: the case of sensory ganglia.

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions

Actions of 5-hydroxytryptamine on ventral tegmental area neurons of the rat in vitro

Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability

An episodic ataxia type-1 mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+.

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia

Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.

Chronic treatment with DAU 6215, a new 5-HT3 receptor antagonist, causes a selective decrease in the number of spontaneously active dopaminergic neurons in the rat ventral tegmental area

ClC-1 chloride channels: state-of-the-art research and future challenges.

Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.

Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties

Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels

De novo point mutations in patients diagnosed with ataxic cerebral palsy.

Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies

ERG voltage-gated K+ channels regulate excitability and discharge dynamics of the medial vestibular nucleus neurones.

Episodic ataxia results from voltage-dependent potassium channels with altered functions

Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1.

Episodic ataxia type 1 mutations affect fast inactivation of K+ channels by a reduction in either subunit surface expression or affinity for inactivation domain.

Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.

Episodic ataxia type-1 mutations in the hKv1.1 cytoplasmic pore region alter the gating properties of the channel ⬇️

Expression and function of a CP339,818-sensitive K⁺ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia.

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.

Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity ⬇️

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.

Heteromeric channel formation and Ca(2+)-free media reduce the toxic effect of the weaver Kir 3.2 allele.

High dose of 8-OH-DPAT decreases maximal dentate gyrus activation and facilitates granular cell plasticity in vivo

Hypoxia Modulates the Swelling-Activated Cl Current in Human Glioblastoma Cells: Role in Volume Regulation and Cell Survival

Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I

K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches

Lethal digenic mutations in the K+ channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay

Megalencephalic leukoencephalopathy with subcortical cysts protein-1 regulates epidermal growth factor receptor signaling in astrocytes

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene

Overexpression of Large-Conductance Calcium-Activated Potassium Channels in Human Glioblastoma Stem-Like Cells and Their Role in Cell Migration

Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration

Role of receptor protein tyrosine phosphatase alpha (RPTPalpha) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels

Role(s) of the 5-HT2C receptor in the development of maximal dentate activation in the hippocampus of anesthetized rats

Seasonal and circadian variations of behavioural response to antidepressants in the forced swimming test in rats

Structure, gating and basic functions of the Ca2+-activated K channel of intermediate conductance

The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma.

The role of the serotonergic system at the interface of aggression and suicide

Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis

Trace amines depress D(2)-autoreceptor-mediated responses on midbrain dopaminergic cells.

Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder